Gwendolyn Strong Foundation

The Gwendolyn Strong Foundation (theGSF) is proud to introduce "Say Hi! AAC". A first-of-its-kind augmentative and alternative communication (AAC) ...

Join Team GSF. Push your physical strength to the limits to help conquer a disease that robs children of theirs. Run, bike, swim, climb... whether ...

March 31, 2008, the day we received Gwendolyn's SMA diagnosis; a degenerative incurable, untreatable terminal illness.

36 Months = 3 Years! A 3rd birthday is a day we thought Gwendolyn would never get to see. Gwendolyn has SMA Type 1 (Spinal Muscular Atrophy), the #...

Gwendolyn is 4 and we are so happy!

Ossining High School's Spirit Week fundraiser for the Gwendolyn Strong Foundation

We were honored to be invited to be part of the MDA telethon in September 2010 -- raising much needed funding and awareness for SMA and the MDA. Th...

This is SMA. Spinal Muscular Atrophy (SMA) kills more young children than any other inherited disease. There is currently no treatment or cure. Res...

Owen_3months_hand

As witnesses to the degenerative cruelty of Spinal Muscular Atrophy (SMA), the leading genetic killer of young children, it is the personal and pas...

SMA - Spinal Muscular Atrophy - kills more babies than any other genetic disease. SMA is currently a death sentence. But, there is enormous HOPE! R...