Miracle for Milana

Milana Marino age 4, daughter of Matthew and Tara Marino, has a rare, life threatening, genetic disease called Niemann-Pick Type C. With this disease she cannot metabolize cholesterol and other lipids throughout her body, effecting her brain and other major organs. This tragic disease has no approved treatments and no cure. Milana is currently in a clinical trial at Children's Hospital of Philadelphia but the main focus right now to maintain the best quality of life possible for her. Milana has been battling this disease, but it has taken a huge toll on her and the hospital visits have been very frequent with medical bills and expenses piling up. Sustaining a quality of life for Milana comes at a very costly price.

Please help us and together we can give Milana the best life possible and support her and her family in dealing with this horrific disease.

No donation is too small! Any support you can give us is so greatly appreciated.

THANK YOU FOR YOUR CONTINUED SUPPORT.
IT MEANS MORE TO US THAN YOU CAN IMAGINE!