60 some odd posts and no one mentions Prader-Willi syndrome, which is CLEARLY not the fault of the parents.
I would love to see what Social Services offered in assistance before resorting to the drastic measure of removing the child. For example, did the child get a FULL medical work-up to rule out some sort of medical/inherited disorder? Were the parents assisted with the help of a nutritionist? Were the parents given clear guidelines? How often did Social Services visit/call the parents? Was it once a month or once every 12 months? A lot of questions remain unanswered in my book.