Tag Archives: travel

Traveling… And some D Stuff too.

Full Disclosure: This is primarily a non-D post, with a couple of D stories included.

The Great Spousal Unit and I traveled to Virginia so I could attend an open house where they’re working on the Artificial Pancreas at the University of Virginia in Charlottesville, Virginia. It was a great opportunity for me. For Maureen, that meant the chance to spend a couple of extra days in one of the prettiest parts of the country. She has a some family there, and there are about 15-20 vineyards between Charlottesville and Staunton (pronounced Stanton), about 45 miles to the west.

So We stayed in Waynesboro, where Maureen’s cousin lives with his family (about 30 miles west of Charlottesville). I wouldn’t normally mention something like this, but we stayed in the absolute best Holiday Inn Express for three nights there. People were friendly, everything was clean. Even the morning breakfast bar was good.

So where was I? Well, let me start with a D story, kind of. This is when I went for my visit at UVA’s Center for Diabetes Technology. Shortly after I arrived, a couple of the other guests arrived… one with a diabetes alert dog. I had never seen an alert dog before, and I was very curious. Plus, I’m a dog person. Almost as soon as they arrived, the dog started alerting its owner. I found out it was a high alert (I only thought they gave low alerts, but no). While we were talking, the dog kept alerting. The owner did a quick BG check, and she wasn’t high. She did mention that her dog would probably have trouble since she’d be at a gathering with a lot of Type 1s. Well, the dog just wouldn’t quit with the high alerts. Then it hit me: I had just eaten lunch before I arrived. I thought… maybe I was the reason for the high alert. So I excused myself from the conversation to go get some water, and I walked to the other end of the hallway. And the dog stopped. I tried to make sure that I wasn’t near her dog the rest of the visit. This person probably thought that I was not friendly, and I feel bad about that. But I wanted to make sure that if her dog gave an alert, it was for the right reasons, and not because I had a few french fries with lunch.

Now on to the travel. It wasn’t all wineries. We spent most of a day in Staunton, birthplace of Woodrow Wilson. Staunton is a beautiful small town with a lot of history. We shopped in the stores downtown, had lunch at Gypsy Hill Park, and got a milk shake at a little drive-in that’s been there for 60 years. We also managed to get in a vineyard visit before heading off to dinner. I really needed these two extra days off. Days like this help me take some of the stress off and recharge the batteries.

The next day was spent touring wineries. We’ve toured Virginia wineries before, many of them in this part of the state, and this was a great day to do it. Virginia has spent a lot of money subsidizing wineries in the state in the last few years, and it shows. There really is something to be said for going to the source and hearing from the people who are directly involved in making the product. And wine tastings ain’t a bad way to spend the day. Well, Maureen got to do the wine tasting, and I got to drive around a lot. But it was fun, and she deserved to get some extra attention for a while.

The fun part of the tour that day involved the Concrete Egg. You read that right: Concrete Egg. One of the new wineries we visited was Stinson Vineyards. We were told they are one of four Virginia wineries aging some of their wines in a 2,700 pound concrete egg. It’s for white wines primarily, and while aging, the wine actually brings in the minerals from the concrete. But in a good way. Gives it a unique taste. Think the difference between tap water and mineral water. They were very welcoming at Stinson, and they let us go back and check out the egg… they were quite proud of it. Stinson is a newer winery in the Charlottesville area, and it looks like they’re doing everything right. And the owner, and everyone we came into contact with there, was a woman. Girl Power in a winery.

My final story is another D story: After dinner Saturday night, it was time for a set change. I pulled out the set I had been using, and went to get everything together to put in a new one. It was only then that I realized that I had forgotten my Quick-Serter… the spring-loaded thing that shoots the cannula into my skin. What to do? I had three choices:

1) Drive the 3 1/2 hours home, immediately
2) Go the MDI route, with only fast-acting insulin available
3) Manually insert the cannula

I had never done a manual insert before, but I had read from others who had done it. I wanted to give it a try. The next set was due to go right in my belly, so I got everything together, and took a deep breath. Do you know that it’s hard to do the Quick-Set manually? I must have tried to shove it in about 8 or 9 times. I didn’t expect the needle to be so dull, but it was. Eventually, I had to get over a little bit of squeamishness, and the site of some extra blood from failed attempts, and I finally got it shoved in there. Literally had to push the thing in there, hard.

But it worked! And it lasted for 5 days. Not something I want to do all of the time, but it’s nice to know I can do it if I have to.

Now on to the pictures!

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Have a great week!
 
 
 

Public Diabetes.

I went to New York on Saturday to hang out with The Great Spousal Unit’s brother and his family. I’ve made no secret of that fact that up until about a year ago, I never took my meter out in public. In addition, I never really wanted to show my pump in public either. I always had it under a big shirt. And I was very careful to kind of turn away from everyone (even if it was friends or family) when I used the pump to bolus or adjust my basal.

It’s not that I really care about anyone seeing me. Anybody who has a problem with it can just shove it, you know? But I don’t want anyone to get sick once they see the sight of blood on my finger. And I’ve certainly noticed how freaked out people get sometimes when they see me using my pump, like I have some sort of really scary problem. Well, it is a scary problem. But that doesn’t make me scary, does it? Anyway, I don’t want anyone to be afraid of me. And I don’t want anyone to look at me with pity. Those kind of things make me feel bad… like it could be avoided if I just hide it away for a while. So until now, I’ve either left the meter at home, or left it on the bus. While I was away, or at least while I was in Manhattan, I was guessing about basals and boluses.

But I’ve been reading posts in the past year or so from many in the DOC who show that testing, set changes, pump adjustments in public are no big deal. It’s just part of what you do. Those posts were powerful, empowering examples for me. I started to realize that at some point, my health and my care had to become a priority. And damn the consequences. So this time, I put my meter in my pocket and used it all day.

I used it at lunch (142 mg/DL). And then about 45 minutes before I got on the bus to go home, I stopped in a small place to grab a sandwich and some iced tea. After walking around all day (that’s what you do in New York) in the 95 degree heat, I was feeling pretty crappy. I wasn’t moving well, and I was thirsty, my mouth was dry. I was certain I was still high. So much so, that I almost didn’t even check. But then I thought: no, I have to know… coming down from 150 requires a different strategy than coming down from 250 or more.

So I pulled out the meter, and right in front of about 35 people, I checked: 52 mg/DL

If I had just bolused based on a guess, how long before I would have gone hypo? What would that have looked like? How would I feel about myself the day after?

I’ll name it: I overcame fear Saturday. Ridiculous, stupid, ego-based fear. Stupid, dumb, vain things that I’ve been feeling and keeping deep inside for a long time. Saturday, it could have affected me in a very bad way.

Don’t be me. Make your health and your care the top priority. Today. Right now. And who knows? Maybe your initiative could serve as an example to someone who’s still hiding their diabetes from the rest of the world.