ALS Association Nevada Chapter pleads for stolen items to be returned
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ALS is 100% fatal and there is no cure…yet. People living with living ALS need your help now—for care, for research, for hope. Give today to help make ALS livable for everyone, everywhere, until there is a cure. | The ALS Association
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Tim Green's ALS diagnosis gives hope to ALS Association of Upstate NY
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Help change the future of ALS. Join our community committed in the fight to treat, cure and care for people with ALS. | The ALS Association
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We’re on a mission to not only discover treatments and a cure for ALS, but also to advocate for and empower people affected by ALS. Join us on our mission to help those living with ALS and their families - give now to make a direct impact. | The ALS Association
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An ALS diagnosis is life changing. Steve from Massachusetts is an ALS advocate and is sharing his experience of what it's like to live with the disease. | The ALS Association
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Join us tomorrow at 8 p.m. EST for a new episode of ALS Matters, an ALS Association produced podcast hosted by Cory Mosley. This week, Cory sits down with Lee Wilson, who is a former ALS caregiver and was recently diagnosed with a genetic form of ALS herself. Together, the two discuss the realities of caregiving and living with different types of genetic ALS from both sides of the experience. Tune in tomorrow night to be part of the conversation! | The ALS Association
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