Tag Archives: type 1 diabetes

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Live. Work. Play: Kelly’s Diabetes Story

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Describing life with diabetes as a “24/7 job” is a common theme in the diabetes community. What with juggling healthy eating, exercise, medication, doctor visits, health insurance costs, etc.—diabetes care sometimes seems to take as much time and concentration as what one does for a living. Continue reading

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Posted in About Us, Life with Diabetes, Staff Stories, Stop Diabetes, Talking Type 1
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Your Rights, One Voice: Kiara’s Story

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Kiara, who is 11 years old and has type 1 diabetes, recently faced an episode of low blood glucose while riding the bus. Although she keeps glucose tabs in her backpack, on that particular day, Kiara didn’t have enough available. The bus driver pulled over and a fellow student gave Kiara a juice box to help. Continue reading

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Posted in About Us, Advocacy, Family, Life with Diabetes, Parents, Safe at School, Talking Type 1, Your Rights, One Voice
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Together for the Win: Our Mission, Football and Diabetes Camp

Team Tackle

Today is the American Diabetes Association’s Capitol Hill Advocacy Day, a time when Diabetes Advocates from across the country gather in Washington, D.C., to urge Congress to make diabetes a priority and invest in diabetes research and prevention. Continue reading

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Posted in About Us, Advocacy, Breaking News, Staff Stories, Stop Diabetes
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Why I Am a Diabetes Advocate: Allison Holdgreve

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When I was 6 years old, my life changed FOREVER when I was diagnosed with type 1 diabetes. Now I am 11, and FOREVER is a long time.
Continue reading

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Posted in About Us, Advocacy, Family, Friends, Life with Diabetes, Stop Diabetes, Talking Type 1
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25 Legends: Hillary Liber

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When I was first diagnosed, I was terrified. My doctor recognized my fear, held my hands in his and asked me what scared me. Continue reading

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Posted in Family, Friends, Life with Diabetes, Red Strider, Red Strider, Step Out: Walk to Stop Diabetes, Stop Diabetes, Talking Type 1
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Your Rights, One Voice: Ashlynn’s Story

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In April 2015, Ashlynn was diagnosed with type 1 diabetes and her access to CREST activities became more limited. Ashlynn’s mother, Audrey, learned that the program would not train its staff to administer glucagon. Glucagon is sometimes necessary when a person with diabetes experiences extremely low blood glucose, also known as hypoglycemia. Continue reading

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Posted in About Us, Advocacy, Family, Life with Diabetes, Parents, Safe at School, Talking Type 1, Your Rights, One Voice
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Living with Diabetes in College: Deanelle

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One of my first such experiences was at the American Diabetes Association’s Camp Carolina Trails in King, North Carolina. Attending camp was the first time I met a large group of people with diabetes. Continue reading

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Posted in About Us, Family, Friends, Life with Diabetes, Talking Type 1
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