Lori’s Story: Aim High…Fly-Fight-Win! Every November on Veterans Day, we honor and remember the veterans who served our country in the Armed Forces. Due to the strong connection between military service and ALS, the Foundation also remembers and honors those …
Faces of ALS: Steve McMichael
Super Bowl Champion Steve ‘Mongo’ McMichael was diagnosed with ALS in January 2021. He points out, “It’s called Lou Gehrig’s Disease. I didn’t know that it was a metaphor too. ALS is going to run the bases on you.” Adding …
Faces of ALS: Cara Gallagher & Easton Stevenson, Support Service Coordinators
The Les Turner ALS Foundation’s Support Services Team often serve as the first point of contact for a person recently diagnosed with ALS and their families to help chart a path forward to address their immediate and future needs and …
Faces of ALS: Remembering Marshall Krolick – One of the Foundation’s Founding Members
When Marshall Krolick passed away in February, the Les Turner ALS Foundation lost one of its longest-standing family members and biggest supporters. As a close friend of Les Turner, for whom the Foundation is named, Marshall was at the hospital …
Faces of ALS: A New Addition to our Support Services Committee
For over 30 years, Cheryl Gallagher traveled the world as a flight attendant for United Airlines. From India to New Zealand, and Cambodia to Vietnam, she reveled in the opportunity to explore new places, take in fresh perspectives and immerse …
Faces of ALS: Working to Make True on a Wish
When Jonathan Brent, MD, PhD, asks his ALS patients what their goals are, the answer is almost always the same: to find a cure for ALS. “What motivates me,” says Dr. Brent, “is how I can make true on that …
Faces of ALS: Hope & Action in the ALS Community
“There is more hope and more action happening right now within the ALS community than I ever thought I would see in my lifetime,” says Deb Paust of Grayslake, Illinois. “It is empowering to be a part of that change.” …
Faces of ALS: Passion, Unabated
For Diane Pospeshil and her family, music and the arts are a lifeline and part of their collective DNA. Beginning with a small dance studio they ran from the basement of their home in Buffalo Grove, Illinois, the family business …
Faces of ALS: My Story of Service
ALS is called a rare disease. But for reasons not yet known, veterans are twice as likely to be diagnosed with ALS compared to the general public. Last week, we as a nation honored our brave veterans for their sacrifice …
Faces of ALS: Running On Kindness and Generosity
«My grandma was one of the most influential people in my life, for so many reasons,» shared Taylor Davis, a member of our Team Race for ALS. «She taught me the importance of being kind and generous to others. During …