By Rhiannon Snaith, 20 September 2023 Indi Gregory is a six-month-old baby girl who has mitochondrial disease, a rare and incurable genetic condition that drains energy from the body’s cells. She also has a hole in her heart, and soon after her birth underwent operations on her bowel, and her brain to drain fluid. DespiteContinue reading “Access challenges in the Family Court: On not being allowed to watch the Indi Gregory hearing “
Promoting Open Justice in the Court of Protection 