The ALS Association is a non-profit organization addressing the needs of persons with Amyotrophic Lateral Sclerosis (ALS) (more commonly known as "Lou Gehrig's Disease").
The following programs and services are provided through our organization:
- ALS patients and families are provided information and resources about ALS as requested.
- Support Groups have been established and maintained providing peer and family support in all three states.
- Adaptive devices and equipment can be provided at no cost through our loan closets, located in the three states.
- Increased public awareness in our communities about ALS through educational talks by knowledgeable staff.
- Supporting ALS advocacy efforts.
- Informing patients and families about clinical trial opportunities.