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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.
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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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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.
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Information and news for those with ALS or Lou Gehrig's Disease - news, research, treatments, chapter events, advocacy, support groups, patient services.
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Provides ALS information for patients, caregivers, and professionals. Includes Canadian statistics.
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Helps spread awareness and raise funds for Amytrophic Lateral Schlerosis, also known as ALS and lou gehrig's disease. Includes research news and events.
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Founded by persons with ALS, this site is the on-line information site for ALS research fundraiser. Find the history, events, news and donate.
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Support for ALS patients, families and care givers in the DC/MD/VA region: information, support groups, equipment loans, and resources.
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Information on the annual walk, photos from the yearly walks, and details about ALS.
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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.
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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.
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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.
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