I have found that it's almost impossible to find decent information. And no one knows about it. I was reading a book about a foster family in the UK and how the foster child was diagnosed with dyspraxia like it was no big deal and now I know why. They actually know what it is there.

I sent this link to DS's IEP manager and teacher. The teacher said she had researched it already but I think she is a first. My experience is that no one has a clue what I'm talking about, even special ed teachers. The article talks about symptoms in adults but it applies to kids as well (IMO)

http://www.dyspraxiafoundation.org.uk/dyspraxia-adults/

Irena, are they looking for more kids for their study or is it just kids in a certain geographic area?
DS has already had 2 MRIs and all that shows up is a possible Chiari I malformation.