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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.

ALS Association

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 ALS patients and their families. Newsletter 3 times/yr. Provides chapter development guidelines.
Write:
A.L.S. Association
27001 Agoura Road, Suite 150
Calabasas Hills, CA 91301
Voice: 1-800-782-4747 or 818-880-9007 information and referral (Mon.-Fri., 7:30am-4pm PST)
Fax: 818-880-9006
Website: http://www.alsa.org
E-mail: alsinfo@alsa-national.org
Verified: 2/12/2013

ALS Support Forum

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.
Website: http://www.alsforums.com
Verified: 2/14/2013

WebMD Medical Reference from the American Self-Help Clearinghouse

Last Updated: February 25, 2014
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.This information is not intended to replace the advice of a doctor. Healthwise disclaims any liability for the decisions you make based on this information.   

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