WS Watch
I have been tracking Williams Syndrome (a genetic condition my son was born with) on the web for a long time. It seems like more information is becoming known all the time.
So, I decided to funnel that info on to a dedicated blog that I have named WS Watch - Updates from the Web on Williams Syndrome. (That is a pretty original name, eh?)
Anyway, if you have any interest in WS I have posted a few helpful (I think) links to articles and other sources of information. For more of my personal view on WS as a parent, you can search this blog (kerux noemata) by the "Williams Syndrome" label.
[Update: I changed the name. It is now called Williams Syndrome Web Watch: Resources and updates from the Web on Williams Syndrome]
what, no link?
ReplyDeleteignore that, found it. i learned lots!
ReplyDeleteWell done my friend. Keep it going.
ReplyDeleteCool.
ReplyDeleteMy younger sister-in-law has WS and my wife will be most appreciative of your research and resources.
Thank you.
ReplyDeleteMy daughter has WS.