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The
Nicholas Woods Friedreichs Ataxia Foundation
is a nonprofit organization dedicated to the research and
aid of those with a very rare disease called Friedreichs Ataxia. The
foundation was inspired by Nicholas Woods, who was diagnosed with
Friedreichs Ataxia in 1996 at the age of ten, and was created out
of the love of his godmother, mother & father and a few caring
community members.
Our goal is to improve the quality and length of life for those diagnosed
with Friedreich's Ataxia, to help provide treatments that eliminate
its symptoms, and to assist the research that will finally find a
cure. We hope to help educate society about this life-shortening,
incurable disease, and bring an awareness that will get the public
involved in helping to find a cure.
Thank you for your support. |
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