Prader-Willi Syndrome and Transparency

By Celia Kitzinger, with Brian Farmer, 21 February 2021

A young man with Prader-Willi Syndrome was at the centre of a hearing before Theis J (COP 13866679, 14th February 2022).

I can only tell you this because journalist Brian Farmer and I made submissions to the judge saying that we should be allowed to report it and she eventually agreed.

The judge had ruled in court that we were “not to identify P’s particular genetic condition“. She’d acceded to the submission of counsel for P via the Official Solicitor (Zoe Harper, Doughty Street Chambers) who said she “didn’t know” how many people had Prader-Willi Syndrome or whether it might risk people being able identify P (in combination with other permitted information such as the part of the country he lives in and how old he is). She wanted to impose a reporting restriction on the diagnosis because she was “cautious“.

I’ve observed more than 280 hearings in the Court of Protection in the last 18 months and I’ve never been in a hearing before where we weren’t allowed to report P’s diagnosis.

The judge asked for comments from Brian Farmer, the PA journalist also present in the hearing. He said: “I struggle to see how that’s an identifying feature. It says it’s a ‘rare’ condition, but a lot of people suffer from it. To say ‘a man in his late teens, in the Midlands, with this condition‘ – how will that identify him?

“Without information about how many people there are with this condition in England, or in the Midlands, or in care, it is not possible to know“, said the judge.

A representative from the Prader-Willi Syndrome Association (UK) (PWSA, UK) was in court to support the family. Like the rest of us who weren’t parties to the case, she had her camera and mike off, but she put up her electronic hand at this point (as she had done earlier to say that she wanted the local authority to liaise with PWSA, UK “because I don’t think the condition has been fully understood“). The judge noted that “there’s a hand up from the lady who comes from the relevant Association“, but “rather than take up time about that” she decided to go ahead and make the order that Prader-Willi Syndrome could not be mentioned.

And that was that.

Or it would have been, had not Brian and I voluntarily devoted several hours each to researching Prader-Willi Syndrome, establishing its prevalence (up to 2000 people in England), and considering the risk that naming P’s diagnosis might lead to jigsaw identification. That risk (and P’s Article 8 privacy rights) needs to be weighed against the public’s Article 10 rights to freedom of information – both about the decision-making process of the Court of Protection and about the apparent failings in care provision for a young person with Prader-Willi syndrome. We both thought that challenging this reporting restriction was the right thing to do.

I contacted Ruth Consterdine, the Support and Training Officer for PWSA, UK (her name was visible on the Teams call during the hearing) to let her know that we would be doing this, and to find out whether she would be able to tell us if the family was likely to object. I heard back that they had “no objection at all“.

I submitted my letter to the judge on 16th February 2022 asking for the prohibition to be lifted (see Appendix [1] below]. The Judge responded by inviting submissions from the other parties by 2.00pm on 17th February. Brian Farmer sent his (very different) letter the following day (see Appendix [2] below). We have reproduced both of our letters in full because we think they are useful examples of how to challenge unnecessary secrecy in the court. (We’ve both previously published other examples, e.g. “He’s Polish: Challenging reporting restrictions“; “Challenging reporting restrictions in the Court of Protection“).

The Official Solicitor then made a submission in response to mine which said, “in summary, having had the opportunity to give full consideration to the issues, it is accepted that the syndrome may be named in reporting on the case whilst maintaining [P]’s anonymity”. A salient fact mentioned in her submission as having influenced this decision is the previous publication of a Family Division case (H v East Sussex County Council & Ors [2009] EWCA Civ 249) to which I referred in my own submission (and which could have been easily found by anyone using the search facility on BAIILI).

I hope in future that the Official Solicitor will give full consideration to any unusual reporting restrictions in advance of the hearing, so that public money is not spent on the court making inappropriate orders which then need to be challenged, with all the cost that entails to the Official Solicitor (in reading and responding to the challenges) and the cost of judicial and court staff time in engaging with the problems this creates. It is not a prudent use of the public purse. And of course it undermines the judicial commitment to transparency that is (usually) so characteristic of the Court of Protection.

Having received submissions from me, Brian Farmer, and the Official Solicitor, the judge then varied the reporting restriction order to permit naming of P’s genetic medical condition, Prader-Willi syndrome.

What is Prader-Willi Syndrome?

There’s a great deal of information available from the Prader-Willi Syndrome Association UK, an organisation “supporting all those affected by Prader-Willi Syndrome, a rare condition causing a near-permanent state of hunger, learning & physical disabilities” (see their Twitter feed: @PWSAUK). They have a website, a regional network of peer support groups, organise training courses for professionals, staff a helpline, and have organised an upcoming one-day virtual conference for adults with Prader-Willi Syndrome on 5th March 2022. Their mission statement is: “Every person living with or affected by PWS has access to the same high level of good quality care, opportunity and support, and the people delivering care, opportunity, support and research towards a cure have the knowledge, training, resource and support to do so in order to cure the challenges of life with PWS“.

Prader-Willi Syndrome is a genetic condition. It’s not inherited, but due to “random events during the formation of egg or sperm cells, or in early fetal development” (Genetic and Rare Diseases Information Centre).

It has a wide spectrum of symptoms but the six most common behavioural features are:

  • Hyperphagia: intense persistent sensation of hunger accompanied by food preoccupations, an extreme drive to consume food, food-related behavior problems, and a lack of normal satiety
  • Temper outbursts: highly explosive episodes in which the person with PWS becomes very angry or upset in a way that seems excessive for the situation and also beyond the person’s control
  • Anxiety: excessive worry and tension often related to schedules/ routines, food planning or food security, persons/items of special interest and excessive concerns about the possibility of change
  • Obsessive compulsive behaviors: repetitive, ritualistic behaviors, collecting and hoarding items, insistence on “sameness,” need to know, ask, or tell
  • Rigidity: ardent inflexibility with certain routines, concepts, or ways of thinking; vigorous resistance to change; black and white thinking
  • Social cognition: difficulties relating to others, challenges with reciprocal social communication, recognizing others’ emotions, empathy and accurate interpretation of social cues.

Prader-Willi Syndrome is in the Rare Disease Database (i.e. it affects fewer than 1 in 2000 people).

Disability rights activist, Gill Loomes-Quinn, says: “As someone with a (different) rare genetic disease, one of the biggest additional challenges (compared with having other, more common impairments – which I also have) is the total lack of public discourse, or even interest, in a given condition (and the effect of that on access to appropriate treatment and support)“.

Commenting on the judge’s eventual decision not to ban us from mentioning Prader-Willi syndrome, Gill Loomes-Quinn says, “this is a good outcome“.

Since its creation in 2008, Rare Disease Day has played a critical part in building an international rare disease community that is multi-disease, global, and diverse – but united in purpose.

Rare Disease Day was set up and is coordinated by the European Organisation for Rare Diseases (“the voice of rare disease patients in Europe”) along with 65+ national alliance patient organisation partners. It takes place worldwide to raise awareness among policymakers and the public about rare diseases and their impact on patients’ lives. working towards equity in social opportunity, healthcare, and access to diagnosis and therapies for people living with a rare disease.

The hearing

This was one of the relatively infrequent hearings when P was in court throughout, visible on screen, and fully engaged in the court process.

While we waited for the judge, various people on screen (both counsel, and P’s Accredited Legal Representative, soon to be replaced by the Official Solicitor) greeted P, introduced themselves and reminded him of previous times they’d met. The judge, likewise, arriving a few minutes late, greeted P and checked he could see and hear her.

P has been assessed as lacking capacity to conduct proceedings, and to make decisions about his residence and care. The issue before the court is where it’s in P’s best interests to live and receive care (and the proceedings were reconstituted as s.21A so as “not to cause any interruption of the public funding“).

Until September 2021, P lived his whole life in the UK with his Aunt V. He was then temporarily placed in a residential placement, which broke down after P tried to abscond through a second floor window and also engaged in self-injurious behaviour.

At a hearing at the beginning of October 2021, the local authority made an out-of-hours application (in the Family Division) for a deprivation of liberty order. MacDonald J approved an order that P could be deprived of his liberty at Care Home A until mid-October 2021. This order was continued for another month at a hearing before Cohen J, and then a further month before Moor J.

In mid-January, Care Home A served notice on P. According to counsel representing P via the Official Solicitor, the current placement [Care Home A] is “at breaking point” with P: “they’ve had to hold a safeguarding enquiry, they’re unable to meet his needs, the police were called four times in a month due to his absconding and a need for protection“.

An alternative placement has not yet been identified.

The case is now being heard in the Court of Protection, rather than the Family Division, due to P’s age.

P wants to leave Care Home A, which is well over a hundred miles from his home. He said that he wants to return home, or to take up a specialist placement option [Care Home B] for people with Prader-Willi Syndrome. Care Home B is also geographically a long way from home, but he believes (and the two aunts in court agree) it will offer him the right kind of care and support. (My understanding is that they don’t have a vacancy at the moment.)

In the hearing, arrangements were made to instruct an independent expert as a matter of urgency, and the plan was to have another hearing in four weeks time.

Neither of the two aunts sounded pleased with what they saw as the delay this occasioned.

Before P moved out, we were told they [the current placement] knew how to deal with the Prader-Willi people. But even though they say they know how to deal with Prader-Willi, I find it not true. This is why all the problems occur now in this home. P needs a setting that has only Prader-Willi people in that home – for the simple reason that with food and behaviour they are all the same.  P would have been much better in [Care Home B] where only people like him are around“. (Aunt V)

The judge said, “it’s accepted he’s going to move from the current placement. We need to find the right placement.”

I would ask you, My Lady, to think like a mother who has spent fifteen years of her life looking after a child. You only want the best for your child. He’s very disturbed in that home. He’s affected physically and mentally. I did not know this would happen. I have said to Ms Harper [Counsel for P] I will take him to my home until the right place is available. I am very concerned about his physical and mental health. I have raised him for 15 years. They are worried about the pros and cons of different placements. I know who P is. I can deal with P. No family is perfect. P has a condition, and I want to help him. He wants to be independent. He sees his brothers going out. He just wants to be normal, like them. He doesn’t want to ‘abscond’. He just wants to be free to go out.” (Aunt V)

And Aunt W expressed similar views:

It is easier to prevent something from happening than to repair the damage afterwards. P is affectionate, lively, smart, talkative. He likes a social life. His all-time ambition is to be a vet. He wants to be treated fairly and equally to others. His behaviour can be very challenging at times – this is why he was taken away from us. But we were under the impression that he would be put in the right place: a Prader-Willi home, where there would be trained professionals, able to deal with him and to meet his needs. What I’ve noticed from my regular calls with P is he’s now very depressed, doing nothing at all, not going out. They say he couldn’t go out because he was upset. He was upset from doing nothing. He has his challenges. They are typical of a Prader-Willi Syndrome person. We don’t know why he was even put in [Care Home A] when all that could have been avoided. He’s put on a lot of weight. The diet and food intake is not controlled. There are no facilities for working out. He’s with a guard all the time. When he’s taken out for swimming or gym, he’s always with a guard.” (Aunt W)

The judge thanked Aunt W for her update which, she said, “will have been heard by everyone responsible for his care“. Her role as judge now, she said, was “to get all the evidence together to make the relevant decision“.

Aunt V added that P now weighs 89 kilos. “He’s never been that heavy. He was 76 kilos and they were warning him he was on the edge of becoming diabetic. I’ve worked very hard to keep his weight down. 89 kilos is really huge.”

At this point P’s electronic hand was raised so the judge asked him to speak. He said: “To be honest, I’m on the same page as my aunties. Since I’ve come into social care, we haven’t had any interest in going to look at places. This place in [City, Care Home B], we knew Care Home B was the best place for me. I feel like being here for four months- This was for me to have a break from my Mum [I think this means Aunt V] and better myself as a person, but I don’t feel like there’s been any help. I feel like I’ve wasted my time in social care, because there’s been no help. There’s been no help at all“.

Thank you,” said the judge. “What you’ve said has been heard loud and clear. My role is to gather information so the court can make a decision about the next stage for your care. You expressed yourself very clearly. Thank you very much.”

The current care home has agreed that P may continue to Iive there until a new placement is available for him. The lawyers will now get expert evidence from a doctor about P’s needs, and explore other possible placements. The next hearing is listed for 10.30am on 11th March 2022 (another directions hearing) and then a final hearing on 28th March 2022.

Celia Kitzinger is co-director (with Gill Loomes-Quinn) of the Open Justice Court of Protection Project. She tweets @KitzingerCelia

APPENDICES:

SUBMISSIONS CONCERNING REPORTING RESTRICTIONS

1. Submission from Celia Kitzinger (Member of the Public)

Dear Judge

I was a public observer in the hearing yesterday concerning the young man with Prader-Willi Syndrome who was at the centre of a s.21A case.

I have received the transparency order which makes clear that the hearing was in public and may be reported subject to an injunction preventing publication of any material or information that identifies or is likely to identify that P is the subject of the proceedings, or that any person is a member of the family of the subject of the proceedings, and any material or information that identifies or is likely to identify where any person listed above lives, or is being cared for, or their contact details.

In discussion with Brian Farmer, the PA journalist present in the hearing, you ordered that it could be reported that P and his family live in the London area and that he is currently residing in a placement in the Midlands.  

You also ordered that the name of P’s genetic disorder, Prader-Willi Syndrome, could not be published.  I would like to ask you to reconsider, and to make it possible for us to publish the information that P has Prader-Willi Syndrome.   

I am making this request after having consulted with Ruth Consterdine, the Support and Training Officer for the Prader-Willi Syndrome Association.  She contacted P’s aunt, Miss V on my behalf and assures me that Miss V has no objections to me making this application.  

My reasons for making this application are as follows:

1.  No evidence was provided in court that reporting that P has Prader-Willi Syndrome risks identifying him – either alone or as part of jigsaw identification with other permitted information.

My understanding of open justice is that it is normally necessary (in a public hearing) for a case to be made as to why information should be withheld from publication, and not that it should be necessary for members of the public to have to make a case as to why information should be available for publication.   In the course of this hearing there were vague and unsubstantiated claims to the effect that it “might” lead to P’s identification, but counsel did not give any evidence to support this, and said they did not know how many people have Prader-Willi Syndrome.  This 2020 Court of Appeal decision (2020] EWCA Civ 580) held that the starting point in civil cases is open justice, and any derogations must be justified as necessary by the requesting party. It should not therefore be necessary for me to provide evidence to persuade you that a piece of information will NOT risk revealing P’s identity in the absence of evidence that it might. However, I have attempted to do so below.

2.  Expert opinion from the Prader-Willi Syndrome Association is that reporting that P has Prader-Willi Syndrome is unlikely to identify him

Ruth Consterdine tells me: “I don’t think there is much danger of the young man being identified, as I understand the other geographical references are ‘the London area’ and ‘the Midlands’. I had my hand raised at the point of discussion, as although it is a rare genetic condition with no cure, there are approximately 2,000 people from birth to 70 years living with it.” (Email correspondence, 14th February 2022)


3. Other published judgments have identified P (a protected party) or children (whose identity is likewise protected) as having Prader-Willi Syndrome – and there is no evidence that this has led to the identification of the person concerned.

There is at least one other published judgment in the Court of Protection concerning a person with Prader-Willi Syndrome (he’s anonymised as FX) which names the diagnosis (see Re FX [2017] EWCOP 36 (19 December 2017)).  There is also at least one published judgment from the Court of Appeal in which a child (whose identity is likewise protected) is specifically referred to as having Prader-Willi syndrome (see H v East Sussex County Council & Ors [2009] EWCA Civ 249 (31 March 2009) (concerning a 12-year old-girl with Prader-Willi Syndrome). There is no evidence that these people were identified following publication of these judgments.

4. The information that P has Prader-Willi Syndrome is integral to reporting this case accurately – and the information that P has a learning disability and a problem with weight gain is likely to lead those with knowledge in this area to identify P as having Prader-Willi Syndrome even if I do not name this diagnosis.

P needs specialist treatment because of Prader-Willi Syndrome – and that was a crucial part of the hearing. His family want him to be able to move to somewhere he can get specialist treatment which (Aunt V says) means  “a setting that has only Prader-Willi people in that home – for the simple reason that with food and behaviour they are all the same.  P would have been much better in [Care Home B] where only people like him are around“. Aunt W said “He has his challenges. They are typical of a Prader-Willi Syndrome person. We don’t know why he was even put in [Care Home A] when all that could have been avoided. He’s put on a lot of weight. The diet and food intake is not controlled. There are no facilities for working out. He’s with a guard all the time. When he’s taken out for swimming or gym, he’s always with a guard“. Aunt V added her specific concern that his weight has increased at the current placement (“he’s 89 kilos, he’s never been that heavy“) and is concerned about the risk of diabetes.  The diagnosis of Prader-Willi Syndrome is integral to an accurate understanding of what the family see as the problem here.  Moreover, if I report information such as that above, the combination of P’s learning disability and his problem with weight gain is likely to lead people with some knowledge in this area to identify P as having Prader-Willi Syndrome in any event. (See for example this NHS website on “Managing weight with a learning disability“, which names two relevant diagnoses: Downs Syndrome and Prader-Willi Syndrome.)

5.  Public interest in diagnosis as a route to social and political action

It’s very unusual (I’ve never seen it before) not to be able to name the diagnosis of someone in the Court of Protection (especially given that determining a lack of capacity requires a disturbance or impairment in the functioning of mind or brain). Diagnostic categories matter because people organise around them.  Campaigns for better understanding of a condition, protests against poor treatment, support events for the people affected and their families, fundraising – all of these coalesce around specified diagnoses. These are exactly the activities apparent on the Prader-Willi Syndrome Association Website.  

In sum, I think that the reporting restriction currently in place, which prevents us from saying that P has Prader-Willi Syndrome, is unnecessarily wide. It curtails the public’s Article 10 freedom of information rights, without any evidence that this is justified to preserve P’s Article 8 privacy rights. The public has a legitimate interest in learning about the problems for people with Prader-Willi Syndrome,  and significant parts of the courtroom interaction dealt specifically with concerns relating to people with this diagnosis, such that omitting reference to the diagnosis makes that interaction either opaque (for those who don’t know about the syndrome) or (for those with the relevant knowledge) reveals what P’s diagnosis is likely to be in any event.  Other published court judgments have said that people (whose identities are otherwise protected) have Prader-Willi Syndrome.  We should be able to publish that information too. 

The prohibition on naming Prader-Willi syndrome has had a chilling effect on open justice.  There is a draft blog post about the hearing which I am not able to publish unless or until this reporting restriction is lifted.  I would also like to add that the time and effort it takes a member of the public, without legal training, to challenge reporting restrictions like these – made in the absence of any evidence as to their necessity – is an onerous addition to the civic responsibility we exercise as we seek to support the judicial commitment to transparency.

Thank you for considering this application.

Celia Kitzinger

16.02.2022

2. Submission from Brian Farmer (Journalist)

Dear Judge,

I’d support Prof Kitzinger’s arguments.

I also want to be able to tell the public that P has Prader-Willi Syndrome.

I’d make the following points.

1:    I think the key issue, when you are balancing P’s Article 8 rights against my Article 10 rights, relates to jigsaw identification. (I’m not asking to name P, or his relatives, or give an exact age or any detailed address.)

2:    I want to report the Court of Protection proceedings and give the public five pieces of personal information about P:

a: He’s a man in his late teens

b: His family home is in the London area

c: He’s currently living in a facility in the Midlands

d: The applicant is the London Borough of Ealing

e: He has Prader-Willi Syndrome.

3:   I think you should consider three questions:

a: Will providing those five pieces of information create an information jigsaw which will enable anyone to identify P?

b: If it will, who would be able to work out his identity?

c: Is there a risk that anyone who worked out his identity would harm him?

4:    I haven’t seen any evidence, but logically the answer to question 3a must be ‘yes’. Providing those pieces of information will no doubt enable some people to identify P: relatives, family friends, neighbours, medical staff/carers. But won’t relatives etc already know P and know that he has Prader-Willi Syndrome, and probably know that he is involved in Court of Protection proceedings – certainly, court proceedings of some kind. My understanding is that P is [in his late teens], has had Prader-Willi Syndrome since birth and has spent most of his life living in London with an aunt. Those around him must know about him.

5:   Is there any evidence that people in that circle of relatives etc have harmed P, or are likely to harm him? Is there any evidence that P will recognise himself in any report and suffer harm as a result? (These are questions I can’t answer). Presumably reporting won’t put him at risk of bullying or teasing at the facility in the Midlands where he lives at present.

6:   I’d also make the point that people in that circle of relatives etc will recognise him even if we don’t say he has Prader-Willi Syndrome, but instead use a phrase like “rare condition”. If there’s a risk of teasing, for example, the risk will exist in any event. And any report would have to say that he had some kind of condition.

7:     Some people will always be able to recognise a P in any report of any Court of Protection hearing: if judges decided that a report could not identify a P to anyone, we’d never be able to report anything. (Likewise, some people will always recognise the child in a family court report).

8:   However, I’d suggest that it would be extraordinarily difficult for anyone outside that circle of relatives etc to put together the five pieces of information and work out P’s identity. How could the man or woman on the bus, even the Ealing bus, complete that jigsaw? There are jigsaws and jigsaws. If I named P’s mother, or gave his address, a child could complete the jigsaw. But who could complete a jigsaw armed only with the five pieces of information outlined in paragraph 2? That’s more than a jigsaw; it’s a Watergate investigation. The website https://www.mangen.co.uk/wp-content/uploads/2018/07/Prader-Willi.pdf   says about 1 in every 15,000 births is affected by Prader-Willi Syndrome. The website https://directory.londoncouncils.gov.uk/directory/ealing/ says Ealing has a population of more than 340,000. But, regardless of how many people live in Ealing or how many of those have Prader-Willi Syndrome, who could solve the puzzle? Sherlock and Mycroft Holmes combined? Bob Woodward and Carl Bernstein? MI5? Why would anyone even try?  In the real world, won’t the bus passenger have other things on his or her mind: What’s for tea? Has she got time to get the gym? Is World War III about to start? Has she got Covid? Why is his brother ringing him again?! I’d say it’s absurd to think that the average person in Ealing would even contemplate attempting to complete the identity jigsaw after reading about P in the Ealing Daily Beast or in Prof Kitzinger’s blog, let alone harm him.

