Providing specialized care for patients in New Mexico who have been diagnosed with ALS, offering a comprehensive, multidisciplinary approach to support their unique needs. Our dedicated clinical team includes experts in neurology, physical therapy, occupational therapy, speech therapy, nutrition, respiratory therapy, and social work. Together, they work collaboratively to enhance mobility, communication, respiratory function, and overall well-being while connecting patients and their families with essential resources, adaptive equipment, and emotional support.

ALS New Mexico proudly operates the largest equipment loan closet in the state, providing essential medical and mobility equipment to families affected by ALS at no cost. This program ensures that individuals have access to vital resources such as wheelchairs, walkers, communication devices, hospital beds, and other assistive equipment to improve comfort and quality of life. Families are encouraged to utilize this free service, which is designed to remove financial and logistical barriers. Once a request is made and availability is confirmed, our dedicated care services team coordinates the pickup and delivery of the equipment, ensuring a seamless, stress-free experience. Our goal is to provide timely support, allowing patients and their caregivers to focus on what truly matters—quality care and daily living."

Through our grant program, we provide financial assistance to help alleviate the costs associated with ALS care. These grants cover a wide range of reimbursable expenses, including respite care to support caregivers, professional counseling for emotional well-being, co-pays for essential medical treatments, home modifications to improve accessibility, and other ALS-related needs. Each registered ALS patient is eligible to apply for up to $2,500 in financial support, helping to ease the financial burden and ensure access to necessary care and services. Our goal is to empower families with the resources they need to enhance comfort, independence, and overall quality of life.

Led by professionals, ALS Support Groups provide opportunities for group members to share their personal experiences and to learn more about living with ALS. Participants learn that they are not alone nor without help or hope. Support Group meetings are free and open to all people living with ALS and their caregivers. Support Groups sometimes feature speakers on relevant topics and are designed to share information as well as strategies for preserving the independence and quality of life of both people living with ALS and their caregivers.

Our ALS Lending Library offers a free and accessible collection of books, movies, and augmentative and alternative communication (AAC) books tailored for individuals and families affected by ALS. Whether you're looking for educational resources, inspiring stories, or entertainment, our library provides valuable materials to support patients and caregivers on their journey. Families can easily borrow and return items, ensuring they have access to helpful information and engaging content without added costs. Our goal is to empower, educate, and bring comfort to those navigating ALS.