Personal Stories: Impossible Moments
This post was originally published on taylordenniswrites.com on November 17, 2020. A couple years ago, I had an appointment at…
My Experience Photographing People with T1D & Their Devices
T1D Exchange asked me to do a photo series portraying diversity within the diabetes community, highlighting people and their devices….
Decolonizing Type 1 Diabetes During Black History Month
Black History Month (BHM) was originally a week-long movement invented by the historian, educator, and activist, Carter G. Woodson in…
Putting The One in T1D: A Love Story
“When did you know that I was ‘the one’?” My fiancé Jason read this question aloud while looking at his…
In Honor of Black History Month, Meet Dalyce
I was in second grade when my name got called to the office. I packed my things, curious about how…
The Impact of Connections for People Living with T1D
There was one weekend during my senior year of high school that I can thank for opening my eyes to…
Living with T1D and Managing Stress During a Pandemic and a Racial Revolution
Emily’s Story: Using Nasal Glucagon to Treat Severe Hypoglycemia
Emily Marcum was excited to take her parents, John and Andrea, on a 10-mile walking tour of Manhattan and Brooklyn…
Bolus Maximus Gives Men with T1D Space to be Vulnerable
I met with Brandon A. Denson and Matthew Tarro, President and Vice President of Bolus Maximus, for a podcast on…
What My Diabetes Diagnosis Taught Me about Health Inequity
The term “health equity” may seem abstract until we connect it directly to personal experiences. Since being diagnosed with diabetes,…
