Navigating Lou Gehrig’s Disease in New Mexico: Resources & Support

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 resources are available to help navigate the complexities of this disease. ALS New Mexico is at the forefront of providing this crucial support, offering a lifeline to those affected by Lou Gehrig’s Disease in New Mexico.

ALS New Mexico: A Vital Resource for New Mexicans Living with Lou Gehrig’s Disease

ALS New Mexico is dedicated to providing a wide array of resources and support for those affected by Lou Gehrig’s Disease in the New Mexico area. Our mission is to empower individuals with ALS, as well as their families, by offering essential services and programs that address the physical, emotional, and financial challenges posed by the disease. See what we’re doing to make a difference in New Mexico.

Key Resources and Support Offered by ALS New Mexico

Care Services:

At ALS New Mexico, we offer personalized care services to meet the unique needs of individuals with Lou Gehrig’s Disease. These services include home visits, care consultations, and connections to specialized healthcare providers. Our team works closely with patients and families to ensure they receive the best possible care and support.

Support Groups:

Living with Lou Gehrig’s Disease can be isolating, but ALS New Mexico helps individuals connect with others who are facing similar challenges. We offer support groups for people living with ALS, caregivers, and family members, providing a safe space to share experiences, gain insights, and find emotional support. Join a support group and connect with others in discussing important topics surrounding ALS, your experiences, and hear from others in the community.

Equipment Loan Program:

As ALS progresses, the need for specialized equipment becomes critical. At ALS New Mexico, we offer an Equipment Loan Closet that provides access to necessary medical equipment, such as wheelchairs, communication devices, and mobility aids. This program helps alleviate some of the financial burdens associated with the disease, and lets you live a full life.

Educational Resources:

In addition to all our other resources, we also offer educational and informational resources for those newly diagnosed with Lou Gehrig’s Disease, and those who have been living with the disease already. You can find access to these educational resources here, and better understand exactly what ALS is and how to navigate it.

Advocacy and Awareness:

In addition to direct services, ALS New Mexico is actively involved in advocacy efforts to raise awareness about Lou Gehrig’s Disease and improve the quality of life for those affected. We work to influence public policy and increase funding for ALS research and care through fundraising efforts, legislative advocacy, education, and community outreach. If you are interested in becoming involved with our advocacy efforts, you can sign up to be an ALS advocate.

Reach Out to ALS New Mexico For Support and Resources Today

Navigating the challenges of Lou Gehrig’s Disease in New Mexico is a daunting task, but with the support of organizations like ALS New Mexico, patients and their families do not have to face it alone. ALS New Mexico’s comprehensive resources and compassionate care services provide vital assistance to those affected by Lou Gehrig’s Disease, helping those living with it maintain their lifestyle and receive the support they need.

If you or someone you know is affected by Lou Gehrig’s Disease, reach out to ALS New Mexico for ongoing support and resources. Together, we can make a difference in the lives of those living with Lou Gehrig’s Disease in New Mexico.