Advance the Future of ALS Research — Funding Opportunity Opens April 15
Maintaining hobbies and passions is vital for individuals living with ALS in New Mexico, offering not only enjoyment but also a sense of normalcy and purpose. Golf, a sport cherished…
APRIL NEWSLETTER 2025 Springing forward together The sun is shining, the days are getting longer, and ALS New Mexico is buzzing with energy! We’re stepping into this new season with…
MARCH NEWSLETTER 2025 THIS ISSUE: CATWALK FOR A CURE ALS AWARENESS DAY AT THE NEW MEXICO STATE CAPITAL 2025 GRANT CYCLE NOW OPEN SAVE THE DATE – SWING FORE A…
ALS New Mexico, in partnership with the ALS Network, proudly announces letters of intent for ALS research funding will be accepted April 15 – May 15, 2025. ALS United members lead nonprofit…
March is an important month for women everywhere, and here at ALS New Mexico, we want to celebrate all the amazing women who help make ALS New Mexico a success.…
ALS New Mexico extends a heartfelt thank you to everyone who made the 2025 Hearts On Your Sleeve Fashion Show a spectacular success! From our generous sponsors and talented designers…
Living with ALS (amyotrophic lateral sclerosis) brings unique challenges, especially during the cold winter months. Cold weather can exacerbate ALS symptoms such as muscle stiffness and difficulty breathing. Preparing your…
As the 2024 legislative session approaches, ALS New Mexico is gearing up to continue its mission of supporting individuals and families affected by ALS across the state. This session is…
Advocacy is at the heart of ALS New Mexico’s mission, and as such we want to highlight a recent victory for our Veterans in our community. On Monday, November 18th,…
November marks National Caregiver Month, a time to celebrate and recognize the tireless dedication of caregivers who support their loved ones facing ALS, also known as Lou Gehrig’s disease. At…