Thank you for being an essential part of this journey and for believing in our mission.
As we mark 40 years of dedicated service to the spinal muscular atrophy (SMA) community, we reflect on our journey and the incredible milestones we've achieved together.
In 1984, a small group of parents founded Families of Spinal Muscular Atrophy (FSMA) with a shared mission: to support one another and promote research into treatments and a cure for SMA. From those humble beginnings, we have grown into Cure SMA, an internationally recognized organization that has devoted over $84 million dollars to SMA research.
This anniversary is not just a celebration of our history; it’s a call to action for the future. We invite you to honor our legacy by making a donation of $40 in recognition of our 40 years of progress. Your gift will directly support ongoing research, advocacy efforts, and vital programs that benefit the SMA community.
Over the past four decades, your support has enabled us to accomplish remarkable feats: