To create a global community free of alcohol-exposed pregnancies and a society supportive of individuals already living with Fetal Alcohol Spectrum Disorders (FASD). Learn More
National Organization for Fetal Alcohol Syndrome (a 501(c)(3) nonprofit)
Updated: The cause has raised $100.
I was diagnosed at the age of 24yrs old and before that day I knew I was different from all my friends but didn't know why or how.
helloo everyone! i recently started doing research on Fetal Alcohol Syndrome. currently im trying to find numerous organizations on FAS. if you know of any, could you please email me names or web sites? thanks in advance!
Updagte of my post on March 13:
It turns out Mareena has 2 mildly dilated ventricles in her brain ........ anyone else have this happen?
Updated: The cause has raised $50.
Thank you for putting this on Facebook! I found out that I had FASD as a young teenager and I appreciate you doing this!
It is important to get information out there to the public. Often this goes so hidden. My parents adopted two boys from Russia..both who suffer from this. The oldest has had several difficult complications. I wish there was a way to help with the research aspect, like from an educational standpoint. I think that once the children are here, there is not enough done to help the parents or adoptive parents cope with this, and all the complications that arrise as a direct result of this. One day I dream of having a school for children like this, where they can obtain actual practical skills that will help them make accomidations for the many issues that can arrise.
On behalf of NOFAS, I would like to thank all of you for your continued support and generous donations!