The ALS Association St. Louis Regional Chapter
About Our Chapter
The St. Louis Regional Chapter was founded in 1984 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 St. Louis Regional Chapter) operates under a shared mission: to help people living with Amyotrophic Lateral Sclerosis and to leave no stone unturned in search for the cure.
We work together to accomplish our mission. The St. Louis Regional 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.
History of The ALS Association St. Louis Regional Chapter
The ALS Association, St. Louis Regional Chapter had its
beginnings in December 1983. That year, a local businessperson, Ronald
Flowers was diagnosed with ALS. When neither he nor his business
partner, R. Scott Davis was able to locate adequate information
regarding the disease. A business trip to New York resulted in a list of
over 200 area individuals who had contacted the NY office for