Introducing... The Dear John Michael Foundation
John Michael Shatzer is a 3 year old boy from Fort Worth, Texas. He was recently diagnosed with Duchenne Muscular Dystrophy. Currently,...
FDA Advisory Committee
Kyle and I are headed to Washington DC in just a few weeks to attend the FDA Advisory Committee meeting to consider the first DMD drug-...
Join Our Walk Team!
Join our team and walk with us in September. Visit the Take Action page or click the picture below.
Two Months
Today marks TWO months since we learned about John Michael's diagnosis. It has felt like a lifetime.. It is hard to remember what our...
William
Today we received some very good news about our second son. After weeks of putting off testing, we finally went through with it....
Please take action NOW
Please take action NOW. Show your support for Duchenne treatments and urge your elected officials to encourage the FDA to approve their...
Speechless
Wow! We are speechless and joyfully overwhelmed by all of the support and prayers. Words can not thank you enough. Lots have messaged me...
Diagnosis
On December 16 2015 just a few days before Christmas, we found out the worst news of our lives. Our two year old son and first born was...
