2013 was a life changing year and where our story begins. It was when we learned that two sets of brothers in our family were diagnosed with a rare form of Muscular Dystrophy called Beckers. In the beginning we faced a lot of unknows and had no idea what the future would look like. Initially as a way to cope, we decided we needed to get the word out and raise awareness for these lifelong debilitating diseases. Our mission is spread the word and raise funding to donate to organizations like the MDA and other research groups working to end neuromuscular diseases and to one day find a cure for all.