The ALS Association (ALSA) is the only national not-for-profit voluntary health organization dedicated solely to the fight against ALS, or Amyotrophic Lateral Sclerosis (often called Lou Gehrig's disease). The mission of The ALS Association is to find a cure for and improve living with ALS.
This website is sponsored by the World Federation of Neurology to link researchers and clinicians worldwide with the goal of finding effective treatment and a cure for ALS.
The Les Turner Amyotrophic Lateral Sclerosis Foundation is the nation's largest, independent ALS organization devoted to raising money for research, patient services and educational materials and to maintaining quality of life for every person with ALS.
Project A.L.S. 511 Avenue of the Americas PMB #341 NYC 10011 tel: 800-603-0270 fax: 212-337-9915 email: projectals@aol.com Copyright Project A.L.S. 2001 ...
The ALS March of Faces is a patient/caregiver governed and operated non-profit organization, dedicated to heightening public awareness of ALS, and advocating on issues that concern and/or benefit PALS (People with ALS).
Information and news for those with ALS or Lou Gehrig's Disease - news, research, treatments, chapter events, advocacy, support groups, more.
The ALS Association (ALSA) is the only national organization dedicated solely to the fight against ALS. .
Voice for Joanie is a totally volunteer organization in southewestern Connecticut which provides computers and voice technology for people living with ALS(Lou Gehrig's disease) ...
The ALS Massachusetts Chapter is a multi-faceted grass-roots organization that carries out ALSA's mission and strategic goals at the community level. The chapter - with supporting services from the National Office - actively pursues The Association's goals. Primarily, ALS MA Chapter exist to serve people with ALS, their families and caregivers.
Home | Facts | Services | Objectives | Newsletter | Other Services | Membership | Donations | Diary | Contact | Mission Statement - To improve quality of life for people living with MND. Home Facts Services Objectives Newsletter Other Services Membership Donations Diary Contact MNDA Carer's Sheets ***** PDF Files for download: Monthly Newsletter Membership Form Donation Form Download Top of Page ...
Local chapter of The ALS Association, serving DC, MD, VA. Patient services, support groups, equipment loans, clinic contacts and information about ALS (Lou Gehrig's disease). Phone: 202-331-1448.
The ALS Family Charitable Foundation Homepage. Home of the Cliff Walk ...
