CASTINE—When a doctor says the words “genetic disorder” and “lifelong diagnosis” about a child, it can cause even the strongest of people and families to lose hope for a normal life.
Tough as it has been, 14-year-old Kelsey Carter never backed down from the fight. The Blue Hill resident and George Stevens Academy freshman has lived with an unnamed, rare genetic disorder that has caused physical, mental and emotional issues, and multiple medical conditions. She and her parents, Jackie and Paul, and her sisters, have traveled around the country for testing, visits with various doctors, and consultations, all without answers. Carter was finally diagnosed four years ago, with a genetic defect called 7q 11.23 duplication syndrome.
“This means that on her seventh chromosome, the lower portion, she has a section of extra DNA pieces,” said Jackie. “Instead of one set from mom and one set from dad, she has a whole extra set in that region called the Williams-Beuren critical region.”
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Stonington select board candidates on why they're running
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Hurvitt to replace England as interim superintendent
Fills in during search for new superintendent
2021 lobster harvest the most valuable in the history of the fishery
75% increase over 2020
Flores receives Presidential Award for excellence in teaching
FLORES: Making connections with students and peers
Blue Hill planning board approves hospital plan
A $25 million investment for the long term
Live at the Grandstand!
Get your groove on at the Grandstand Stage with a wide variety of live events throughout the fair.
Despite the rain, Stonington still has to haul water, fixes leak
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The Odd Fellows pitch in
Helping a neighbor, painting a house
Just For Kids holds its last graduation
Terri-Lee Jones retires
Fishermen's Wives donate $10,000 to Blue Hill YMCA
Safety programs, swimming lessons on tap