Manzano Volleyball Team Honors Coach with ALS
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…
ALBUQUERQUE, N.M. — A Manzano High School volleyball team is raising awareness about Lou Gehrig’s disease, or amyotrophic lateral sclerosis, after their coach was diagnosed with it. Fred Ader is…
Election day is almost here, and ALS New Mexico wants to ensure you have a stress-free and seamless voting experience. When you vote, you are offering your voice and advocating…
Lou Gehrig’s Disease, also known as Amyotrophic Lateral Sclerosis (ALS), is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord. Living with Lou Gehrig’s Disease…
New Mexicans are rallying together this August to celebrate the 10th Anniversary Ice Bucket Challenge. New Mexico is making waves in the fight against ALS! This August, we’re commemorating the…
Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig’s Disease, is a progressive neurodegenerative disorder that affects nerve cells in the brain and spinal cord. This debilitating condition leads to…
As we reach the halfway point of 2024, it’s time to reflect on our progress and celebrate our achievements. We’ve had a busy and exciting first half of the year,…
On January 1st of 2024, Katie Crouch assumed the esteemed role of CEO and President at ALS New Mexico, marking a significant milestone in her dedicated service to our community.…