Gabriel was never well enough to have an operation. But through the foundation we named after him, we have been able to fund operations that put smiles on hundreds of young faces
On September 19, 16 years ago, my son Gabriel went to heaven. He was born with a rare chromosomal disorder called trisomy 13. He had cleft lip and palate, had a hole in his heart, and was severely vision- and hearing-impaired.
Gabriel was never well enough to have an operation. But through the foundation we named after him, we have been able to fund operations that put smiles on hundreds of young faces. Gabriel’s Symphony Foundation is a reminder of his life and the inspiration he is to all of us who love him.
Know more about Gabriel’s Symphony Foundation on Facebook:
https://www.facebook.com/GabrielSymphony/
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