Thank you for supporting Angie's Hope - an organization that has been working to raise funds and awareness towards a cure for Spinal Muscular Atrophy (SMA) for the past 13 years. 100% of the proceeds from this fundraiser will go to Cure SMA, a non-profit doing research for a cure for SMA. Any donation, big or small, is greatly appreciated!

This year, in light of the COVID-19 pandemic, Angie's Hope sold t-shirts to spread the message of protecting vulnerable populations. Cure SMA has been supporting SMA families during the COVID-19 crisis by providing care packages, keeping patients up to date on best practices as a vulnerable population, and hosting/planning virtual webinars and conferences. We want to support these efforts, as well as ongoing research on SMA. While the deadline for t-shirt orders has passed, we appreciate your continued support and donations!

Cure SMA is dedicated to the treatment and cure of Spinal Muscular Atrophy (SMA)—a disease that takes away a person’s ability to walk, eat, or breathe. 8 million Americans carry the gene that causes SMA , and it is the number one genetic cause of death for infants.

Since 1984, we’ve directed and invested in comprehensive research that has shaped the scientific community’s understanding of SMA. We are currently on the verge of breakthroughs in treatment  that will strengthen our children’s bodies, extend life, and lead to a cure.

We have deep expertise in every aspect of SMA—from the day-to-day realities to the nuances of care options—and until we have a cure, we’ll do everything we can to support children and families affected by the disease.

Learn more about how you can help us reach a treatment and cure at www.cureSMA.org.