A night of hope and celebration with Paul Lisnek
The 37th annual Hope Through Caring Gala is set to be an unforgettable evening, and we’re thrilled to be joined again by Paul Lisnek— WGN’s own Emmy Award-winning television host, political analyst, and longtime supporter of the Les Turner ALS Foundation—serving as our emcee!
Paul’s distinguished career spans decades in broadcast journalism, where he has interviewed presidents, governors, and political leaders. His dedication to storytelling and community impact, including his past coverage of Les Turner events, makes him the perfect host for this inspiring night. “This organization has moved me so much,” says Paul, “it’s a place where I’m dedicated to making a difference.”
Join us for our March ALS Learning Series
Discover how observational studies are driving ALS research forward with Dr. James D. Berry, Chief of the MGH Division of ALS and Motor Neuron Diseases. Learn how these studies accelerate drug development, uncover biomarkers, and refine clinical trial design to create lasting resources for the ALS community.
This webinar is made possible at no cost by the generous support of the Gilbert & Jacqueline Fern Foundation, Biogen, and Mitsubishi Tanabe Pharma America.
Click the link to register now.
The Les Turner ALS Foundation has joined 39 other neuromuscular advocacy organizations in opposing the NIH’s 15% cap on indirect costs for research grants. This policy threatens the progress of lifesaving ALS and neuromuscular disease research by limiting funding for essential lab operations, clinical trials, and training for future scientists.
NIH-funded research has been instrumental in identifying the causes of neuromuscular diseases and developing nearly 30 FDA-approved treatments. Without adequate funding, research could stall, labs may shut down, and the hope for future breakthroughs could be delayed indefinitely.
We are calling on the NIH to reverse this harmful cap and protect the critical research that brings hope to those living with ALS.
March Madness is almost here, and that means it’s time for the Young ProfessionALS Group NCAA Bracket Challenge for Charity. Compete with friends, enjoy the excitement of the tournament, and support the ALS community—all while vying for cash prizes.
Purchase up to six brackets, with a maximum of three for the men’s tournament and three for the women’s. After signing up, you’ll receive an invite to join the Les Turner ALS Foundation group on CBS Sports. Brackets go live on Selection Sunday, March 16, and must be finalized before the first round begins—March 20 for men’s and March 21 for women’s.
Top winners will take home prizes, including $500 for first place in both men’s and women’s brackets. All proceeds support ALS care and research.
Don’t miss your shot—sign up today and be part of the madness!
Guide Spotlight: ALS + Mobility
As ALS progresses, mobility challenges can make everyday tasks more difficult. With the right equipment and support, you can maintain independence and continue engaging in the activities you love.
Our ALS & Mobility Guide provides expert-backed information on walking aids, leg braces, wheelchairs, transfer equipment, and home modifications. Learn how to choose the right tools for your needs, work with your ALS care team, and explore insurance options for durable medical equipment.
From rollators and ankle-foot orthoses to power wheelchairs and patient lifts, this guide helps you understand what’s available and how to make the best choices for your mobility needs.
Click the link below to read the guide, also available in Spanish:
