Charlotte Hampton SMA Research Memorial Fund
$3,805 raised
61 contributors
4 Years running
Charlotte Kennedy Hampton was born on June 21, 2012, a full-term, healthy baby girl. On December 18th after noticing Charlotte's head control was not very good and she appeared to have "floppy" arms and legs Charlotte's parents took her to a ...
Charlotte Kennedy Hampton was born on June 21, 2012, a full-term, healthy baby girl. Months after she was born, her parents started noticing Charlotte's head control was not very good and she appeared to have "floppy" arms and legs. Charlotte's parents took her to a neurologist at the advice of their pediatrician. On December 18th, Charlotte was diagnosed with a genetic disorder. That day will forever change their lives as they learned that their beautiful baby girl had a rare genetic disorder called Spinal Muscular Atrophy (SMA) type I. This is the most aggressive form of the disorder and they were informed that their smiley, happy daughter would most likely not live to see her second birthday. Since that day, the Hampton's lives have been filled with trials and struggles while trying to enjoy every last minute with their precious gift from God. As one might expect due to the complications from this disorder, there have been, and will continue to be, a large amount of medical expenses endured by the family. Any help or donation to them will be much appreciated! Thank you to you all for your prayers. Miracles happen every day. Charlotte is God's little miracle to us all. "For I know the plans I have for you, declares the LORD, plans for welfare and not for evil, to give you a future and a hope." Jeremiah 29:11
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