BENEFITING: Kawasaki Disease Foundation
What if your child is sick and you know it, but nothing is found. The doctors send you home and your child doesn't get better, just gets worse. Your child doesn't move nor talk, he/she is just there. That is what parents of KAWASAKI DISEASE patients deal with. THE SCARY UNKNOWN of this disease and what your infant or toddler's futures hold.
I was diagnosed with KD in 1990 at the age of two. My mom and family was sent home then told I had 1 of 4 diseases. 2 fatal and 2 were not. As my grandmother drove home from visiting me in the hospital, she saw a rainbow and knew God was saying I will survive. The next day I was diagnosed with KD and given treatment. I have had no aneurisms (Praise God). But running a support group in Alabama has allowed me to meet any people and hear there horrifying stories. All money raised will be sent straight to the KD Foundation in hopes to funding research to find a cure and cause of this nightmare. To read more about this disease or kids stories go to www.fkfoundation.org or my page on facebook Team Kawasaki Disease - AL.