Muscular Dystrophy Association

DBA
MDA of Utah
A voluntary health organization that advocates on behalf of people with muscular dystrophy and related neuromuscular diseases that take away physical strength and mobility. It also funds research for promising treatments and provides people with quality care. The organization also offers support groups and camps for children and youth dealing with a neuromuscular disease. Informational materials are offered through their website.
Description:

Provides a summer camp for children with any neuromuscular disease covered by the organization's program. Summer camp provides a full range of recreational camping activities geared to the special needs of those with neuromuscular disease.

Eligibility:
Youth ages 8 to 17 affected by muscular dystrophy, ALS or related muscle-debilitating diseases and their families.
Service Hours:
Vary
Intake Procedure:
Visit the website or call for more information.
Fees:
No cost
Service Contact Information:

US

camp@mdausa.org mda.org/summer-camp
Description:

Financial assistance for the repair of manual and power wheelchairs, leg braces, and communication devices. Operates an extensive equipment loan closet where clients can receive durable medical equipment at no charge. Items available include power wheelchairs, manual wheelchairs, bath equipment, canes, walkers, standing frames, etc.

COVID-19 Update: following all CDC and state guidelines.

Eligibility:
Individuals affected by muscular dystrophy, ALS or related muscle-debilitating diseases and their families.
Service Hours:
M - F 8 am - 4 pm
Intake Procedure:
Call for information.

COVID-19 Update: following all CDC and state guidelines.
Fees:
No cost
Service Contact Information:

US

Description:

Adult and pediatric support groups that provide a safe place to gather resources, interact meaningfully with others, and exchange valuable information with others in the neuromuscular disease community. The support groups offered include adult and pediatric community support groups, ALS community support groups, and gene therapy community support groups.

Eligibility:
Individuals affected by muscular dystrophy, ALS or related muscle-debilitating diseases and their families.
Service Hours:
M - F 8 am - 4 pm
Intake Procedure:
Call or complete the community support group form on the website.
Fees:
No cost
Service Contact Information:

US

mda@mdausa.org mda.org/care/community-groups
Description:

Information about medical centers for individuals living with muscular dystrophy, ALS, and other neuromuscular diseases to access expert multidisciplinary care, clinical trials, and connect with MDA and the neuromuscular community. Also offers one-on-one support via phone/email for information about programs and resources.

Eligibility:
Service Hours:
24/7
Intake Procedure:
Visit the website.
Fees:
No cost
Service Contact Information:

US

mda.org/care/mda-care-centers