2019 Dallas Walk-n-Roll
Welcome to My Personal Page
Please help my family support the Troxell family. Their sweet little boy Brock is such a bright spot in life. I'm supporting Cure SMA because spinal muscular atrophy is the number one genetic cause of death for infants, and approximately 1 in every 50 individuals is a genetic carrier for SMA. But there's great reason for hope. We know what causes SMA and what we need to do to develop effective treatments.
Thanks to dedication of our community and the ingenuity of our researchers, we know we have the first-ever approved treatment that targets the underlying genetics of SMA. But our work is not done. We know what we need to do to develop and deliver effective therapies. And we're on the verge of further breakthroughs that will continue to change the course of SMA for everyone affected - from infants to adults - and eventually lead to a cure.
I've chosen Cure SMA because they are uniquely positioned to direct funds to where they can make the greatest difference as quickly as possible. They've already invested $70 million in research and have funded half of all the ongoing new drug programs for SMA.
Cure SMA is an irreplaceable resource for famlies facing SMA. They also provide vital support for nearly 4,000 families annually through informational packets, newly diagnosed care packages, local Cure SMA Summit of Strength programs, Annual SMA Conference, and equipment.
To support me, just click the donate button and follow the steps!
Thank you again for your gift to support my efforts to fund vital research and family support programs for those affected by SMA.