The Faces of Eosinophilic Disorders.
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My tough man, Will and me!

This is how Will is fed. We hook a tube up to his 'button' and pump special formula in. He also has a lot of granulation tissue surrounding his 'button' that we have to burn off with silver nitrate.

Happy Valentines Day!

This is how Will eats. Sometimes when he is feeling really bad, we have to hook him to a pump that very slowly pumps his formula in.

Colin eating his special formula, Neocate 1+ Colin has Eosinophillic Colitis.

Colin. Isn't he so sweet?!

Keegan on his way into the operating room at Cincinnati Childrens Hospital.

Chayce with his feeding tube supplies. Chayce and Keegan (above) are brothers.

This is Kaitlyn. She is 3 years old and also has EE. Please keep her in your prayers, she is having a feeding tube surgically placed this week just like Wills.

Kaitlyn at the hospital for her scope.