Thanks for that link.
Once again, they are talking absolute nonsense. From the abstract:
For the purposes of this abstract, we are defining gender incongruence as characterised by a marked and persistent incongruence between an individual’s experienced gender and assigned sex.
Without a definition of what constitutes "an individual’s experienced gender", this is completely meaningless.
The Plain English Summary is no better:
Gender incongruence is when a person feels their gender identity differs from the sex that they were given at birth. Some people with gender incongruence want their bodies to be more like their gender identity.
What is a gender identity? Without a definition this too is meaningless. And saying that children are given a sex at birth? In a medical document?
In the recent past, doctors sometimes used medicines to stop puberty....The idea was that GnRHa might give young people time to think about their identity without worrying about their bodies changing during puberty.
Why? Wouldn't going through puberty enable them to establish their identity as their brains mature? Have they not considered that keeping adolescents in an immature childlike state means that they are still going to be making their decisions as children?
And why is it so important to 'think about their identity'? They can't change sex and children don't understand what it will be like to be an adult man or woman. Children don't have an adult understanding of fertility or sexual function which is what these drugs interfere with.
Children think it's all about stereotypes. Adults are encouraging them to think their bodies need modifying because of their preferences. Doctors want to do more unethical experiments on children.
However, we don’t know if GnRHa are safe and helpful for young people with gender incongruence.
On their own admission, these drugs might not be helpful and they don't know if they're safe, but the proposal is to experiment on even more children anyway.
We also do not know enough about how identity and feelings develop for young people with gender incongruence as they grow up and what treatment is helpful.
Why not? The Tavistock has already done one experiment and failed to keep proper records or follow-ups. Is this going to be any different? Why not try to track down the missing information from the previous experiment instead? I'm sure they could do that for less than £10m and it would avoid more harm being done to even more children.