Medical and Treatment Expenses for Cooper

Hi everyone! As most of you know, on June 15th, Cooper was diagnosed with an extremely rare genetic disorder; Infantile-Onset Unverricht-Lundborg Disease. In Cooper’s case, he is 1 of 5 people in the world to have his specific gene mutation. Because of the rarity of this disease, there is very little known about the future, potentially treatment and side effects. Based on what we do know, we do not expect Cooper to walk, talk or do much of anything on his own. He will be 100% dependent on his g tube for feedings & on Bradley and I for his everyday care.

Bradley and I have made a promise to Cooper that we will do absolutely everything we can to give him the best shot at life That’s where we need your help! Medical expenses are astronomical and some of the best doctors and potential treatment opportunities are not local. Bradley and I are in communication with a few doctors who are hopeful & we are hoping that you all will help us help baby Coop. If it’s a dollar or positive energy sent out way, we love & appreciate each and every one of you! Follow our journey on Facebook; Cooper’s Corner