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Michael's Apert Syndrome Journey at Gillette Children's
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Since infancy Michael has been treated for Apert Syndrome at Gillette Children's. Shortly after Michael’s birth, doctors diagnosed him with Apert syndrome, an extremely rare condition that affects about 15 of every 1 million U.S. babies.
Apert syndrome is a genetic disorder caused by a mutation on a single gene. Thanks to his surgeries and treatments at Gillette, Michael is developing normally. His parents say he's a bright, happy child, with a delightfully mischievous personality. And he’s always smiling.
In 2014, Michael was chosen by Children’s Miracle Network Hospitals as the 2014 Minnesota Champion child representing Gillette Children's Specialty Healthcare. The Children’s Miracle Network Hospitals Champions’ program recognizes children, like Michael, who have triumphed despite severe medical challenges and brings attention to the important work being done at Children’s Miracle Network hospitals such as Gillette.
Apert syndrome is a genetic disorder caused by a mutation on a single gene. Thanks to his surgeries and treatments at Gillette, Michael is developing normally. His parents say he's a bright, happy child, with a delightfully mischievous personality. And he’s always smiling.
In 2014, Michael was chosen by Children’s Miracle Network Hospitals as the 2014 Minnesota Champion child representing Gillette Children's Specialty Healthcare. The Children’s Miracle Network Hospitals Champions’ program recognizes children, like Michael, who have triumphed despite severe medical challenges and brings attention to the important work being done at Children’s Miracle Network hospitals such as Gillette.
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