My husband and I work hard to manage our son’s condition so he feels good, learns the ropes and has a long, healthy, happy life. But also so diabetes isn’t the focus of his world—there’s plenty more for a first-grader to think about. Still, that weekend a nasty cold, a clog in his insulin pump, and other factors led to a series of high blood sugars and, consequently, vomiting and dehydration. We were shades away from hospitalization.
Category: Living
The College Diabetes Network (CDN) started here at UMass five years ago. It was created by Christina Roth who has Type 1 diabetes, and was then a UMass student searching for peer support. Her first meeting was attended by just a few people, but she understood how great the need was for diabetes peer support in college. She turned CDN from a little group on one campus into a national program.
During my senior year in high school, I once made the tragic mistake of leaving my purse on my car while I drove out of the campus parking lot. Whoever found that purse and turned it into lost and found (thank you, former classmate!) uncovered a satchel filled with loose insulin syringes and half-full tubes of cake icing, my preferred low treatment at the time.
I’ve always loved to travel, and so when I was diagnosed with Type 1 diabetes at the age of 22, one of my biggest fears was that the disease was going to keep me tethered to home. Thankfully, nearly 14 years later, I’ve learned that diabetes doesn’t have to limit my adventures, as long as I’m thoughtful and prepared – and I’ve been fortunate enough to travel to far-flung places including China, Croatia, Cambodia, Vietnam, Siberia, Mongolia and Tibet. Here are my top 15 tips for how to take your broken pancreas on the road, whether you’re headed someplace exotic, or just relaxing on a beach.
JDRF, the leading research and advocacy organization funding type 1 diabetes (T1D) research, and Tidepool, a Silicon Valley-based non-profit organization committed to reducing the burden of T1D, announced a partnership supported by JDRF funding for data access technology for people with T1D who use insulin pumps and continuous glucose monitors (CGMs) through a device agnostic cloud platform.
Sierra Sandison became a role model, symbol, and icon to the millions of people with Type 1 diabetes all by deciding (in an admittedly somewhat hesitant way at first), to do something so simple and yet so complicated it’s hard to fathom: wear her insulin pump in clear sight while competing.
In the diabetes world, I saw numerous commentators extolling the need for a parallel ice bucket challenge to raise money for diabetes research. This made me wonder why the idea of "making a difference" is almost universally equated with fundraising for research to the exclusion of all other needs in the global diabetes community.
College life with diabetes can get complicated and overwhelming. The College Diabetes Network (CDN) is a resource whose sole focus is to help students as they navigate through the wonderful chaos of college. CDN just reiterating "doctors office advice", it connects you with your peers so that you can share real experiences and find what works best for you.
Novo Nordisk has decided to discontinue all its research and development (R&D) activities within inflammatory disorders while increasing efforts within diabetes prevention and treatment, obesity and diabetes complications.
The decision to discontinue all R&D within inflammatory disorders follows a review of Novo Nordisk's strategic position in the therapeutic area after...
you’re in a lecture hall with 100+ people, taking a final exam. Not a sound can be heard except for pencils scratching on paper, the occasional cough, and BEEPBEEPBEEP or BUZZ! BUZZ! from your CGM or pump. It’s absolutely mortifying! Not only do you have to deal with subsequent stares and glares from your neighbors, but you also have to figure out which diabetes problem is causing the device disturbance in the first place – all while taking an exam that you spent the past week studying for. Can it get more overwhelming?