Month: March 2025
People living in California can help fund amyotrophic lateral sclerosis (ALS) research when filing their state taxes. The California ALS Research Network Voluntary Tax Contribution Fund allows Californians to contribute…
The ALS Network, in partnership with ALS United, proudly announces that letters of intent for ALS research funding will be accepted April 15 – May 15, 2025. “We are honored…
On Thursday, March 27, the ALS Network hosted an engaging Lunch and Learn session with our Policy and Advocacy Manager, Allison Nadeau, MPH, MBA. Attendees gained an inside look at…
Process to turn skin cells into motor neurons detailed in 2 papers Scientists have developed a novel method to efficiently grow motor neurons from skin cells, which may serve as…
Tuesday, 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…
Erin Taylor was born in Whittier, California, in 1999. When she was 17, she moved to Salt Lake City, Utah, to attend college. Always creative and hard working, she juggled…
Thursday, March 27 at 1 p.m. PT/ 10 a.m. HT – Hosted by our partner, Mitsubishi Tanabe Pharma America, this webinar highlights the importance of building a strong support system…
JERSEY CITY, N.J. March 12, 2025 – Mitsubishi Tanabe Pharma America, Inc. (MTPA) today announced the presentation of eleven abstracts covering research in amyotrophic lateral sclerosis (ALS) at the 2025…
Our March eNewsletter is in your inbox now, or you can view it online! This month, we celebrate Women’s History Month by honoring amazing women who make a difference throughout…
Fifteen nonprofit organizations across the U.S. formed a new ALS group, ALS United, to better address the needs of people living with amyotrophic lateral sclerosis (ALS) and drive advances in…