News

UMass Medical Center officials said the late Gov. Paul Cellucci’s last campaign — battling the disease that killed him — raised nearly $2 million that is helping researchers zero … ...
Beverly native Pete Frates died peacefully Monday after a seven-year battle with amyotrophic lateral sclerosis, but his legacy will live on forever with the impact he made on ALS research and ...
He didn’t just want to stand up an entirely new ALS advocacy group, or secure more funding for ALS research, or expand access to treatments for the roughly 15,000 Americans with ALS, or provide ...
ALS is a cruel disease. It gradually robs a person's body of its motor skills until the ability to walk, talk, stand and eat are gone. About 5,000 people in the U.S. are diagnosed every year ...
Discover the Power of Community as the ALS Network Highlights Care Services, Advocacy, and Research during ALS Awareness Month. PR Newswire. LOS ANGELES, May 6, 2025.
The event aims to support those living with ALS and to fund research, advocacy, and care services. ALS, often referred to as Lou Gehrig’s disease, is a progressive neurodegenerative condition ...
Leading ALS advocacy group roiled by infighting over money and priorities. ... The money is invested in research, clinic certification, and lobbying, among other activities.
Market 32 and Price Chopper have announced the launch of an in-store fundraising campaign to support the Muscular Dystrophy ...
The disease hit one Santa Rosa County woman close to home after her stepfather lost his battle, turning her tragedy into advocacy. Mandi Bailey leads the Veterans ALS Action Committee.
LOS ANGELES, May 6, 2025 /PRNewswire/ -- May is ALS Awareness Month, and the ALS Network is committed to raising awareness and understanding of the devastating disease that has no known cure. This ...
Hundreds in Napa set to ride for ALS research and celebrate 20 years of advocacy. Diagnosed almost two years ago, Napa’s Howard Mattfield’s team of 36 will walk and ride Saturday in support of ...