Please help Gabriel with CFC expenses.
$255 raised
26% of $1k goal
3 contributors
3 Years running
Gabriel W. Morrison was born Nov. 5, 2009 to Chris and Jimi Kate Morrison who now live in Chattanooga, Tn. Gabriel was born with CFC, cardiofaciocutaneous syndrome. A rare syndrome only 200-300 individuals have worldwide. It took Jimi Kate ...

Gabriel W. Morrison was born Nov. 5, 2009 to Chris and Jimi Kate Morrison who now live in Chattanooga, Tn. Gabriel was born with CFC, cardiofaciocutaneous syndrome. A rare syndrome only 200-300 individuals have worldwide. It took Jimi Kate years of doctors appointments and even moving to Baltimore, MD to get a diagnoses for Gabriel. To learn more about CFC you can go here http://www.cfcsyndrome.org/syndrome.shtml to learn more.

I am Jimi Kate's "mother Kate Clifton" who is reaching out in hope we might get some help with a few items Gabriel needs that would make his life more comfortable. Chris and Jimi Kate work very hard at always being there for their boys, they also have another "son, Xayden," who will be two in July.

Gabriel has problems with his hips and muscles preventing him from walking. There is a new device called an Upsee (fireflyfriends.com/upsee) that allows a child to walk together with their parent. We are hoping this will build and stretch the muscles in his legs. 

Gabriel also has a problem with staying overheated and skin sensitivity. This is common with CFC patients. We have done endless research on diapers that would keep Gabriel most comfortable. Sherpa cotton and wool have proven to have the best air circulation that would prevent rashes, sores, and help stay cooler.

Both these items are not cheap "any help, even $1" would be greatly appreciated. I know the economy is not at its best. 

Thank you,

Kate Clifton

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