Foundation to Honor Robert Ives and Steve Gleason at Virtual Hope Through Caring Gala

lesturner Home Page, Press Releases

Both Men Continually Help Raise Funds and Awareness, Advocate for Change While on their Own ALS Journey The Les Turner ALS Foundation will host its 34th Annual Hope Through Caring Gala on Saturday, March 20, bringing together supporters for an elegant …

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 …