Dream of Accessible Transportation Comes True for New Jersey Family Living with Duchenne
Josvin and his family are relieved to have reliable transportation for medical appointments.
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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!
Josvin and his family are relieved to have reliable transportation for medical appointments.
Victor, Christian, and Alan Cruz look forward to unencumbered travel to medical appointments and daily activities.
The Petz family’s van opens opportunities for family trips, safe everyday travels, and countless memories.
Ethan Hoot has more freedom and independence to explore his childhood with accessible transportation.
Massachusetts residents Natalie, Paul and their 29-year-old son Max Gaudenzi have been navigating a life with Duchenne muscular dystrophy since Max was diagnosed at a
Fourteen-year-old Cooper Klein from Pasadena, Maryland, lives with Duchenne muscular dystrophy, a progressive neuromuscular disorder that weakens his muscles and affects his lungs and heart.
The Partin-Rockwood Family has three boys living with Duchenne and autism who are excited for new adventures.
Ellis Bautista and his family celebrate the arrival of safe and accessible transportation.
Daniel Toy and his family look forward to many adventures and memories thanks to new accessible van.
The Fialkowski Family celebrates the ability to safely transport their family again.
The Kim Family starts a new journey of safe and accessible transportation.
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
Jett Foundation, Inc.
65 Cordage Park Circle
Suite 130 | Plymouth, MA 02360
781-585-5566 | [email protected]
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Your gift helps Jett Foundation provide programming and opportunities, such as Camp Promise, to many families impacted by Duchenne muscular dystrophy each year.