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 …

September 2020 Foundation eNews

lesturner Foundation eNews, Home Page, Research & The Les Turner ALS Center, Support Services

Join our 10th Annual Les Turner Symposium on ALS Registration is now open for our 10th Annual Symposium, hosted by our own Les Turner ALS Center at Northwestern Medicine. This year’s event will be held virtually on Nov, 9, and …

August 2020 Events eNews

lesturner Advocacy, Events eNews, Home Page, Research & The Les Turner ALS Center

$20,000 Triple Your Impact Challenge We’re kicking this Events eNews off with a new ALS Walk for Life Team Challenge! Starting today, the first 10 teams to register, raise $1,000 AND recruit 10 walkers will receive a $3 to $1 match ($2,000 …

August 2020 Foundation eNews

lesturner Advocacy, Foundation eNews, Home Page, Research & The Les Turner ALS Center, Support Services

New and Improved Clinical Trials Webpage While it may feel like much in life is on pause at the moment, there is exciting news in the ALS clinical trials and studies space, including information on the upcoming HEALEY ALS Platform …

Introducing the First-Ever ALS Platform Trial

lesturner Home Page, Research & The Les Turner ALS Center

The Sean M. Healey & AMG Center at Massachusetts General Hospital is launching the first-ever ALS platform trial aimed at advancing the development of ALS treatments. Our Lois Insolia ALS Clinic at the Les Turner ALS Center at Northwestern Medicine …