At Cure SMA, everything from our funding priorities to our day-to-day decisions are driven by our vision, mission, and values.
Our Vision & Mission
Cure SMA leads the way to a world without spinal muscular atrophy (SMA), 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 individuals with SMA and their families the support they need for today.
Our commitment to a 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 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, individuals with SMA, and their families. Together, we are—and always will be—stronger than SMA.
There is no “right way” to live with a disease like SMA. Every person’s experience is different, and it’s every person’s right to decide what SMA means for them.
Thanks to the Cure SMA community, no person is ever alone in facing this disease. We offer unconditional support to people with SMA and communicate openly and honestly, giving them clear and accurate information.
Our work is not done until we have a cure, and we’ll remain strong in our fight no matter what challenges come our way.