Support for ALS patients, families and care givers in the DC/MD/VA region: information, support groups, equipment loans, and resources.
The ALS Association Connecticut Chapter is a not-for-profit voluntary health organization dedicated to fight against ALS through research, patient and family services, and information dissemination.
Information and news for those with ALS or Lou Gehrig's Disease - news, research, treatments, chapter events, advocacy, support groups, patient services.
Dedicated to raising public awareness of ALS and advocating on issues that will benefit PALS (People with ALS) and their families, through self-empowerment resources.
Helps spread awareness and raise funds for Amytrophic Lateral Schlerosis, also known as ALS and lou gehrig's disease. Includes research news and events.
Supports ALS research and assists patients with the high costs associated with treating and living with their illness, and raises awareness of the needs of ALS patients. Find disease information and how you can help.
Information on the annual walk, photos from the yearly walks, and details about ALS.
Seeks to find the cause of, and a cure for, ALS and improve the quality of life for people living with this disease. Includes the chapter services and information.
Working to help Texas families touched by Amyotrophic Lateral Sclerosis, also known as Lou Gehrig's disease, by providing support, information, awareness, education, advocacy and hope through research.
Non-profit organization dedicated to increasing public awareness of Amyotrophic Lateral Sclerosis (ALS, Lou Gehrig's Disease)and improving quality of life for the ALS community. Find disease information, events and service details.
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