9:   I’d argue that, in essence, the current restriction is preventing me from telling some people what they already know.

10:   What are the consequences if the media can’t tell people that P has Prader-Willi Syndrome? I’d say that would constitute a serious infringement of my right to impart information and the public’s right to receive information.

11:  If journalists can’t refer to Prader-Willi Syndrome, there can be no debate about the case and its implications for people with Prader-Willi Syndrome; and there can be no contribution from any Prader-Willi Syndrome organisation or society; and these public Court of Protection proceedings won’t be transparent.

12:   Shouldn’t everyone who has a relative with Prader-Willi Syndrome know about the case? They might want to raise the same kind of concerns that P’s relatives have raised. Shouldn’t social services staff from other councils know about the case? They might have a suggestion for a placement.  Shouldn’t other lawyers and other Court of Protection judges know about the case?

13:   If you decide lessons about the care of people with Prader-Willi Syndrome should be learned, they can’t be learned if no-one can mention Prader-Willi Syndrome.

14:   Even members of Ealing Council won’t be able to debate the council’s approach to people with Prader-Willi Syndrome in the light of any ruling you give, because they won’t know that the case is about someone with Prader-Willi Syndrome.

15:    Mr Angry of Ealing won’t be able write to the Ealing Daily Beast and demand a better approach to Prader-Willi Syndrome from the council, or the Government.

16:   Isn’t public debate about conditions like Prader-Willi Syndrome in the public interest? Isn’t public debate about the funding of care for people with Prader-Willi Syndrome, and availability of placements, in the public interest? Isn’t public debate about the difficult issues Court of Protection judges have to grapple with, when dealing with conditions like Prader-Willi Syndrome, in the public interest? (I think I can answer those questions: my answers are yes, yes, and yes).

17:  I’d argue that the balance clearly falls on the side of Article 10 and that the restriction preventing the mention of Prader-Willi Syndrome should be lifted.

(If I can help with anything else, or answer any questions, just let me know. And thanks for considering this so promptly. Much appreciated).

Brian

Brian Farmer, Reporter, Press Association

17.02.2022

A response to ‘The politics of the pandemic…’: COVID-vaccination of a disabled man

By Alice Hodkinson, 19th February 2022

A recent blog post (The politics of the pandemic in the Court of Protection) reports and comments on a hearing before Deputy Circuit Judge Rogers in Nottingham (Case no. 13816452) at which the judge ruled that an autistic learning-disabled man in his 30s, living in a care home, should be vaccinated against COVID-19, in spite of his sister’s concerns that vaccination was not in his best interests.

I was asked to look at the blog about this case following an interaction on Twitter where I expressed my distress at the overwhelming opinion that vaccination is a good thing in all circumstances and that any dissenters were just wrong. 

Often on Twitter any opinion expressed contrary to the current paradigm is met with abusive personal responses that don’t look at the issues themselves but just react aggressively against any view contrary to their own apparently entrenched view. 

Of course, I have my own biases: I am a GP and A&E doctor who has seen quite a number of coronavirus sufferers, but also people who had come into A&E too late with other conditions, some of whom died. I have also experienced first and second hand the harms of the pandemic response in terms of family illness, difficulties and disagreements. 

In my medical practice I endeavour to follow evidence-based medicine; this means I am not always on the side of the medical establishment that can be focused on one specialist area while missing the bigger picture. Occasionally the medical establishment is simply entrenched in practice that should have changed

I have found the response to coronavirus distressing because it has not appeared to follow the evidence that we had available at the time. Neither how we treated children nor how we treated the elderly were sensible responses; indeed, the deaths amongst the elderly were tragically high while children bore a high burden of the lockdown for no benefit to their own health. Now that we appear to be coming to the end of the pandemic, dissenting academic voices are becoming more prominent and I can be more open about my own reading of the evidence. 

These vaccine cases are fascinating for many reasons, and I enjoyed reading the blog, reminding me why I took a Masters in Ethics and Law a few years ago. This case was only ever going to be decided one way, as case law usually supports vaccination in the case of disagreement unless the protected party can be shown to have, or to have had, a clear personal perspective, such as that of the protected party in the case of Re SS (Re SS [2021] EWCOP 31).  But this case was unbalanced in terms of the people involved in the case and how the evidence was framed, and I am not entirely sure that it was in this particular person’s best interests to be vaccinated. I must make clear, though, that I only have the blog for my information: I was not present for the hearing itself. 

Also, for clarity, I was vaccinated against COVID-19 in January and March 2021, having decided early on that it was my duty to aim to protect other people, rather than myself. I didn’t realise at the time that the vaccine wouldn’t stop me spreading it to my vulnerable relatives or patients. I have been vaccinated against all the usual infections, have my ‘flu jab every year and my children are fully vaccinated.

 I found this blog difficult to write as I am one of those who find myself abused on social media for having opinions that might be different from the prevailing narrative. 

The case

The subject of this case is a 39-year-old man with “severe intellectual disabilities and severe Autism Spectrum Disorder” who lives in a care home. 

He cannot consent to vaccination, but would have been vaccinated in his “best interests”,  if it were not for the objection of his sister who strongly opposed his vaccination. It is reported that he is in good health but his behavioural and learning disabilities, his residence in a care home and any other conditions or medications statistically increase his likelihood of doing poorly if infected with coronavirus.

He had already been exposed to coronavirus in his home; indeed, he was the only resident not to develop symptoms of the virus even though he was unable to wear a mask or to distance himself from others. It is very likely, therefore, that he has met – and his immune system has interacted with – the virus already. 

While vaccination may well be in his best interests, there are enough uncertainties to consider that this is not as clear cut as it might appear: these include his previous exposure to COVID 19 infection and the controversies over the epidemiology of the vaccines themselves, as questioned by some prominent scientists.

Risk of infection for P

So, what is the risk of infection for P? Before one is exposed it is difficult to say for certain, given there have been some deaths in very young people while there have also been cases of remarkably few symptoms in some elderly people. Broadly, however, the older and more generally unwell, the more likely one is to do worse or die from a COVID infection. On balance, the risk is low for P as he is young and said to be in good health, although undoubtedly with a higher risk than a person of a similar age without disabilities.

However, things change once someone has had the infection: we can say for certain what the risk has been for that individual from that episode. Given that P had little or no illness from interaction with the virus in his home, the risk to him from future infection is most likely to be reduced, with the caveat that a more deadly immunologically distinct variant might arise which would put him at risk along with the rest of us, vaccinated and unvaccinated alike.

We do know that previous infection confers some protection, and it appears that second infections are usually less severe[1]. It is also known that vaccination as well as infection appears to add to protection from further illness, if not from infection.

For P, as he had very few or no symptoms, we can reasonably reliably say that he is unlikely to be particularly unwell from the same or another similar variant of COVID-19 coronavirus. This is also supported by studies on coronaviruses from before the 2019 pandemic started.

Risk of vaccination for P

What about the risk of vaccination? The risk of significant vaccination injury appears to be very low, in the region of 10 in 1 million, although absolute numbers vary with the source of information.

There have been, however, concerns raised by some well-known statisticians and epidemiologists about whether there are overall mortality benefits from the vaccine, but these have been unpublished; journals that were very happy to publish their other work have decided not to publish these particular data. It may be that medical and science journals do not want to publish anything that could be used by the anti-vax or COVID-denying groups; however, not having these data in the mainstream literature means that it is not peer reviewed and not criticise,d and we cannot learn from it in a scientific forum. Thus it remains a grey area. There are papers are available online via Professor Fenton’s web page, a man we certainly can’t label as uninformed, antivax or a COVID-denier, or any of the other ad hominem attacks that people who question the current paradigm have levelled at them. 

Clearly, if vaccination is in P’s best interests, then he should have the vaccine. We do not know, before he has the vaccine, if he will have a reaction. We do know that he has not shown any effects from his exposure to coronavirus, so the balance of the risk and benefit to him individually has shifted, even if all he gets from a vaccination is the pain of the jab, the distress of being restrained and a few days of a sore arm for each vaccination he is given.

Altruistic vaccination?

If it could be argued that it is in his best interests to be vaccinated because it reduces the risk to others, then this could be a reason to vaccinate: case law has allowed altruism to be a reason for some treatments (Re Y (Bone marrow donation [1996 2FLR 787])

In this instance, we cannot demonstrate an altruistic benefit to P: the Delta strain was infecting vaccinated people in the UK; Omicron is even more easily transmitted; vaccination does not give sterilising immunity (preventing future infection) although it does appear to reduce severity and the likelihood of catching the disease by a small amount. Vaccinating P will not prevent infection of other residents in his home, so this cannot be a justification for vaccination. 

P’s sister

Reading the blog, I felt quite sorry for P’s sister. It appears that she was seen as a disingenuous figure, not having her brother’s best interests at heart, with ulterior motives for her opposing his vaccine. This is an impression that I did not read in the case description myself. Indeed, I cannot see why anyone would go through court proceedings unless she was very much trying to do her best by her brother. 

She provided a spreadsheet of information about the vaccine that is described as “non-expert” by one of the barristers in the case, Victoria Butler-Cole. And this of course is the trouble: the question of who decides what information is valid, what is true, who is an expert or non-expert, and it cuts to the heart of the information wars that we have had since the start of the pandemic. If professional epidemiologists, statisticians, Bayesian modellers, professors of risk information, evidence-based medicine and theoretical epidemiology can be blacklisted, finding themselves unable to be published then how can we know where the facts truly lie? We are in a world where an expert in evidence-based practice for 30 years can be “fact checked” by an unnamed employee, on the basis of the current paradigm. Indeed, the British Medical Journal (BMJ) itself has been fact-checked (see here and here). This leaves us in a knowledge desert, where none of us can know fact from fiction with many an expert voice silenced.

P’s sister, CT, started with the view that it was this vaccine that she did not trust, from a concern that it has not been widely used and reviewed as yet. This is entirely reasonable given that there was such a short time from developing and trialling the vaccine to its widespread use. When it was being rolled out, I think most of us believed it would be used for those at highest risk and not on low-risk young people – as serious side effects would most likely be much higher per life saved in the young. 

I would agree that some of P’s sister’s arguments are likely to be a misreading of the statistics.  It appears to be clear that those who are vaccinated are at much lower risk of dying of COVID-19, but there were more vaccinated people in ITU with COVID than unvaccinated, simply because so many people had been vaccinated by then. On the other hand, what we don’t know is the true effect of the vaccine on all-cause mortality, if, as Professor Fenton describes, there has been widespread misrepresentation of vaccination status. 

That CT changed her tactics to looking more at best interests, rather than problems with vaccination, seems to me a straightforward and sensible thing to have done, given she realised that the initial approach would not work. I don’t see this in anyway as disingenuous. It seems quite reasonable, particularly as she was a litigant in person and did not have a legal expert to support her preparation. 

Dr Rogers, GP

From what was written about Dr Rogers, I also feel sympathy for his position. For me it is not at all illogical or “ironic” that he should want to help out in a health crisis to take up his registration again to help his colleagues. Indeed, it is entirely logical. One set of beliefs about helping in a crisis does not mean one has to believe everything that comes out from the authorities about that crisis. 

What is striking is that we failed, in most countries, to protect the very elderly and very vulnerable. The suggestion to put in focussed protection for these groups was dismissed, perhaps causing terrible loss of life[2]. Dr Rogers supports the use of Ivermectin for the treatment of Covid, it having shown some promise last year. It was added to the PRINCIPLE trial run from Oxford University but the results have not yet been published, that I can find. There are articles in the scientific press that support its use, but on balance it looks like it is not effective, or sufficiently effective, to be used – unless further evidence comes to light. Given that there isn’t yet an answer to the Ivermectin question, and the questions over the effectiveness and harms of lockdown, judging him for his view about these seems a little premature. 

Dr Rogers is indeed on the team of the UK Medical Freedom Alliance. I had not come across this group before, but they certainly have a point that we should be fully informed, free to accept or decline intervention, there should be absolute transparency on drug and vaccine data, and that there are ways we could have handled this pandemic better. The information on their website is certainly compelling and concerning if genuine, as it appears to show that the responses to COVID did very little indeed. Questioning the current pandemic paradigm might look entirely logical given the inconsistencies of the data, particularly as much has not been published, either from censoring of information or from lack of transparency from the pharmaceutical companies. This of course is difficult to prove, but is not unknown in medical science, as seen in the long-running battle of the BMJ editor to get the full information about statin trials run by the drug companies. 

Dr Rogers’ statement on COVID-19 not being a disease of the young is broadly correct, certainly at the start of the pandemic, and we knew this from the information we had from China two years ago. It is still the case that COVID-19 is causing very little disease in the very young, although it is causing infection. Those who do poorly are children with underlying health problems which makes them very vulnerable, and for these it seems sensible that they should be vaccinated. Dr Rogers also describes the vaccine as being ineffective – which is only partially true in that it doesn’t prevent infection. It does appear to prevent serious illness given that it is almost universal that it is the unvaccinated in ITU with COVID-19. (It is probably not surprising that the COVID vaccinations are not sterilising, in other words they do not prevent infection, given the failure to find a vaccine against the common cold, for example, and other coronaviruses, thus far; indeed, perhaps it is surprising that COVID vaccines work as well as they appear to.)

Dr Rogers is not an expert in any particular field, being a GP. GPs are, at their best, advocates for the individual person based on their individual needs and beliefs. Even retired, he was probably more of an expert than the people in the court room. 

Returning to P’s sister…

I don’t think that criticisms of P’s sister are entirely justified. CT would have liked P to have one blood test rather than vaccination, which is not a straw man argument; his having three vaccines, including booster, could be much more distressing than one blood test. Sadly, blood tests are not guaranteed to demonstrate prior infection (they usually look for antibodies only rather than other markers of immunity), so he may have ended up with the blood test as well as vaccinations. 

If one starts from the principle that the risks are fairly well balanced, as I have tried to argue, CT’s answers become entirely reasonable. I am not surprised she feels bullied and victimised, as the questions aren’t that relevant to P’s situation, but more to a general risk of COVID to the wider society. So even with the inquisitorial court proceedings, CT will be affected by the accepted paradigm and feel that she has to fight from a “child ego state”.

It appears to me, reading this case report, that all the bloggers were critical of CT. This might be that I am reading it from the position of understanding her view, given that I am not a fan of vaccinating someone who probably won’t benefit and might be harmed.  But the information that Celia reports (in one section of the the blog) regarding CT’s scepticism of childhood vaccinations brings another layer to this case. It appears that CT does not trust any vaccines, even ones that have been proved to be safe, effective and neutralising: some of the most important ones worldwide are polio and measles, both of which cause devastating illness in the very young. This undermines her case that her argument is purely about the COVID vaccination. Yet she still had a valid case that it wasn’t necessarily in P’s interests to be vaccinated, or at least, that it was finely balanced. 

Conclusions

It is a reasonable conclusion, as argued above, that P is likely, given his prior exposure to COVID infection, to be more at risk from vaccination than from re-infection, even with waning immunity or a more pathological strain. 

Along with many people in the country who have had one or more mild or asymptomatic infections with COVID, vaccination of P appears to be a waste of effort and resources when at that time we could have been concentrating more efforts on vaccinating the elderly, frail and sick who couldn’t get to vaccination centres. 

Vaccination appears to have been a good tool to build immunity and prevent deaths in those at risk of severe illness. Whether it has helped us to transition to living with an endemic virus I don’t believe is clear. There are still some scientists and doctors who appear to believe that having a vaccination reduces the risk to other people, but the Omicron wave has demonstrated this is not the case given the incredibly fast spread at the end of last year.  When the Secretary of State decided not to mandate vaccines after all there was an outcry on Twitter, even from doctors, that they would not want to be treated by an unvaccinated health care worker – this without evidence of harm to others from unvaccinated people. 

CT is trying to do the right thing for her brother, and I can see her rationale. However, the case was only ever going to be found in favour of vaccination, so she put herself through quite a bit of trauma for no likelihood of the outcome she wanted. 

But the major issue here is that we are not a nation, a world, where scientific debate is being allowed at the moment, where differing interpretations of the data can be shared and debated in an open and constructive manner. We cannot know for certain where the reality lies; those who think they do are surely mistaken.

Let me be clear: I also do not know where the evidence points, because the evidence is not reliably available to examine. I do not know this because the supremacy of evidence-based medicine has been lost, which is personally devastating, as I wonder what will happen to evidence, debate, scientific method and freedom to explore uncertainty. 

The Open Justice Court of Protection Project has published blogs about other vaccine cases. 

The following  paragraph is taken from a blog about a case (COP 12770223) before DJ Mullins via MS Teams on 23rd December 2021.  It concerned “a man in his 30s with severe cerebral palsy and learning disability (MK) who has yet to receive even a first COVID vaccine because his mother objects”. 

Looking through the chronology of the case, the judge said.  “It’s not my role to point the finger at any individual or organisation, but it doesn’t make comfortable reading.  Vaccination was first considered in February or March 2021 and here we are in December and there hasn’t been any resolution – and no vaccination.  And now he has COVID. Though he seems to be doing relatively well?”

Again, this is a disabled man who is managing well with the infection. As well as his disabilities he also needs kidney dialysis, so he is clearly a vulnerable person who we would expect to do badly from COVID infection: an early vaccination would have been sensible. But as it turned out, he wasn’t vaccinated and was not particularly unwell from the infection. Perhaps he was simply lucky not to have caught the infection until it was the Omicron variant; maybe he has inherited a robust immune system; maybe we are wrong about who is likely to do badly with COVID. Whatever the reason, now that he has had COVID, unless we see the return of more pathogenic variants, it would seem that COVID does not present such a risk for him that vaccination is definitely in his best interests. In the event of more pathogenic variants then all of us, vaccinated or not, could be at risk of illness. As reported in a subsequent blog posthowever, the judge inevitably decided that vaccination was in his best interests.

In the fullness of time, I hope that some more settled science emerges so that we can learn what factors are important in a healthy immune system and how to manage a future pandemic more effectively to protect the vulnerable much better than we did in these last two years, while also preventing so much damage to people struggling in our wider society. 


Alice Hodkinson is a GP in the East of England. She worked in Emergency Medicine (A&E) for most of the pandemic but is back now working in general practice. She completed a Masters in Medical Ethics and Law at King’s College London in 2018 and the Diploma in Tropical Medicine and Hygiene in 2021. She tweets @HodkinsonAlice


[1] Spicer et al 2022. Protective immunity after natural infection with severe acute respiratory syndrome coronoavirus-2. International journal of infectious disease. 114: 21-28; Gazit et al 2021. Comparing SARS-CoV-2 natural immunity to vaccine-induced immunity: reinfections versus breakthrough infections.;  Abu-Raddad, L.J. 2021. Severity of SARS-CoV-2 Reinfections as Compared with Primary Infections. N Engl J Med 2021; 385:2487-2489; Kojima, N & Klausner, JD. 2021. Protective immunity after recovery from SARS infection. Lancet; West et al, 2021. A case of COVID-19 reinfection in the UK. Clinical Medicine (London) 21(1): e52-e53. Note: some of these publications would not have been available at the time of the hearing. 

2 The Great Barrington Declaration shows there is no consensus from the scientific and medical communities that the measures put into law were reasonable and sensible.

Photo by Martin Sanchez on Unsplash

No decision without representation

By Celia Kitzinger, 11th February 2022

Mr M (who’s been diagnosed with schizophrenia) has ulcers on both his legs. The one on his right leg is getting worse and becoming “malodorous”.  

He refused to allow doctors to assess him when he was admitted to hospital back in October 2021.  

Outpatient appointments were made, but he did not attend them.  

He’s declined to admit the district nursing team to his home and has not attended GP appointments.  

There is no information about the condition of his leg since the end of October, except that the community mental health team (who have visited him) are concerned.

The local authority has made an “urgent” application to the court that it would be in Mr M’s best interests to take him into hospital against his wishes for assessment. This would almost certainly have to involve restraint and deprivation of liberty.

The hearing was before Mr Justice Peel on 8th February 2022 (COP 13883671) and lasted a little over one hour.

The hearing

There were two advocates in court: Ulele Burnham acted for the local authority and Emma Galland for the hospital trust.  

There was no legal representation for Mr M, nor was he in court himself.  The judge said, right away, as soon as this became apparent: “I’m highly unlikely to do anything of substance today, without him being represented”.

There were no position statements (since the case had been fast-forwarded to the ‘urgent’ list) and on the basis of what I heard in court it was very unclear what the evidence was to rebut the presumption that Mr M has capacity to make his own decisions about whether or not to allow clinicians to examine his legs. I think the court determined that whatever the evidence was,  it was sufficient to give the court “reason to believe” on an interim basis that Mr M lacks capacity in this matter (s. 48 Mental Capacity Act 2005).  But the judge also commented that “the Official Solicitor may have a view about the capacity evidence”. 

There was also no medical evidence before the court.  Although the hospital trust was a respondent, they made clear that the hospital had last seen Mr M at the end of October 2021, when he was discharged without any assessment having taken place (because he refused it), with care in the community and outpatient appointments offered.  There was no more up-to-date medical evidence they could provide about the state of his legs.

The judge made it clear that, despite the “serious concern” about Mr M’s health raised by Ulele Burnham (for the local authority), he would not make substantive orders today. 

Judge:  I understand you want to achieve an assessment as quickly as possible.  For me to be satisfied with that, there has to be some opportunity for Mr M through the Official Solicitor, to make representation.  I find it hard to see on the basis of what I’ve read that I could do otherwise. The Official Solicitor needs to be present for these sorts of discussions doesn’t she?

Burnham: My Lord, I would say not.  She’ll be on notice for this application.  It should be rare for this to happen, but it is the concern of the local authority that he should get to hospital quickly.

Judge:  What does ‘quickly’ mean? This has been going on since October.  I appreciate the situation is getting worse, but are you telling me that this very second Mr M needs to be taken to hospital for assessment, with a deprivation of liberty as part of that, since it appears, based on previous events, that he would not go willingly.  These are very dramatic and significant orders to make in his absence.

Burnham: The problem is that the condition has been getting worse. There is a risk of amputation. There is a risk of death.  The local authority seeks as best it can to do its duty and it simply doesn’t know how serious the position is.

