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Just the other day I was speaking with a group of co-workers about different life changing events in the life of someone with diabetes. As we sat there and talked about it I began to reflect on my own. I thought about the different times in my life such as diagnosis time, school, relationships, complications, and work. All things that every person living with diabetes can relate to, or will eventually deal with.

Where were you when you were diagnosed? What were you doing that day or at that particular time in your life? Were you at work? Were you at school? Did you go into a coma or diabetic ketoacidosis? Was your vision so blurry, that like me, you realized you couldn't see the picture on the t.v.?
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Several times a year, our social calendar involves an event in which each of us is expected to contribute food to be shared by all. In some parts of the US, this is known as a "covered dish dinner"; in ours, it's called "pot luck". Depending on the event and the organizer, there will be greater and lesser degrees of coordination regarding courses, types of dishes, and quantities to be contributed -- let's face it, unless it's a same-dish/recipe cook-off, even folk without diabetes would rather have more selection than five different pans of mac 'n' cheese, two different types of fried chicken, and twenty apple pies. When you add diabetes, food allergies, and other dietary restrictions into the mix, planning for success can get a bit rough.

 

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Every day, I live my life with diabetes the same way. I test my blood sugar, I treat lows and I change infusion sets. It is a part of me. Sometimes, it is all of me. I get frustrated on a regular basis with the highs and lows or the way it interrupts my entire life from school to dating to sleep.
It amazes me though when I look back on all those days. It makes me smile. As frustrated as I get and all the tears I cry, I don't remember diabetes as my past. Surely, it's there. I just don't remember the daily parts of the disease. (READ MORE)

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Ever since I can remember, I've been a dreamer. Not only do I get lost in vivid day dreams, but my subconscious takes over in the darkness of night with raging images. Over the years, I've come to realize that I have a history of especially strange dreams.

 

They are a mix of nightmares, unrealistic events, and practical moments. I've had some that were premonitions, predicting coming events. Others were so far out of the box that I don't expect anything to resemble them in real life.

 

But the one thing that my mind usually keeps out of my dreams is diabetes and pain. No nightmare has ever involved diabetes complications, seizures, or even diabetes moments. It's so ingrained in my daily life that my brain doesn't find the need to remind me of it in my sleep.

 

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The JDRF Promise Ball is coming up in just a matter of two weeks! I can't believe it's already here. I don't feel prepared at all. Sure, I've been fundraising for months and getting all that in order. But the rest of me isn't prepared to take a night to remember diabetes for the past year of my life.

 

Last year's Promise Ball was absolutely amazing. I took three of my friends with me; we got to dress up, valet park my car and eat a fancy dinner. As amazing as it was, it still brings me to tears today (almost one year later). Because the most amazing part was seeing how much was raised in one single night to find a cure for diabetes.

 

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What an awesome, great, fabulous, wonderful time I had this weekend in St. Louis, MO. I attended a family retreat put on by the Juvenile Diabetes Research Foundation. The event offered people associated with our disease MANY opportunities. There were tons of kids, parents, and loads of helpful information. If you are someone who has diabetes or someone who has a relationship with a person with diabetes then I would highly recommend becoming a part of your local JDRF chapter if you have not already. There are literally hundreds of them around the globe and the nation and you will get everything you need from them.
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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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2007 is behind us now. It blurred by and stamped in key moments that will surely be remembered. My past year with diabetes stacks upon only a few others since I was diagnosed. 2008 will mark four years since that day in the hospital and it seems like I'm always learning something new. Each highlighted moment in this year taught me a little more about how I successfully live with diabetes. (READ MORE)

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A topic came up on one of the diabetesteentalk forums which got me thinking. The topic was about how diabetics miss days from school or work because of doctor's appointments, seizures or ketones. There were alternating perspectives. Some chose to think that if you miss for diabetes related events, you should be excused or allowed time off without feeling guilty. Others chose to think that you have to suffer through at work or school and should not miss because of diabetes. After all, it is a self managed disease. (READ MORE)

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My friend L's mom died over the weekend. I've known L as long as I can remember, probably close to 30 years. We were girl scouts together in grade school, played flute together in middle school and while I played the piccolo in the high school marching band, she twirled along as a majorette. Though we were never "best friends," we've kept in touch over the years through mutual friends.
L and her parents are in the background of many of my childhood memories. Her dad, R, was the high school band director and I remember her mom, J, at girl scouting events going back as far as the first grade.
It's always sad when someone dies, but what makes this even more sad is that L's dad died a few years ago. She's too young to lose both her parents. (READ MORE)

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