Month: March 2026

2026 MLB Lou Gehrig Day With the ALS Network

March 31, 2026 Comments Off on 2026 MLB Lou Gehrig Day With the ALS Network

Each June 2 and throughout the month of June, we honor the legacy of Lou Gehrig and all those impacted by ALS. We look forward to our annual partnership with…

Keeping Hope High – An ALS Network and MMD Partnership

March 31, 2026 Comments Off on Keeping Hope High – An ALS Network and MMD Partnership

The ALS Network is proud to partner with MMD Shops, a leading California cannabis retailer, and a few of their top brand partners Heavy Hitters, Papa & Barkley, and Almora,…

End the Legacy’s 2026 Genetic ALS & FTD Community Summit

March 31, 2026 Comments Off on End the Legacy’s 2026 Genetic ALS & FTD Community Summit

After two incredible summits in 2024 and 2025, End the Legacy’s 2026 Genetic ALS & FTD Community Summit is returning to Sacramento, CA, September 24–26, 2026. Hosted by ALS Network,…

Celebrating National Doctors’ Day and Women’s History Month

March 27, 2026 Comments Off on Celebrating National Doctors’ Day and Women’s History Month

Monday, March 30 is National Doctors’ Day. Women’s History month is a great opportunity to celebrate women ALS clinicians and scientists. These dedicated individuals work tirelessly for people living with…

Brooke Eby Honored with Advocate of the Year Award

March 26, 2026 Comments Off on Brooke Eby Honored with Advocate of the Year Award

The ALS Network is proud to announce Brooke Eby has been named the recipient of the 2026 Dean and Kathleen Rasmussen Advocate of the Year Award, recognizing her extraordinary commitment…

Spotlight on… Patti Hancock

March 23, 2026 Comments Off on Spotlight on… Patti Hancock

Born in Sacramento, CA, Patti was raised by parents who valued education, and taught her perseverance and determination. At the age of 12, she sustained painful injuries and broken bones…

Women Who Carry Hope Forward

March 16, 2026 Comments Off on Women Who Carry Hope Forward

When Beth Greulich’s husband, Geoff, was diagnosed with ALS in January 2023, their world shifted overnight. What followed, however, was a powerful reminder of the strength found in friendship. Beth’s…

ALS Community Funding Letter

March 9, 2026 Comments Off on ALS Community Funding Letter

Our ALS community came together with a unified message to Congress: sustained investment in ALS research is essential to accelerate treatments and move us closer to cures. The ALS Network…

ALS News Today Named 2026 Presenting Sponsor of ALS Network’s ASK ME Webinar Series

March 9, 2026 Comments Off on ALS News Today Named 2026 Presenting Sponsor of ALS Network’s ASK ME Webinar Series

LOS ANGELES – March 9, 2026 – ALS News Today will serve as the presenting sponsor of the ALS Network’s ASK ME educational webinar series throughout 2026, supporting a year…