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 diagnosed with Duchenne Muscular Dystrophy- the most severe type of MD.
We are experiencing an unbelievable amount of heartache, anger, confusion, and fear. Our sadness deepens daily as we learn more about our future with this terminal disease and the struggles that John Michael and our family will have to face. We are searching for hope, treatments, and ultimately a cure for John Michael and all the young boys who are dealing with DMD.
We need your help in raising awareness and funding for research to help find a cure. We will never stop fighting for our son who is the light of our lives. Please follow and share our story!