Judge: That’s exactly the problem you are dealing with.  You were right to bring this application, but you don’t have medical evidence, so you’re dealing with this slightly in a vacuum, and that makes it very difficult for you to put forward any cogent evidence that if he doesn’t have an assessment this afternoon it might have life-changing consequences.  It’s the absence of up-to-date clinical evidence, combined with the absence of Mr M who isn’t here and isn’t represented, that prevent me from making the orders you are seeking today.  I can’t see how I could be persuaded to go down that route.

The judge went on to detail what could be done today: directions for medical evidence from the hospital, appointing the Official Solicitor as a litigation friend for Mr M, and making arrangements to bring the case back to court “in pretty short order”.  

Ulele Burnham suggested provision of a “transition plan” in time for the next hearing. The judge asked what that meant.  “How he’s going to be conveyed or transported, and are we countenancing restraint, and what would we do if he physically resists”.  “That seems sensible to me”, said the judge.

Other matters to address before the next hearing include: What would the assessments entail?  What restraint might be necessary not just for “conveying” him from home to hospital, but also to overcome any resistance to having his legs assessed? What treatments might be possible?  What about his future care and residence?  And I think a third party disclosure order was made (or perhaps only discussed and postponed for consideration at the next hearing) concerning Mr M’s medical records.

The judicial decision

In a closing statement, Mr Justice Peel said it would be “wholly inappropriate to make substantive orders of the sort requested by the applicant in the absence of representation of the patient and in the absence of up-to-date medical evidence.  It is apparent to me that the furthest I should go is to make directions enabling the case to be brought back next Monday, by which time the Official Solicitor will be engaged. Once the Official Solicitor is involved, I suspect this case will take shape rapidly.

He pointed out that if there were to be “a true emergency” before the date of the next hearing, then it could be brought back in the proper way for an out-of-hours or emergency hearing.

The next hearing is listed for 10.30am on Monday, 14th February 2022.

Celia Kitzinger is co-director (with Gill Loomes-Quinn) of the Open Justice Court of Protection Project. She tweets @KitzingerCelia

Four commentaries on Re PH before Hayden J

By Sam Green, Daniel Clark, Claire Martin and Imogen Goold, 10th February 2022

Editorial introduction by Celia Kitzinger

Four commentators give their impressions of a case in the Court of Protection before Mr Justice Hayden (Case No.1354439T Re PH). 

We’ve already published a blog post about the most recent hearing (“A home not a hospital”) and about several earlier hearings in this case.

It came back to court in 2022 (after a long history of previous hearings) on an urgent basis, because PH, who has an acquired brain injury, was refusing to allow himself to be fed via his feeding tube.  He said he’d “had enough”, having lived in hospital – despite being ready for discharge – since 2019.  He was desperate to live somewhere that felt like a home and to have some privacy.  

The Health Board had applied for a declaration either that PH had capacity to decide for himself whether or not to accept tube feeding, so his decision should be accepted even if it led to his death; or alternatively that he lacked capacity to make this decision but that it was not in his best interests to force-feed him contrary to his wishes since this is both medically counter-indicated and also “demeaning and traumatic” for PH. 

Towards the end of the hearing on 7th February 2022, the Health Board withdrew that application.  It was no longer necessary because PH had decided to resume his feeds, and had done so since being taken to see the new home to which he will move towards the end of February.

So, PH has a hopeful future.

Reports of the case (in earlier blogs –  in reverse date order: “A ‘secret’ hearing on life-sustaining treatment”;  “Capacity to refuse intensive care”, “When academic theory becomes reality”, “Delays in finding an acquired brain injury placement”, and “Inviting family into the decision-making process” had caused considerable interest.  It was very unfortunate that the hearing on 2nd February 2022 had not appeared in any court listings (hence the term ‘secret’ in the title) and I managed to attend only because I was coincidently in Newcastle (for a different hearing) and able to make it to the courtroom on time.  

The hearing of 7th February 2022 did appear in the listings and although seven (I think) observers managed to attend, there were problems for others who did not (at least four, to my knowledge).  The hearing was originally listed for 10.30am and appeared from the listings to be attended (i.e. not marked as “hybrid” or “MS Teams”) such that observers would only be able to attend if they went to the physical courtroom.  In fact, I’d heard (unofficially) that it might actually be hybrid and I told potential observers about this.  We then heard that the hearing would be delayed until 12.30pm, and then, at about 11.30am, one of us received an email from court staff saying it was being moved earlier again, maybe as soon as 11.45, though in fact it started  at 12noon.  The effect of shunting the hearing from 10.30am to 12.30pm then back to 12noon that some of those who’d hoped to observe in the morning but had afternoon appointments found they were unable to observe; but others, who hadn’t been able to observe in the morning, were excited at the possibility of observing the hearing once we knew it had been rescheduled for the afternoon.  Unfortunately, though, late emails to the RCJ staff (who ask for requests to observe to be with them by 9.30am on the day of the hearing if possible) did not yield responses – and I didn’t learn this from some people until it was too late.  The video administrator and Mr Justice Hayden’s clerk did everything they could to help with the situation (thank you!), and I was pleased that so many observers did gain admission, although obviously disappointed for those who did not receive the link to the hearing on time.  As is sadly often the case, the court’s aspirations for transparency flounder in practice, despite everyone’s best intentions.

Four reflections on the case in the #NotSecretCourt follow. The first is by Sam Green, a barrister who did not observe the hearings but chose to comment on a blog post about the hearing of 2nd February 2022, and we reproduce his commentary here. The second is by Daniel Clark (a paid carer); the third by consultant clinical psychologist Claire Martin; and the fourth by legal academic Imogen Goold. These latter three commentators all observed the hearing on 7th February 2022.

1. Competing aims, by Sam Green

Overall, there is a sense of competing aims among the legal professionals involved in this hearing.

The lawyers are seeking decisions from the judge. 

The judge,  perhaps recognising that no decision he can make is likely to affect the outcome for PH, is attempting to use his authority to mediate the best outcome for him. 

It is an excellent example of how the CoP can work best and how it differs from traditional courts.

It is also a reason it is a worry that CoP decisions become precedents despite the repeated assertion that every case rests on its facts.

This case follows a string of cases which have at their heart a similar theme: faced with a situation P cannot control,  they react by refusing nutrition. Judicially these cases boil down to whether they are simply refusing nutrition because they’ve had enough or because they want to force another to act differently. The former is generally capacitous the latter generally not. 

Above all,  the theme of these cases is agency – people who feel agency has been robbed from them asserting it in the most extreme way possible. In this case “He feels he has been a creature of the state” and he is “understandably…flexing his muscles

Hayden J encourages them to recognise that they do have agency and to help them exercise it.


I made a video about another case heard by Hayden J in a similar legal situation which can be viewed here.

I said before a ruling couldn’t affect the outcome for PH. What I meant was that if the judge held PH had capacity, then he can refuse nutrition. If the judge held that he did not have capacity it was accepted that there would be no attempt to force nutrition on PH so, practically. what difference would it make.

Instead, Hayden J chose to use the time more effectively, narrowing differences, cajoling, encouraging, arranging practical progress.

My favourite bit in the report from the 2nd February 2022 hearing is this:

JudgeHas the plan been put before PH?

HillmanNo.

               (c. 20 second silence)

Hillman: Your Lordship is asking me why not?

JudgeNo. I’m letting the question float through the ether. Why is it that everyone knows the plan except the person it most affects?

Sam Green is a barrister and mediator at Normanton Chambers.

2. Respecting the thoughts and feelings of P, by Daniel Clark

Although I had not observed any of the former hearings in this case (this was only the second time I have observed a Court of Protection hearing) I was reasonably familiar with the situation before the hearing began. I had read previous blogs about this case which, in chronological order, can be found: hereherehere, and here. Given the content of the previous hearings, I am so glad that I had the opportunity to observe a hearing with such a positive tone.

Celia Kitzinger had contacted me with the details of this hearing around 11am, which had been listed for 10.30am, but which she’d heard was actually starting at 12.30pm.  I’d not received any response by 11:35, so Celia forwarded my email to a named member of the court staff she thought might be able to help – and also told me that she’d heard more recently  that it was due to start earlier. This led to a mild panic on my part as I rushed around ensuring that I had everything I needed whilst waiting for the link to arrive. Thankfully, I was ready on time, and the hearing started at midday.

In contrast to the first hearing I observed, which was exclusively online, this hearing was hybrid. Mr Justice Hayden, Counsel for the Health Board (Roger Hillman), and Counsel for the Official Solicitor (Victoria Butler-Cole) were all present in the courtroom. Joining the hearing remotely were PH and a psychiatric nurse. There may have been other parties who I missed, as I was unclear who everyone who was joining the hearing remotely was. In the hearing that was exclusively virtual, parties to the case had their role in the case posted next to their name. That did not happen in this case. 

Being a hearing that did still rely on technology, I did naturally have a technological difficulty of my own. I struggled to hear the initial exchanges, as the audio was fairly faint. This did, however, resolve seemingly of its own accord, and I was able to both see and hear the hearing clearly.

Background to the case

PH is a man in his 40s who, in 2016, drank highly corrosive hydrogen peroxide, resulting in oesophagectomy (removal of part of his oesophagus), splenectomy (remove of his spleen), a tracheostomy and colostomy, and the insertion of a PEJ through which he receives nutrition and hydration. Following a seizure in 2019, PH was diagnosed as having an acquired brain injury. He has been assessed as lacking the capacity to make decisions about his care and residence. 

In the last hearing, on 2nd February 2022, PH had been refusing nutrition (not hydration). An interim placement had been found for him but he wanted the opportunity to visit it himself to see whether he liked it. Hayden J made an order that PH should be taken to see the house. 

Bringing PH to the centre

The hearing began with Counsel for the Health Board (Roger Hillman) being asked to describe what had happened so far with regards to acquiring a place for PH to live, in order to help observers to understand the case. I was grateful for this, and it showed to me that the Court of Protection is serious about its commitment to open and transparent justice.

Whilst listening to the summary, it struck me, once again, that it is a truly intolerable situation for somebody to be living on a surgical ward for a year-and-a-half despite being medically fit for discharge. This was brought home to me by Hayden J’s observation that “we’re giving this man the first opportunity for privacy in a year-and-a-half“. I cannot imagine how this total lack of privacy for so long would have felt. 

Despite all the previous setbacks, somewhere has been found that will allow PH to have his wishes met. This even extended to ensuring that there was somewhere else for his care staff to stay, which was still in the house but also allowed PH his own space. They could be “out of his hair“, as Counsel for the Health Board remarked. 

It was reported that upon visiting the house that it was proposed he would temporarily move to, PH began once again to accept nutrition via his PEJ tube, having chosen not to for 10 days prior. He was actually going to have a feed prior to the visit but decided not to, due to the risk of his stoma leaking on the journey. This was a clear indicator that PH was happy with this new house, and he has continued with his feeding regime since. 

What really struck me about this hearing was the fact that PH’s thoughts and feelings were brought to the fore. There were repeated references to the fact that this would only be an interim placement because PH wanted to be close to home, to his family and friends. In doing so, something important to PH was recognised, and that guided decision making. This placed him front and centre, and acted as a reminder of the importance of an individual’s own views when best interest decisions are formulated. 

Community access was also clearly important to PH. Hayden J remarked that moving to this house would allow him to get a new hairstyle that he wants, which I thought was a good reminder of the small pleasures that have been denied to PH but that so many of us take for granted. I also reflected at the time that this demonstrates how well Hayden J has come to know PH, beyond his support needs and the importance of being close to home. 

Concluding remarks

My first care job was in neurological rehabilitation, supporting people to work towards their eventual discharge. When thinking about the next step, it is quite easy to focus solely on where can meet somebody’s needs, and how close they would be to their family (if they want to be). It is, however, so important to see beyond those issues – as important as they are. 

I distinctly remember one individual, an avid cook, who told us how important it was that she could be close to her favourite supermarket. This way, she could go out and get her favourite foods with ease. Ordering online, she told us, just isn’t the same – you never know what you’ll miss, what new tastes will pass you by. By chance, I was actually in that chain of supermarket a few days after she told me this, and I remember thinking at the time how these simple acts become so much more important when you can’t do them. As a young and inexperienced carer, this experience made a significant impact on me. 

Overall, I found observing this hearing to be very moving, as PH’s next steps were decided upon in a way that included him. His thoughts and feelings had been brought to the fore, and he was recognised as the expert in his own life. 

Towards the end of the hearing, PH gave Hayden J a thumbs up to signal that he was happy with the direction of travel. After the challenges of the last few years, I feel extremely relieved for him. 

Daniel Clark is a paid carer.  He is also deputy director of Backbench, an unaffliliated open platform blog that publishes a range of articles about current affairs. He has recently completed an MA in Political Theory. He tweets @DanielClark132

3. A hopeful resolution, by Claire Martin

I haven’t observed any of the other hearings for PH. I have read the blogs about his case and the media reports of Hayden J ‘slamming’ the Health Board for their lack of adequate care. I managed to get the link for this hearing after being unable to observe a different hearing today and I was really pleased to be able to join at what was a very hopeful resolution for PH. 

PH was on screen throughout this short hearing and he looked to me to be relieved about the current situation – which is that a suitable place to live (off the hospital ward) has been found for him as an interim measure, whilst the search for a permanent home continues.

For 10 days (until 4th February) PH had been refusing nutrition: it seemed he had lost hope.  Counsel for the Health Board mentioned that PH had a history of refusing nutrition and Hayden J corrected this in relation to the current situation:

“… denial of feeding had been the history of this case – but this time the motivation was different – he’d run out of steam, lost a will …” [Judge’s emphasis]

I notice in a previous blog about this same case, by Gaby Parker, that P had been given a diagnosis of ‘emotionally unstable personality disorder – impulsive type’, exacerbated by his brain injury. There is always a high risk for people (given this label) that all of their actions and takes on their experiences are put down to such a diagnosis (known as diagnostic overshadowing) so I was very pleased to hear Hayden J say (in relation to Health Board efforts to find a place for him to live) that he didn’t “doubt the energy or sincerity of the effort [to find somewhere suitable] but nevertheless it was not entirely suitable for P and his resistance to it was not entirely unreasonable”. 

As Gaby Parker had reflected in her previous blog:

I wondered whether P’s complex psychological needs (which included emotional and cognitive issues as well as self-harming behaviours) had led to an over-shadowing of his ‘normal’ distress in the face of unwelcome healthcare interventions and his right to have an opinion about these. There was a sense that he had been silenced in his care, both literally and metaphorically; I felt distressed reflecting on the many ways that being silenced in this way would be experienced by any person who had been through significant trauma. It was apparent that P’s opinion had not been weighted highly in decisions made about him …. .”

What struck me the most about Hayden J’s interaction with PH (and I have noticed this before when observing the Vice President’s hearings) is that he treats ‘P’ in each case as an individual and not a diagnosis. 

The judge does not seem to seek to attribute P’s views and behaviours solely to any diagnosis, especially psychiatric/psychological diagnosis. He ensures that the relational interplay between the health and social care organisations and each P is noted. This means that ‘behaviour’ is not located in P (or conversely only in the clinicians/teams/organisations) but in the relationship between them. Given the location of power in a patient-to-system dyad, I think this is vital in CoP cases. It conveys to each person at the centre of a case that they matter as a person in the CoP. 

I wish PH all the very best for the next part of his life and hope that the system continues to listen to him, as Hayden J has managed to listen to him throughout his lengthy court case. 

Claire Martin is a Consultant Clinical Psychologist, Cumbria, Northumberland, Tyne and Wear NHS Foundation Trust, Older People’s Clinical Psychology Department, Gateshead. She is a member of the core group of the Open Justice Court of Protection Project and has published several blog posts for the Project about hearings she’s observed (e.g. here and here). She tweets @DocCMartin

4. A constructive approach, by Imogen Goold

This was my first experience of watching a COP hearing, and I was struck by the collaborative, constructive approach taken by all concerned. There was clearly a genuine commitment on the part of everyone involved to ensure Mr PH’s wishes were understood and respected, and that he was found accommodation that was not merely sufficient, but a home where he would feel happy and comfortable. 

I was also struck by the thoughtfulness with which Mr Justice Hayden approached PH’s motivations for refusing feeding. 

When Mr Hillman suggested that Mr PH was using refusals to exert some control over his situation, I was impressed by the fact that His Honour gently, but firmly, pointed out that while that was his motivation for past refusals, the current one was of a different character. As he said, PH wasn’t trying to manipulate his situation or press for his wishes to be met, but this time instead he had ‘run out of steam’ and lost his will. This was an important insight, because it drew attention to the fact that this refusal evidenced something different – his loss of hope, which was perfectly understandable given the parlous situation in which he found him. It was important because it meant the focus was on whether, if PH’s wishes were fulfilled, he might turn a corner. 

And, in fact, it turned out to be the case. Once suitable housing had been found, he had agreed to feeding, and he was clearly feeling more positive about his future. This, of all that I saw, really impressed upon me how the constructive approach and the attention paid to his wishes, despite his lack of capacity to make his own decisions, led to an outcome with which the Official Solicitor understandably said she was ‘delighted’ to agree.

Imogen Goold is Professor of Medical Law at the University of Oxford. She tweets @ImogenGoold

Photo by Jeremy Bezanger on Unsplash

A home not a hospital: Service delivery goals for PH

By Eleanor Tallon, 9th February 2022

My experience of this hearing (COP 1354439T) on 7th February 2022 could not be more different from my previous attempts to observe a public Court of Protection hearing (which I blogged earlier).

Not only was it straightforward to gain access to the hearing itself, but also I was able to observe a clear and compelling exemplar of the  functions and influence of the Court of Protection and see  how legal scrutiny can accelerate and steer the delivery of services to its optimum.

The hearing was about Mr PH.  The ‘cliff-hanger’ ending of the last blog post about this case (from the hearing a few days earlier) was that arrangements had been made for PH to be taken, as he requested, to view a care setting he could move into. If he liked it, he would hopefully decide to resume taking nutrition – after having refused it for the previous 10 days.  So I wanted to know whether the visit had been successful.  Had he liked the property? Was he accepting food again?

Background

PH is a 41-year-old male affected by a brain injury (acquired after a fit). He has ‘emotionally unstable personality disorder’ and several complex physical conditions. 

I have keenly followed PH’s journey over the course of the preceding months by reading several (very insightful) blogs written for the Open Justice Court of Protection Project: in reverse date order: “A ‘secret’ hearing on life-sustaining treatment”;  “Capacity to refuse intensive care”, “When academic theory becomes reality” and “Delays in finding an acquired brain injury placement”.

PH has been living in a side room on a hospital ward for over 18 months, although (with the exception of a couple of acute medical incidents) he has been ready for discharge throughout. Court applications were initially focused on finding him a suitable placement outside of hospital, in rehabilitation or other care settings, though this has been amidst a difficult landscape of resource constraints and the impact of COVID. Moreover, various emergencies have intervened and preoccupied the court.

Over this time, several decisions have been needed about PH’s  care and treatment. For some of these decisions, PH was assessed as lacking capacity, and best interests decisions were taken. 

For other decisions (such as the decision to refuse to go to the Intensive Care Unit), PH was deemed by Mr Justice Hayden to have the capacity – and PH’s capacitous decisions have been respected – thus eloquently demonstrating principle 5 of the Mental Capacity Act 2005; that a person shouldn’t be seen as lacking capacity simply because their decision appears to be unwise.

Mr Justice Hayden has made very public criticism of the Health Board responsible for PH’s care because of the lack appropriate rehabilitation support and because PH has remained in unsuitable accommodation, on a hospital ward.  The effect of this seems to have been that meetings were set up, and the issues escalated in a more timely fashion. 

In last week’s hearing, the Health Board presented a concrete interim plan: a bespoke care placement in a purpose-built house at the edge of a village. The house more closely resemble a ‘home’, in that PH will have his own private living space complete with a bedroom, kitchen, lounge and bathroom all upstairs, with 2 bedrooms (for ‘live- in’ carers) and an office downstairs (it sounds similar to a supported living ‘home’, though presumably would still be classed as a residential home in terms of the CQC registration). 

Today we learnt that PH had very recently visited the home and he says he likes it.

The proposed placement is envisaged to last a maximum of 6 months, and is located near to PH’s home town with options for visits to family and places of interests.

The long-term plan is for PH to return to live in the community, with his own tenancy (ideally in his home town) having regained some self-care skills in the interim (e.g. “attempts to improve his manual dexterity – impaired by brain damage –  so that he can meet some of his own care needs”).

This seems to reflect Mr Justice Hayden’s words back in October when he stated he felt “considerable optimism that his needs would be better met in future”. The fruition of a better outcome (albeit short term) seems to have been due to enhanced proactivity from the Health Board in identifying suitable resources, as well as an alternative lead psychiatrist to treat PH. 

Could it be there was more robust action due to media coverage and the spotlighted glare of accountability which follows high profile court proceedings? In any event, the progress was welcomed by all.

The hearing on 7th February 2022 before Mr Justice Hayden

The two barristers in court for this hearing were Ms Victoria Butler-Cole (as counsel for PH via his litigation friend the Official Solicitor) and  Mr Roger Hillman (counsel for the Health Board). Mr Hillman was asked to provide a summary and update of events so far.

Judge: We had a busy and stressful week last week: it is helpful to have that update. And we have members of the public on the platform who would like to know what happened.

Hillman: Your Lordship will recall that an urgent treatment application was applied for on 31st January and we came back again at the beginning of February.  The reason for the urgent application was because PH had decided to refuse to allow himself to be fed.

Mr Justice Hayden intervened at this point in response to counsel having used initials (rather than PH’s full name)  and instructed that ‘in this court we call him Mr H (full name used).”  He reminded everyone that the Transparency Order prevents use of his full name in any publication about the case, and that means that his name can be used in court without risk of compromising his privacy.

From this point on, I felt a sense of the highly respectful, professional value base with which Mr Justice Hayden conducts himself in relation to others. I admire his intervention. I find it so depersonalising, for example when individuals are referred to simply as ‘the husband’ or ‘the daughter’, and I’m sure that Mr Justice Hayden is expressing the same value base when he clarifies how PH is to be referred to in this hearing.

