Awareness
In celebration of Rare Disease Day, Bionews is launching the Community Connection Travel Scholarship, awarding two scholarships (up to $2,500 each) to help rare disease patients or caregivers attend advocacy or…
On a quiet Wednesday afternoon in Beverly Hills, LA Living Magazine partnered with The ALS Network to host an intimate charity luncheon rooted in connection, compassion, and action. Held at…
Every ticket sold, every cup brewed, and every item worn helps raise vital funds that bring care and hope to the ALS community. Our partners help turn everyday purchases into…
HONOLULU (HawaiiNewsNow) – Hundreds gathered to help raise money for amyotrophic lateral sclerosis (ALS) in Kapiolani Park Saturday morning. The ALS Network hosted the 13th Annual Hawaii Walk and Roll…
The ALS Network is honored to announce its role as Charity Champion for the inaugural season of the Impossible Dreams podcast, launching on Tuesday, October 7, 2025. Hosted by acclaimed…
Dear Friends, I am grateful for your steadfast support of the ALS Network and invite you to read our new Impact Report. We are excited to share how your partnership powers our mission-critical…
The ALS Network is honored to celebrate the 5th annual Lou Gehrig Day and our continued partnership with Major League Baseball in paying tribute to Lou Gehrig’s enduring legacy and…
In honor of May as ALS Awareness Month, the ALS community collaborated with various local government representatives in Hawaii and California to raise awareness. ALS Awareness Month in Hawaii On…
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…