@fighterpilots, thanks for tagging me and I’m more than happy to continue the discussion, even if the OP has left the room!
Yes, of course, my daughter was seen - following her appointment with her properly credentialed school psychotherapist- by appropriately qualified (and separate teams) who made the separate diagnoses. Interestingly, all of the practitioners involved worked jointly for the NHS/CAMHS and private organisations.
We were fortunate that my DD’s school funded the assessments so we could bypass the multiple-years waiting lists for our local CAMHS service.
I do agree with you that there is a strong overlap between the ‘symptoms’ of developmental trauma and those of ASD (actually, the NHS are now referring to it as ASC as it is a ‘condition’ rather than a ‘disorder’) but there is strong heritability for both ADHD and ASC (about 75 per cent for the former and between 40 and 80 per cent for the latter). Given that adopters don’t have access to the medical records of birth families, but we are told (usually) about substance abuse and chaotic lives, there is a prevailing school of thought that birth parents may self-medicate with drugs and alcohol to manage mental health issues and neurodiverse conditions such as ADHD. Both of my DD1’s birth parents were addicted to drugs and alcohol - I have written here previously that she is registered blind due to her in utero experiences - and her birth father died in prison (all of this information is known and owned by my DD). Neither of her birth parents succeeded at school, nor did they ever manage employment or ‘normal’ lives - and I can’t help but wonder if that was because they were undiagnosed for the conditions they had and subsequently passed on to their birth children?
I always seem to end up as the bad fairy at the celebration on the adoption board here (!), but I have always found it helpful to listen to and read of the experiences of those who are further ahead of me in their adoption journeys (I started the process 15 years ago now and DD1 was placed with me 13+ years ago).
I think the point I mostly want to make is that we all end up being the experts on our own individual children. I truly would not medicate my child unnecessarily but the difference in her since starting ADHD medication is remarkable - she masked for so long because she is academically able but now the pressure is on in Y9, she started to unravel. I/she have found it helpful to have proper diagnoses and to begin to try to understand the workings of her very complex brain, rather than everything being ‘because adoption’. I do agree that her pre-natal (horrible) experiences and her removal at birth, plus her two foster placements before she was a month old, and her placement with me are all factors in how she relates to the world. I am always mindful to remind every single adult working with my child that she is complex due to her sudden and unexpected sight loss at the age of 11, her birth history, her adoptive status and now her ADHD/ASC/PDA diagnoses.
In short, I believe it’s lazy and short-sighted to attribute every single difficulty in the life of an adoptive child to ‘developmental trauma’ and then offer adoptive parents a plethora of panaceas such as parenting courses or NVR training; sometimes, there are genuine medical reasons why children behave in the ways they do. And, in the same way my mother takes medication for her severe arthritis, I will continue to opt for medical interventions to help my DD1 control her diagnosed conditions. And if the net result is a more harmonious family life for all of us, then, for me, as a single adoptive parent of two, that’s a win-win.