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Hope Loves Company is an American 501(c)(3) non-profit organization founded in 2007 that focuses upon providing resources and emotional support to the children and grandchildren of amyotrophic lateral sclerosis (ALS) patients. It is the sole non-profit in the United States with the purpose of providing support and resources to families affected ...
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 ...
A New Era of Support and Engagement for ALS Patients One of the most exciting new features of the app is the introduction of Pathfinders, a service that connects individuals newly diagnosed with ALS to experienced guides from the community. Pathfinders are here to help patients navigate the complexities of their diagnosis and offer guidance and ...
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 ...
ALS patients experience severe symptoms as the fatal, rare disease progresses. Patients shared how they're fighting for better treatment to be available faster.
Jan. 28—A Spokane clinic designed for patients with amyotrophic lateral sclerosis, or Lou Gehrig's disease, has received designation as a certified treatment center of excellence. The ALS clinic ...
It came on Sept. 26, 2019 — amyotrophic lateral sclerosis (ALS), or Lou Gehrig's disease. ALS causes progressive ... Care on multiple fronts: ALS patients see variety of specialists in one-stop ...
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]
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