Become a Partner

Jett Foundation is a world leader in Duchenne muscular dystrophy.

We build a stronger patient community by collaborating with corporations and businesses with similar values and goals to improve education, awareness, and health outcomes for individuals living with Duchenne around the world.

Partner With Jett Foundation

Our team at Jett Foundation will work with you and your company to customize the partnership. Let us explore with you how, together, we can serve a community full of unmet needs.

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    Our Impact

    October 23, 2023
    The Benson Family celebrates their new safe and accessible vehicle
    August 22, 2023
    The Daniels Family receives a safe and accessible van through Accessible Vehicle Fund
    May 30, 2023
    A guest blog from Declan Hickey, an 18-year-old with Duchenne muscular dystrophy and previous participant in Jett Foundation’s Jett Giving Fund
    January 4, 2023
    The Fritz family receives their new safe and accessible vehicle through Jett Giving Fund
    December 10, 2022
    Futrell family receives financial assistance through Jett Foundation’s Emergency Fund
    July 26, 2022
    “We moved to Colorado four months ago because my husband got a job with housing on a ranch. Then we were told the ranch was being sold, and we had only a few days days to move,” says Gail Neal.
    May 19, 2022
    “As a parent of a son living with Duchenne, the mission of my wife and myself is to do whatever we can to help our son enjoy every moment of life,” says Todd.
    April 13, 2022
    A Connecticut father reached out to Jett Foundation for assistance with putting food on the table for his family. Jason is a proud father of two boys. His son, Justin (12), was diagnosed with Duchenne muscular dystrophy at just 18-months-old.
    April 6, 2022
    “For four years, I have stressed about how to deal with getting a safe vehicle. This is life-changing” says Michelle, mother of Kelvin Jones. Kelvin is a young man diagnosed with Duchenne muscular dystrophy from Johnston, Ohio.
    March 28, 2022
    “As our boys keep growing, we run into more barriers for transporting our family in a safe manner. Having two boys with Duchenne is incredibly difficult,” says Ember Thomas, the mother of two boys who have Duchenne muscular dystrophy.

    Accessible Vehicle Fund Applications Open