This week the New York Times published an article bringing to light the constant struggles facing all Duchenne patients and their families. The article brings much needed national attention to the disease. I’ve posted the link below, please take some time and read it.
Matt
Lacking Cure, a New Tack on a Muscle Disease (New York Times)
Our new web site is live (yahoo!). We had most fun pulling together pictures of the boys for use on the site.
Want to see more? Visit our Flickr site to see others that didn’t “make the cut” (but are still very cute!).
Through our smilelines, our Foundation blog, we will keep you up-to-date with Foundation news, event announcements, and research updates.
