Jett Foundation is a remarkable brand that aims to empower people and families impacted by Duchenne muscular dystrophy (DMD). Founded in 2001 by Christine and Stephen McSherry after their son Jett was diagnosed with DMD, the foundation has since raised over $16 million for biomedical research and shifted its focus to direct service programming for affected families. Committed to making a difference, Jett Foundation offers transformative programming, educational opportunities, and ongoing support for every stage of the Duchenne journey.

Their one-of-a-kind direct service programs and educational activities have proven to be instrumental in meeting the needs of families impacted by Duchenne and other neuromuscular disorders across cities and towns, regardless of location or financial situation. Driven by values such as empowerment, community, family, tenacity, and integrity, Jett Foundation is dedicated to advocating for individuals and families living with Duchenne. With a passionate team, supportive board of directors, and an extensive network of partners, they work tirelessly to provide support, raise awareness, and fund research to ultimately find a cure for Duchenne muscular dystrophy.

To stay connected with Jett Foundation, you can sign up for their newsletter and updates, donate to their cause, or explore volunteer opportunities. Experience the magic of their transformative programs and become part of their family today