The nerve damage was extensive and the surgeon cut out the scar tissue which had gone right into the 3 branches of the nerve, and then put in neural tube implants which will serve as a mini pipeline to reconnect the nerves. I am still experiencing burning pain in my foot, and have also started having horrible shooting pains that go into various areas of my foot, and sometimes my toes. Sometimes, they are like electric shocks, but most of the time it is a stabbing, intense pain that lasts about 5-10 seconds and then subsides. Sometimes I feel as if I'm having an electrical storm in the bottom of my foot! I had really hoped that this surgery would help me get rid of the pain, but so far, it's actually worse than it was pre-op. Is there anyone else who may have had a similar surgery? What was your experience? Does this pain eventually "settle down"? I certainly would appreciate some input on this. Thank you.
From what I understand, when the nerve is done growing and finds the end (for example, of your finger) the nerve pain should settle down.
If I did damage the nerve again, and have another neuroma, my next option is to bury the nerve into a bone in my hand. The nerve will then think it found the end and should stop sending pain signals.
I hope this helps. Hang in there.
I noticed you had surgery back in December and I am curious to know if you had complete recovery by now - 4 months later?
In mid May of 09, I had surgery again to help the entraped nerve and help the tarsal tunnel syndrome. The operation was a success, but the patient... I am now suffering from numbness almost entirely in my foot. My heel feels like a piece of wood when I try to walk on it. I continue to have shooting pain often like electrical shocks.
I am being treated with Lyrica, but it does not help much. The pain is constantly with me. I've been told it may take up to a year for it to go away.
Rose, I too, would like to hear from someone who is further along their recovery time than I am.
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I had surgery to remove planters facititis on the flexor longus tendon he cut the tibial nerve i am exsperienceing almost the exact feelings my big toe is numb my foot stings and burns it is so numb it doesn't feel like a foot,,,chronic pain.I went to a dr.lineaweaver in brandon,ms.that ordered a NCS &EMG i find out tommorrow if he can do anything to help me.The Dr.never told me he cut my nerve,i am a hairdresser with 0insurance i know what you are going thru.This dr lineaweaver said he was going to put a pipeline in the side of my foot i am scared to death because during all this the incision came open woundcare debreeded,,well what they called debreeding a 2inch hole in the surgical site 2months after the surgery i contracted m.r.s.a. from the woundcare almost died with a 2inch hole with m.r.s.a. in it.I thought when i had taking all 2months of vancomyacin treatments i would be ok with my foot now this is what i have to look forward to.I hope i have helped you feel somewhat at least not alone.GOOD LUCK!
Rose64 I recently had a similar surgery on 11/29/2012.I had the same experience! How are you feeling now ? 4 years later
I have had a severed tibial nerve for about 8 years now. I had surgery 3 months after the injury to repair the sheath which the nerves grow in so they could grow back into my foot. The problem is the nerves are fibres which grow where ever they want to - not where they used to be, so I have feeling in the foot but it doesn't tell me where I am feeling something. If you were to tap the bottom of my foot with your finger I would feel a general sensation all over the sole of my foot. As my surgeon said it's better than no sensation because the ability to feel pain when the foot is injured is very important.
Having said all that I am able to jump and run as well as I would be able to had I not been injured. I still have the stabbing electrical shocks but the brain gets good at filtering them out so I only notice when I think about it.
The biggest issue for me is I developed a back injury due to poor posture and I have only just realized why. After I stared walking again I could only feel the edge of my foot. It was/is painful to walk on this edge so subconsciously I have been inwardly rotating my bad (right) foot to reduce this pain when I walk. Doing this caused my right hip to twist forward. It also gave me a flat right foot. With a forward/lowered right hip back trouble was sure to occur eventually.
Today I noticed with my heels flush to the wall my right big toe was a full centimetre longer than my left toe but all the other toes were the same length. I had never noticed this before and I initially thought I had uneven foot size. Then I noticed I had no arch in the right foot. When I twisted my ankle to put an arch in the foot the toes suddenly were the same length. Not only that but my hips were no longer rotated. I have tried walking in this position and it hurts on the strip of my bad foot where I am still able to feel, but my pelvis is straight again.
I think everyone who has tibial nerve disfunction will eventually develop this problem. Be aware of the arch in your foot. It has to be there even if it feels wrong :)
If anyone wants to contact me about this you can find me on linkedin. My ID there is Mike Donelly (in Bulgaria)
Hi, how are you doing now?
Hello, Cant Believe I found someone else.. I know how you feel!!!! I have had two nerve grafts from an open right calcaneal fracture. First graft failed. The second graft is about 5-6 inches above my ankle. Its off the shelf nerve 12 inches long with two branches coming off of it. Like you I feel as if my foot is plugged into a power outlet. I have pins and needles along with a constant burning sensation all the time. I just started getting the intense pains which are wow will stop you in your tracks. I have no feeling on the entire bottom of foot. Last nerve graft was on 9/13 surgery number 12. It was surgery number 13 in 9/2014 to cut heel back off and realign, and toes 2,3,4 had to have pins in them to keep from curling under(hammertoe). I have noticed it getting worse. This is a very complicated surgery and problem. I live in Houston so today I have made two appointments. One with Baylor's group and the other is Memorial Hermann Mischer Neuroscience center. I am curious if anything can be done without surgery or the crappy meds that I now stopped taking. This unfortunately is something that is very hard to know the outcome on. Due to this being a foot and the pounding it takes even after months of non weight bearing that graft or transection once we start bearing weight with it being such a delicate hair like graft is taking a beating every time we walk, stand, etc,etc. I would like to hear how you are doing now as this has been posted over a year ago. Thanks..
Hello Rose:
I had surgery last Friday and am experiencing identical symptoms. Did it go away? Thank you
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