Travelling is often considered one of the best ways of taking a vacation. That’s why most people use the saying “getting away from it all” when they go somewhere. But for someone with Type-1 Diabetes, travelling can present its own set of headaches and problems that often just doesn’t make it worth one’s while to take a trip. I’ve posted often before about what people should bring with them or carry in their vehicles while travelling, especially in the winter. But while rounding the corner on 1,600 posts, who the hell remembers what I provided three or four years ago. By virtue of this, today’s post will focus mostly on my own experience and what you should bring with you, if you have Type-1 Diabetes.
I think there’s a distinct irony in the fact that until about ten years ago, travel was no big deal. A couple of boxes of insulin, a box of syringes and my glucometer with a full jar of strips and I was off to the races. My biggest issue was worrying about getting through security at an airport with all the sharps in my bag but besides the occasional longer time to get processed through, I’ve honestly never had a problem. But these days while being on pump therapy, I fnd myself needing to pack and carry about a dozen separate components, most of which act off of one another so forgetting one is just as bad as having brought nothing at all. I still aheva bit of an extended wait time at airport security and often need to be patted down since I have medical devices attached to my body, but I still don’t have significant issue in that area.
Whether I’m driving or flying, the main nissue comes with proper preparation and packing before the trip even happens. For example, we’ll start with the most important piece of equipment, which is my insulin pump. What’s nice about the pump is I use a model that has continuous glucose monitoring and tracks my blood every five minutes, making micro-adjustments as I go through my day. This can be exceptionally important while travelling since, as you all know, absolutely EVERYTHING affects blood sugars. But the pump itself uses four separate components (including the pump itself) that need to be changed out every three days. Time and insulin calculations can make the difference between having a smooth trip or scrambling to the nearest pharmacy to try and figure out if they carry what you need. For the pump, this includes the insulin reservoir, the infusion set and the bottle of insulin. It’s kind of hard to travel WITHOUT the pump, since its attached to me. In ten years of being on pump therapy, I’ve yet to leave the house without it.
My CGM, or continuous glucose monitor, is even worse. It uses five separate components, including the inserter, adhesive bandage, the sensor, transmitter and charging cradle. Every time I cahnge this bad boy, I need to put the transmitter into the charging cradle for about an hour. Then all the other components come into play. A small price to pay for well-controlled blood sugars but if you’re keeping score, we’re slowly creeping towards a dozen separate pieces of equipment I need to drag with me when I travel. This is why the calculation is important. For example, I’m currently sitting in a hotel room in Saskatoon where I travelled for my scheduled eye injections. Although I’m only away from home for a little over 24 hours, I checked how many units of insulin I had left in my pump and “assumed” I would have enough to last until I get home. But it’s surprising how many carbs were in that burger and fries I had the previous night. By the time I rolled out of bed about an hour ago, I only had five units left. Thank the light I brought a spare set of everything…
And that’s the take away lesson for today. Bringing extras of everything, even when you don’t believe you’ll need them, will avoid problems and make your trip smoother and less stressful. Calculate how many infusion sets and CGM sensors you’ll need and double it. After all, it may not just be your schedule or your usage you have to contend with. What if you have a set failure? What if you sit in a hot tub at the hotel and fry your sensor? What if your infusion set gets ripped out by something? These are all things that I’ve had happen to me. Always bring more than you need and that includes your insulin. Bearing in mind that I’m aware that not folks are in a position and have the additional resources and equipment to always carry extra, of course.
Over the years, a key component I’ve always carried with me is a full bag of skittles or gummy bears. yes, you read that right… While some folks use orange juice ro something similar, that shit takes FOREVER to work on me, if I’m having a low. If boarding a flight or travelling a long distance on the road, you may find yourself in a compromised position if you have a low and suddenly can’t get immediate access to something sugary. If you’re travelling the vast expanses of Canadian highway with hours between stops when you suffer a low, that bag of skittles could mean the difference between carrying on safely or finding yourself in a seriously compromised position.
All of this should be pretty common sense, especially if one has had Diabetes for any significant amount of time. On a final note, keeping a small, basic first aid kit with you is always a good idea. Basic kits will usually come with small bandages, adhesive tape and bandaids. People with Type-1 Diabetes are prone to infections when an injury happens. That cut you got while hiking or the knee you scraped falling off your bike, can become a problem quickly, if left untreated for a significant period of time. Quickly cleaning it and slapping a band aid on until you get home can make all the difference. Unexpected injuries can occur while travelling, as well. These are just basic steps to try and take some of the stress off of travelling. Given the added steps and effort it takes, sometimes it doesn’t seem worth travelling. But it also isn’t worth staying hidden at home to avoid that effort. Not my style. Diabetes shouldn’t prevent you from doing anything you want to have a happier life. Food for thought… ☯️
