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People with diabetes, and those touched by diabetes, follow their journey with the disease through a myriad of winding emotional paths. Depression is very common for those newly diagnosed, sadness can rear its head at different stages in the game, and a little humor and humility can even find the door to expose itself from time to time. The keys for controlling those doors are littered all over the place and on  Wrld Diabetes Day today, you can follow this map of internet hotspots. Expose diabetes for all that it is, good and bad, and then share it with others. Find an emotion and embrace it!

 

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Sometimes I really want my friends to know about my diabetes. Other times, I really hate that they know anything about it at all.
My mom always told me to be open about being diabetic so that my friends would know how to treat lows and what to do in case of emergencies. She's right (why are mothers always right?!?). My friends need to know where my glucagon is in my house. They need to know the symptoms of low blood sugars. My friends need to be prepared for the emergency situations that come about when you're diabetic. (READ MORE)

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Last Friday, November 14th, marked World Diabetes Day, and the Blogabetes bloggers marked the day in style. I wanted to make sure you didn't miss their musings, so here's a quick recap!

Scott Marvel wrote a great list of ways to celebrate and get involved with World Diabetes Day - check out his suggestions here!

Lindsey Guerin gave us some insight on how she sprinkled diabetes education into her day.

Michelle Kowalski wrote a poignant post about how emotional this World Diabetes Day was for her.
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I have officially started my new job and I am excited about the potential that lies ahead. For a while now I have been chasing after the opportunity to work for this company and I'm at a point where I feel comfortable sharing more about it. While I am employed full time with my new job I will also continue to do some personal training and be a blogger for dlife. So anyway, enough of the dancing around,I am now a full-time employee of the Juvenile Diabetes Research Foundation (JDRF) and I am really happy about it.
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The problem with living with diabetes 24/7 is that you forget the details of the disease. It becomes like breathing or eating. You only remember the major moments...the great food you enjoyed or the time you got pulled under by a wave and struggled for the surface and air.

 

And that's exactly how diabetes is for me. After sixteen plus years of this disease, I can't remember the finger pricks or the insulin shots or any of the in between. It just zooms past my memory because I don't find a need to remember these minute issues (and my brain would constantly be on overload if I tried to remember 6+ finger pricks a day for the past sixteen years).

 

But today, I'm finding the need to remember these issues. Since I'm back on MDI's for the time being, I've been submerged into the life of insulin injections and many more finger checks. The ups and downs of diabetes are now important. The details are important.

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How often has this question been debated?
Olivia doesn't care what she's called. She calls herself diabetic often. I'm the one with the issue. I always say that she has diabetes. To me, calling her a diabetic makes her only her disease.
On dLife a couple of weeks ago, Jim Turner said that he was always a diabetic, that diabetes was what he thought about, what was going on in the background all the time, no matter what else he was doing. He was, first and foremost, a diabetic.
I can understand that thought process, but I don't agree with it. Yes, diabetes takes up a lot of space in the brain and it's not something that can be shoved aside and forgotten. You always have to take it into consideration. But you take it into consideration along side your life. Your life as a person. A person with diabetes, yes, but a person with a life. A person who is a sister, daughter, student, drama queen and soccer player as well as a person with diabetes. (READ MORE)

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I had no idea the firestorm I would create with one of my last blog posts. The readership and number of comments, though, show me that I hit the nail on the head.

 

We hate diabetes. And that’s OK. I think it’s healthy to say to this disease that I hate it. I do. And I won’t apologize to anyone for feeling this way or for saying how I feel.

 

I was furious this morning when I read Andy’s post claiming that he loves diabetes. I felt attacked and had a how-dare-you-talk-to-me-like-that attitude. But, I think I understand where he’s coming from now. I think he was just trying to help.

 

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When I was little, I imagined a perfect life. I picked careers, pretended to make life-changing decisions and pictured my future. Nothing was affected by realistic needs and the facts of my life. I could be anything and never worry about discrimination in the workplace. I could live anywhere and not stress over medical access or insurance. My mind was limitless.
Now I make these life-changing decisions for real: I pick future careers, places to live and potential spouses. Now I have limits. My decisions factor in my diabetes and my future with diabetes. I look at things like job requirements, insurance benefits and personal reactions to my diabetes. Everything is affected by it. (READ MORE)

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Back in November I wrote a song called "Not By Choice" for World Diabetes Day.

 

The words I wrote were pulled from my memories of how it felt to be diagnosed and not know what type one diabetes was. Thoughts like, “why did this happen to me?” “What did I do wrong?” And I blamed myself for a long time too.

 

Then I found this community online. The Diabetes O.C. which we affectionately call it and a community I mention often. When I found this group of other people with diabetes who had those same feelings, I realized that we could help one another and not give up hope.

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Because I was diagnosed at age 14, I can only speak about not having diabetes from the perspective of a child. I lived 14 years free of diabetes. As a young kid, I did experience a few random episodes of hypoglycemia, but never did I imagine myself becoming a person with diabetes. I didn't even know what the word was. I remember one distinct conversation that I had with a friend's mom. She was talking to me about a guy that we both knew named Curtis. Curtis was a soccer referee and before I knew about my diagnosis, I remember her telling me that he was, "a diabetic and that he had to take shots everyday". Looking back I can remember my exact feelings and reaction to this. (READ MORE)

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