Below you will find various graphics and resources to use leading up and during our World Duchenne Awareness Day celebration.
Your toolkit for spreading the word in your local community!
View past webinar recordings from our 2021 webinar series by clicking a topic below.
View past webinar recordings from our 2020 webinar series by clicking a topic below.
Read Dan and DMD with one or all of our special guests!
Check out “The Red Balloon,” a teacher’s guide to introducing Duchenne muscular dystrophy and reading Dan and DMD in the classroom!
Features more than 250 common genetic terms pronounced and explained in an easy-to-understand way by leading scientists and professionals at the National Human Genome Research Institute.
An exhibit produced by NIH. Cracking the genetic code allowed us to study diseases at the molecular level, which is increasing our knowledge of potential preventions and treatments for diseases.
A public service provided by the Genetic Disease Foundation, a nonprofit foundation supporting research, education and the prevention of genetic diseases.
A nationwide-network of genetics experts available by telephone to help patients and providers harness the power of genetics to achieve the promise of personalized healthcare.
A publicly funded medical genetics information resource developed for physicians, other healthcare providers, and researchers that promotes the use of genetic services in patient care and personal decision making.
Everything you need to know to successfully fundraise for Jett Foundation and Duchenne muscular dystrophy.