Cure SMA is dedicated to the treatment and cure of spinal muscular atrophy (SMA), the number one genetic cause of death for infants. We fund groundbreaking research and provide families the support they need for today.
Our Vision & Mission
Cure SMA leads the way to a world without spinal muscular atrophy, the number one genetic cause of death for infants. We fund and direct comprehensive research that drives breakthroughs in treatment and care, and we provide families the support they need for today.
Our commitment to a treatment and cure is not just about seeking solutions—it’s also about creating them. We’re working with some of today’s sharpest minds to advance a diversity of approaches and champion the most promising discoveries and methods.
As relentlessly as we pursue a treatment and cure, we are also strategic. We know the fastest way to a future without SMA is to take a comprehensive, unbiased approach to research and maintain a balance of optimism and realism.
Our community is everything to us. We would not have made it this far in our fight without the invaluable contributions of our researchers, doctors, and families. Together, we are—and always will be—stronger than SMA.
PO Box 268122
Weston, FL 33326
Jennifer Miller Smith, president
Patti Kirner, treasurer
Fiorenna Fuentes, committee member
National Contact Information:
If you have a general question or your question isn’t covered below, we are happy to help connect you with the right person. Call our national office at 800.886.1762 or email firstname.lastname@example.org and let us know how we can help.
Our mailing address is:
925 Busse Rd
Elk Grove Village, IL, 60007