Eleven years ago Kate was born with a condition called Sagital Synostosis, and required surgery to reconstruct her skull.
At the time there was no Dell Children's Medical Center in Central Texas, thus we had to search outside of our community to find the right doctors who would operate on Kate and give her a fresh start in life.
We donate 5% of all speaking fees that I earn to funds we have created at both Dell Children's Hospital and Rady Children's Hospital (where Kate was operated on in San Diego), and each February we celebrate Kate with this online fundraiser.
Today Kate is doing great, but one in 3000 children are born with some type of cranio-facial abnormality. We ask you to support the research for this important cause.
Thank you for your support of this great cause!
Thom, Sara, Jackie and Kate Singer
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