Our son appears to have developed what used to be known as Regressive Autism (now PDD-NOS) very, very gradually, when he was around 2 years old. As of summer 2021 he is 6.
This site is just some notes, made by me, his dad, on what we have been doing to help him and get him back to being able to see us again, play with toys and, one day, speak to us. As of late 2018 he sees us mostly (many days with good eye contact) and can concentrate on toys to play with them for a while again. It is wonderful to see. We wish so much to hear him speak again.
It's a long road but I feel very strongly that there is "a road" to follow whereas most standard medical opinion is that this is a psychological disorder and has no treatment. Just writing "has no treatment" makes me pretty angry - there are thousands of parents who have made a huge difference to their childrens' conditions via "biomedical" interventions and also thousands of enlightened doctors who have helped them.
Wait. Who am I? Well see my page on another little site I have: Who Is This Guy?
This site is purely a personal site and nothing here is meant as advice. Do your own research, make your own decisions.