The ALS Association is the only national non-profit organization fighting Lou Gehrig’s Disease on every front. By leading the way in global research, providing assistance for people with ALS through a nationwide network of chapters, coordinating multidisciplinary care through Certified Treatment Centers of Excellence, and fostering government partnerships, The Association
builds hope and enhances quality of life while aggressively searching for new treatments and a cure.
builds hope and enhances quality of life while aggressively searching for new treatments and a cure.
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