Our Mission
Our mission at Jett Foundation is to extend and enrich the lives of individuals affected by Duchenne muscular dystrophy and other neuromuscular disorders.
We fulfill this mission by partnering with individuals and families through empowering educational programming, transformational direct service experiences, and by accelerating the development of life-changing treatments.
About The Community Webinar Series
This year 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.
No one ever expects Duchenne and there is no correct way to tackle a diagnosis, but we can always better prepare. This webinar series is an opportunity to be better equipped with more knowledge, resources, and tools for those real-life, often unanticipated, scenarios.
Logos
Jett Foundation Logos: Red PNG | Red PNG with tagline | Black PNG | White PNG
20th Anniversary Logo: Color PNG
Community Webinar Series: Color PNG
Social Media
We encourage your organization to engage with us on social media. Our Facebook audience alone encompasses over 5,500 actively engaged followers. Like, comment on, and share our posts to enjoy mutually beneficial digital exposure as we work to promote the series and your organization’s work in the Duchenne community.
Jett Foundation’s Social Handles: Facebook | Instagram | Twitter | LinkedIn
Jett Foundation Hashtags: #FightDMDTogether, #StrongerThanDuchenne, #Duchenne, #JettGivingFund
