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How often do you worry about diabetes complications?

May 24th, 2012
Category:
Type 1Type 2Oral MedsInsulin & Pumps
ChildrenFoodHighs & LowsRelationships
ComplicationsEmotionsIn the NewsFitness
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We found 7 result(s) that match your search "pancreatitis":

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My mother had diabetes the last 20 years of her life. She was insulin-dependent but she wasn't Type 1 or Type 2. Mom had acute pancreatitis throughout the early '70s and had 90% of her pancreas removed just after the Blizzard of '77 in Buffalo. There was later some speculation that she had some beta cells left or some regenerated because Mom would have horrendous blood sugar swings seemingly out of nowhere.
I remember once going to a mall in a big city 2 hours from home a couple years after the surgery and ending up having an ambulance called for her. Mom kept eating sugar packets thinking she was low, and kept getting worse and worse. As I remember it, when she got to the hospital she was extremely high. (READ MORE)


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I mentioned the other day that there were some issues with my health during my blogging hiatus, and I thought I should share a bit about what was going on during that time.

 

I've written previously about the trials and tribulations that I've had with oral medications; they've either worked great as far as blood glucose control is concerned but had horrible side effects that I couldn't handle, or they just didn't work well at all.  It's been an on again/off again struggle for the last couple of years and, unfortunately, I dealt with more of that during my time away.

 

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In observance of D-Blog Day, diabetes bloggers all over the world have been asked to identify six things they'd like people to know about diabetes. The following are mine:

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It's my last day of Accutane. I've officially finished five grueling months of the "miracle drug." I cannot say that I'll miss it.

 

The first two months weren't unbearable. Increasingly dry skin, headaches, and off and on joint pain. Easy enough to handle. Even with the rising insulin resistance that started within two days of starting the drug.

 

Month three was a hurdle. A big one. Rashes on my arms, migraines, constant back pain, and the fatigue. Oh, the fatigue. Month four and five have been difficult as well. Muscle cramps, unquenchable thirst, insomnia, and all sorts of dryness. On top of that extensive fatigue.

 

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I am not a number. -- "Number 6", The Prisoner

 

One of the questions asked in a recent #dsma chat had to do with the people we live and work with who are familiar enough with our diabetes care to support us, make sure we have appropriate food and drink as needed, who know how and when to administer glucagon, and what to tell the folk at 911 about us. Some debate arose over the common patient-community designation of these individuals as "Type 3s".

 

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The scheduling nurse from the Mayo Clinic called today and said the doctors have agreed to see me. And get this: I have an appointment in two weeks. Yep, two weeks! They're not squeezing me in, they're not making exceptions. I have a regular appointment.

 

So, I'm sort of stuck between really excited and fairly skeptical. I've made it pretty clear that I have high expectations for my endocrinologist. So on one hand I feel like the Mayo Clinic is the best of the best and my expectations will be met and on the other hand I feel like these people are still doctors in one of the largest cities in the country and likely see a ton of patients and why will they treat me any differently than Dr. S did?

 

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I've had off and on bladder pain for several years now. The endometriosis surgery that I had in November was supposed to have fixed it, but I'm not so sure it did. Sunday, I developed vice-like bladder pain that would not go away with ibuprofen. I started drinking tons of water then headed to the doctor on Monday.

 

The doctor said that my white blood count in my urine was slightly elevated, but nothing else showed signs of an infection or kidney problem. I was prescribed 10 days of antibiotics just in case, which I started immediately.

 

My bladder pain had gone away on Monday. But by Tuesday night (two whole days into the antibiotics and lots of cranberry later), my bladder pain had turned into kidney and side discomfort. Just a general malaise. I wasn't feeling up to myself, just out of sorts.

 

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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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