Every story matters. From the moment of diagnosis to the time you conquered the overnight basal rate to the moment when you realized that the CWD community has your back, every story in your diabetes life matters.
Do you have a story to share about your experiences with diabetes? We want to hear from you! Tell us your story using the form below and we'll consider it for inclusion in the CWD Stories section of our website.
I have lived with type 1 diabetes for as long as I can remember. I had just turned two when I was diagnosed, and although I’m sure it was difficult for me as a toddler, it was much harder for my parents. They had to manage my blood sugars using tools that were much more […]
I became a type 1 diabetic in 2013 at age 51. I feel lucky to have great medical care and I have a wonderful husband who is very supportive. The month I discovered I had T1 was a chaotic experience. I had lost 10 pounds in 2 months; the same 10 lbs I had earnestly […]
Sometimes it feels like my daughter has had diabetes for 100 years even though it’s really only been nine. In the early days after her diagnosis, I couldn’t imagine how a tiny glass vial full of insulin would become her lifeline and how without that vial pictures like this one might not be possible. When […]
Hi, I am Maddie. I play the flute, I love singing, I like swimming, I have a younger brother, two rescued greyhounds, and I have type 1 diabetes. I attended my first Friends for Life conference in 2016, after my parent’s bribed me with a trip to Disney World. I could not begin to imagine […]
I don’t ever remember a life without diabetes. Some people might say that’s good, though. I certainly didn’t have a sudden lifestyle change when I was a child or even worse a teenager. I was diagnosed with type 1 diabetes when I was just 18 months old. I just turned 13 this month, though, so […]
I was diagnosed with T1 diabetes when I was in the 7th grade years and years ago. Treatment at that time was archaic, i.e. glass syringes, boiling supplies for sterilization, clinitest tablets for blood sugar testing, limited supply of insulin types, little community support, etc. Despite the limitations, I made my way through a normal […]
I’ve been a diabetic for 9 years and a sabre fencer for 6. I was motivated to find a sport originally to become more active, but eventually I became more focused on fighting stigma associated with type 1 and actual athletic performance. I am ranked in top 40in the US under 17, fence for international […]
I’ve been living with T1D since 1983. My sister was diagnosed six months prior and now her daughter and grandson are all in the T1D family. My first 10 years were pretty bad. My A1C was around 10% (which apparently isn’t perfect) and the BG roller coaster swings rivaled Disney’s Space Mountain. The thing that […]
My daughter was diagnosed with type 1 on December 10, 2018. About a week later, I was sitting in a Mexican fast food restaurant because it was easy to carb count, and started google searching about type 1. I came across Kerri Sparling’s blog, “Six Until Me,” where she wrote her thoughts about living with […]
I’m trying to find the words to sum up last week. I keep coming back to “exhale.” To be surrounded by family that eat, sleep (or don’t sleep), and breathe the literal highs and lows is a powerful thing – for all of us. Even though we are surrounded by a great support system, this […]