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Elder
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[Welcome to Neuro Talk. MrsD does know alot about PN. I also have followed her advice as I was DX's with PN, but only on certain areas of my body.
Her information was agreed with, with my physiatrist. I take some suppliments and low and behold I am better a year later. You do need to get DX's. There are clinics, that treat, according to what you can afford. Your hospital advocasy dept. maybe able to help you find someone to see you even with no insurance. I was in the same boat, no insurance. It may take a bit of effort, but you do need to be seen. If you can, keep a journal of all that you are experiencing. Even the post you sent us. This can help your doctor determine what is wrong. If this is interfering with your life, be assertive and find that good doctor to help you. There is alot of hope regarding PN. I do wish you all the best as you move forward with this. NT will be here to support you every step of the way. ginnie ![]() |
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"Thanks for this!" says: | krystar2k9 (03-05-2013) |
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