Hillman: Mr H decided to refuse to allow himself to be fed (he is PEJ fed) for a period of 9 days. He became very emaciated and lacking in energy due to a sustained period of fasting. He has a background of occasionally refusing to allow himself to be fed and making a stand if he is unhappy about what is being proposed. He is in the circumstances of a man with very little control, trying to draw attention to the fact that he’s unhappy about a problem. By day 10 the Board became very worried.

Judge: Mr Hillman, denial of nutrition as an exercise of personal autonomy is part of the history of this case.  But this time the motivation was different. (PH) wasn’t trying to achieve anything, he had simply ‘run out of steam’, lost his will,  having lost a close friend in a road traffic accident.

Mr Hillman corrected himself in light of the judge’s observation. He went on to clarify that at times PH  took stands and at that stage PH had said he did not want to die and that he was unhappy and was making it clear that he did not want to go to the placement that was proposed for him, a rehabilitation unit.

Judge: To place this in context, there is a strong body of professional belief that the arrangements [in the proposed rehabilitation unit]  fell considerably short of what was needed

Hillman:  We thought something rather good had been put together, with therapies that would meet his needs.

Judge: That wasn’t intended as a criticism. I don’t doubt the energy or sincerity of the effort but nonetheless it fell far short of the ideal  and (PH’s) resistance to it is not entirely unreasonable.

Hillman: The desire of all staff is to discharge him from the surgical ward where he’s now been for a year and a half and not to have him remain there on an ongoing basis, with the risk of infections.  The general wish was to have a step-down scheme, first at [Rehab Placement] with therapies provided, and  then in due course a move thereafter to a  community placement in his home town. On the 31st January Your Lordship strongly pressed (the Health Board) to revisit the options available and examine alternatives to [Rehab Placement] given that PH was so opposed to it. There were two interdisciplinary meetings on Tuesday [i.e. the day after the hearing on 31st January] following that regarding accommodation. On 2nd February, the Court was told that the Health Board had identified a placement for up to a maximum of 6 months –  not a hospital in the ordinary sense  but a residential home, a four-bedroom house which is suitable in terms of the lay out and his needs regarding treatment and care. Accordingly, the Health Board proposed that if it could be agreed and if PH were happy to move there and receive 24-hour care – there will be a full team and care provided –  he would have dignity and privacy akin to living in a private home.

Mr Hillman went on to describe the living arrangements and how staff could be ‘out of his way’ and the judge interposed, “giving this man his first  opportunity for privacy for a year and a half”.

Counsel for the Health Board recounted how PH went to see the premises in person (following the s.48 order made by the court) – despite some reluctance initially from the Health Board due to the identified risks to his health after not eating for a period of 10 days, and being extremely emaciated and tired. There was a risk mitigation plan in place; ‘special care’, a wheelchair, and ambulance transport was arranged. 

Hillman: It was agreed by Your Lordship that it was in (PH’s) best interests to see it.

Judge: Put like that it sounds like rather a reckless plan approved by me, but the reality is (PH) was dying. That has to be balanced with the paucity of the alternatives.

Hillman: The balance of risks dictated that he was approved to see the premises. He was taken in a wheelchair by the psychiatric nurse and she prepared a report for Your Lordship.

Mr Justice Hayden then enquired whether Nurse D was present at the hearing. At this point both Nurse D and PH appeared together on screen (turning their camera on after having it switched off). It was reassuring to see that PH seemed bright and alert and seemed to be intently following the discourse.

Nurse D then confirmed that PH had taken a feed following his visit to the care setting – and that he had actually agreed to have a feed prior to the visit but he did not want his stoma to leak during the ambulance journey, so had decided to wait for his feed until his return from the viewing.

At this point, it was announced by Mr Hillman that PH was in full agreement with the plan. 

Hillman: (PH) was pleased to tell everyone that he was happy with the house. The important thing is it felt like a house – it’s not like a hospital and more like a home. That’s what he told everybody after viewing the premises on Thursday, and after that he continued to go ahead with the refeeding programme, which has continued to date, I’m pleased to say.

Mr Hillman explained that a memorandum would be drawn up on what the Health Board are going to provide and this will be in simple language so that PH can understand. A care plan and transition plan will  be confirmed by way of an advocates meeting on 14th February with a view for the move to take place on 25th February or thereabouts.

It was reiterated this was, in essence, a half-way house pending a permanent home nearer to or in his home town. It was discussed that the council (of his home town) would also be involved and would need to provide an update at the end of March as to progress made in relation to obtaining a tenancy for PH and what part they are taking in working with the health board to meet his health and social care needs.

Reflections on Mr Justice Hayden

Mr Justice Hayden executes his role as judge flawlessly, and further to this he serves as a role model for how practitioners should approach their work within services for people. 

There is a very vivid imprint of person-centred practice. He has clearly built rapport through his direct engagement with PH, and he made comments which reveal this. For example, Mr Justice Hayden alluded to PH’s wish to get ‘a Mohican haircut’.  He also playfully remarked, after learning that it had been PH’s birthday a few days earlier, that PH is ‘looking good for 41’ (and PH responded with a smile and a self-deprecating shake of his head ).

Furthermore, Mr Justice Hayden’s compassionate closing statement directed towards PH, almost moved me to tears. It came across as so authentic and empathetic.

Judge: Mr H, if all goes well this may be the last time we meet. You’ve  made a very significant impression upon me. I hope it won’t come as a surprise to you that when I was told that you’d started to take nutrition again, I couldn’t have been more delighted.  In a challenging week,  it was a real ray of sunshine and I was hugely pleased to hear it. There may be a slightly easier period coming up in terms of the pandemic and better weather, and moving to the new house and re-emergence with your family. So 2022 could be a good year for you, I hope that it is. If I don’t see you again, I wish you the best for the future and for (your partner) who has been a great support for you, and I’m sure will continue to be. So from me, the very best of luck for the future. 

PH: (Gives a thumbs up and his facial expression appears sanguine)

Judge: I also want to thank Nurse D for playing an invaluable part in this case. And a debt of gratitude is owed to Dr R for his discrete and major personal input. I’m extremely grateful. PH turned a corner last week and Dr R and Nurse D were very much  instrumental in that. 

Nurse D: Thank you, My Lord.

Dr R: Thank you, My Lord.

Judge: Thank you all very much and good luck.

Reflections from the perspective of a Best Interests Assessor

As a Best Interests Assessor (within the remit of Deprivation of Liberty Safeguards), I too have followed cases over prolonged periods of time. 

These have included  s 21A appeals, and also cases where a ‘part 8’ review is required (which is when an unplanned reassessment of the DOLS authorisation is needed due to major change such as a significant increase in restrictions). There is also case continuity in situations where I have recommended that specific conditions are added to the authorisation, which have been approved by the supervisory body (the local authority) as a requirement for the care provider to meet, and I have needed to monitor these conditions repeatedly.  

I can certainly relate to situations in which I have developed empathy and felt frustrations for the individual I have assessed, especially when they are faced with a lack of alternative options (due to limited resources). 

Clearly Mr Justice Hayden has much more persuasive power than a Best Interests Assessor, but I can reflect on how having some level of oversight from a professional who is somewhat independent, and who can initiate communication with separate bodies (i.e. care home management, local authority, health commissioning) can be pivotal in ‘making things happen’ for P, that wouldn’t have necessarily happened without such intervention.

This is why I believe that the Court of Protection is so vital in promoting and protecting the rights of those who cannot always get their voices heard.

Ultimately, every person is an individual with their own story, their own belief system and their own balance sheet as to what is in their best interests. Yet we have a system where often outcomes depend on what services / funds are available to a person, rather than what would actually be best for them. In deciding best interests, we should always be focused on what they want (within a reachable distance), and balance that with a holistic assessment of their strengths and the challenges they face.

PH seems to be a spirited man, who values his autonomy so vehemently that he was almost willing to give up on life itself, rather than live a life without having any control over what was happening to him.

It seems that he has had an arduous and abhorrent experience within hospital (and possibly other institutions of care), and his clear wish is to live in his own domain and be sovereign over it; to have his own privacy and to guard his freedom as far as possible.

Surely this must be what many of us would fight for, if it were taken away from us? Particularly as there is a consensus that these are basic human rights (the rights to liberty and privacy are ratified under Article 5 and Article 8 of ECHR, which is the foundation for the legal framework of the Deprivation of Liberty Safeguards).

Dr Lucy Series reflects (here) that the experience of living in an institution can be crushing to a person’s sense of autonomy and self-identity. How would we feel if we were faced with a plethora of rules and regulations over all our daily routines, and there was an omnipresent authority which influenced every part of our lives, from goals we should achieve down to how our ‘home’ is decorated.

With his solid strength of will (and the impeccable governance of Mr Justice Hayden), PH was able to overcome some of the barriers faced by many people who find themselves in health or social care institutions, and there is an optimistic ending to this chapter.

However this is not typical (in my experience)  of the majority of cases, and it seems there is no easy answer within the climate of austerity and scarcity of provision, particularly in relation to specialist mental health provision(see Oliver Lewis’ blog here). 

I am hopeful that the actions taken in this case (as in others) builds on the recognised need to push forward the agenda to have bespoke person-centred care and to facilitate a person’s wishes as much as possible, regardless of whether or not they have capacity to make their own decisions about residence and care.

Eleanor Tallon is a Best Interests Assessor and Specialist Practitioner in MCA and DOLS with a background in Social Work.  She tweets @Eleanor_Tallon

Photo by Evan Smogor on Unsplash

Why members of the public don’t ask earlier to observe hearings (and what to do about it)

By Claire Martin, 8th February 2022

Judges have suggested repeatedly over the last 18 months – to me, and to other observers – that we should ask to observe hearings in a timely fashion, giving judges (and advocates and court staff) more warning that we want to be there in court.

It happened again last week, during a remote hearing (COP 13607901)  before HHJ Thomas in Birmingham on Thursday 27th January 2022.

As I joined the hearing at 10.30am, the judge was talking to counsel, one of whom then observed that I had joined the platform.  The judge said to me: ‘because you only applied last night at 5.30[1] when all of the staff had gone home, I haven’t had time to consider your request’. She asked me to leave and said I would be contacted if I were to be allowed access.

I was permitted to re-join after some portion of the hearing (I think a costs hearing) had been completed, at 11.29am (so an hour later).

At that point the judge addressed me again, saying that I was “welcome, of course”  but explaining that “the court office is only open from 9-5”, so communications received outside of those hours aren’t processed.  When the office opens the next morning, she said, there is “a lot for staff to do”.  Her suggestion for my future requests to observe hearings followed: “So, Dr Martin,  if you would be kind enough, the earlier you can give notice the easier it will be“.

This blog post is a response to that suggestion – which I’m sure was intended to be helpful.  It must be especially frustrating for judges who fully support open justice and want to ensure a positive experience for public observers, to be unable to provide smooth and timely access to hearings because they have received the request too late for them to engage with the issues.

The problem of late requests to observe hearings

It’s very inconvenient for judges to receive messages from members of the public asking to join remote hearings just minutes before (or sometimes minutes after) those hearings are due to start.

In fact, it’s more than inconvenient. It distracts their attention from the substantive business of the hearing.  

Partly it’s the technology. District judges doing telephone hearings, already exhausted by the task of calling out to 8 or 12 different people on a conference call, are now facing the task of adding yet more numbers to call.  Court staff setting up video-hearings who may well be preoccupied with helping P or P’s family with dodgy connections from borrowed iPads, or doctors in hospitals with unhelpful firewalls, now have members of the public needing to be sent links, and possibly also struggling with connections.  These problems are exacerbated when requests are last-minute.

Partly it’s sorting out issues of transparency and reporting restrictions.  When advocates learn there will be observers – this still seems to come as a surprise to some! – there’s often a sudden flurry of concern about whether the hearing is actually “private” or “public”.  And why (they sometimes ask) if COP hearings are supposed to be public, is there a Remote Hearings Order saying that the hearing is “private” and that Practice Direction 4C has been disapplied – and what needs to be done about that?  There’s a Transparency Order to locate, or create.  Sometimes there’s anxiety about informing Litigants in Person, P and P’s family about our unexpected (and possibly unsettling) presence, hurriedly, at the last minute, as the hearing is about to begin. The start of the hearing “proper” can be delayed while transparency matters are sorted out.  

Sometimes this all seems too difficult, too late in the day, and judges decline to admit us. 

Why don’t we ask sooner?

Quite simply, I couldn’t have asked for this hearing sooner than I did, because I didn’t know it was happening.

We can’t apply to observe hearings unless we know about them – and that usually means we can’t apply until they appear in the daily cause listings.  Those are overwhelmingly our source of information about hearings in the Court of Protection.  Mostly, that means (as in this case) that we learn about the hearings late afternoon or early evening the day before a hearing.

This hearing before HHJ Thomas was posted on Courtserve[2] the afternoon of the day before the hearing, sometime between 4-5pm Wednesday 26th January 2022.  I emailed the Court of Protection hub (in Birmingham) at 5.30pm that day, as soon as I saw the listing after I had finished work. 

Many observers (like me) will not finish work until at least 5pm, when – as the judge informed me – court staff have then clocked off. And that’s the soonest we can check the listings for the following day and request a hearing.

I wasn’t the only one who tried to observe this hearing. Eleanor Tallon (a Best Interests Assessor and Specialist Practitioner in MCA and DOLS) also tried to observe this hearing and blogged about the experience here.  Like me, she was admitted to the hearing, but the Judge then said that as I had only requested access at 10.50pm the evening before, she had not had time to go through formalities. She then referred to Claire Martin, another public observer (and core member of the Open Justice Court of Protection Project) who was also observing the proceedings and requested that we ‘kindly leave’. So that was that. Abrupt as it was, I duly obliged, and felt slightly down beaten at this point.” 

In a personal communication (with permission to quote), Eleanor Tallon said: “It did feel like I was being told off and sent on my way. It was quite abrupt.”  In fact, she understood the request to leave to mean she was excluded from this hearing altogether, and she did not return. 

It seems that the experience of trying to ensure open justice for this hearing was an unhappy one for the court and for observers alike.

The systemic problem

My experience of courts, the legal system and attending hearings is limited to being a COP observer during the pandemic. I have had the privilege of observing over 30 hearings and my impression is that most judges are supportive of open justice (including the judge at this hearing). So, it is not that open justice isn’t supported, in theory, by people in the system, but that open justice, in practice, is hard to achieve, systemically. 

Observers are frequently excluded from allegedly “public” hearings  – often because nobody replies to our emails –  or does so after the hearing is over, apologising for not responding sooner due to pressures of work, or computer problems, or the relevant person being on sick leave.  But I don’t think it’s part of a nefarious plot to keep hearings secret and stop us observing them.

And when judges tell us they only received our request to observe a hearing 10 minutes before the hearing was due to begin, or 10 minutes afterwards, or after the hearing was finished, it’s not that we’re deliberately sending in late requests to annoy the judges or disrupt the court process. We probably asked the evening before, or first thing that morning, and either there was a delay in busy court staff forwarding our request, or the judge was in an earlier hearing, or otherwise engaged, and not able to check their emails.

Unfortunately it doesn’t help to advise us to put in our requests sooner.  

At present, with the system as it is, it is rarely possible for observers to request to observe a hearing until the evening before.  We depend on the listings, which don’t appear until around 4.30pm.  Occasionally CourtServe does list hearings for a few days in advance, but this is relatively unusual, and our experience is that very often these ‘advance’ notifications don’t yield observations, because the hearings are subsequently vacated.  Our best chance of getting a hearing that isn’t vacated is to apply to observe one that is on the list the day before the hearing is supposed to happen (and even then, a large number are vacated on the day).  

Sometimes we’ve observed an earlier hearing in an ongoing case and know when the next hearing is likely to be (because the listing date was discussed in court at the end of the earlier hearing), so we can make a request well in advance.  We’ve seen, though, that this runs the risk of our email requesting access being buried in court staff inboxes, necessitating a further email nearer the time.

Very occasionally, we’re informed of cases by P, by people connected with P, by Litigants in Person, or by counsel for one of the parties.  This assists us with making timely requests – although the vagaries of court listings mean that even parties don’t necessarily know much in advance when a case is to be heard, before which judge, or (now) whether it will be remote, hybrid, or attended, all of which affect our ability to observe and hence whether or not we can make a request..  Moreover, open justice should not, of course, have to rely on ‘inside’ (privately communicated) information about upcoming cases.  

What to do about it

The judiciary has stated its commitment to open justice over and over again and we have no reason to doubt that the Court of Protection aspires to transparency and seeks to support public observation of hearings.  

The problem is the gap between aspiration and reality.

For most members of the public, their observation is the first time they’ve ever been in court.  It can feel daunting, nerve-racking, anxiety-provoking, stressful.  If people feel chastised by judges for late applications, if they’re “told off”, “down beaten” and “sent on [their] way”, it may be the last time they try.  Even for me, as a seasoned court observer, it feels upsetting to be advised (albeit, I accept, with the best of intentions) to make my requests to observe “earlier”,  by a judge who seemed simply not to realise the practical impossibility of doing so.  I would if I could! 

This is a matter we will be raising at Court of Protection User Group meetings.  We’d love suggestions as to how best to manage the situation going forward. 

Claire Martin is a Consultant Clinical Psychologist, Cumbria, Northumberland, Tyne and Wear NHS Foundation Trust, Older People’s Clinical Psychology Department, Gateshead. She is a member of the core group of the Open Justice Court of Protection Project and has published several blog posts for the Project about hearings she’s observed (e.g. here and here). She tweets @DocCMartin


[1] This judge correctly identified the date and time at which I had made my request. Sometimes judges have claimed that we asked  (for example) “five minutes ago” – based on when the judge received the request, as (belatedly) forwarded to them by court staff, without reference to the date and time at which we sent the email to court staff (usually after office hours the night before).

[2] For an explainer blog on how to use Courtserve click here.  The other court listings are similarly not available before around 4.30pm the afternoon before they are due to take place. First Avenue House listings usually go up between 4.30 and 5pm. The Royal Courts of Justice cause list is often available somewhat earlier (around 4pm) and asks:  “Please can requests be emailed the day before the hearing or, if possible, no later than 9:30am on the day of the hearing.”

Photo by Sonja Langford on Unsplash

A ‘secret’ hearing on life-sustaining treatment

By Celia Kitzinger, 7th February 2022

This is the first hearing in more than two years that I’ve observed in a physical courtroom, rather than remotely via phone or video-platform.

It’s a case (COP 1354439T Re: PH) that’s been before Mr Justice Hayden repeatedly over a long period, and I’ve watched several previous hearings over MS Teams.  But this time I was there in person, sitting in a physical courtroom in Newcastle County Court on 2nd February 2022. 

It turned out to be a ‘hybrid’ hearing.  

Along with the judge and court staff, counsel for the protected party (Ian Brownhill of 39 Essex Chambers) also attended in person. 

Counsel for the Health Board (Roger Hillman of Exchange Chambers) attended remotely, as did the protected party himself, a nurse who acted as his advocate, his consultant psychiatrist, and the instructing solicitors. (I think there may also have been others whose roles I missed.)

Background summary

We’ve blogged about hearings in this case several times, most recently in “Capacity to refuse intensive care”, and previously (in reverse date order), “When academic theory becomes reality” “Delays in finding an acquired brain injury placement” and “Inviting family into the decision-making process”).

In summary, the protected party, PH, is a man in his 40s who drank highly corrosive hydrogen peroxide in 2016, resulting in oesophagectomy (removal of part of his oesophagus), splenectomy (remove of his spleen), a tracheostomy and a colostomy and the insertion of a PEJ, a percutaneous feeding tube, into his small intestine.   

He’s been assessed as having an “Emotionally Unstable Personality Disorder, Impulsive Type”, exacerbated by an acquired brain injury, following a fit in 2019. Capacity assessments have determined that he does not have litigation capacity, nor does he have capacity to make decisions about his residence and care, or (at the end of last year) to make decisions about treatment for his broken hip. 

There is however some disagreement between the Official Solicitor and the Health Board as to whether or not PH has capacity to make his own decisions about clinically assisted nutrition and hydration.  (A consultant psychiatrist says that he does.)

PH is currently refusing nutrition (but not hydration) not because he wants to die but because – as Hayden J put it – “he’s had enough, and this situation is compromising his dignity”.

The situation is that he’s still in hospital, despite having initially been ready for discharge (with intermittent medical emergencies) since the end of 2019. Previous hearings before the court have been concerned (first, and ongoingly) with finding him a suitable place to live, and also with his refusal of medical treatments (intensive care, and clinically assisted nutrition).

Following a hearing I did not attend on 13th October 2021, it was reported in the media that Mr Justice Hayden “slammed” the Health Board and spoke of “substantial and alarming failures” in PH’s treatment.  But at that time, the response of the Health Board, and of the new psychiatrist treating PH, led Mr Justice Hayden to feel “considerable optimism that [PH’s] needs would be better met in future” and that this marked “a new beginning”.  At the end of October 2021, it had been agreed that PH was due to transfer from the general surgical ward at the Hospital to a mental health rehabilitation unit run by the Health Board.

The move was delayed by an accidental fall in early November 2021 when PH fractured the neck of his femur, which required hip replacement surgery. It had been hoped that PH would have recovered sufficiently to move to the rehabilitation unit in early February 2022 but he was unhappy with the proposed placement and had stopped eating.

So, some 18 months after the case first came before Hayden J, the Health Board is seeking a declaration from the court either:

  1. that PH does have capacity to refuse nutrition and that his wishes not to continue to be fed should continue to be respected, even if this means his death; OR
  2. that PH lacks capacity to refuse nutrition and that it is not in his best interests to attempt to feed him nutrition against his wishes and so he should be allowed to die. This is on the basis of advice from a consultant respiratory specialist who gave evidence that any attempts at sedation to overcome PH’s resistance to being fed nutrition itself runs a high risk that it will so suppress his respiratory function that it may well prove fatal in any event. Physical restraint to force-feed PH would be “demeaning and traumatic” for PH and “should not be contemplated as it would be destructive of his dignity and self-respect”.

