Walk n’ Wheel to End ALS
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 all people impacted by the disease. ALL ALS brings together people living with ALS, families, caregivers, researchers, clinicians, and partners from government agencies, industry, and…
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 ALS helps them move forward with greater clarity and confidence. When symptoms appear and uncertainty grows, understanding what to expect during the ALS diagnosis process…
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 more importantly, to donate and raise awareness for amyotrophic lateral sclerosis. While the challenge was global, its impact continues to ripple locally, including right here…
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, and support that makes daily life safer, more comfortable, and more connected. Why Your Support Matters ALS is a relentless disease that impacts mobility, communication,…
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 those who care for them. When you search for ALS support Albuquerque, here’s what you should know about connecting, sharing, and sustaining strength together. Why…
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 Wednesday, November 13th at 7:00 p.m. EST, MTPA will hold its last patient and caregiver webinar of 2025, “Understanding RADICAVA ORS® and How to Get…
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 ALS?” here’s an accessible guide to the disease, how it’s diagnosed, and the support options available in New Mexico. What Is ALS? ALS is a…
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 painters, art auctions, and a decades costume party, our ALS arts event is a great way to connect with the community and help raise awareness…
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 skies filled with hot air balloons. I could brag all day about how magical this season is. But fall also holds a special place in…
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 coordination, and community engagement. She is a highly organized, self-motivated professional with a strong background in nonprofit development, volunteer coordination, and project management. Most recently,…