That's great news Eidsvold!
Jimjams yes I did read that article, and thought it very depressing, especially after watching the programme about Oxfordshire social services a few weeks ago. My sister lived in wandsworth when her ds was born 14 years ago, and he has downs syndrome. She said it was exactly the same then as it is now, and if she hadn't been lucky enough to afford a good lawyer she wouldn't have got anything either.
I just hope the services we are getting now stay as good. The only thing I can grumble about is the length of time social services are taking to get ds a bathing seat. We were referred in October, had a home assessment in December, got sent an incorrect seat in January, had to wait 5 weeks for it to be collected, got sent a highchair instead last week, and am now waiting for that to be collected, as well as praying for the seemingly very rare bath seat. It has had me ringing up getting cross but they seem a bit incapable imo. If it isn't here by next week I am going higher up to complain. It's impossible to wash ds without 2 adults present at the moment and it's getting beyond a joke. Still only 1 thing to moan about can't be that bad can it?
Also took ds to the special needs dental clinic today for the first time,and was very impressed. The dentist had a (now grown) child with cp herself, and was completely understanding of him and his ways. She said the first few times he visits will be just playing until he gets used to her and will let her touch him. Managed to get a peek at his teeth though and she said they were good, so a house point to me .