Our mission at Jett Foundation is to extend and enrich the lives of individuals affected by Duchenne muscular dystrophy and other neuromuscular disorders.
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!
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.
Provides consumer-friendly information about the effects of genetic variations on human health.
For a quick look at enrolling or soon to be enrolling investigational drug studies in Duchenne and their enrollment criteria, check out our Clinical Trial Cheat Sheet below.