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The ALS Association is an American nonprofit organization that funds global amyotrophic lateral sclerosis (ALS) research, provides care services and programs to people affected by ALS through its nationwide network of clinical care centers, and works with ALS advocates around the country for state and federal policies that serve people living with amyotrophic lateral sclerosis (ALS), also ...
We invite everyone in the ALS community, from newly diagnosed individuals to long-term patients and caregivers, to explore the new features and benefits of this comprehensive app. About EverythingALS EverythingALS is committed to accelerating the discovery of new treatments and a cure for ALS through innovative research and community engagement ...
PatientsLikeMe launched its first online community for ALS patients in 2006. [7] From there, the company began adding other communities for other life-changing conditions, including multiple sclerosis (MS), Parkinson's disease, fibromyalgia, HIV, chronic fatigue syndrome, mood disorders, epilepsy, [8] organ transplantation, progressive supranuclear palsy, multiple system atrophy, and Devic's ...
The Les Turner ALS Foundation is a non-profit organization based in Chicago that provides amyotrophic lateral sclerosis (ALS) patient services; supports events, education and awareness about ALS; and funds ALS research. [2] Since it was founded, it has raised over $64 million. [3]
ALS patients experience severe symptoms as the fatal, rare disease progresses. Patients shared how they're fighting for better treatment to be available faster.
Navigating your way through difficult legal issues such as long-term care, estate planning, or social security benefits, as an aging American without adequate support is an overwhelming and...
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