This case is about trying to draw a near-invisible line in the sand about what healthcare can and should be offered to young people and what should be denied. This is an arbitrary distinction: a child can be informed of any consequences and be expected to fully consent to any other life-saving treatment where possible, but we’re expected to believe this is magically untrue of treatment around gender dysphoria. At the heart of this case lies a mission to run roughshod over the legal precedent of Gillick competence.
With waiting times creeping into the years, gatekeeping of options for young people with gender dysphoria – whether intentional or not – is already causing acute distress to a population who deserve and demand robust and proper care. If our response to young people in distress is to compound these feelings, we are failing them. These people know themselves, know their bodies and know what it right for them individually. Where there exists Gillick competence, they consent in the fullest terms, after several consultations with the NHS’s only service for them, to the treatment which is right for them. Some young trans and non-binary people may choose to take puberty blockers until a time where they can safely and legally access medication which may help them feel more congruent in their gender.
Either a young person can consent to their medical treatment when presented with all known information about that treatment, or they cannot. These are highly individualised conversations which cannot be reduced to simple talking points or a reductive rolling back of enshrined rights through the courts. If we were, as a society, to allow for children to be stripped of their agency when choosing what’s right for them, we set off a dangerous domino effect of others deciding what is and isn’t right for all of us. If this case is successful in removing Mrs A’s child’s right to consent to medical treatment, the line in the sand is removed: A loss to trans youth is a loss to all.