Our mission at Jett Foundation is to extend and enrich the lives of individuals affected by Duchenne muscular dystrophy and other neuromuscular disorders.
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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.
For a quick look at enrolling or soon to be enrolling investigational drug studies in Duchenne and their enrollment criteria, check out Jett Foundation’s Clinical Trial Cheat Sheet.