Foundation Advocating for COVID-19 Vaccination Prioritization for Individuals with ALS

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As we turn the calendar to 2021, the Les Turner ALS Foundation is taking proactive steps to help ensure that those living with neuromuscular disease, including ALS, are given priority access to COVID-19 vaccines and treatments. On Wednesday, January 6, Illinois …

Advocacy Announcement: ALS Disability Insurance Access Act

lesturner Advocacy, Foundation Blog, Home Page

Foundation Blog: Advocacy The Les Turner ALS Foundation has joined with several other national ALS patient advocacy organizations (ALS Association, I AM ALS, Muscular Dystrophy Association and Team Gleason) in a letter to U.S. House of Representatives’ leadership requesting that …