Christina
I've got a 3 year old boy with fragile x and a sister, who although she has the full mutation is unaffected. I was lucky and got an early diagnosis and my son has been receiving speech therapy, occupational therapy, physio and Portage from when he was about 18 months. He now attends nursery with 1-1 support and is doing brilliantly. Its not all doom and gloom just a lot of hard work.