Hi all,
We've recently been approved for adoption and are currently getting to grips with the challenges of matching and linkmaker.
We have said that, for us personally, we do not think we would be prepared to adopt a child with diagnosed FASD but we are very taken by a little girl, on linkmaker, who is just due to turn three, whose mother drank heavily during pregnancy.
The child has none of the facial features or delayed growth usually associated with FASD. She is also hitting all her development milestones, and is bright by all accounts.
We know that FASD Is often diagnosed later in life, we also know it to a spectrum of presentations, but we are finding it difficult to find any clinical information or research or any advice that would allow us to understand the risks.
We attempted to open a discussion with the SW but they have declined as our profile advised we would not consider a child with FASD.
To a lay person, it just seems that if a 3 year old child who is under review and assessment for presentation of FASD has none of the markers then the risk of FASD and, in particular, the risks of the more severe forms of FASD are likely to be low and we would have at least wanted to know more information to be able to understand that risk fully.
if there is any advice, or information sources anyone can direct us to, Then it would be hugely appreciated
Thanks so much in advance,