Super Cohen's Crusade

Cohen is a miracle, he is the most amazing little boy full of joy and faith. He has had 15 procedures/surgeries under anesthesia in the OR and he is only 4 years old. Can you imagine never being able to eat but yet being able to smell fresh bread baking, pizza, Italian food ohh yummy Italian food, steak on the grill, bbq. I'm sure at this point your tummy is rumbling, but you get to fill it with all those amazing foods. Well Cohen gets to smell it but never taste it and instead, his belly only enjoys ice and his body is fed through his heart with a tube filled with a special formula just for him. Ice is his only "food' that hits his belly, yummy cold tasteless ice, but to him it's amazing... it's his BBQ, pizza and yes it is even fresh bread. I wish I could tell you why he cannot eat but even the best doctors at Cincinnati Children's Hospital cannot. You see Cohen has such a rare disease that no one and I mean no one can figure him out. February 28th is rare disease day. Let's blow him away with a gift that can help releive the family from some burden. To learn more about him please visit his Facebook page. Super Cohen's Crusade. #supercohen. For all those that know them and have said to themselves I wish I could help Cohen or I wish I could help Carrie. Here is your chance. I know I have said over and over I wish I could do something and now I am. They do not know I am setting this page up and if you know them, you know they wouldn't be happy with me. You would never know by talking to them that they struggle or that they need help, but Cohen's medical bills are larger than you can imagine and with no end in sight. Every time they have to run to Cincinnati, and I mean pick up and jump in the car at last minutes notice cost them at least $500. I want to try and help take some burden off of them. So who's with me??!?!