Safe and Accessible Transportation for North Carolina Family
Arian Mooring is an 13-year-old boy living in Goldsboro, North Carolina, with his grandparents and younger brother, Slayden. Diagnosed at 15 months old, Arian is
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The critical work that Jett Foundation does in the Duchenne community is completely dependent on outside donors.
In order to continue providing education, resources, advocacy, and many programs for the Duchenne community, we need you and your community’s support.
A third party fundraising event is when a business, organization, community group, school, or individual plans and hosts a program or an event that benefits Jett Foundation. It is planned and executed independently of Jett Foundation and Jett Foundation’s staff.
Below are just some ideas of the many ways that you can raise funds and awareness for Jett Foundation in your local community!
Arian Mooring is an 13-year-old boy living in Goldsboro, North Carolina, with his grandparents and younger brother, Slayden. Diagnosed at 15 months old, Arian is
The Benson Family celebrates their new safe and accessible vehicle
Pamela and Marvin West live in Ravenna, OH, and are the parents to two boys, Dakota (15) and Duane (9). Dakota is living with Duchenne
The Daniels Family receives a safe and accessible van through Accessible Vehicle Fund
A guest blog from Declan Hickey, an 18-year-old with Duchenne muscular dystrophy and previous participant in Jett Foundation’s Jett Giving Fund
The Fritz family receives their new safe and accessible vehicle through Jett Giving Fund
Futrell family receives financial assistance through Jett Foundation’s Emergency Fund
“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.
“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.
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.
“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.
“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.
Jett Foundation, Inc.
65 Cordage Park Circle
Suite 130 | Plymouth, MA 02360
781-585-5566 | info@jettfoundation.org
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Tune in on February 29 to hear from our panel and moderators on how they are accomplishing goals and living life to the fullest!
Your gift helps Jett Foundation provide programming and opportunities, such as Camp Promise, to many families impacted by Duchenne muscular dystrophy each year.