The main reason for doing this type of surgery is to prevent neurological disability, for example the loss of muscle function that could have come from that
nerveNerve biopsy
Nerve conduction velocity root or spinal cord being damaged/compressed for a long time. I do not know if you had evidence of
nerveNerve biopsy
Nerve conduction velocity damage by exam or EMG preop.
This does not necessarily mean that the pain will go completely, and there will be pain for a period postop .Sometimes a bone or disc fragment may remain in the surgucal space and cause residual symptoms. This can be evaluated with an MRI. Otherwise there may still be some nerve root (but not spinal cord because of the space created by the surgery) compression at that or another nerve root. You neurosurgeon should be able to tell from his examination and/or a postop MRI scan. If you develop weakness or clumsiness in both legs or inability to pass urine, this should be evaluated straight away in case of spinal cord compression.
Good luck
I've had a CT scan and MRI, both of which are fine. My surgeon says this is nerve inflammation and that it will go away. I'm in such agony that I'm now going to the pain service at the hospital. They are giving me Lyrica and Elavil and I have had two Lidocaine Challenge procedures.
Have any of you experienced these problems post surgery? Did the problem resolve on its own? How long on average did it take? Right now I'm worse off than I was before the surgery, although I had no quality of life before and I had to do this.
Help! I'm finding it hard to cope. Still mostly using a walker because the left foot feels unstable; not walking the 6 miles I should be working on. I'm basically housebount. I'm only 52 and I need to get back to work someday soon, I hope.
Thanks for listening.
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Now I'm getting really concerned about the numbness in my read end and the problems I'm having with my bladder and bowel function; not knowing when I am finished with either. I know it's called "saddle hyperesthesia" but I've not been able to find good info about it on the internet so far.
My foot does not feel any different than it did six weeks ago when I had the surgery.
I wish you luck.
Tks for listening.
I had 2 appointments, 2 weeks apart, and my surgeon gave me a local lidocaine and depo injection directly in the area of the rods where I had my fusion. I felt wonderful, from my back, through my hip, leg, and my foot for 45 minutes, and then all pain came back. After the second injection, the doctor told me that because I didn't get a better response that it wasn't just an inflamation (inflammation) around the rods or surgical area, that it was the rods inpinging on nerves and surrounding areas and my body was possibly rejecting the material also; therefor, we are scheduling surgery for removal of the hardware at both levels, but the titanium sylindrical cages will have to stay in the disc space as it is a good, solid, fusion now after 2 years. I am so excited to finally have them removed, the fusion/reconstruction of the lumbar area was necessary, but am now glad to get things out and on the road to the right recovery! YEAH! It pays to bug the daylights out of doctors until they finally listen, make them take all necessary tests, and get things accomplished...hang in there to all who believe that its not in your head!!!