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The symptoms for this:
1.extremely painful burning sensation, like a 2 or 3d degree sunburn
2. over most/all of my body
3. skin hot & dry & dark red during the episodes only
Any ideas on what it could be?
I did tell my doctor about it during one of my visits. And I emailed her over the holiday about the dark red color of my skin. She was not real sure what to make of it either.
Thanks,
HootyView Thread

Diabetic neuropathy is very painful. I had it for three years before my PA dx'd the diabetes [2003>, then I went to my neuro because he kept misdiagnosing my problems with my legs and feet. [I also changed doctors a number of times since then.> I was already an established patient of my neuro, so I did not need his say-so to go to her.
Currently, I am on 1600 mgs of neurontin daily for my neuropathy. I might go back to my neuro early next year, as I think it may be time for a bigger dose ? Keep walking even if it is painful, it will help in the long run.
There are numerous meds for diabetic neuropathy, so if the med you have is not working, it is good to discuss it with your doctor/s and try either a higher dose if the med can be done in higher doses, or different meds. Sometimes multiple meds could be the answer.
I have read on here that keeping one's sugars under control is helpful to relieving neuropathic pain. My sugars have been under control for a long time, but if it helps, I cannot tell it is helping. Then again, the nerve pain and damage could be worse, so perhaps it is. My meds help, but they are not 100% on relieving the pain. Perhaps they are about 80% or so.
Keep walking all you can, and do not give it up.
HootyView Thread

Those things are also such puny and stingy portions, and no thanks. They LOOK disgusting to me. Food has to look and taste good to me. If stuff looks disgusting, I cant eat it. [i.e., cooked greens, liver, etc . Eeewww.>
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HootyView Thread

Oh yeah, drug companies have programs to help you with meds, but sometimes they still expect a person to pay part of the cost, and they do not even have enough means to do that. I know when I was waiting for my disability to be approved, I had $100 a month to live on. There was no way I could pay even the smallest copay for meds. Sometimes I was able to find help with my meds, and sometimes not. The drug companies live high in their Ivory Towers and are totally clueless on the hardships they create for people. Looking for help to buy meds, pay utilities, groceries, house payments etc is very degrading. I would gladly work, but my health interferes with that, despite my best efforts. At least now I have insurance, even though I still have to fight them on some things.
I have had to cut corners with insulin and syringes in the past too. Even so, last month I was without my seizure meds for over 2 weeks because of it. Disability is less than half of minimum wage; and they keep giving away our SS monies to illegal immigrants and other non Americans... GRRRRRRR..
HootyView Thread

this is an ILLEGAL law just passed by Congress and Obama secretly.
HootyView Thread

And as others have noted, many other things can cause nerve damage including toxic chemicals in your enviornment. I was raised on the east coast in a large industrial city. My dad built lots of model airplanes and we inhaled the glue a LOT. Toluene is a known carcinogen and causes many health issues. There are all kinds of toxins that I was exposed to growing up, so...
HootyView Thread

I think insulin would give you a LONGER lifespan than the pills would, and a healthier outcome also.
HootyView Thread
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