This Health Board had initially sought this declaration at an “emergency” hearing a few days before (on 31st January 2022).  That hearing (which I’m told continued until 7pm) was adjourned after Hayden J spoke privately with PH who told him that he wanted an agreement in writing with the Health Board about leaving the hospital to go to a home for him to live where he could have privacy.  If such an agreement were possible, it was suggested that PH might agree to resume accepting nutrition.  The case had been adjourned for these possibilities to be explored.  

Hayden J had not at that point made either of the two alternative possible declarations sought by the Health Board.

A “secret”  hearing

I’m describing it as a “secret” hearing because (despite apparently having been arranged two days earlier, at the hearing on 31st January 2022),  this hearing didn’t appear on any of the daily court lists for Wednesday 2ndFebruary 2022 – not on the Royal Courts of Justice list where Hayden J’s hearings normally appear, and not on the County Court Civil and Family Courts “Court of Protection” list in CourtServe under the “Newcastle” tab, which was where I expected to find it.  

If a hearing doesn’t appear on the court lists, there’s usually no way for anyone not involved in the case to even know that it’s happening, let alone ask to observe it[1].  

I was in Newcastle in person for a different hearing (attended, in-person) before Mr Justice Hayden – one that was (more-or-less) correctly[2] listed on the Newcastle County Court COP list, for 2pm that day.  I’d known about that one for a while because arrangements for it were made at the conclusion of an earlier hearing, back in November 2021, in the same case.  

Newcastle is one of the courts closest to where I live, and as ‘attended’ in-person hearings are slowly replacing the remote online hearings we’ve become accustomed to during the pandemic,  I was keen to observe a hearing in a physical courtroom.

After arriving (early) in Newcastle, I heard from Ian Brownhill, one of the barristers involved in the 2pm hearing, that there was an 11am hearing before Mr Justice Hayden in which he was also involved. 

I checked the listings again.  Nothing. 

I emailed the judge’s clerk asking whether or not there was an 11am hearing and requesting that, if there was, it be publicly listed.  I knew people in Newcastle who’d read blogs about this case would be interested in observing the hearing. 

Although she confirmed that the hearing was happening, and indicated that she would endeavour to ensure it was listed, I don’t think it ever appeared in the lists.  

It wasn’t there when I walked into Newcastle County Court at around 10.30am and checked the lists pinned up on the boards after passing through the airport-style security scanners. 

The court staff on the ground floor couldn’t find it on any lists when I asked about an 11am hearing before Hayden J.  They directed me up to the second floor to the waiting area outside the courtroom where Hayden J’s 2pm hearing was listed as taking place.  They suggested I ask the staff there.  

The staff on the second floor didn’t know of any such hearing either – and were also anxious that I’d turned up without (in their words) “asking permission” since (under COVID restrictions in place in the court) the courtroom only holds six people plus the judge and court staff.

Then Ian Brownhill emerged from one of the small ‘consultation rooms’ around the perimeter of the waiting area.  Yes, the hearing was going ahead at 11.am in the same courtroom as Hayden J’s 2pm hearing.  He emailed the judge’s clerk (copying in me and the other barrister in the case, Roger Hillman) asking for permission for me to enter the courtroom. Permission was immediately granted (and I was also sent the MS Teams link, since it turned out that the hearing was hybrid).  

Once I knew the hearing was happening, and was able to get my request to observe it before the court, everything went smoothly.  I absolutely don’t believe that the court was trying to prevent me from observing this hearing.

This case has been heard in ‘secret’ before on at least one other occasion – in November 2021.  Back then, the judge’s clerk sent me an email (unprompted) at about the time it was due to start, alerting me to the hearing which, she said, had erroneously not appeared on the lists. I was otherwise engaged and didn’t read the email until hours later, so didn’t watch that hearing, but it was clear to me then that despite the hearing having been unlisted, I was welcome to attend.

Once the hearing got underway, I learnt that this case had also been heard a few days earlier in the Royal Courts of Justice on Monday 31st January 2022 as an ‘emergency’ hearing.  Had I known about it, I would have observed it then.  I didn’t because it wasn’t on the lists when I checked on the previous Friday (which is when Monday’s cases usually appear), nor on the Monday morning.  I didn’t check again on Monday afternoon, but the judge said that the RCJ cause list had been amended at some point in the afternoon shortly before the hearing started – presumably as soon as was reasonably practicable under the circumstances. I understand there were no public observers, but given that it actually appeared on the lists,  I don’t characterise the Monday 31st January hearing as “secret”.

But it does concern me that there are hearings taking place which are never listed (anywhere) and so without any possibility of members of the public observing them –  except under very peculiar circumstances such as led me into this hearing. 

This isn’t a one-off experience.  I’ve encountered unlisted hearings before. On a couple of occasions family members contacted me, asking me to observe their hearings, giving me COP case numbers, judge names and dates/times for the hearings, and – despite attending them after family members negotiated access for me – I was unable to find these hearings listed anywhere on CourtServe.

Of course, given that I succeeded in attending this “secret” hearing  and am blogging about it now, there’s an argument to be made that it wasn’t “secret” at all. I want to distinguish between “secret” (unlisted) hearings and “private” ones. It’s the absence of information that the hearing was even happening in the first place that renders it “secret” –  in the sense of not known by the public, and not available on the lists for them (us) to know. Knowing that a hearing is happening and that it is “private” is very different. Even “private” hearings – from which members of the public are excluded – are nonetheless listed on public websites; they’re not “secret”. 

I should add that there was in fact a “private” part to this hearing when the protected party was offered, and accepted, the opportunity to address the court without being observed by members of the public.  I was entirely content with being asked to leave the courtroom for this “private” exchange.

“Secret” hearings seem often to be, as in this case, a consequence of administrative error.  When the error is discovered, I have seen the courts act rapidly (if not always effectively) to try to ensure that it’s rectified and that the public is alerted.  I’ve been sent (unsolicited) links to unlisted hearings I haven’t been able to ask to observe. I’ve never been refused entry to an unlisted hearing. I’ve never felt, when observing an unlisted hearing “ah hah! I can see why they didn’t want to let us know about this one!”.  

Secret hearings are not part of a sinister conspiracy to evade transparency, and conduct justice behind closed doors  – but of course the effect (excluding the public) is just the same as if they were.

To my Newcastle colleagues who would have liked to observe this hearing and who saw in it a unique opportunity to observe the Vice President of the Court of Protection hearing a serious medical treatment case, in person, just down the road from where they work, a case they’d read about over several blogs….  I’m sorry it didn’t work out.  

I’d imagine the court is too.

What happened at the hearing on 2nd February 2022?

The hearing opened with the information that there is now a skeleton plan in place for a home that PH can move to – and a video of the property was available, although due to encryption problems nobody seemed able to send it to the judge.  This would be a temporary home for PH for maybe 6 months, while something more permanent was organised for the long term in the geographical area where he wishes to reside.

Judge:     Has the plan been put before PH?

Hillman:  No.

                 (c. 20 second silence)

Hillman:  Your Lordship is asking me why not?

Judge:      No. I’m letting the question float through the ether.  Why is it that everyone

                  knows the plan except the person it most affects?

Hillman:  The plan has only been finalised in the last few hours. We have wanted to 

                  avoid putting down things we would later need to resile from.

The psychiatrist (Dr R) was called as a witness and reported that he’d met with PH the day before and updated him. They’d talked at length about the new property and Dr R had shown him pictures from Google maps.  “PH replied he’d like to visit. It was explained to him that he’d need to be somewhat heavier in weight.”

Shortly after this the judge addressed PH, saying: “PH, you can hear that. Until you’ve put some more weight on, you’re not going anywhere.”

There was some discussion of the property. It’s a two-story house, with four bedrooms, one with en suite facilities to a good-sized wet-room.  On the ground floor there are 2 bedrooms and an office.  Staff caring for PH  (it’s a condition of the use of the premises that he continues to receive 24/7 care) would be downstairs “out of his hair so to speak” and “not in his living apartment”. 

Ian Brownhill (cross-examining Dr R) asked how much weight PH would need to put on before the visit could be accomplished.  “That’s difficult because we don’t know what weight he is today… If he were to eat or accept feeds over a period of five days, a visit would be possible” (Dr R). 

Ian Brownhill suggested it might be possible to “do a deal” with PH – to which the judge took exception: “I don’t like that term.  He can if he wants accept nutrition. What I am trying to do is not negotiate, but let him have options to choose between” (judge).

On (not) making the declarations sought

The ongoing dispute about whether or not PH has capacity to make his own decision about nutrition (the Official Solicitor thinks not; the Health Board thinks he does) was not explicitly addressed in the hearing, but caused problems in making the declarations sought.

Mr Justice Hayden asked counsel for the Health Board: “Are you asking me to resolve the issues in paragraph 6 [of your position statement]. It seems rather difficult to do so in time.”

Paragraph 6 was the paragraph seeking a declaration from the court either 

  1. that PH does have capacity to refuse nutrition and that his wishes not to continue to be fed should continue to be respected, even if this means his death; OR
  2. that PH lacks capacity to refuse nutrition and that it is not in his best interests to attempt to feed him nutrition against his wishes and so he should be allowed to die.

I am not instructed to abandon that point”, said counsel for the Health Board, “and I understand My Learned Friend [Ian Brownhill, for the Official Solicitor] opposes it.  Starkly, what should we do if PH decides not to eat and not to accept nutrition and hydration.  We would ask the court to give a declaration so the Board knows what to do.”

Counsel for the Health Board outlined the two alternative possible declarations he was seeking.  

Hillman:  Your Lordship on Monday made the comment that in effect either he has capacity and should say what should happen to him and not be made to be fed, or if he doesn’t have capacity, I suggest it’s not in his best interests to compel him to have food – partly for medical reasons, partly because of his respect and dignity.  Considering the use of force to compel him to be fed would be appalling.

Judge:  I don’t think anyone is suggesting that sedating him and forcing him to be fed is in his best interests. I think I was pretty clear about that on Monday.

Hillman:  With the greatest respect, My Lord, I don’t believe you were. The issue was parked rather than being dismissed out of hand, and hence I feel a need to raise this matter now, as the clinicians could use some guidance. It’s the belief of Dr R that PH has capacity to decide on accepting nutrition and hydration or not. In the event that you are not so persuaded and it becomes a best interests decision, sedation is medically counter-indicated. And the use of physical force is such an appalling prospect in terms of trauma, loss of dignity, and humiliation of PH that we don’t wish to go down that road at all.

Judge:  What is ambiguous is why such a declaration is necessary. I am trying to empower PH to have the maximum options to assert his own autonomy. When he started refusing food, it was not as a bargaining tool at all.  Dr R said it was simply that he’d had enough – as he put it, that his dignity was being compromised.  It came off the back of a series of issues in his own life when he’d become upset, not least because a close friend had died. It wasn’t a device to get his own way. It wasn’t an attempt to compel the Trust. If he is able to agree the way forward today- Not ‘agree’.  If he decides to go to the proposed placement, does the declaration achieve anything other than to undermine PH’s autonomy?

HillmanAll I’m asking is that the Health Board be empowered to continue to respect the autonomy of PH. That is in effect the outcome of the declaration we are asking you to make.

Judge: When you say the Health Board needs to be empowered, what greater empowerment could it have other than the consent of the patient, freely given. Why does it need a court declaration?

Hillman: Because there is still a view that this man may not have capacity to make this decision, and I wish it beyond doubt that a failure to compel this man to accept nutrition is lawful, and that the Health Board would be doing the right thing by not compelling this man to be doing something he doesn’t want to be doing.  If we are not able to move forward in a consensual way, which is absolutely the wish of the Board.

Ian Brownhill (for PH via the Official Solicitor) said “the OS agrees with Your Lordship’s decision not to make the declarations sought” because she was “uncomfortable with the declaration that PH has capacity to refuse nutrition”. He suggested that “What’s happening here is that Mr Hillman’s submissions are designed to protect the Health Board, not to protect PH”.  

The judge demurred, rejecting the proposition that the Health Board was “cynically protecting themselves”, and pointing out their reliance on psychiatric opinion.  He asked what was required to assess whether PH had capacity to make his own decisions about nutrition – what matters PH would have to be able to weigh and balance.  The resulting to-and-fro touched on a lot of issues (involving comparisons with political hunger strikers and anorexics, and touching on capacity to choose an assisted death in Switzerland) without resolving anything.

JudgeLet’s assume for the sake of argument that the presumption of capacity is rebutted. What declaration do you want then?

Brownhill:  I don’t seek a declaration. There is no available option for treatment to put before the court.

JudgeGiven it’s clearly his expressed wishes to refuse food, you would not wish to impose force-feeding upon him?

BrownhillIf someone said they wanted PH to be held down and force-fed, I would take instruction from the Official Solicitor. But it’s not an available option.

Judge: I don’t think it’s an ethical option. He feels he has been a creature of the state, and there could be no more graphic example of that than being held down and force fed.

BrownhillWhat was disturbing to us on Monday was the switch to a palliative care plan.

JudgeThe word ‘palliative’ sometimes generates more heat than light. What it means is ‘pain relief’. If he’s going day after day after day without food, he’s going to need pain relief. So where, at what point then, are you separating from the Board in terms of a plan for PH?

BrownhillOne, we don’t think there should be a positive declaration that he has capacity. Two, we don’t think the Board should stop offering him the opportunity for re-feeding and continued nutrition and hydration.

JudgeI don’t think that’s a difficulty.

BrownhillTo put it in the vernacular, we don’t want people to give up on him.

JudgeI’m sorry to be pedantic, but recognising his wishes is not ‘giving up on him’.

The judge then turned to PH and his advocate-nurse, Nurse D, (who were together in the same room, and visible via video-link).  Nurse D said that PH did want to visit the proposed new home, but disagrees with the view that he should gain weight before doing so.  He wanted (she said) to reassure Ian Brownhill that he is being offered food, but he doesn’t believe it’s necessary for him to accept nutrition at the moment. 

The judge then offered PH a “private session with no members of the public present” which he accepted, and I left the courtroom, re-joining after the lunch break.

Viewing the property

After the lunch break, Nurse D, who’d not been able to send the video of the house over to Hayden J, played it to us on her mobile phone, holding it up to the screen and walking us through the outside parking space, the ramp to the front door, through to the kitchen, the bedrooms, the wet room, the rural view from the window.  After she’d shown it to the court, PH asked to see it as well.

Dr R then updated the court about his conversation with PH in the lunch break.  PH, he said, “refuses to eat before visiting the placement. He’s agreed he will eat after seeing it, if he likes it.  He walked the length of the corridor and back to prove his fitness: he believes he can survive for a further week without eating. He asked to go  to the property this afternoon – which is difficult because of organising the ambulance and so on.  I imagine he’s quite tired, although he says he’s not, and he’s becoming increasingly angry.”

The judge asked for confirmation on the last point: “Did you say increasingly angry?”  “Correct, My Lord”.

The judge then said that, although he didn’t want to find himself in a position where PH was “manipulating the situation”, he could understand why he would want to “flex his muscles”. “If the reality is that, come what may, if he doesn’t go to [the new property] that he will risk his health and ultimately his life, then the risk of taking him there has to be evaluated against the alternative even worse option”.  He asked Dr R, “Is it more reckless to take him to view the property, or to leave him in the hospital?”  Dr R said, “We can’t guarantee that it’s safe [to take him], but I did think last week we could persuade him to eat before taking him there, but that’s becoming less and less likely.”

Ian Brownhill then suggested consulting the Official Solicitor, Sarah Castle, about making a s. 48 order allowing PH to make the visit on the following day, and the court adjourned to allow this consultation to take place.

Mr H,” said the judge, “you are making us all work very hard today, but I’m going to see if I can grant your wish to go tomorrow”.

PH did a thumbs up.

When we reconvened at 16.10 (having been in a different in-person hearing in the same courtroom in the interim), Ian Brownhill reported back:  “Considering what PH has said, and that he wants to visit the property and doesn’t want to die”, Sarah Castle as Official Solicitor supported the making of a s.48 order today, “allowing for him to visit as soon as is reasonably practical”.  “I don’t suppose anyone would disagree with that,” said the judge.  The order, said the judge, should say something like “it shall be lawful and in PH’s best interests, having regard to all the circumstances of the present situation and identifying and balancing the competing risks, for PH to be taken to view the property at….”.   It will have immediate effect, without endorsement.

The judge then said he was not going to make any determination of the capacity issue today – not least because the case would be heard again in just five days time, but also because “it would not be right for me to determine that today, given what’s going to happen tomorrow.  It would undermine PH’s sense of his own autonomy, without impacting on anything”. 

The judge closed the hearing by addressing PH:  “Tomorrow they are going to take you to [new property] to see if you like it.  I hope the message will come back to me that you like it, that you see it as a good stepping stone back to [where you want to live long-term] and that you decide to take some nutrition.  It is your decision, in your hands.  It is your life and I’m letting you be in the driving seat. I hope you’re a good driver. We’re all rooting for you.”

Postscript on observing in-person in a hybrid hearing  

As soon as the hearing opened, I realised that my view of the judge and the various parties was compromised in this in-person hearing compared with watching hearings remotely. 

The judge was a long way away even in this small courtroom, and my view of him was impeded both by the barrister seated in front of me (especially when he stood up to address the judge) and also by the judge’s own computer.  The judge spoke quietly and I often had to strain to hear him – if I’d been watching at home, I’d simply have turned up the volume on my laptop.

Since I was seated behind him, I only had a back view of the barrister in court.  I couldn’t see his face when he was speaking.

My view of the people attending remotely was also much less satisfactory than at home.  There were two screens on the right-hand side of the courtroom on which they appeared via video-link, but I had to rotate 90 degrees in my seat to see them, and it was challenging to watch them as well as simultaneously typing notes on what they were saying.  At home I have one laptop with the video-link open directly in front of me on a shelf raised about a foot above my desk and another laptop on my desk beneath it for typing my notes, so both the court participants and my own notes are easily visible.

I found a solution which I’m sharing here because it might help others.  Since I’d also been sent the link to watch the hearing remotely, I experimented with opening that on my laptop with the sound turned off.  Then I had a much better (close-up) view of the judge, and could see the faces of both counsel (instead of merely the back of the co-present barrister). It didn’t solve the problem of lack of volume control for the judge, but was otherwise fairly satisfactory.  Unlike at home, though, it meant having two windows open on the same (small) screen, which isn’t ideal.

One more point for court observers:  the desks were all supplied with sockets for plugging in laptops. Mine didn’t work.  Nor did the sockets at the adjoining desk, as I discovered in the afternoon hearing, when the instructing solicitor for one of the parties attempted to charge up her laptop.  Fortuitously, I had an extension lead with me, and she and I both plugged our laptops into that, and ran it to a socket in the wall.  I recommend coming to court prepared!

Finally, the court staff in the waiting area told me I should in future phone in advance to check whether or not there’s room in the court if I hope to observe in person. The Newcastle courtroom Hayden J sat in was suitable (under COVID measures) for only six people in addition to the judge and the court staff.  I was lucky with the hybrid hearing described here, since it was just Ian Brownhill and me in the physical courtroom, but the afternoon hearing on the same day didn’t have space for everyone, and some participants (including solicitors) took part via a video-link from an adjacent consultation room.  I don’t actually know whether court staff would be in a position to tell someone about seating availability (or ‘book’ them a seat) in advance of a hearing: if you try it, please send me some feedback on what happened!

Celia Kitzinger is co-director (with Gill Loomes-Quinn) of the Open Justice Court of Protection Project. She tweets @KitzingerCelia


[1] There are also what I call ‘semi-secret’ COP hearings.  These are actually listed in CourtServe, but not under the Court of Protection tab, so it’s not apparent to anyone looking for COP hearings that they’re happening. I find them by trawling through the lists of towns and cities, and then through sub-tabs which are usually lists of judges. It takes me more than an hour to do this each day, so it’s not something I do regularly – meaning that if hearings are not listed under the COP tab, we’re unlikely to publicise them via the Open Justice Court of Protection Project, and they’re highly unlikely to attract observers from amongst members of the public.  To give a sense of the scale of the problem, I’m writing this on Sunday 6th February 2022, and there are no COP hearings listed under the Court of Protection tab for Chester, Mold, or Medway. I have just spent an hour scouring the listings and I found a COP hearing listed before The Honourable Sir Jonathan Cohen (no less!) not under the COP heading, but as as the fourth hearing if you scroll down under the “Daily Family” tab embedded beneath the “Chester’ tab. There’s also a COP hearings before HHJ Howells under the “Mold” tab, and before HHJ Cove under the “Medway” tab – neither of which is reproduced under the COP tab. Three ‘semi-secret’ hearings!

[2] Only “more-or-less” because it omitted any information about whether the hearing was remote (e.g. via MS Teams), or hybrid, or whether the public could only observe if they attended in person.

Cross-examining a GP in a COVID-vaccination hearing

By Celia Kitzinger, 4th February 2022

Editorial note: The judgment is published here: A CCG v. DC & MC & AC [2022] EWCOP 2. The parents subsequently appealed the decision, and the appeal was heard by Hayden J MC & Anor v A CCG & Anor [2022] EWCOP 20. (See postscript to this blog for what happened.)

The parents of a 20-year-old profoundly learning-disabled man (DC) asked the judge not to make the declaration sought by the Clinical Commissioning Group (CCG) that it was in their son’s best interests to receive COVID-19 vaccination.  They believe there is insufficient medical evidence to justify vaccinating him.

The advice to vaccinate DC came from a GP, Dr H, who is also employed by the CCG in a management role with responsibility for vaccine roll-out in his area.  This GP had first made contact with the parents in February 2021.  He discussed their concerns about COVID vaccination, and they were “unconvinced” that vaccination was in their son’s best interests. 

There was then a substantial delay before the matter reached court. This is a common feature of the COVID vaccination cases I have watched.

The matter came up again in July 2021 as part of a routine review, and led to a best interests meeting involving DC’s parents, his continuing healthcare case manager, representatives from his care home, and Dr H. 

