For our birthdays, Brad and I took a much-needed vacation… a Western Caribbean cruise.
This was cruise number six for us. It was originally supposed to be a couples’ winter escape. Our decision to take this trip was actually made while sitting in a winery in Madison with our friends in November. Tickets were booked and we were planning our escape when our friends found out that they are expecting (yay!). They weighed the risks and decided to do what is best for them and their baby and cancelled the trip. Every place on our travel itinerary had a CDC travel warning about Zika for pregnant women. Whenever you travel, double check no only the security warnings about your destination, but also the health warnings.
So Brad and I went by ourselves. It was incredible and relaxing. It was nice to get away from winter for a little while. I have a few pictures from our trip to share with you. Enjoy!
First order of business when on board: Lunch at Park Cafe
I’m wearing blue today, as I do many Fridays during the year. People must really think that I like the color blue. While I do like blue, the color means a bit more to me.
November is Diabetes Awareness Month… it’s a global awareness month. November isn’t really a month for people with diabetes, because we’re well aware of the realities of this disease each and every day.
November is for you, dear friend without diabetes. It’s a month specially set aside for you to be aware of diabetes. To learn about the realities people like me face every day. To learn the truths about the different types of diabetes. To change your mind, your language and your attitude about the word “diabetes.”
The two most prominent diabetes organizations are working hard this month to help spread awareness and enable advocates.
So my diabetes gadgets were Out of Warranty and I had planned to keep it that way as I wait for better technology. Hope draws closer as people are actually being enrolled in the first tubeless artificial pancreas trials (wish one of the clinics were here in Cleveland!). But I’m halfway back under a warranty.
My Dexcom gave the dreaded, “transmitter battery low, reorder soon” message. So I called my medical supply company. After a slightly frustrating conversation where I had to repeat myself four times and spell the word “low” the lady said she’d get the paperwork in for me to get a new Dexcom G4 system. “Since I’m getting a whole new system, let’s put in paperwork for the Dexcom G5 please.” (Because who wants new-old technology?)
She put in the order and I anticipated full transmitter battery death was imminent and prepared to fly blind for a week or so without my CGM. Thankfully, that didn’t happen.
I feel like I’m in a perpetual state of conflict over the perception of my life with type 1 diabetes.
Because I choose to not hide my diabetes, I found myself at a party with my Dexcom sensor fully visible on my arm, talking to a friend’s husband. He was asking me the questions that I’m used to answering. The ones I get on a regular basis from family, friends, acquaintances and strangers. The questions were about what my equipment does, what I can and can’t eat, etc.
Then came the familiar one, “So as long as you do what you’re supposed to, it’s not a big deal. Right?”Continue reading →