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Joy in Jackson’s Journey

Each year I like to go into the local schools and do a presentation about Jackson and allow the students to meet him, to research and learn about Duchenne Muscular Dystrophy and to put a face to the disease.

This year we had a little bit more than 32 questions that local 7th graders wanted to know about DMD and about Jackson. They are wonderful questions and I feel like instead of only answering a few the day of the presentation, I figured I would answer them here in case they wanted to see how I answered all of the rest that we didn’t get time to cover.