Thank You for Your Support at the 2025 Hearts On Your Sleeve Fashion Show!
Facing ALS can feel isolating—but you don’t have to go it alone. Across New Mexico, and especially in Albuquerque, there are vital support structures for people living with ALS and…
As we approach the end of the year, the Muscular Treatment & Patient Alliance (MTPA) is hosting one final opportunity for connection, learning, and support for our ALS community. On…
Amyotrophic lateral sclerosis, or ALS, remains one of the most daunting neurological disorders today. But for New Mexicans seeking answers, awareness and connection matter. If you’ve ever asked, “What is…
We have an exciting announcement: ALS New Mexico will be hosting our first ever Arts for ALS New Mexico event on Thursday, October 30th, 2025! Featuring live music performances, live…
SEPTEMBER NEWSLETTER CHILE SEASON IS HERE! Fall in New Mexico is unlike any other. Every year, we’re gifted with crisp mornings, the scent of chile roasting, piñon fires, vibrant fiestas, and…
We are excited to introduce you to Maria Montoya, who recently joined our team as the Development and Engagement Manager! Maria brings over 13 years of experience in administration, event…
Living with ALS brings enough challenges—your home shouldn’t be one of them. That’s why ALS New Mexico, with the generous support of the Pitre Family Foundation, is proud to offer…
At ALS New Mexico, we are proud to work in partnership with ALS United to bring critical research developments to our ALS community. Through this collaboration, we aim to ensure…
Neuromuscular Advocacy Organizations Oppose Health Care Cuts June 16, 2025
May is ALS Awareness Month, a time to honor those affected by amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s disease. This progressive neurodegenerative disorder impacts nerve cells in…