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If you experience pain as a result of your diabetes, what have you found to be the best way to alleviate it?

May 27th, 2012
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We found 10 result(s) that match your search "kidney problems":

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www.google.com

 

"pink fingernails; blood under fingernails"

 

As early as 400 BCE, Hippocrates taught that the nails reflect the condition of the inner body. It is true that abnormalities of the nails can often provide early clues to common medical problems or severe systemic diseases.

 

Red or deep pink: Can indicate a tendency to poor peripheral circulation.

 

Half white/half pink: May indicate fungal infection or, more seriously, kidney disease.

 

(READ MORE)


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I started the pump in October last year with an A1c of 7.3. At the time, that 7.3 was my lowest A1c since before being diagnosed. Growing up, my A1c levels were anywhere from the 8.0's to the 13.0's. Between "sugar free," a lack of diabetes knowledge in the world and being a kid, I never could get my averages right. The three years prior to going on the pump I decided to be an idiot and "take a break" from diabetes. I stopped checking my blood sugar and just blindly did my insulin. I had no idea that my blood sugars were getting into the 500's sometimes. I stopped going to the doctor. What was the point? They were going to tell me the same thing I already knew but just wasn't willing to do. (READ MORE)


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Diabetes has made me a hypochondriac. Every ache, every pain, every change is some condition, disease or syndrome. Now typically I don't truly believe I have any of the things I so often "self-diagnose," but I have to admit that I am constantly living in the shadow of my diabetes. (READ MORE)


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The title reads "Cancer drugs halt type 1 diabetes in mice." My first response is: oh my gosh! How can this be??!??!! Then I read further. I can feel the emotions starting to get the best of me.

 

Do I break out in song? Do I start dancing around the room? Do I cry? What if this is it? What if this breakthrough is the one that we all have been striving for?

 

The article explains that research has shown two cancer drugs, Gleevec and Sutent, to halt type 1 diabetes occurrence in mice. It also says that up to 80 percent of the mice with type 1 diabetes went into remission from the drug. Eighty percent!

 

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I read today about a woman who boluses for every jelly bean, grape and kernel of popcorn she eats. And I can't help but think "why?"
I mean, I know why, but why don't I have that mindset? What has happened to me that I eat a handful of mini vanilla wafers without a second thought? Ok, I do give it a second thought, but I don't use the fast-acting insulin that I have readily available. What exactly is it with me that I can't always bring myself to use that?
I'm a grazer, and I've speculated that perhaps I'm afraid. Afraid that I'll take too much or too little for my grazing, I guess. I, frankly, don't really know what it is. It's not like I'm afraid of needles or anything. I,I just don't get it. I get so frustrated at myself for seeming not to care. (READ MORE)


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I should have known he'd ask about diabetes. Of course he would, I mean he's a rep for an insurance agency for Pete's sake. (Who is Pete, anyway?)

 

I'm on the hunt for short-term health insurance. My new job has a 90-day probation period, which means I don't get health benefits until Sept. 1. I'm currently covered under COBRA, but the premiums are nearly $900 a month for me and the kids. That really puts a dent in the wallet. And really all I need at this point is catastrophic coverage since I have enough pump supplies and meds to get me through and the kids have all had their well-child checks and are up to date on all their shots.

 

The rep had a few questions, he said, before he could get me a quote. I should have just hung up then because I knew he was going to ask about diabetes and I knew that would be the end of it. But I stuck through it, just in case.

 

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Yesterday I posted about my toe problem and I wanted to dig a little deeper into the fear that accompanies any little thing like a spot on my toe.

 

Ever since I was diagnosed with this stupid disease I have be told horrible stories of all the complications that can happen to me. Going blind, losing a limb, kidney’s failing, heart disease, neuropathy, stroke and more. All very real and very scary stuff.

 

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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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This morning, I checked my email as usual. JDRF had sent a clinical trial list to me. I tend to check the list every now and then to just see if there is anything I qualify for and anything that works for me. I've contacted a few over the years but never commited to anything (usually they are out of state and I can't afford the travel expenses).

 

Today was different though. I clicked on two studies. One involved a new kind of insulin. I wasn't too thrilled about the way it sounded. Another really caught my eye though. Islet cell transplants.

 

I've looked at transplants a lot through the years. Way back when, they started using seaweed and all sorts of things to help the body accept the transplants. I've heard good and bad stories from it. I've always been interested, but never quite sure what it would mean for me.

 

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I received this news article by email a few weeks ago. I was actually sitting in the middle of the Mediterranean as I read it. I turned to my mom and said "Oh great, something else to worry about."

 

Diabetes complications are not news to me. My parents and doctors shielded me for many years thankfully. But when I hit the appropriate age, words like DCCT and kidney transplants became part of the diabetes lingo. Slowly, they infiltrated my diabetes lifestyle. The risks, the fears, it all slowly built up over the years.

 

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Julia
JuliaJulia lives behind the Tofu Curtain, in the Pioneer Valley, in Western Massachusetts. It's a nice place. She likes it there. Her eldest daughter, Olivia, has type 1 diabetes. She's also 13. It's a real toss-up as to which is more difficult -- the diabetes or the teen-age drama. (Read More)
Carey Potash
Carey PotashCarey is a full-time hater of diabetes. The benefits stink. His 7-year-old son, Charlie, has been giving he and his wife the finger since November of 2003. Carey's parenting humor has appeared in various websites and print magazines. He resides in the suburbs of Philadelphia with his wife and three children. (Read More)
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