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May 26th, 2012
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When I was in high school I played volleyball. Like most schools, we had a junior varsity and a varsity team. I believe I was a sophomore (maybe I was a junior,it was a long time ago) when I started playing for JV and varsity. OK, so I actually played for JV and mostly warmed the bench while the varsity team played until the coach got mad at a player and decided to send me in.
At any rate, I was called a floater, as were the other girls who played for both teams. Until I got involved with the diabetes community, my definition of floater was a person who moves between two high school volleyball teams. It wasn't until I started frequenting the Diabetic Mommy web site that I learned there are actually more definitions for this word. (READ MORE)


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I've always loved my hair. I used to say it was one of my best features. Once I understood and appreciated my curls, I learned how to take care of them. Throughout college and before having kids, I had long (mid-back length), curly hair.

 

I started cutting my hair shorter around the time No. 1 was born. I would go back and forth between wanting it short and wanting it long. The Mr. has always liked my hair long, and I think for the most part I prefer it that way.

 

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I'm meeting a friend of a friend for lunch on Thursday. I've never met either of these friends in real life, but we've chatted via e-mail for years and months.

 

I "met" C. after I e-mailed her about her blog. She is a writer/editor (like me) and has type 1 (like me), so we had some instant connections. I asked her a professional question and we just kept talking, bouncing ideas off each other, chatting about family, etc. (She's writing a book, by the way, about pregnancy and pre-existing diabetes.)

 

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"I know diabetes shouldn't be a connection, but it is," M. said as I was telling her about my lunch with S. today.

 

"But it really is," I said. I knew what she meant. That we should all have better things to be connected by than health issues. But it is what it is.

 

"You know, whenever I meet someone who rides horses we have that instant connection, even if there's nothing else there's that," she said.

 

"Yes, exactly," I said, nodding.

 

I was standing at the entrance to her cube, where I often stand to chit chat with her, discussing how I met S. and how our lunch went.

 

"We talked a little about diabetes, but... well, it certainly wasn't the focus of our conversation," I said.

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As an informed person with diabetes and an active member of several online diabetes communities, it's important for me to "get out into the real world" and make connections with other people with diabetes and with people and associations whose purpose is to support us medically, psychologically, and socially. In addition to real-life meet-ups with members of my various diabetes online networks, I go to health fairs and community events to make contact, inquire about the state of diabetes-care support and diabetes advocacy programs, and have even given a presentation about how diabetes online communities positively effect the lives and health levels of people living with all types of diabetes. 

 

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Yesterday I posted a picture on Facebook of Dexcom with a flatline, showing 100 mg/dL and a trend arrow going nicely straight with a caption that said "Beyond cool."

 

I didn't expect many -- or any, really -- people to comment or "like" the picture considering I don't have that many D friends on Facebook and many of my non-D friends likely don't know what to say when I post diabetes-related stuff.

 

When I checked on the photo later in the day I was slightly surprised (which isn't even the right word, but will do for now) at the one person who did "like" the photo. I don't know why this caught me so off guard, but it did. I couldn't figure out how he would know this was significant.

 

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It's no secret that several of us who blog here at dLife are active in a number of diabetes-oriented online forums and social networks -- what we refer to as "the Diabetes Online Community" or "the DOC" -- and that in the process, we've learned which people, which groups, and which venues are doing what in terms of offering emotional support, medical and lifestyle advice, places to gripe and complain, and ways to use our various talents to make living with diabetes easier (or less difficult, depending on your point of view) for ourselves and others to manage.

 


I must also mention here that I have been, for the most part, a satisfied user of Freestyle glucose meters since I adopted the Therasense Freestyle several months after my initial diagnosis, upgrading to the Freestyle Flash almost as soon as it came out, and eventually to the Freestyle Lite (which I currently use).

 

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If you have only one day to see the Tour of Somerville, Monday's the one to aim for. The Borough of Somerville puts on a day-long festival that starts with a Memorial Day parade before proceeding to a family fun-ride and the day's races. Vendors of cycling gear, healthy-lifestyles, and other stuff are set up on the lawn in front of City Hall; club team tents are lined up on the lawn along the side street; and the whole area is punctuated with local fraternal organizations selling burgers, hot dogs, and other "hand" foods while spectators line the barriers along the route. It's also the day Team Type 1 - sanofi-aventis plays "meet the public" in a big way, signing posters and team cards under the Sanofi tent as well as racing in three or more of the day's criteriums.

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Last night, I participated in #dsma, a Twitter event for the diabetes online community. It happens every Wednesday at 9pm EST. I've joined in a couple of times before, but never gotten into it like last night. I've been really focusing on Twitter the last few weeks and finding connections with the DOC.

 

#dsma is crazy. It's fast paced. That hour goes by like lightning as you're trying to read all the other tweets, submit your own, and truly make an impact with fellow D tweeters. It's insightful and it's thoughtful. For that hour, you are thinking about the diabetes community, how to connect, how to integrate different ideas, how things apply or don't apply.

 

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First DBlog Week Prompt: It seems the most popular thing about Diabetes Blog Week is that it helps us find blogs we weren’t reading yet and connect with some new blog friends. With that in mind, let’s kick off Diabetes Blog Week by making some new connections. Think about the d-blogs you read that you think we may not know about and introduce us to one that you love!! Let’s all find a new friend today!    Special thanks to Gina, everybody’s Diabetes BFF, for helping me title this post!)

 

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Lindsey Guerin
Lindsey GuerinLindsey is a typical, yet unique, Texas girl who loves shopping, movies and reading. She loves to travel and take risks. She dreams of diabetes cures, never-ending cheesecake and her own airplane. The rest you can discover in her blog! (Read More)
Michelle Kowalski
Michelle KowalskiMichelle Kowalski, a writer, editor and photography hobbiest living in Phoenix, was diagnosed with Type 2 diabetes in February 2005. In January 2008, as part of her quest to start on an insulin pump, Michelle learned that she actually has type 1 diabetes. (Read More)
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