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Thank you for betting against ALS at our first-ever Virtual All in for ALS Casino Night, hosted by our Young ProfessionALS Group! The evening was filled with laughter, inspiration, fun and, most importantly, support for people living with ALS.
Because of your support, we raised over $16,000 (and counting)! Don't forget, online donations are still being accepted until December 31, 2020!
Thank You to Our Sponsors!
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For fast updates on the event, follow the Les Turner ALS Foundation's Young Professionals Group on Facebook
To get involved in more YPG events, visit lesturnerals.org/get-involved/young-professionals-group
About the Les Turner ALS Foundation
Founded in 1977, the Les Turner ALS Foundation is one of the longest-serving independent ALS groups in the country. For over 40 years, we have taken an individualized approach to ensure each person living with the disease receives the best quality of care and access to the most promising therapies. We treat each person like family, supporting them every step of the way, and provide their loved ones with answers and encouragement.
About ALS
Amyotrophic lateral sclerosis (ALS) is a terminal, progressive disease that causes muscle weakness, difficulty speaking and swallowing and, generally, complete paralysis. ALS can, in some cases, also cause changes in intellectual function, mood, behavior or personality. While technically considered a "rare disease," experts predict an individual's lifetime risk of acquiring ALS is about 1 in 300, by the age of 85. There is no cure, yet.