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Why We Fundraise

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. There’s great reason for hope. Thanks to the dedication of our community and the ingenuity of our researchers, we now 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.

We are experts in every aspect of this disease—from what it means for families to the genetics and the nuances of treatment options—and we offer unconditional support.

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

If you have any questions or need any assistance please email us at fundraising@curesma.org or call at (800) 886-1762.

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