Every step you take and every dollar you raise helps make a difference. Your fundraising supports ALS research, multidisciplinary care, support services, equipment, grants and resources for families across our community. Register and start fundraising today: p2p.onecause.com/alswalkforlife

Who's on your Walk team this year? Whether it's family, friends, coworkers, or neighbors, the ALS Walk for Life is the perfect day to come together, make memories, and support the ALS community. Join us October 24 at Soldier Field: p2p.onecause.com/alswalkforlife

Need plans for October 24? We've got you covered. Join thousands of supporters at Soldier Field for a fun, meaningful day on Chicago's lakefront. Walk with your team, meet new people, and be part of something that truly makes a difference. Register here: p2p.onecause.com/alswalkforlife

Registration is now open for the National ALS Registry 2026 Annual Meeting! Join the ALS community on August 19–20 to learn more about the Registry’s ongoing work to advance ALS research and support the ALS community. Register: www.zoomgov.com/webinar/regi...

Every team has a story. For Gary Kravitz, it's a 22-year tradition of honoring his mother through the ALS Walk for Life. Now it's your turn to create your own. Join us on October 24 at Soldier Field. Register today: p2p.onecause.com/alswalkforlife

Thinking about traveling with ALS? Join us for practical advice, personal experiences, and a live Q&A designed to help you travel with greater confidence. Register: us02web.zoom.us/webinar/regi...

Never been to the ALS Walk for Life? This is your year. Expect an inspiring community, an unforgettable walk along Chicago's lakefront, and hundreds of people coming together for something bigger than themselves. Register here: p2p.onecause.com/alswalkforlife

Les Turner ALS Foundation joined 34 patient advocacy organizations in urging the federal Office of Management and Budget to withdraw a proposed rule that could weaken the biomedical research infrastructure supporting people living with neuromuscular diseases. Read: lesturnerals.org/neuromuscula...

Travel didn't stop after Craig's ALS diagnosis. Hear Craig & Emily Mandell share their experiences and practical advice for traveling with ALS. Register: us02web.zoom.us/webinar/regi...

Meet Kari Brouwer, OTR/L, an Occupational Therapist at Northwestern Medicine. Join Kari on July 23 for practical tips on planning and traveling with ALS. Register: us02web.zoom.us/webinar/regi...

Learn how the ALS Turbocharged Living Scale offers a new way to measure quality of life and focus on what matters most. Join us Thursday, June 25, at 12pm CT. Register: us02web.zoom.us/webinar/regi...

Meet Peggy Plews-Ogan, MD, physician, educator, and ALS advocate. Learn how the ALS Turbocharged Living Scale was developed and the impact it can have on people living with ALS. Register: us02web.zoom.us/webinar/regi...

Join us Thursday, June 25, at 12pm CT for a live webinar with Peggy Plews-Ogan, MD. Learn how the ALS Turbocharged Living Scale offers a new way to think about quality of life beyond physical function. Register: us02web.zoom.us/webinar/regi...

Support for ALS families across Illinois is growing. Thanks to $300,000 in newly approved state funding for ALS care and research, more people will have access to the care, services, and support they need throughout their ALS journey. Read more: lesturnerals.org/together-we-...

Thank you for being part of the 2026 Lew Blond Memorial Run/Walk. From the 5K and 1-Mile Walk to the Little Lew Dash, it was incredible to see the community come together in support of the Les Turner ALS Foundation and in memory of former Maple School teacher Lew Blond.

Tomorrow’s the day! We’re excited to gather with the ALS community for Lou Gehrig Day with the Chicago Cubs at Wrigley Field. Check if there are still tickets available: e.givesmart.com/events/OQR/

Meet Juan Reyes and Kelly McGinn. Juan is involved with I AM ALS and Kelly is an active member of Her ALS Story. Learn how advocacy, resilience, and community can shape life after diagnosis. Register: us02web.zoom.us/webinar/regi...

Meet Rob Akins and Tina Cascio. Learn how advocacy, outreach, and service helped shape their ALS journeys. Register: us02web.zoom.us/webinar/regi...

Join us Thursday, May 28, at 12 pm CT for a live ALS panel with Juan Reyes and Kelly McGinn. Learn how support and advocacy can create strength after diagnosis. Register: us02web.zoom.us/webinar/regi...

Join us Thursday, May 28, at 12 pm CT for a live ALS panel with Rob Akins and Tina Cascio. Learn how connection, advocacy, and community support can make an impact after an ALS diagnosis. Register: us02web.zoom.us/webinar/regi...

Join us as we gather with the White Sox and Cubs for two special games in support of the ALS community. Chicago White Sox vs. Detroit Tigers – Sunday, May 31 at 1:10 p.m. CT Chicago Cubs vs. Athletics – Tuesday, June 2 at 7:00 p.m. CT Tickets: lesturnerals.org/events/lou-g...

Meet Melissa Diaz-Viera, LCSW, advocate and research contributor in the ALS community. Join her Thursday, April 23, at 12:00 p.m., CT. Learn how lived experience shapes ALS decisions. Register: us02web.zoom.us/webinar/regi...

Meet Danielle Burks, LCPC, founder of Journey to Healing. Join her Thursday, April 23, at 12:00 p.m., CT. Learn about the emotional side of ALS care decisions. Register: us02web.zoom.us/webinar/regi...

Meet Matt Creen, a longtime member of the ALS community. Join him Thursday, April 23, at 12:00 p.m., CT. Hear real perspectives on ALS care decisions. Register: us02web.zoom.us/webinar/regi...

Join us this Thursday, April 23, at 12:00 p.m., CT for a live discussion on informed decision-making in ALS. Learn about the medical, emotional, and practical considerations of tracheostomy and invasive mechanical ventilation. Register: us02web.zoom.us/webinar/regi...

Learn how tissue donation supports ALS research and what the process involves. Join us Thursday, March 26, at 12:00 p.m., CT. Register: us02web.zoom.us/webinar/regi...

Meet Dr. Lyle Ostrow, Associate Professor of Neurology at Temple University and founder of the ALS Postmortem Research Core. Join him this Thursday, March 26, at 12:00 p.m., CT. Register: us02web.zoom.us/webinar/regi...

Join our Living After Loss Bereavement Group, a supportive space to connect with others who understand, share stories, and honor the memories of loved ones. RSVP: supportgroup@lesturnerals.org

“We have an ongoing effort at the Pranger ALS Clinic to increase enrollment so we can get a clear picture of who is getting ALS and the magnitude of the disease, which we believe is grossly underreported.” - Dr. Steven Goutman, researcher. Learn more at cdc.gov/als. #ALS #ALSClinic

ALS affects more than just health — it affects daily life, family, and the future. Our Support Services Team is here to listen, guide, and connect you to the resources you need — from clinical education to financial assistance and end-of-life planning. Please email supportservices@lesturnerals.org