
Care Gets a Lift: How Kevin Carbone Got Back to the Water with Help from Jett Foundation
Jett Foundation’s Equipment Assistance Fund brings water therapy back to the Carbone family.
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Our Family Workshops bring together clinicians, researchers, and families impacted by Duchenne in many cities each year. Community Webinars better prepare our community through virtual speakers and presentations.
Jett Foundation knows and understands that getting a diagnosis like Duchenne is far from easy. We have worked to create a package for families on this journey –through its highs and lows.
Our Community Webinar Series is focused on ensuring that our Duchenne community is better prepared for those unexpected moments, challenging medical decisions, and difficult stages when on a Duchenne journey.
This program aims to spread awareness about Duchenne and the programs and services that Jett Foundation provides through community ambassadors, who are individuals with Duchenne, parents, family, and more.

Jett Foundation’s Equipment Assistance Fund brings water therapy back to the Carbone family.

A message to Jett Foundation from Kristina Pham, mother of Simon and Steven Dinh, who’s family received an accessible vehicle after participating in Jett Foundation’s

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.
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.