Category Archives: Safe at School

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Your Rights, One Voice: Jennifer and Allie’s Story

Safe_At_School_082316b

During the summer we were even more lost. We became increasingly concerned about the upcoming school year—we knew we could not spend each day in class with Allie. My husband and I felt as though we were drowning in a sea of uncertainty and confusion. Continue reading

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Posted in About Us, Advocacy, Family, Parents, Safe at School, Talking Type 1, Your Rights, One Voice
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Your Rights, One Voice: Jazmyne’s Story

SAS_2016_6-27

One day at school in late January 2016, 7-year-old Jazmyne Codes, of Moncks Corner, South Carolina, received her insulin dose an hour late. The assistant principal informed her mother, CaTasha, of the incident. When CaTasha asked why that happened, she was told that the regular school nurse wasn’t available. 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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Your Rights, One Voice: Andrés’ Story

SAS_2016_5-23

When Adriana asked about diabetes care in the afternoons, she was told by a few of the camp directors that they could not offer any options for afternoon care. They did not propose anything to ease her concerns. Adriana wondered who would be there for Andrés after the camp nurse left each day — and if he could even attend at all. Continue reading

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Posted in About Us, Advocacy, Life with Diabetes, Safe at School, Talking Type 1, Your Rights, One Voice
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Your Rights, One Voice: Kiara’s Story

SAS_2016_ 4-25

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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Your Rights, One Voice: Ashlynn’s Story

SAS_ 2016_3-29

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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Your Rights, One Voice: Kevin’s Story

SAS_2016-2-22

Sandy of Encinitas, California, needed some help on behalf of her son Kevin, a seventh grader. Kevin, who has type 1 diabetes, had a 504 Plan in elementary school, but it didn’t carry over to his new school. He needed a new 504 Plan to ensure that he would be treated fairly, stay medically safe and have the same access to education as his peers in middle school. 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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Your Rights, One Voice: Kamdyn’s Story

Kamdyn Wilds YROV

On Kamdyn’s second day in the program, her blood glucose level began to drop a bit, but was still within a normal range. Chelesa explained over the phone how to give Kamdyn some gummies to treat the dropping blood glucose. Continue reading

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