Coolest Way to Be a Hero
The Access for All in ALS (ALL ALS) Consortium is a nationwide effort, funded by the National Institutes of Health (NIH), that aims to make ALS research more accessible to…
An ALS diagnosis can bring uncertainty and many questions, but you and your family are not alone. Throughout New Mexico, families often find that learning about the early stages of…
A single viral campaign changed the ALS landscape forever. The ALS ice bucket challenge first swept social media in 2014, inspiring millions to dump buckets of icy water over themselves—and…
Giving Tuesday is more than a day—it’s a movement of generosity that transforms lives. For families living with ALS in New Mexico, every dollar you give provides critical care, equipment,…
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…