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Old 05-27-2010, 01:37 AM #1
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Angry Not pain ????????????

I found this in a newsletter for people with inflammatory neuropathies, it was written in 2002 so I am hoping the writer has different ideas now. I felt very angry when it read it. NOT PAIN??? The writer obviously does not have peripheral neuropathy


"When a patient complains of pain, I ask "What is the quality of the pain?" Many will complain of
burning sensations or pins and needles but such is not pain. It is uncomfortable but is not the pain
when you have a tooth abscess. "

Hugs to everyone and it is real pain!
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Old 05-27-2010, 06:44 AM #2
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Default Yes--it is just a different type of pain.

That tooth abcess pain is nociceptive pain, but those who have experienced the burning, stinging neuropathic pain are unlikely to confuse it with anything else.

It is hard to describe it to people who haven't experienced it, though, due to its dysesthetic quality.
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Old 05-27-2010, 08:41 AM #3
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The last neuro I went to (with the constant buzzing and intermittent burning and aching in my feet) asked me, "does it affect your quality of life?"

Nawwwwww, I just came to see you because I enjoy the 90 mile trip to Jacksonville!!!!!!!!!!!!
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Old 05-31-2010, 07:19 AM #4
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I too suffer from PN with some days better than others. I'm on Topamax and Neurontin plus Ibuprofen. Honestly? They don't do much for me that I can really tell.

Even when trying to explain to nonmedical people the feeling of walking on hot sand, broken glass, pebbles in the the shoe, burning in the arms, legs, hands, and feet they just don't get it. Shaving is a whole other story with the sensitivity from the blade across my face and the feeling that it is red hot against my skin. Oh! Let's not forget to mention I also have spastic involuntary movements which provides an additional challenge to shaving causing nicks.

Now, when you describe these symptoms to a doctor, not to mention an almighty neuro, and they look at you like you're nuts and question your mental state, what the he** are they good for?

After over 10 years of dealing with these symptoms, regular doctors and stupid, uncaring, desensitized neuros, I have little respect for western medicine. And NO, more drugs are not the answer!

I've resigned myself to deal with it quietly, not complain, and go with the flow. Why not complain? Simple! 50% don't care and the other 50% are glad to hear it. Moral of this story? We have to take responsibility for ourselves, be the most pro-active healthcare advocate for ourselves, and do what makes us feel the best we can while we can. Most of all, continue to look for our own answers because we never know where they will come from. Case in point, Lorenzo's Oil.

OK! I'm done for now. Thank you for your patience and tolerance of my rant.
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Old 05-31-2010, 07:38 AM #5
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Quote:
Originally Posted by NeuroNixed Craig View Post
Case in point, Lorenzo's Oil.

OK! I'm done for now. Thank you for your patience and tolerance of my rant.
What is Lorenzo's Oil?
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Old 05-31-2010, 08:17 AM #6
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Lorenzo's Oil is a true story of a child with an unidentifiable disease and no cure. The mother, specifically, and father refused to believe modern medicine and doctor's, did an enormous amount of personal internet research thus developing the cure, Lorenzo's Oil.

Their son's name is Lorenzo. There is much more to this great story so Google it for more information. I use it as an example modern medicine, much to their own disbelief, do not know everything they think they do.
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"Thanks for this!" says:
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