The parents oppose vaccination on the basis of its potential risks and what they consider to be an insufficiently individualised risk assessment. They’re concerned about myocarditis as a side-effect of the vaccine (especially given their son’s family history of heart disease).  Because of their son’s very low body weight, they believe that – if he has to be vaccinated – a ‘child’ dose (i.e., a third of the adult dose) would be safer. They also want their son to have a blood test to establish whether he has natural immunity: he may not need the vaccination after all. The CCG has refused both a ‘child’ dose of the vaccine, and a blood test to check for antibodies[1]

Since it had not proved possible to resolve the issue, the CCG applied to the court in early December 2021 and the hearing was initially listed for 17th December 2021.  Due to funding difficulties, the Official Solicitor was unable to instruct solicitors or counsel to attend the hearing, so it had been relisted for January 2022.

The case (COP 13860597) was heard remotely before His Honour Judge Burrows, sitting at Manchester Civil Justice Centre on Monday 17th January 2022. 

There were a lot of things happening in this hearing that I found of interest (listed below), but I’m only going to write about the first of them in this blog post:

  • Cross-examination of the GP by counsel for DC’s parents – the focus of this blog post
  • Cross-examination of DC’s father by the other parties – with counsel for the parents raising “objections” to several questions (for another blog)
  • Contradictory claims from different advocates as to whether DC (who has never had capacity to make medical decisions) would decide to be vaccinated if he were able to do so.  In this hearing, as in others I’ve observed, counsel made efforts to ventriloquise an imaginary capacitous DC – sometimes literally putting words into his mouth, eg. “As his Dad, can you not see some circumstances in which DC might say ‘actually I don’t want to risk being one of those people who succumbs to this and dies of it’?” or “Would DC have decided ‘actually I would quite like to know if I have natural immunity?’” and “Would DC have said, ‘I want to examine why people of my weight mostly have a lower dose’ – my submission is he’d be concerned about that”.  It was hypothesised that a counter-factually capacitous DC would be strongly influenced by his parents (and sister), none of whom had been vaccinated, and would, like them, decide against vaccination – especially as “he’s only alive now, at the age of 20, because of his parents’ care, so he would give a greatly enhanced weight to their views” (counsel for the parents).  Alternatively, it was suggested that, at 20, he is at the age at which children tend to rebel against the position taken by their parents, or simply form different views. Or that he’d altruistically decide to be vaccinated from “community spirit” to prevent transmitting the virus to others in his care home. Or that he’d choose to be vaccinated so as to be permitted to engage in community activities and avoid being isolated. I notice that some of these speculations made their way into the judgment.
  • Lack of clarity concerning substituted judgment vs. best interests. Counsel for DC’s parents proposed that the weight that DC (if he were capacitous) would give to any given argument for or against vaccination “is the weight Your Honour should give it, because Your Honour is stepping into DC’s shoes”. In his closing submission, counsel informed the judge that he should “stand in DC’s shoes” and make the decision that DC would make, drawing on Montgomery as evidence that “individuals have a number of different reasons for making decisions”.  In his closing summary he referred the judge to §20 of his position statement: “the substituted judgement that must be made on behalf of the patient is one in which the court seeks to put itself in the shoes of the patient and make the judgement he would be likely to make even if, as in DC, he has never had the capacity to make those judgements before. This is not the same as the court substituting its own view of what is in DC’s best interests”.  Counsel for the Official Solicitor said, in her closing statement, that although counsel for the family “repeatedly refers to the court putting itself into DC’s shoes, of course that’s not the test for best interests” – and followed this up with a long extract from Lady Hale in the case of Aintree v James [2014] AC 591 (also picked up in §26 of the published judgment).

A proper expert?

Dr H is a General Practitioner and adult safeguarding lead at his practice. He is also the Medical Director at the CCG and responsible for the roll-out of the vaccine in the CCG’s area.

The parents’ view is that the GP, Dr H, the only medical expert involved in making the best interests decision, and the only medical expert before the court[2], does not have sufficient expertise or detailed knowledge of their son.  They asked for adjournment so that that an appropriate expert could be appointed. 

They described Dr H’s best interests assessment as “formulaic”.  The nineteen questions they had submitted to him “have largely been unanswered at the best interests meeting and since” – possibly because Dr H is unable to answer due to “his lack of involvement in DC’s care”. In their view, Dr H “does no more than repeat government guidance which is directed at the generality of individuals of DC’s age and which cannot bear on the individual question of DC’s best interests”. 

They had hoped to find independent experts: a paediatric respiratory physician to report on the particular effects of DC’s medical conditions in considering the risk/benefit analysis of vaccination; and a toxicologist to report to the court as to the relevance of DC’s low body weight to the dose he should receive (if the judge were to decide on vaccination). They have not been able to locate relevant experts for their case.

Having failed to find experts themselves, they were now seeking a s.49 report instead, because (as their counsel put it)  “if Your Honour makes an order, they don’t have a choice. They have to identify someone”.  The judge pointed out that this begs the question as to whether there is an appropriate expert and could lead to “a wild goose chase by proxy”. 

The CCG saw no need for additional expertise. They took the position that the treating GP was “precisely the right level of person” to make a judgement about whether or not vaccination is in DC’s best interests and that “only when relevant counter-indications are identified” should a different expert be involved: in this case there are no “relevant counter-indications”.  

Counsel for the parents had also filed statements relating to other cases, some of which they wanted to be admitted as evidence.   These statements appeared to the Official Solicitor “be to fulfilling the function of expert evidence despite which none of the various statements has been filed with the court’s permission or in the prescribed form…”.  Two were statements from Clare Craig and Dr Peter McCullough filed in entirely separate judicial review proceedings (R (AB) v Secretary of State for Health) which challenged the authorisation of COVID-vaccines on people under the age of 18. (Permission for judicial review had been already refused on the papers).   Another was a statement from Marek Pawlewski in an injunction application in the High Court matter of Dr Sam White v Stephen Lightfoot, on data about the risk of certain batches of the vaccine appearing to cause a greatly elevated risk of death.  The Official Solicitor did not see the relevance of these statements, one of which is “more on the broad issue of government roll-out to adolescents and is not concerned with adults like OB”, and another of which is “of unknown provenance” from someone who “prefers not to say where he works” and describes himself as “a data scientist”. She did not want to “allow collateral challenges in ongoing JR proceedings to colour decisions about what is in DC’s best interests”.  Additionally, the CCG was concerned that this evidence could not be tested in court via cross-examination.

Failure to comply with court rules for expert evidence is common to several of the  COVID-19 hearings I’ve observed (see also “Naming a putative ‘expert’ in a COVID vaccination case” and “The politics of the pandemic in the Court of Protection”) though none has as yet been as explicitly in violation as the doctor permitted (extraordinarily) to give evidence in the case of  Z v University Hospitals Plymouth NHS Trust & Ors (Rev 1) [2020] EWCOP 69).   

The outcome was that the judge did not agree to adjourn the hearing – not least because the case had taken so long to reach court in the first place, and was now urgent (he said), given the risk of serious illness or death to DC. He also decided that the additional material submitted by the family was not admissible as evidence. He left open the question of whether or not he would make a s.49 order (i.e. ask the CCG to locate a relevant independent expert), but ultimately concluded that this was not necessary.

The question of whether or not Dr H was an appropriate expert in this case was – as will be shown below – an issue the parties tackled in oral examination.

Position of the Parties

The three parties in the case were the applicant CCG, the protected party DC via his litigation friend the Official Solicitor, and DC’s parents. 

There was no dispute that DC lacks capacity to make decisions about his care and treatment, including COVID vaccination: final declarations regarding DCs lack of capacity had already been made following the December hearing.  

The sole focus in this hearing was on whether or not vaccination was in DC’s best interests.

The CCG’s position

The CCG (represented by Philip De Berry) believes DC is at risk of becoming very ill if he contracts COVID and so it’s in his best interest to be vaccinated with an adult dose of the Pfizer vaccine in line with the professional opinion of Dr H, following government guidance. 

Counsel referred to Hayden J’s judgment in SD v Royal Borough of Kensington and Chelsea [2021] EWCOP 14 and said it was “not the court’s role to arbitrate between different medical opinions” [3] (e.g. concerning vaccine dosage).  The applicant’s submission was straightforward, he said:

“DC fits clearly within the parameters of public health guidance.  He is plainly clinically vulnerable – by reference to three separate factors: respiratory illness, neurological impairment, and learning disability. There is no dispute that he is vulnerable to COVID because of these three features. The clear public health advice is that he should be vaccinated in the absence of any contraindications, as set out clearly in the Green Book.  The contraindications don’t apply to DC. So, the case is clear and straightforward that vaccination is recommended based on public health advice and the court doesn’t need to look beyond that.”[4]

The Official Solicitor’s position

Counsel appointed by the Official Solicitor to represent DC’s best interests, Nicola Kohn, also took the position that he should be vaccinated against COVID-19 as soon as possible to protect him against serious illness or death.

She pointed out (in response to Philip De Berry) that the court does adjudicate between competing medical views – in serious medical treatment cases, for example.  But it is somewhat different to ask to the court to adjudicate between competing theories that are (a) not presented via live evidence (and so cannot be cross-examined) and (b) not presented by clinicians who are proposing to give such treatment.  She referred to the case of Re AVS, in which the judge had considered the matter of receiving evidence on a treatment (in that case, Pentosan Polysulphate [PPS]) that no one was actually proposing to offer:

… it strikes me as unlikely in the extreme that the court would order a clinician to undertake a medical intervention which he, the clinician, did not believe to be in the best interests of the patient. Absent a clinical opinion that the continued administration of PPS would be in the best interests of the patient, therefore, it seems to me that the current proceedings would be doomed to failure.” (§24 Re AVS)

The point, she said, was that it may be appropriate for the court to adjudicate between competing clinical options proffered to the court, but it is “trite law” (that’s the lawyerly way of saying everyone already knows this!) that the court can only decide between available options, and cannot adjudicate between competing theories.

The competing options, for me, are either that DC has or doesn’t have the vaccination?”, asked the judge.  

The Official Solicitor confirmed that was the case.  “There is a suggestion in the parents’ evidence that there should be a consideration of Ivermectin, notwithstanding that it is not an authorised treatment in the UK.  And a re-evaluation of the vaccination based on DC’s weight and an adaptation of the dosage. With respect, the court is quite right. The only options are authorisation of the vaccine as offered, or not.”

The parents’ position

The parents were represented pro bono (i.e., without having to pay for their legal team) by Francis Hoar of Field Court Chambers.  

Francis Hoar has made quite a name for himself in relation to COVID-19, not just as a barrister representing the views of his clients, but also in publicly articulating his own views (e.g. in an article and a blog post challenging the legality of lockdown restrictions). He has acted in a range of COVID-related cases in other courts including R (Dolan) v Secretary of Statein which the Court of Appeal decided in December 2020 that lockdown regulations were within the government’s statutory powers and did not breach the European Convention on Human Rights. According to his website, he “is currently acting in a Judicial Review of the original ‘quarantine’ regulations (now before the Court of Appeal), a claim against a school trust’s mask policy and an impending claim against a care-home’s vaccination policy” (accessed 29thJanuary 2022).  

He’s not a barrister I’ve seen before in the Court of Protection, and (as I’ll illustrate in this report) his style of advocacy was considerably less “inquisitorial” and more “adversarial” than is usual in this jurisdiction.

The parents’ position as expressed in their position statement, and as it emerged over the course of the hearing, was that their son should not be vaccinated against COVID because DC is not at any great risk either of contracting COVID, or of becoming seriously ill if he does, and that the risks of vaccination for someone with their son’s complex medical conditions outweigh the risks of contracting COVID.  They made the following claims:

  • DC is unlikely to contract the virus because he’s unable to move without assistance, which means that (unlike people in other vaccinations cases before the court) there is no risk of his being unable to be distanced from people known to be infected or who appear to have symptoms.  
  • DC is unlikely to become seriously ill if he does contract COVID because of his age cohort: the government’s Green Book estimate of the infection fatality rate for young persons between the age of 15 and 44 – including those with pre-existing conditions – was one death for every 2,932 young people infected.
  • DC is at risk of side-effects from vaccination, especially of myocarditis and blood clots (there’s a family history of heart problems and strokes), and there may be other medium- and long-term side-effects that aren’t yet known because the vaccines are still in an  “experimental” phase.
  • The CCG proposes administration of the adult dose of vaccine, but DC (despite being 20 years old) weighs only the same as an average 10-year-old child (around 31 kilos). His parents consider the adult dose of the vaccine to be potentially dangerous (but the CCG refuses to vary the dose).
  • Proper analysis of the risks and benefits of vaccination for DC requires a blood test to establish whether he has natural immunity. (The CCG has refused this.)

In addition, they had apparently raised the possibility of alternative treatments (Ivermectin was mentioned) although this was not before the court.

Counsel “accepted fully” that there were only two options before the court: [1] To vaccinate DC (with the dose proposed by the GP) and [2] not to vaccinate him.  

Insofar as Your Honour will be satisfied that there is not sufficient evidence that it’s in DC’s best interests to make the order requested – which is for two adult doses, plus booster, plus further doses in line with government policy – there is no middle ground to administer a child dose.  The only option would be not to vaccinate if Your Honour decides it’s not in DC’s best interests to receive all the standard doses. Insofar as Ivermectin is concerned, there is no application from the family for alternative treatments, but it may be that Your Honour considers the treating physicians to have not sufficiently considered alternative treatments, and that it’s therefore not in DC’s best interests to vaccinate him. There is no competing medical evidence before the court.  What we have here is simply an assertion of government guidance by doctors, and on the other hand scientific evidence of the risks of myocarditis, yellow card effects and so on.  That’s not competing medical evidence. It’s simply evidence that’s not refuted by other evidence before you. I accept that as you don’t have experts before Your Honour, you can’t make determinations about natural immunity.  I invite the court to note that one of our points is that it is not in DC’s best interests to give the vaccine without testing for natural immunity because if he does have natural immunity then vaccination would not give a benefit.  We invite the court to make an order not for vaccination or to make an order for vaccination conditional upon DC not having natural immunity.”

Evidence from the GP 

I am writing this blog report having just attended a weekend workshop organised by Inner Temple on advocacy training for Bar students. I was there to talk about open justice, but one of the things attendees were learning – and I was learning alongside them – was how to cross-examine witnesses. Consequently,  I am looking at my record of this cross-examination in a new light[5].

The aim of cross-examination is to elicit information that can later be used in closing submissions.  Successful cross-examination is often said to include:

  • Ask only questions to which you already know the answers.
  • Don’t ask the witness to report again on material covered in their written witness statement (there’s a risk of them saying something different!) but you can ask them to confirm parts of their written statements.
  • Only ask about one fact per question.
  • Keep questions short and to the point.
  • Ask only questions that lead to information you want to use in your closing submission.
  • Ask only ‘leading’ (yes/no) questions. (Apparently some law schools are requiring tag questions – “isn’t it?”, “aren’t they?” etc – in all cross-examination, though this practice was not endorsed by the barristers present at the weekend event.)
  • Keep control of your witness: don’t let them make speeches or ramble (obviously yes/no questions help with this).
  • Use plain English (avoid Latin and fancy legal terminology).
  • Know your way about the bundle so that you can quickly take a witness to relevant statements.
  • Begin and end your examination on a ‘winning note’.

The cross-examination of the GP in this case seems in many ways to exemplify the principles students were taught at the Inner Temple advocacy weekend, and it was exciting to see ‘real life’ examples, to flesh out the role-play.

Cross examination by Francis Hoar (for DC’s parents)

The cross-examination by Francis Hoar was  notably less “inquisitorial” and much more “adversarial” than is commonly the case in the Court of Protection.  

Here’s how the cross-examination began. I’m guessing that the ‘winning note’ is to discredit the GP’s knowledge of his patient.

FH:  Your involvement with DC started in early 2021.

GP:  Yes

FH:  And you have confirmed that you have not seen DC.

GP:  Yes.

FH:  And you haven’t treated DC for anything, is that right?

GP:  No. I have treated him for a number of minor issues, but I haven’t seen him face-to-face.

FH:  And your colleague, Dr Y, has also treated him, also remotely, for skin issues.

GP:  Yes.

FH:  But neither of you has treated him for anything related to his chest or neurological issues.

GP:  Correct.

This interaction casts doubt on how well the GP knows the protected party at the centre of the case, thereby undermining his expertise and damaging his credibility: he’s never seen DC face-to-face, and neither he nor his GP colleague have ever treated DC for the medical problems that may have the potential to cause difficulties with the vaccine (or serious illness with COVID infection).

According to the parents’ position statement: “the only clinician who was present [at the best interests meeting] was Dr H, who does not appear even to have met DC before the meeting… It does not appear that the specialist Consultants who lead the delivery of DC’s care were consulted and they did not attend the meeting”. 

Cross-examination seems designed to underscore that point.  Here’s how it continued:

FH:  Turning to the best interests meeting notes [of 24th September 2021]. You see the list of participants. You were the only medical practitioner there.

GPYes.

FHYou said to the parents that you had no doubts that the potential benefits outweigh the risks of vaccination.  

GP:  Yes

FH:  You said that 9 out of a million had a risk of serious thrombo-embolic events.

GP:  Yes.

FH:  When you said that, what information did you use to make that statement?

GP:  The Joint Committee on Vaccination and Immunization guidance.  As a GP, I work to the guidance I’m given. The reading I’ve done supports that that’s correct, but I’m not going to pretend I’m an expert.

[…]

FH:  Did you mention at the meeting the elevated risk of myocarditis?

GP:  No. At the time we had that meeting the risk of myocarditis was unclear and unquantified. It has come to prominence since that meeting.

FHThat’s not correct, is it.  Elevated risk of myocarditis was specifically mentioned by the JCVI on 3rd September and it was one reason why the JCVI said that although there was a marginal benefit, the risks were not quantified and so they couldn’t recommend the vaccine for 12-15-year-old children[6]. Is that fair?

GP:  I don’t see how that’s relevant since OB is not 12-15.

So, now it appears that not only does Dr H not know his patient very well, but also he doesn’t regard himself as an expert on the side-effects of vaccination. Counsel goes on to cast doubt on his understanding of the evidence behind the JCVI guidance which Dr H is charged with implementing.  According to Francis Hoar (although he didn’t provide the source of this information), at the time of the best interests meeting at which the GP has said he did not mention the elevated risk of myocarditis, there was evidence in the public domain of myocarditis in young men of DC’s age, and this evidence had been “relied on” by the JCVI.

FH:  Were you aware that the evidence on which the JCVI relied was extended to ‘young men’ including those over 20 years old?[7]

GP: No. I wasn’t following information about younger people, because it wasn’t relevant to my practice. I was not undertaking vaccination of that age group at that time.

FH: So it’s right then, isn’t it, then, at that meeting, when you were discussing DC, his weight is the median weight of a 10-year-old boy. Do you agree?

GPI was treating a man of 20.

FHI wasn’t asking you that Doctor. I am asking you about his weight.

GP:  I don’t have that data to hand. I don’t doubt it, but I don’t know.  

FH:  Let me take you that [in the bundle]. This is taken from public domain sources and shows that 30kg is the median weight of a nine-and-a-half-year-old boy.

GP:  That is the correct reading of that graph.

FH: So, we have a 20-year-old with the weight of a 10-year-old.  You did not inform yourself of this prior to the meeting.

The GP is beginning to sound somewhat truculent and defensive by this point and the judge intervenes.

Judge:  Can I stop you there Mr Hoar. This doctor has been very candid. His role is to roll out the vaccine. He bases his decision-making and the information he gives to those who would be receiving the vaccine on the JCVI guidance. You said that in relation to 12-15 year old children, on 3rd September, the JCVI had indicated there might be a problem of myocarditis and the evidence relied on by the JCVI indicated that it might also be the case for young men.  Was the JCVI guidance also warning that young men might be at risk of myocarditis?

FHAs far as I know there wasn’t JCVI guidance relating to 18-plus young men, no.  But on the other hand, it was in the public domain, and recognised by the JCVI that the risk pertained to young men and not just boys. I agree that no criticism can be made that he wasn’t aware of that. But what I’m suggesting to you, Dr H, given that we have a particularly vulnerable young male and his parents are not thinking it was in his particular best interests, is that it was up to you to be up-to-date with the evidence for him.

GPMy responsibility as DC’s GP is to try to find what it in his best interests. As it clearly says in my statement, I balanced the risks of the vaccination and the benefits of the vaccine and they very much stand in favour of vaccination. I acknowledge I was not aware of the specific risk of myocarditis.  It was not raised in that meeting, as I recall it.  

FHIt was raised at that meeting.  Please turn to the second page of those minutes.  [DC’s father] explained his thinking and had looked at the safety trials and asked about myocarditis.

GP:  I apologise. It was mentioned but it didn’t really register with me. I do apologise.

The effect of this series of question is to suggest that the GP took what could potentially be characterised as a rather cursory approach to establishing his patient’s best interests. The father’s concern with myocarditis, specifically raised at the meeting, “didn’t really register” with him, and he’s found himself having to apologise for having forgotten about this. He did not follow up on the father’s concerns by reading up-to-date evidence on myocarditis. 

In the following exchange, counsel for the parents adds to this implied criticism the fact that the GP did not report age- and disability- stratified risks for myocarditis, but rather relied on a population-wide statistic.

FH:  Dr H, your recommendation was ‘it’s obviously in his best interests on a risks-benefits analysis’? I put it to you that the only way you can arrive at that conclusion is to put on the one hand his risk of being infected and becoming very ill versus on the other hand the risks of the injection.

GPYes.

FHSo you have to take into account the age- and disability- stratified risks.

GPYes.

FH: So it’s not appropriate, I suggest, to say “a nine in one million” chance of myocarditis, which is across the whole population, when the risk may be very different for different stratifications. Do you agree?

GPYes, but that stratification wasn’t available at that time. I have to be pragmatic. I have to manage my time.  I have to share the guidance shared with me.  When JCVI think the risks are of sufficient importance to be part of my consideration or informed to my patients, I do my best to do that.

At this point, it seemed to me as an observer that counsel for the parents abruptly changed direction and asked a question that (to me) seemed to come out of the blue.

FH: Are you aware of the Montgomery and Lanarkshire Health Board[8] case on informed consent, which meant a less paternalistic approach to patients?

GP:  I am aware of my responsibilities around informed consent.

FH:  Are you aware of the Supreme Court case?

GPIt was not in my mind at the time but I was aware that there had been a Supreme Court case.

