Bringing DIY To Our Daughter’s T1D (By Closing The Loop)

It’s a little bit after six in the morning, and I find myself, as I do most mornings, at work at Remington Park. The sun is just peeking over the horizon and the racetrack is beginning to come alive. Horses snort and buck on the mechanical walkers, grooms move to and fro saddling and bridling the ones headed to the track for training, farriers and jockey agents and veterinarians begin their morning rounds, while the trainers and assistants organize their days. I sit in my truck sipping coffee, having completed my early morning chores and preparing myself for another busy day. A quick glance at my Pebble watch brings a smile to my face, as I see the impossibly straight line and the reading of 113 mg/dL, which tells me that my daughter is sleeping peacefully in her bed as she has all night, and is safe. Continue reading

The Power Of The Reveal (Finally Telling My GF I Had T1D)

I was diagnosed with type 1 diabetes at age 6 and was told that I took it like a champ. I was not afraid of the injections or the frequent blood tests while I was hospitalized. When the doctors told me to look away I would usually tell them no, I’m not afraid. In fact, my only major problem was I missed being home with my family and toys.

At that age I was pretty open with the fact I had diabetes. I would often inject or test in front of family and friends and they would be in awe at my bravery. When I returned to school, my classmates and teachers were informed about my health issues and they all looked out for me. Anytime I the opportunity arose, I would show off my needles and other diabetes gear. Continue reading

How To Fuel Your Way Through A 24-Hour Swim Relay

My sister convinced me to sign up for a 24-hour relay swim to raise awareness for Multiple Sclerosis (MS).

Swimming I like, raising awareness for charity I enjoy, and a new challenge beckoned. Doing this 24-hours after flying back from a Boston marathon trip – this would be fun. Continue reading

Q&A with Amy: Running the Boston Marathon in Range, the Whole Race!

It’s great connecting with past podcast guests (see episode 19). I got word that Amy McKinnon was traveling the world again, motivating me to get in touch. Amy was kind enough to give us insight into her recent completion of the Boston Marathon (no small feat).

Q: What adjustments in your game plan did you make for this marathon, compared to past races?

A: Leading up to Boston I had a couple of injuries that took me off my feet completely for a few months, so I wasn’t where I wanted to be with my fitness level prior to a race. Because of this, my pace would be a lot slower, so I changed my race plan completely. I decided to focus on keeping my BGLs in range the entire race while enjoying the atmosphere of the crowds and running the prestigious Boston Marathon. I went into the marathon with a very light-hearted approach, compared to my usual competitive self.

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Ask Us Anything #3 (Type 2 Clarification, Lows, Exercise, and Parenting) | Amber and Ryan | Real Life Diabetes Podcast 42

Finally, the long-promised, definitely under-delivered Ask Us Anything podcast is back. The questions rolled in from Oregon, LA, NYC, and a suspected location below the Mason-Dixon line. Of note, we looked back at those practices we loved from our parents… and those we would advise against, kindly. As it turns out, low blood sugar symptoms change over time, and we covered our own evolution. Par for the course in most episodes, we politely disagreed about the distinction between type 1 and type 2 diabetes. Continue reading

A Stroll Through My Life Of Low BG Reactions

Over the past three years of binge reading other PWD’s posts and interviewing people who live with diabetes, the common theme has been our ability to recognize low BGs changes over time. In my adolescent years, my nose would feel numb and I would get shaky. At that point in my life I was checking my BG every once in awhile so my body took the reigns and made sure I knew something wasn’t right. It was all about trial and error – I feel woozy and am shaking so I would down a packet of honey or four and start to feel better. Continue reading

Making It In NYC… As A Dancer… With T1D

I was born in Vancouver, BC and at 18 months old I was diagnosed with Type 1 Diabetes. I consider myself lucky to have grown up in Canada where majority of medical supplies are covered and you don’t have to beg your insurance company on your hands and knees for equipment, like insulin pumps and CGMs. I think I’m even luckier to have parents who were not afraid of my diabetes and let me join numerous dance classes at a young age. I’ve always had a passion for dancing and performing and I knew that I wanted to make it my career as I got older. I also knew that NYC was the place with the most opportunity to make it happen and that is why I moved to the Big Apple. Continue reading

Searching For Embrace (Inspiration Will Eventually Show Up)

Living with diabetes is far from easy–checking BGs multiple times a day, giving yourself insulin injections, and changing pump sites every three days (at least you’re supposed to…). I was diagnosed with T1D at the age of two. Luckily, I was raised by wonderful parents who taught me very early on to be independent, giving my first injection at the age of four and learning the carb vs. insulin ratios at six.  Continue reading

Does Diabetes Phantom Pain Really Exist?

I’m completely aware I sound crazy, but I’ve experienced a new diabetes scenario since jumping on board with the Dexcom G5. I want to be clear as I stated in a recent post, Losing My T1D Technology Virginity, the insertion of the device did not/does not hurt so this recent discovery had me questioning how my mind is processing a foreign object/device being attached to me… Continue reading