ALS (Lou Gehrig's Disease)
This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site.
National. 39 chapters and support groups. Founded 1985. Dedicated to finding the cause, prevention and cure of amyotrophic lateral sclerosis. Aims to enhance the quality of life for people with ALS and their families. Newsletter 3 times/yr. Provides chapter development guidelines.
The ALS Association
1275 K Street NW, Ste 250
Washington, DC 20005
Voice: 1-800-782-4747 or 818-880-9007 for non-medical information and referral
Online. Provides a free community of support for anyone directly or indirectly affected by ALS (Lou Gehrig's disease) and MND (motor neuron disease) including caregiver support.
Online. 550+ members. Support, information and sharing of experiences for persons with amyotrophic lateral sclerosis (Lou Gehrig's disease) and motor neuron diseases, their families and friends. Also includes primary lateral sclerosis, progressive muscular atrophy and multifocal motor neuropathy.