FHAnd that this means that the Bolam test would no longer apply.

GPYes, because the guidance changed.

FH:  So you have a responsibility to provide – absent informed consent from the patient – information to the people who would decide, namely his parents[9].

I was rather thrown by these questions about informed consent, since there was nobody to “consent” in this case (certainly not the parents), but rather a best interests decision to be made. Unless I have misunderstood, the point seemed to be that the GP had not provided sufficient information about the medical risks of vaccination to the parents. But they are not proxy decision-makers for DC. I was puzzled by the relevance of Montgomery in this context and posted a question on Twitter about this: “It’s not really relevant as it is about consent from people with capacity”, responded Victoria Butler Cole QC (@TorButlerCole): “There is a more obvious point which is that to contribute an informed view to a best interests process you need to know the relevant risks and benefits of the treatment in question to the person concerned.”

The overall direction of questioning aimed at demonstrating the GP’s lack of “expertise” when it came to deciding whether or not DC should be vaccinated concluded like this:

FH:  We are talking about an extremely complex patient. Not an average 20-year-old man, or someone with one or two conditions, but a multiplicity of conditions. Do you agree?

GP:  Absolutely.

FHYou said the aim is to vaccinate all adults in the population – again you generalise.

GPYes.

FHYou can only give the generality of the advice. What you couldn’t do is give an evaluation based on DC because you hadn’t seen him. It was based on your experience as lead clinician in the roll out of vaccination for adults.

GP: Yes.

FH: You’re not an expert paediatric physician or paediatric neurologist. Is that right?

GPYes.

Counsel for the family then asked a series of questions that seemed directed to specific concerns the parents had raised.

The parents took the view that DC was not at risk of becoming seriously ill because he is so young. Counsel asked the GP whether  “the age curve applies” whether or not there are other medical conditions – “so someone like DC, with his conditions, but older, would be at greater risk” (“yes”).  

The parents wanted DC to be tested for natural immunity.  Counsel asked the GP about the general principle relating to natural immunity and vaccination, referring to the Heaf test:  “daisy pricks to ascertain natural immunity so you wouldn’t need the BCG injection – it’s not a novel position, is it” (“not at all”).  Have you evaluated the evidence about natural immunity and vaccination?  (“I didn’t have any evidence: we were on a learning curve”).

The parents believe that DC is not at risk of contracting COVID because he can readily be “socially distanced” from others (also meaning that he is unlikely to infect others).  Counsel questioned the GP about the safety of other residents in DC’s care home, stating that this should not be part of a best interests consideration.

GPWell, there are multiple consequences for him of not being vaccinated. His ability to socialise with other residents is impacted upon by his vaccination status.

FHThat’s a decision of the care home though, isn’t it.

GP:  Yes, I’m not passing judgment. I just stated in the meeting that it might impact on other aspects of his care.

FHDC is immobile.  Given that he cannot move around save with the help of others, there can’t be any concern about social distancing.

GPI don’t know enough about the movement of people into the communal areas and the movement of people around the building, so I don’t know enough about how it might impact on his quality of life. His interaction with others may be less.

FHGiven that he cannot move save with the help of others, and given that we know that vaccinated people in the care home have had COVID over the Christmas break, why – looking at it from a medical view – why should DC have to be isolated when he returns from visiting family, when others would not.

GPThat’s the JCVI guidance.

FHDo you agree with it?

GPIt’s not my job to agree or disagree with it. The guidance is written by people who are better educated than I am.

Later questioning moved to point out an error in the GP’s witness statement, and to explore the consequences of the way that COVID vaccination is currently licensed for use.

FH:  You said the vaccines are lawful but that clinical trials will end in 2022.  It’s 2023.

GP:  I don’t doubt your information.

FH:  As a result of the authorisation, it’s not possible to sue the manufacturer if there are adverse consequences, except under very special circumstances.  And government compensation is limited to £120,000[10].

GPYes, the only person you can sue is the government.

JudgeThere were two questions. The question was whether the fact that this vaccination has been brought in under circumstances where is there a special exemption from civil liability – whether someone is consenting or not – is that something a reasonable person would take into account in deciding about vaccination?

GPA reasonable person should be thinking about their health, not about financial consequences if they sue someone subsequently.

FH:  The 2015 Supreme Court decision in Montgomery means that it is not for you to decide what a reasonable person should or does take into account, or what they may think when making a decision. You need to give them all the information.  While your view is that they shouldn’t take into account that they wouldn’t’ be able to get compensation from the manufacturers, some people may disagree. So it’s important to inform people of their very limited right to sue.

GPIt’s not in the guidance that I should inform people of this.

JudgeThe vast majority of people don’t sit down with a GP and discuss the risks and benefits of vaccination. They attend a vaccination centre and are provided with a sheet of information[11].

GPYes, there’s always a clinical supervisor available.  Within that sheet, there’s nothing saying you’d not be able to sue the manufacturer if there were adverse effects.

JudgeSo, if someone says “I’m happy to have this vaccine, but what I’m worried about is not being able to sue”, would you be able to explain?

GPYes. I’d say there is a very limited amount of government compensation and you can’t sue the manufacturer.

And the parents are of the view that their son should not receive the full adult dose of the vaccine due to his low weight. The GP pointed out that there is no lower weight restriction for administration of Pfizer in the official guidance: “I am there to apply the guidance, not to challenge it”. If the guidance were to change, then he would do “whatever JCBI is saying is most appropriate”. 

The final line of questioning from Francis Hoar – and the ‘winning note’ to end on – related to the failure of Dr H to consult with experts involved in DC’s care.

FHIt’s right to say that when DC was last seen by his respiratory consultant, neurologist, and physiotherapist – you didn’t speak to any of those before the best interests meeting.

GPNo.

FHOr subsequently.

GPNo.

FHAnd I’m going to suggest that you should have done, given the complexity of this patient and the fact that the vaccine is new.

GPThe experience of hospital specialists in relation to COVID vaccination is very low and the conversations I have had have been with my clinical colleagues in the vaccination service who have the experience of giving the vaccine.

FHThey don’t have specific experience of DC or his diagnoses. You and your colleagues in the vaccination service are simply going by government guidance, which is what you’ve being going by throughout.

GPYes. I’m a GP. I’m not an expert on everything.

One feature of Francis Hoar’s cross-examination is that at no point did he treat the GP as an expert – for example, by asking him questions about whether he’d expect DC to become seriously ill if he were to contract COVID, or what the likelihood is that DC already has natural immunity and the implications of that for decision-making about vaccination. Instead, Francis Hoar focused on how Dr H himself had behaved in the past – what he had (and hadn’t) said in the best interests meeting, who he had and hadn’t consulted – and asked about his knowledge of medico-legal matters (including correcting a factual error in his statement).  

Watching this cross-examination it seemed that the goal was very clearly to discredit Dr H as an expert. It did not seem that counsel intended to use anything Dr H might say in evidence as contributing to consideration of DC’s best interests. 

Correcting witnesses, telling them what they “should” have done, and phrases like “I put it to you…” are rarely deployed in the Court of Protection.  There’s another example of robust cross-examination (from Joseph O’Brien) in our blog post on “When expert evidence fails” which is worth reading for comparison. It was an effective demolition of expert evidence and led to a new independent expert being appointed by the court (who as it turned out came to the opposite conclusion about the protected party’s capacity).

In the current case, Francis Hoar’s cross-examination laid the groundwork for a significant part of his closing submission (the other significant part related to what DC would decide for himself in relation to vaccination if he had capacity to make that decision).

In his closing submission,  Francis Hoar said that the court “cannot put a great deal of weight on Dr H’s evidence”.  The reasons he gave derived in large part from this cross-examination.

He did not consult with DC’s multi-disciplinary team. What he exhibited in evidence is that he is very familiar with giving normal guidance on vaccination regarding risks that are known, but not in giving specific advice to individuals he hasn’t seen and hasn’t treated, except for online in relation to minor issues.”

Cross-examination by Nicola Kohn (for DC via the Official Solicitor)

The Official Solicitor did some work to ‘rehabilitate’ Dr H as an “expert”.

Unlike counsel for the parents, counsel for the Official Solicitor treated Dr H as an expert able to answer questions about the risks and benefits of vaccination for DC.  For example:

NKIn your evidence this morning you said DC is ‘extremely vulnerable’ and quoted from the Green Book which shows he falls into three of the clinical risk groups: he has a respiratory condition, a neurological condition, and he’s in long-term residential care.  Can you elucidate for the court what are the risks to DC if he contracts COVID.

GP: That’s why I’m so categorical that the balance of is in favour of vaccination. Each of those vulnerabilities increases the risk of serious illness for him if he contracted COVID. The risks of vaccination that have been raised – they do exist but are tiny in comparison.

NK:  I don’t want to overplay it, and I know this is upsetting for the parents, but is there a risk of death?

GPYes. We’ve had a patient with less vulnerability than P in our practice die.

At one point she said he’d been “self-effacing in [his] evidence” – to Francis Hoar – in having said “I’m just a GP”.  She asked: “For how long?”  “Thirty years”, he replied.  

She also addressed the issue of whether he had consulted other ‘experts’ by asking him whether the members of the vaccination team (with whom he’d discussed this case) were – “civil servants or doctors?”.  The answer was that they were mostly doctors, plus some public health consultants.

So, on the basis of the Official Solicitor’s cross-examination, Dr H is an experienced GP who has consulted relevant medical colleagues about the case. 

When asked about the absence of evidence from any specialists, Dr H said, “the questions being asked are effectively challenging the scientists in the JCVI, rather than specialist doctors’ knowledge.  No other expert, unless they have a specific agenda would offer any other advice.

In her final submission, the Official Solicitor accepted the CCG’s submission that “the GP is the correct discipline to assess whether DC should have the vaccine. There is no justification for any further medical advice. It is not at all clear who to ask, what to ask, how it would help, or how long it would take” (Philip de Berry).  She said likewise:  “this is not a case where we can say ‘oh, if only we had the evidence of X person’ – someone named and identified.  I would submit that the court should make a final decision now, and not seek more evidence”. 

How did the cross-examination influence the judgment?

The judge decided there was no need to involve any further experts in the case, and that he had enough evidence to decide that vaccination (with the full adult Pfizer dose) plus boosters in line with government guidance was in DC’s best interests.

He made this decision despite, in large part, accepting the information derived from Francis Hoar’s cross-examination of Dr H, the GP.

It seems to me that Francis Hoar’s cross-examination was “successful” to the extent that it revealed the limits of Dr H’s expertise and exposed the extent to which Dr H was essentially toeing the official government line put out by the Joint Committee on Vaccination and Immunization.  

The cross examination succeeded in this goal by using the standard methods identified above: i.e., by asking closed questions to which counsel already knew the answers, deriving information for subsequently use in a closing statement, and so on.

In his judgment, HHJ Burrows shows that he saw and accepted what Francis Hoar wanted him to understand concerning the limits of Dr H’s expertise:

Having heard Dr H respond to cross examination from Mr Hoar, it seems very clear to me that he did not feel able to engage with some of the points put to him about risk and benefits. It is obvious to me that the CCG’s evidence rests on the official-line towards the vaccine. Dr H was not before me to look behind the official guidance and advice, but simply to ensure that he applied it faithfully. When some figures which are emerging from vaccinations in certain groups (Israel and the US Armed Forces, for instance), were put to him Dr H did not attempt to question them by reference to any research carried out elsewhere. This is no criticism of him. He is a G.P. and CCG Medical Director with a task of ensuring the vaccine is effectively rolled out. (§40, Re DC [2022] EWCOP 2)

The problem (for Francis Hoar and for the parents) is that the court routinely makes decisions based on the official guidance and expects no more of a GP except that he applies it faithfully.  

This position was laid out originally by Mr Justice Hayden:

“My task is to evaluate [P’s] situation in light of authorised, peer reviewed research and public health guidelines and to set those in the context of the wider picture of [P’s] best interests“. (SD v Royal Borough of Kensington & Chelsea [2021] EWCOP 14)

In this case, HHJ Burrows also drew on a decision in the Court of Appeal (albeit obiter) as to the approach the Court should take on vaccination cases involving children: “It favours the Court being guided by Public Health England and the Green Book: see Re H (a child) (Parental Responsibility: Vaccination) [2020] EWCA Civ 664 Eleanor King, LJ” (§33, Re DC  [2022] EWCOP 2).

So Dr H, who relies on public health guidelines and the Green Book, and applies official guidance “faithfully”, is in fact – as counsel for the CCG claimed from the outset – an entirely appropriate expert in a case of this kind.

A cross-examination can be technically flawless in its execution, in the sense of eliciting the information (and creating an impression of the witness) that counsel wishes subsequently to use in closing submissions.  But it can ultimately fail because those submissions are simply not compelling for the judge.

POSTSCRIPT

Mr Justice Hayden heard the parents’ appeal against this decision on 3rd May 2022 (MC & Anor v A CCG & Anor [2022] EWCOP 20). A few days before this appeal, DC contracted COVID-19 and was quite ill. In light of this development Hayden J reviewed the framework put in place for vaccination. In his judgment (§28) he comments that the original decision was “unimpeachable” and “but for the intervening Covid-19 infection, the appeal would have been dismissed.” Given the “parents’ almost palpable anxiety” about vaccination, which Hayden J considered would lead to DC becoming distressed in turn, making this a factor in DC’s best interests, Hayden J took the rare course of ordering further evidence about the nature of the vaccinations required and the effect of post viral natural protection before reaching a final conclusion. The appeal was adjourned to permit this. I don’t know the subsequent outcome.

Celia Kitzinger is co-director of the Open Justice Court of Protection Project. She tweets @KitzingerCelia


[1] Family concerns to establish whether their loved one might have ‘natural immunity’ are common to several of the cases I’ve observed, with the implied or explicit expectation that evidence of natural immunity would obviate the need for vaccination.  The parents’  position in this case was characterised by the Official Solicitor as “one of scepticism regarding the efficacy and risk of the currently licenced COVID-19 vaccination programme adopted in this country” – although they “do not profess themselves to be anti-vaccination per se and in fact protest the opposite”.  This seems to be a recurring pattern across several COVID-related hearings I’ve observed – with family members seeking to refuse vaccination characterised by the court as “anti-vaxxers”, a label that they themselves reject (e.g. Part 3: “Is P’s sister an ‘anti-vaxxer’, in this blog post: “The politics of the pandemic in the Court of Protection”).

[2] Another GP from the same surgery (Dr Y) had been asked by the CCG to give a written ‘second opinion’ and that document was also before the court.

[3] What Hayden J actually said in SD v Royal Borough of Kensington and Chelsea [2021] EWCOP 14 was: ““it is not the function of the Court of Protection to arbitrate medical controversy or to provide a forum for ventilating speculative theories. My task is to evaluate V’s situation in light of the authorised, peer-reviewed research and public health guidelines, and to set those in the context of the wider picture of V’s best interests.” (§31, my emphasis)

[4] I’m grateful to Claire Martin who also observed this hearing and shared with me her detailed and comprehensive notes of what was said in court.  I have benefited enormously from the opportunity to compare my record of the spoken word against hers, but accept ultimate responsibility for the quoted material in this blog post. It is as accurate as I can get it, given that we are not allowed to record hearings. There are many extracts quoted in which Claire and I had identical word-for-word records of what was said. There are others where one of other of us missed a word or phrase, or recorded something with slightly different phrasing and I have had to select one or the other. For example (to show the extent of divergence where we differed): Claire’s notes read: “FH: It’s right to say that when P was last seen by neurologist and physio – you did not speak to any of them prior to BI meeting. (GP: No). FH: Nor since. (GP: No). FH: I’m going to suggest you should have done.”  My version of the same exchange goes like this: “FH: “When P was last seen by his respiratory consultant, [missed one consultant] and physiotherapy consultant, you didn’t speak to any of those before the BI meeting. (GP: No.) FH: Or subsequently. (GP: No.) FH: And I’m going to suggest that you should have done, given the complexity of this patient and the fact that the vaccine is new.”)

[5] I am enormously grateful to Oliver Lewis and Leonie Hirst for inviting me to participate in the Inner Temple Advocacy Weekend.

[6] That is in my view an accurate and fair summary of the JCVI statement of 3rd September 2021.

[7] I’ve had a search for this evidence and can’t find it. There are only 3 research references cited in the JCVI statement of 3rd September 2021 and I can’t see evidence in any of them relating to myocarditis in young men post-vaccination. There’s a note at the bottom of the statement saying “Some of the data considered by JCVI were unpublished analyses from the studies cited above” – but I would not know how to obtain this data and wouldn’t expect a GP to do so.  There are certainly publications post-dating the Best Interests meeting of 24th September 2021 (e.g. “COVID-19 Vaccination–Associated Myocarditis in Adolescents” which finds post-vaccine myocarditis with “quick clinical recovery and excellent short-term outcomes” in males aged 12-20; published in November 2021). A study of the entire Israeli population found that “definite or probable cases of myocarditis among persons between the ages of 16 and 19 years within 21 days after the second vaccine dose occurred in approximately 1 of 6637 male recipients and in 1 of 99,853 female recipients” (“Myocarditis after BNT162b2 mRNA vaccine against COVID-19 in Israel”, published 2nd December 2021).

[8] Montgomery v Lanarkshire Health Board [2015] UKSC 11

[9] The parents are not, of course, the decision-makers. 

[10] Here’s the government website concerning Vaccine Damage Payment

[11] The current version of the Information for UK Recipients of the Pfizer vaccine is available online (click here). It does not include the information that you cannot sue the manufacturer or that government compensation is limited to £120,000.

Photo by Steven Cornfield on Unsplash

Not quite there yet: My first three attempts to observe a Court of Protection hearing

By Eleanor Tallon, 28th January 2021

It could be said that my ‘Open Justice’ observer experience didn’t get off to a very good start.

I tried from 8.20am on the 26th January 2022 to access a hearing before Mr Justice Hayden, which was at 10.30am. I had no response and continued to contact the court by phone, but to no avail, until Celia Kitzinger came to my aid and emailed the judge’s clerk directly on my behalf. Following that,  I was sent login details to a viewing via ‘Cloud Video Platform’ at 11am, though there was no access to this, and it turned out the hearing had been mistakenly listed on the RCJ website as ‘hybrid’ (meaning both remote and in person access), when it was actually only open to observation in person. 

I had some free time the next day so I tried again.  

On the evening on 26th January, as soon as I spotted  a case listed on the Open Justice Court of Protection Project Twitter feed, I emailed the Birmingham Court, as instructed, to request access to a hearing the following day (27th September 2022, COP 13607901, before Judge Thomas).  I then followed up the request the next morning with a reminder, and received an email to say that the Judge would consider my request.

Further to this I received access and log in details and whilst frantically trying to gain entry, I had a very helpful phone call from (an administrator possibly?) from the Birmingham Court who helped me to navigate the technology and I successfully gained access (this seemed like an achievement in itself!). 

The hearing was already underway, and the respondent’s counsel was in full flow, going through the details of various complaints made against the Local Authority. Mid -way through her delivery, the Judge stopped her and highlighted that ‘Ms Tallon has joined the proceedings’.

The Judge then went on to say that as I had only requested access at 10.50pm the evening before, she had not had time to go through formalities.   She then referred to Claire Martin, another public observer (and core member of the Open Justice Court of Protection Project) who was also observing the proceedings and requested that we ‘kindly leave’. So that was that. 

Abrupt as it was, I duly obliged, and felt slightly down beaten at this point. 

The advice from Celia had been that it was typical to request access on the morning of the hearing (as listings aren’t usually available until the evening before then) and I thought I had been one step ahead of the game by sending in my request the evening before.  Clearly not – for this judge, anyway.

Thankfully I had already created a Plan B and had received access details for an 11.30am telephone conference hearing before Judge Hilder, so I swiftly moved onto finding out about the etiquette for phone hearings (seeking further advice from Celia, again gratefully received) and writing up my experience thus far. 

I was just about to dial in to the phone conference to observe the hearing before Hilder J when I saw an email to say I could re-join the Birmingham hearing – I hadn’t realised I was going to be allowed back in! 

At that point I felt it was worth committing to the phone hearing,  and it turned out that it was in relation to a DOLS application (which I was pleased to hear as it felt like familiar territory). I was quickly admitted to the call, and as Celia had explained, the transparency order was explained to me by Judge Hilder.  I asked if I could have a copy of the transparency order  sent to me via email (as advised by Celia, who prefers to see transparency orders before publishing blogs about hearings).  Judge Hilder  politely declined to send me the transparency order and made it clear that the contents of the hearing could not be published. Therefore, I presumed there no prospect of sharing the content of that particular case with any other members of the public.(As it turned out, the phone hearing only lasted 15 minutes.)  

It was odd to be part of a phone hearing, in that I’m very experienced as a Best Interest Assessor in attending virtual meetings (usually via Teams or Zoom) but have never in 13 years of professional life been part of a phone conference. It felt incredibly disconcerting not to have a visual picture of others and not to have the greatest sound quality, especially in respect of Judge Hilder. I think this was felt too by the Judge as she made a point of requesting a video conference for the next hearing. 

Despite this shaky start, I am not discouraged.  I actually now feel more equipped and confident about completing a successful observation next time, though I’m not sure I would have got even over the first hurdles were it not for Celia’s help.   

I do think there is room for improvement in terms of allowing and facilitating public access to Court of Protection hearings (and our right to report from them) – and it seems there may be disparity between different judges in terms of how well they understand and implement access for  public observers?

I hope to report back on a successful observation soon!

Eleanor Tallon is a Best Interests Assessor and Specialist Practitioner in MCA and DOLS.  She tweets @Eleanor_Tallon

Photo by Zach Vessels on Unsplash

Capacity and elective caesarean

By Samantha Halliday, 26 January 2022

I have written extensively about court-authorised obstetric intervention[i] but I’ve always relied upon reported decisions. 

I am acutely aware that as Rosie Harding has commented: “When only the judgment is available for academic scrutiny, we cannot be clear as to the ways that the various submissions were framed”.   That being the case, I was very keen to observe this hearing (COP 13865837) before Sir Jonathan Cohen on 21 December 2021 in the Court of Protection.  

