About Our Chapter
The South Carolina Chapter was founded in February 2006 to serve the needs of those living with Amyotrophic Lateral Sclerosis and their caregivers.
The ALS Association is the only national not-for-profit health organization dedicated solely to the fight against ALS. ALSA covers all the bases — research, patient and community services, public education, and advocacy — in providing help and hope to those facing the disease.
The ALS Association (National Office and the South Carolina Chapter) operates under a shared mission: to lead the fight to cure and treat ALS through global, cutting-edge research, and to empower people with Lou Gehrig’s disease and their families to live fuller lives by providing them with compassionate care and support.
We work together to accomplish our mission. The South Carolina Chapter focuses primarily on helping local patients and families live with ALS while the National Office focuses primarily on research and advocacy. The Chapter supports the National Office through revenue sharing and research contributions. The National Office supports the Chapters by providing up-to-date information and materials.
Our accomplishments are made possible by the generosity of others. From the smallest donation to the largest gift, donors touch the ALS community with hope for the future.
We gratefully appreciate the support of the following Foundations for their support of our Care Services programs to improve the lives of people with ALS and their families in SC.
SC State Covid Relief Fund
Dabo's All In Team Foundation
Daniel Island Foundation
Bank of American Trust
Elizabeth Calvin Bonner Foundation