Help fund HadIt.com. Please note HadIt.com is NOT a non-profit, there is no tax deduction for helping to fund HadIt.com Veteran To Veteran LLC
We have been very lucky since 1997 in being able to fund the site from advertising and my own pocket. Unfortunately my pockets are empty and revenue for the site is down. So if you want to help keep the site funded please use the button below and help fund the site.
Posted 17 July 2008 - 04:06 PM
Posted 17 July 2008 - 06:15 PM
Do you have back trouble? Did yout MRI show any cervical, or lumbar back degeneration?
Nerve block 4 weeks ago and pain worse. Had them in past without any success, hoped for improvement, but notta. What about fibromyalgia also...where else is all your pain? Trigger points with fibro yet many people have probs with feet too. I think sometimes peripheral neuropathy can be evident without examination, testing confirmation, ie(EMG), that is just my opinion. There are some nerves that have neural impulse synaspes that misfire, esp if compression of nerves.
OTC meds don't touch the pain. Hydrocod. or fentanyl patches may help to manage it but not always and not a cure. Then you have to worry about the s/e of meds esp. with the other meds you take...esp watch for antidepressants with pain meds.
I had an EMG today because my feet hurt so much. The VA said there was no nerve damage in my feet or pinched nerves. So I guess I am cured. Can you have peripheral neuropathy and yet not show any damage on an EMG? I have miserable pain in my feet and sometimes lose my balance, but VA now says my nerves are fine. Feelings of numbness,pain and tingling are not totally objective. I worry the VA will decide I do not have diabetic neuropathy and cut off my pain meds. I have been for a lot of tests this last two weeks and my subjective pain is not really reflected in my objective findings from MRI and EMG, but I still have miserable pain in my feet and back. I get sick of doctors telling me that my findings are normal and, yet, I hurt, and the VA does not adequately treat my pain. I don't believe that these pain doctors know what they are doing, and just want big bucks to do procedures like nerve blocks that may or may not work.
Posted 17 July 2008 - 06:46 PM
I've had the EMG's too, and I think the nerves can be damaged but not damaged and/or compressed enough to show up on EMG. Unfortunately if it doesn't show up on a test, most doctors say there is nothing there and sometimes seem to take satisfaction from that fact.
Have you talked to the podiatrist?
Posted 17 July 2008 - 07:12 PM
Posted 17 July 2008 - 07:15 PM
I would recommend you have them check you for RSD (Reflex sympathetic distrophy); another name for this is CRPS (Complex regional pain syndrome).
My spouse was diagnosed with this condition (RSD) from a botched bunion surgery.
From what her pain specialist tells us, many doctors are not familiar with this condition or don't know how to diagnose it and will say that the "pain is in the patient's head" or something like that.
I wish you the best.
Posted 17 July 2008 - 11:08 PM
Anyway, they won't come right out and say anything possitive as to what is the source of my extreme pain, but since physical exams show varifiable weekness, they have given me a scooter to use when I have to remain on my feet for any amount of extended time. go figure.
I rate a cart, but they can't say the neuropathy is the cause, or the minor DJD disease is the cause, or the osteoarthritis is the cause, or if the Sacoidosis is the cause, or even if a combination of all of them is the cause. Non of these are SC or have any likelyhood of ever being SC, so why do they still hem and haw around it?
I too am on anti-inflamatoies, one is also for pain and take the Hydrocodone also. I'm suppose to take one tablet of it four times a day, but the pain is so great at night when I try to sleep, I double up and take two before bed time and again mid way through my night, just so I get enough sleep. I also take a sleep med and a psych med at bed time, otherwise I would get very little if any sleep until I drop from extreme exhaustion.
I wish you luck in you endevevors to manage your pain, I know how it is.
Posted 18 July 2008 - 12:02 AM
Posted 18 July 2008 - 06:40 AM
Posted 18 July 2008 - 08:10 AM
I had an EMG today because my feet hurt so much. The VA said there was no nerve damage in my feet or pinched nerves. So I guess I am cured.
John999, I have misspoken. I said I had an EMG. I had a nerve conduction test that proved PN. My symptoms are the same as yours.************** "Can you have peripheral neuropathy and yet not show any damage on an EMG? I have miserable pain in my feet and sometimes lose my balance, but VA now says my nerves are fine. Feelings of numbness,pain and tingling are not totally objective."*************
My pain got worse over time and near the end of my work life the feet were swollen and painful by 9am, with 8 more hours to go. Ricky may have hit the nail on the head. "John did you have a simple emg or nerve conduction study? ". I also have bad disc shown by an MRI. I turned that in to VA as I knew they would get it anyway from SSD. I understand that pain of PN goes down the front of the leg and disc the back of the leg. I have some of both (lucky me).Point is all my success with doctors stems from that one nerve conduction test. I gave copies to ever doctor I saw, they all put it in their notes. I have a good tolerance for pain. Had a burst appendix that was not found for 10 days. People are different. 98.6 is a rule of thumb. You might run 97 or 99 and be normal. I am sorry for your pain. The reason I had the MRI is because the doctors did not seem to think that PN should be so bad. I had hope that it was something that could be fixed!I think I would go to the best nerve doctor in Tampa and get an IMO nerve test. Hard for them to argue with FACTS. Surround & Overwhelm. Do you think Overwhelm comes from the German?
Posted 18 July 2008 - 09:15 AM
Edited by otey2171, 18 July 2008 - 09:21 AM.