Nearly everyone on the staff at T1D Exchange is directly affected by type 1 diabetes (T1D) — living with it themselves or supporting a family member, friend, or partner with the disease.
Here are just a handful of the diagnosis stories from our team at T1D Exchange:
“I was starting the second semester of graduate business school in Philadelphia and began displaying all the common symptoms of T1D. I knew these symptoms from a work project two years prior, but at 24 years old, people I told (including physicians in my healthcare management major) said I was too old to have type 1 diabetes and too young for type 2.
When my vision became so blurry the next day that I couldn’t read the presentation in class, I immediately went to student health and told them, ‘I think I have type 1 diabetes’. My blood sugar was almost 600 mg/dL.”
I went to a CVS Minute Clinic which gave me a glucose test — it was 609 mg/dL. I was rushed to the hospital for further testing.
After getting stabilized with intravenous fluids and insulin, and education sessions at Joslin Diabetes Center, I was ready to take on my new life as a T1D! I love working within the T1D community and advocating for those living with T1D.”
I was rushed from a doctor’s office to the emergency room only to find out my blood sugar was over 1200 mg/dL. After a week of monitoring, intravenous fluids, and education in the hospital, I finally was able to celebrate my birthday.
Twenty-two years later, I’m still advocating and living my best life despite having T1D.”
I was unable to perform in school despite my best efforts, causing me to fail out of music school.
A few weeks after the semester ended, my friend’s mom (who has T1D) took one look at me and said, ‘Can I check your blood sugar?’ From that moment on, I’ve dedicated my career to T1D research!”
What’s your diagnosis story? Share with us in the comments!
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