The mission of the Jett Foundation is to increase worldwide awareness of Duchenne muscular dystrophy with the purpose of raising and appropriating funds for research that will realize a cure for this fatal disease and programming that will ensure children with Duchenne have the opportunity to enjoy a full life.
Array (  => stdClass Object ( [code] => 32 [message] => Could not authenticate you. ) ) If you are seeing Rate Limited Exceeded please go to our Twitter Options page and follow the instructions under the header Twitter API Token.
If you’d like to receive emails from the Jett Foundation, please sign up for our email newsletter.
What? On Wednesday, September 7th, please join Jett Foundation and the Duchenne Community in celebrating World Duchenne Awareness Day, by alighting the Charles River with red to symbolize our community’s commitment to providing safe and effective treatments for those affected by Duchenne. We invite ALL who are impacted by Duchenne to attend- patients and their […]
July 8, 2016
Boys, Not Statistics A drug for muscular dystrophy works better than we reported. Jack Willis, center, Nolan Willis, right, and Max LeClaire, bottom, attended the opening for Sarepta Therapeutics global headquarters in Cambridge on June 2, 2014. Jack Willis, center, Nolan Willis, right, and Max LeClaire, bottom, attended the opening for Sarepta Therapeutics global headquarters […]