HEARTS ON YOUR SLEEVE FASHION SHOW
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 an opportunity to build upon the successes of the past year and advocate for the critical funding needed to sustain the programs that make a…
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, the U.S. House of Representatives passed the Senator Elizabeth Dole 21st Century Veterans Healthcare and Benefits Improvement Act. Not only does this show that our…
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 ALS New Mexico, we want to celebrate the work of all the amazing caregivers in our community by offering resources and support to better assist…
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 the head coach for the Manzano varsity team. People say he’s a big part of the volleyball community not just for the Monarchs, but also…
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 for what you stand for and can help make change when it comes to ALS advocacy in New Mexico. In this blog we discuss what…
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 presents significant challenges, not only for those diagnosed but also for their families and caregivers. In New Mexico, a supportive community and a range of…
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 10th anniversary of the Ice Bucket Challenge with a renewed commitment to supporting our fellow New Mexicans battling Lou Gehrig’s Disease. Thanks to the incredible…
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 the loss of muscle control, making daily activities increasingly difficult for those affected. Understanding ALS and its impact on individuals, particularly in New Mexico, is…
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, and we’re proud of what we’ve accomplished.
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. For the past eight years, Katie has illuminated our organization with her unparalleled passion and unwavering dedication, propelling us towards remarkable growth and success. Under…