The Gwendolyn Strong Foundation (GSF) was born out of Bill and Victoria Strong’s firsthand experience with their precious daughter, Gwendolyn. Gwendolyn was born perfectly healthy in October 2007, but was diagnosed with the terminal disease Spinal Muscular Atrophy (SMA) Type I at 6-months-old.
As witnesses to the degenerative cruelty of SMA, Bill and Victoria are personally and passionately dedicated to leaving no stone unturned in raising awareness about and funding research for SMA and supporting families who are impacted by SMA and other life-altering diseases.
Here is where you come in. Help GSF win $20K for research for SMA by voting for the next two days. That's it. It's quick and free!
1. VOTE — TODAY and TOMORROW by going to www.VoteForSMA.com and voting for the Gwendolyn Strong Foundation (GSF)!
2. SHARE — Help multiply your one vote! Forward this email to at least 25 contacts, post http://VoteForSMA.com on Facebook, tweet about it, blog about it, spread the word!
3. Lastly, you can vote once per day on each of your internet devices. So vote on your desktop, vote on your laptop, vote on your ipad and phone, TODAY and TOMORROW.
Thank you for your vote and support!