It concerned an application by an NHS Trust (King’s College Hospital NHS Foundation Trust) for a declaration that a young woman (JK) lacks capacity to decide either the mode, or location of her baby’s delivery and that it would be in her best interests for her to deliver in hospital by caesarean.

Context

JK is 21 years old, and at the time of the hearing she was 36 weeks pregnant. At the time of the hearing nobody knew of her whereabouts.  

Asked by the judge to outline the issues before the court, Eloise Power (acting for the applicant Trust) characterised JK’s life to date as “tragic in the utmost”, noting that Katie Gollop QC (acting for JK via the Official Solicitor) had described it as “Dickensian”. She agreed, she said that “Dickens could scarcely have devised a worse scenario.”  

A vulnerable adult, JK is not suffering from a mental disorder, marking out this case from many of the other cases concerning court authorised obstetric intervention that are regularly determined by the Court of Protection.  However, she has a history of Foetal Alcohol Syndrome and her cognitive ability has been assessed as between 5 – 11 years.  She lives in supported accommodation, but her attendance at the unit has been erratic and she has been absent for a number of days, with her current whereabouts unknown.  She has missed “at least 13” ante-natal appointments and has been aggressive and violent towards healthcare professionals. It was reported that throughout the pregnancy she has abused alcohol and drugs, testing positive for cannabis, crack cocaine and morphine.  Foetal growth is restricted leading to a risk of foetal distress in labour.  

JK gave birth to twins 2 years ago by an elective caesarean section.  The twins were placed with her adoptive mother at birth, but the relationship between JK and her adoptive mother (A) has broken down and A has said that she is not in a position to parent the child JK is expecting. It was noted that the child would be taken into care upon birth.  

The hearing

JK was not present at the hearing, indeed her whereabouts are unknown and she has not been seen since 15th December, almost a week ago.  She was represented via her litigation friend, the Official Solicitor (Katie Gollop QC), although neither she nor any agent of the Official Solicitor had not been able to speak to JK directly.

The central question for the court was whether JK had capacity to make her own decision about where and how to deliver her baby.  

An adult with capacity has the right to refuse any treatment, no matter how unwise that decision may appear.  Treatment without consent will give rise to both tortious and criminal liability.  S.1(2) Mental Capacity Act 2005 sets out a rebuttable presumption that a person has capacity, so the starting point is that as an adult JK should be assumed to have capacity to make her own decisions.  

Acting for the Trust, Eloise Power reported that JK’s capacity had been assessed on 9th December 2021 by Dr S, the consultant obstetrician, who concluded that JK lacked capacity to make decisions for herself in relation to mode of delivery.  During her previous pregnancy,  JK had chosen to give birth to her twins by caesarean section and was deemed to have capacity to do so.  A significant difference between the two pregnancies relates to JK’s drug use.  During her first pregnancy she had tested positive for cannabis, however throughout this pregnancy she had abused alcohol and drugs, testing positive for cannabis, crack cocaine and morphine. 

Two witnesses gave evidence on the issue – JK’s support worker and a consultant obstetrician.

The consultant obstetrician’s evidence on capacity

Giving evidence on behalf of the Trust, Dr S (a consultant obstetrician) stated that whilst JK had capacity to make choices about her maternity care during the first pregnancy (when she was cared for by the same Trust), alcohol and drug abuse meant that she was unable to make similar decisions now as she is unable to concentrate for long enough to allow a discussion of the issues.  

On 8th December 2021 JK was reported missing and brought to the hospital by the police using the power under s.136 Mental Health Act 1983 to remove a person appearing to be suffering from a mental disorder and in immediate need of care or control to a place of safety.  The following day Dr S assessed JK’s capacity observed by the duty psychiatrist (Dr P), in the presence of JK’s named midwife and a safeguarding midwife.  Unfortunately, Dr P could not be contacted to give evidence, however a detailed account of the consultation on 9th December was given by Dr S.

Dr S testified that she had assessed JK’s capacity, forming the opinion that JK did not have the capacity to decide upon the mode of delivery because she could not weigh the risks posed by a vaginal delivery after a caesarean, against the risks of a caesarean delivery; however, she concluded that JK retained the capacity to decide to leave hospital. 

Capacity is decision-specific, so it is not unusual for a person to have capacity to make one decision, but to lack capacity to make a more complex decision.  However, assessments relating to JK’s capacity to decide to leave the hospital are telling in that they clearly indicate a fluctuation in JK’s capacity.  Previously the police had brought JK to the hospital on 30th November where she was found to lack the capacity to decide to leave the hospital, only to regain the ability to make that decision one day later.  This suggests that JK’s capacity is impacted by the influence of drugs and alcohol, leading Katie Gollop QC, acting for the Official Solicitor to argue that the two-stage capacity test (s.2(1), s.3 (1) MCA 2005) had not been satisfied and that a further capacity assessment is necessary. 

JK’s support worker’s evidence as to capacity

Dr S stressed that JK was unable to understand and weigh the risks of a vaginal versus a caesarean delivery. However, evidence given by JK’s support worker (K) emphasised that she is able to take decisions, although K noted that JK is under severe pressure due to the fear that her much wanted baby would be taken away from her and that this is impacting upon her attention span.   

K has not been able to discuss delivery options with JK, but felt that her cognitive ability was greater than suggested and that JK would consent to a caesarean and delivery in hospital if the benefits were explained to her.  JK’s support worker demonstrably has a good relationship with JK. She explained that she had become aware that JK was pregnant around June 2021 and that she believed ‘we really lost her’ around August 2021 when JK realised that her baby would be taken away from her.  She said that JK had named the baby, that she wanted the very best for her baby, but that she did not want to lose her.   In her view, this overwhelming fear meant that JK would not engage with healthcare professionals and led to her being verbally abusive and aggressive towards them.  She emphasised that the loss of trust had far-reaching consequences for JK’s ability to focus, reducing her ability to discuss what was happening and to plan for the birth.

Katie Gollop QC set out the Official Solicitor’s position that she was “not in a position to say that the statutory presumption set out in s.1(2) of the Mental Capacity Act 2005 is rebutted in respect of litigation or subject matter capacity.”  She expressed concern that the Official Solicitor had not been able to speak to JK directly and that support workers at JK’s placement may believe that she has capacity to make her own decision about mode of delivery.  Katie Gollop QC argued that an interim order should be made so that if, or when JK is found a further capacity assessment can be performed.  This would allow an assessment of her capacity at that time, rather than relying on the now rather dated assessment from almost two weeks ago.

This argument was rejected on behalf of the Trust by Eloise Power who argued that the court should give weight to the professional expertise of the healthcare professionals who were present and conducted the capacity assessment on 9th December 2021, emphasising that the consultant obstetrician is the lead for perinatal health and is experienced in dealing with similar cases.

She juxtaposed Dr S’s testimony with that of JK’s case worker, noting that whilst K has knowledge of JK, she is not trained in mental capacity assessments.  Whilst she recognised that it was unfortunate that JK was not able to speak for herself, Eloise Power argued that there was more than enough evidence to rebut the presumption of capacity and indicated that if the court were not satisfied that JK lacks capacity to make this decision, she would invite the court to exercise the inherent jurisdiction to allow a caesarean to be performed in line with clinical advice.  

Best interests

In comparison to the evidence presented relating to JK’s capacity, there was little discussion of her best interests.  This is significant because an individual who lacks capacity should be treated in accordance with her best interests.  Katie Gollop QC reminded the court that best interests are not limited to best medical interests, instead they include consideration of the individual’s wishes and feelings.  However, because she had not been able to speak to JK direct she had “no first-hand knowledge of her wishes and feelings about how she wishes to deliver.”  Therefore, the Official Solicitor was able only to state that JK’s “purely medical interests” would support the performance of an elective (in the sense of planned) caesarean.  On behalf of the Trust, Eloise Power stressed that JK had chosen to give birth to her twins by caesarean section, lending support to the argument that she would consent to a caesarean if she were in a position to do so. 

Decision

Sir Jonathan Cohen recognised the great importance and highly personal nature of the decision the court was faced with, saying “the court is being asked to take about as personal a decision as it could be asked to take about the birth of JK’s child and I’m acutely conscious that it is her body that the court is being asked to make orders about.”  

Having described JK’s life as “one of extreme disorder,” saying “she suffered from about as a disruptive and abusive childhood and adolescent as can be imagined” he proceeded to summarise the evidence presented to the court.  The judge detailed JK’s frequent absence from the unit over the last month, her failure to attend ante natal appointments and the hostility she displayed towards the midwives who came to the unit on 15thDecember, when she is described as “verbally aggressive towards the midwives, shouting, swearing and screaming.  She looked unkempt. The midwives were unable to complete an antenatal healthcheck.” 

Sir Jonathan Cohen noted that the Director (K) of the supported living accommodation where JK lives has provided considerable support to JK, but that K had told the court that once midwives started visiting the unit JK lost trust in the staff.  He noted that K did not know what JK would want, but that she had told the court that JK was very scared of losing her child again.  

He emphasised the experience of the professionals who conducted the capacity assessment on 9th December and stressed that JK had not been intoxicated or scared at the time, concluding that the assessment was conducted in relatively favourable condition to JK.  

Sir Jonathan Cohen described K as “doing her best to assist the court, albeit that she herself does not have medical training, or mental capacity assessment training”, juxtaposing her lack of specialist knowledge with that of the health care professionals who conducted the capacity assessment on 9th December.  Nevertheless, he noted that K had said “if things were explained properly to JK she would be able to understand them.  She doesn’t understand 100% about risk and she sometimes says now I understand, but she can’t hold on to too much information.  She had never spoken to JK about the delivery process.  … Her ability to understand has got much worse, she said she couldn’t even have a 5-minute conversation with JK, couldn’t even ask her what she would want for breakfast.  Her mood has got much worse she said, she has lost trust in people.  Then to me she said … she’s under great pressure at the moment.  …obviously it weighs on her the thought of the loss of her baby.  The pressure simply does not let her concentrate on herself or on  her baby.  She would not listen to anyone on 15th December, the last time she was seen, her ability to sit down and listen to explanation has gone.”

The judge emphasised the familiarity of Dr S, the consultant obstetrician with these type of cases and that she has special responsibility for perinatal mental health.  He addressed the fact that JK had been found to have capacity to determine mode of delivery two years ago in her previous pregnancy, but that the capacity assessment on 9th December 2021 found that she lacked capacity to determine the same.  “She did not appear to be suffering from the effect of drugs at that time and was not intoxicated, or scared.  The problem was more that she simply  lacked the attention span, she couldn’t discuss the risks and benefits for long enough before becoming verbally aggressive and shouting.  …. She is in a very different place….”  

The change was he said attributable to her chronic use of cocaine.  She is a chronic user of drugs and alcohol and that combined with the potential loss of her child simply stops her making any decisions as to her healthcare.”  

Turning to the arguments made by Katie Gollop QC on behalf of JK via the Official Solicitor, he accepted that this problem should have been foreseen.  However, he rejected her position that when/if JK were found a further capacity assessment should be undertaken and that if she were found to have the necessary capacity to determine how to give birth her wishes should be respected.  

In considering the Official Solicitor’s position that there is insufficient evidence that JK now lacks capacity (2 weeks after the assessment), and that it may still be possible to support JK so that she can make her own decision, the judge accepted the Trust’s argument that there is insufficient time for this: the caesarean is scheduled to take place in two days’ time and in any event, nobody knows where JK is.  

Sir Jonathan Cohen dismissed the possibility that JK might now have capacity for the following reasons “I particularly refer to the long term diagnosis … about her cognitive ability and the other aspects of her psychiatric make up [FAS, epilepsy and depression]; I look at her history since January 2019 and the history of erratic behaviour no doubt in large part also due to substance abuse; I look at the assessment of 9th Dec 2021 carried out in what are rightly described as relatively favourable conditions to JK in circumstances when she was neither intoxicated, or scared.  I refer to the attention span deficit which there is no reason to think that there is any likelihood of improvement.  I refer to the evidence read of the visit on the 15th December 2021 by the midwives on the last occasion that she has been seen.  All those factors lead to the clear conclusion that the prospect of capacity being regained is illusionary and becoming ever more so, I say becoming ever more so because the pressure on JK is only going to increase as the date for delivery gets ever nearer.  And I am clear therefore that she lacks capacity.

I regard the prospect of her engaging voluntarily in any capacity assessment as so remote as to be one that the courts simply cannot put into the balance at all.  I therefore conclude that when I look at s.3 MCA that JK is unable to make a decision for herself because s.3(1)(b) she is unable to retain the information relevant to the decision and unable to weigh the information as part of the process of making the decision.”  

Having concluded that JK lacks capacity, Sir Jonathan Cohen went on to consider JK’s best interests.  Where an individual lacks capacity, she must be treated in accordance with her best interests.  The judge said There is no dispute that if I were to make a finding of incapacity, the OS accepts that a caesarean section under general anaesthetic would be the appropriate course to take.” Summarising his assessment that it would be in JK’s best interests for a caesarean to be carried out he said: “JK has a scar on her uterus from her previous caesarean section, there are risks that the scar might rupture from a spontaneous and induced vaginal birth; the baby that she is carrying is a vulnerable child, growth restricted and on the 3rd centile; JK is unlikely to cooperate in a long induction or vaginal birth and she is at the risk of absconding during a vaginal birth; there are risks that analgesia will not be effective on her due to drug abuse; and she is at more risk of perineal trauma due to non-compliance.  If she were to abscond the risk of infection would grow.  And says the obstetrician, the baby is at risk of distress in labour due to growth restriction and there is a high chance in any event that she would need an emergency caesarean.  All of us who do these cases that an emergency caesarean section is the most dangerous thing of all for a mother and her unborn child.  And therefore I come to the clear conclusion that it is in her best interests for a caesarean section to take place.”  

In determining JK’s best interests the court is required to consider her “past and present wishes and feelings” (s.4(6) Mental Capacity Act 2005) and Sir Jonathan Cohen emphasised that JK had previously chosen to deliver via caesarean section, noting that in her current medical conditions the advantages of such a delivery are much greater than they were at the time of the twins’ birth.  He concluded that it “Appears likely, if able to express informed wishes and feelings, that she would consent to the operation.”

Therefore, Sir Jonathan Cohen granted the declarations sought, authorising restraint if necessary for conveying JK to the hospital and during the birth.

Reflections

As Hale LJ recognised in Montgomery v Lanarkshire Health Board [2015] UKSC 11, the way in which one gives birth is an intensely personal decision: indeed Sir Jonathan Cohen echoed this at the start of his judgment.  

However, if the woman is judged to lack the necessary capacity to make this decision, it will be transferred to a third party who has only to consider (but not give effect to) the woman’s wishes and feelings.  As Lady Hale said in Aintree University Hospitals NHS Foundation Trust  v James [2013] UKSC 67 “The purpose of the best interests test is to consider matters from the patient’s point of view. That is not to say that his wishes must prevail, any more than those of a fully capable patient must prevail. We cannot always have what we want.”

 In 2017 the Law Commission recommended that the best interests checklist set out in s.4 Mental Capacity Act 2005 should be amended to ensure that “particular weight is given to the person’s ascertained wishes and feelings when a best interests determination is being made “ (Mental Capacity and Deprivation of Liberty, 2017) .   

In this case, JK lacked a voice.  Whilst the Official Solicitor represents those lacking capacity, her role is to represent JK’s best interests, not her.  Indeed, the Official Solicitor had no personal knowledge of JK and so no direct knowledge of what she would have wanted.  K, her support worker provided a detailed account of K and said that JK would be very able to speak to the judge, that she knows her own mind and is able to take decisions if supported, but at the time of the hearing JK was missing.  She had not been seen by the Official Solicitor and took no part in the proceedings.  The role of the Official Solicitor is to represent P’s best interests, not to act as her advocate representing her views.  Nobody spoke on behalf of JK’s values, wishes, feeling and beliefs  – she, her situation, was discussed by others.  Her own voice was noticeably absent.  

The fact that she had previously decided to be delivered by caesarean does not mean that she would want to deliver in the same way again:  indeed, that was the very situation that Mrs Chowdry found herself in in Rochdale Healthcare NHS Trust v C [1997] 1 FCR 274 where she proclaimed that she would rather die than have another caesarean.  Moreover, it seems to me significant that during her first pregnancy JK trusted the healthcare professionals caring for her.  This pregnancy was very different: at the time of the hearing she had missed multiple ante-natal appointments and it was reported that she did not trust the healthcare professionals caring for her as she thought they would take her baby away.   

In any event, it is impossible to know what JK would have wanted.  Her support worker believed that she would consent, if the risks were explained to her; it was suggested that during the capacity assessment she had at least acquiesced in agreeing to have a caesarean, but the fact that her wishes were a matter of conjecture is deeply regrettable.  

As a side note, it is worth remembering that the best interests’ assessment should focus upon the individual concerned –  that is JK, not her foetus – and to that end the risk to the foetus due to its restricted growth is not relevant to the assessment.  However, in this, as in other cases of court authorised obstetric intervention, the woman’s best interests were linked to the desire to deliver the baby as safely as possible, the judge suggesting that it is likely that if JK had been able to express informed wishes and feelings she would have consented to a caesarean.  

The underlying philosophy of the Mental Capacity Act 2005 is that individuals should be empowered to take decisions for themselves wherever possible, and therefore s. 1(3) Mental Capacity Act 2005 requires that all practical steps be taken to enable the individual to take the decision for herself without success before she is deemed to lack the capacity to decide for herself. 

As a vulnerable woman, it was foreseeable that JK would need to be supported, to be assisted to make a decision.  Such support can be provided, but it takes time, time that is not available two days before the procedure is scheduled to be performed.  

This type of case needs to be identified much earlier in the pregnancy, with appropriate support provided to enable the woman to make her own decision, rather than falling back on what might be considered the normative position, that she would consent to major surgery to ensure the safe delivery of her baby if she were able to do so.

Given the Official Solicitor’s position that the presumption of capacity had not been rebutted, I was disappointed that the court was unwilling to accept the argument that an anticipatory and contingent order be made, requiring JK’s capacity to be re-assessed before the caesarean is performed.  Sir Jonathan Cohen stressed the specialist expertise of Dr S and that the capacity assessment on 9th Dec 2021 was carried out in “what are rightly described as relatively favourable conditions to JK in circumstances when she was neither intoxicated, or scared.”    However, it must be remembered that JK had been delivered to the hospital the previous day by the police for the second time in less than a fortnight.  It is likely that she was very anxious, certainly she was vulnerable and angry, it is difficult to imagine that the situation was conducive to a calm discussion of the relative risks of a vaginal delivery.  

 In NHS Acute Trust, NHS Mental Health Trust v C [2016] EWCOP 17 it was agreed that the patient’s capacity to make decisions and the methods authorised by the court should be actively reviewed: however in this case the court accepted that the presumption of capacity had been rebutted, that JK lacked capacity. 

 In United Lincolnshire Hospitals NHS Trust v CD [2019] EWCOP24 Francis J made an anticipatory, contingent declaration on the basis that a patient with capacity might become incapacitious.  

In the case I have focused on in this blog a similar order could have been made, providing for JK’s capacity to be assessed so that if she were found to have capacity her own decision about mode of delivery would apply.  

Like so many of its predecessors, this case was framed as urgent.  But JK was not due to give birth imminently – she was 36 weeks pregnant and so birth would normally have been expected in around four weeks.  What was imminent was the caesarean that had been scheduled for her in two days’ time.  Evidence was not provided at the hearing that the caesarean was immediately necessary, although the clinical evidence was that it would be dangerous for JK to give birth outside a medical setting, both for herself and the foetus, and that an emergency caesarean would be the most dangerous option of all.  Nevertheless, that an order might be necessary in this case was foreseeable, that JK would need support was foreseeable; the risk of JK disengaging from antenatal care and deciding to deliver in secret, without medical support was all too apparent as long ago as August.  This case should not have been allowed to become the subject of an urgent hearing.  

Indeed, Katie Gollop QC reported that the Official Solicitor is in something approaching a state of despair about pregnancies such as JK’s.  She pointed out that “It is a tragedy that those who most deserve the most skilful, time intensive, patient, relationship-building, multi-disciplinary attention that the NHS can provide find themselves deprived of that consideration because of medical delay.”  

As Lieven J noted in University Hospitals Dorset NHS FT v Miss K [2021] EWCOP 40 It is wholly unacceptable that NHS Trusts routinely put the Official Solicitor in such an impossible situation where she cannot do the job she is instructed to do, and where her role effectively becomes a tick box exercise. This is a waste of resources and wholly unhelpful to P’s best interests.  It is also unfair on the court.”  

At the request of the Official Solicitor, the judge agreed to include a recital to the order recording that the Trust has provided an assurance that the director of governance will be issuing a revised policy and some Mental Capacity Act training to staff in the hope that this might send out a message to other Trusts that there is a need to identify such cases as early as possible and to avoid the recurring situation whereby action is taken too late to facilitate support for the individual and proper representation of their interests.  

This is not a novel suggestion, guidance was issued by Keehan J in NHS Trust & Ors v FG [2014] EWCOP 30emphasising that “Urgent applications … must be limited to those rare and few cases where a genuine medical emergency has arisen and an immediate court order is necessary. I do not consider a failure to plan appropriately and/or a failure to identify a case where an application to the court may be required constitutes a genuine medical emergency.”  It would appear that this message has not yet got through…

As a legal academic it was fascinating to observe the proceedings and to see how such cases are determined, to observer the way in which evidence is presented, how the barristers framed their positions, and how the judge determined the case.  These cases are terribly sad and undeniably hard, but I saw nothing but compassion for JK from all involved and join them in hoping that things went as well as possible for JK and that she is receiving the support she undoubtedly needs.  

Dr Samantha Halliday is Associate Professor in Biolaw at the Centre for Ethics and Law in the Life Sciences at Durham Law School. She tweets @DrSamHalliday


[I] See for example S. Halliday Constructing the Foetus as a Patient: A Comparative Analysis of Compelled Obstetric Intervention; S. Halliday Autonomy and Pregnancy: A comparative analysis of compelled obstetric intervention, 2016, Routledge; S. Halliday, “Court-authorised obstetric intervention: Insight and capacity, a tale of loss” in Childbirth, Vulnerability and Law: Exploring Issues of Violence and Control, 2019, Routledge).  

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