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Damage to the spinal cord and nerve roots

I had my 1 yr. follow up with my neuro-surgeon a couple days ago from a C5/C6 fusion. I had a disc that was herniated and was pushing against my spinal cord. I had the surgery and a good share of pain and issues since. Fast forward to last week, I had x-rays done and we had our talk after the examination. The doctor told me that because of the herniated disc was compressing my spinal cord, my spinal cord had been damaged in that area C5/C6. On the MRI, the area of the fusion looks cloudy around the spinal cord which is normal apparently when there is a fusion in that area. The NP for the neuro-surgeon and the physiologist said that the spinal cord in that area looks like it is still crowded and damage is still showing up. They also believe the nerve roots are probably damaged also. On the xray, everything looks good despite an accident at work that affected my head and neck. THe NP said that there really isnt much they can do about the pain except deal with it and maybe do Botox injections. I am allergic to cortisteroids so I am seriously limited. I am afraid of what botox would do to me. I am totally against those! I am not finding much about this online. Most spinal cord "injuries" affect people to greater points than mine. I can still walk and do most things. I can be pretty clumsy, cant walk in a straight line to save my life, cant stand with my eyes closed without tipping over, and have poor fine motor skills but I can do most else.
Tracie C
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Comments

  • Sorry you're still going though this. Are you able to get a second opinion from a NS in another town, just to make sure they agree with the assessment? I was offered a myelogram if I wanted confirmation it was decompressed.
    My physiatrist discussed botox injections for my muscles (so arms and legs) because of my spasticity. Scary, scary idea! I can understand your fear.

    ACDF w/Corpectomy C3-6 12/8/14 ; Laminectomy C3-6  5/19/2016

  • I haven't seen any information about this issue. Just being a rare case makes things difficult. I don't want a life on medications to stay at a functioning state. I don't know if it pays to have an EMG done and I am not fond of the thought of a RFA done. Especially when I have heard so much negative feedback, here and elsewhere.
    Tracie C
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  • I have an EMG tomorrow. I am a bit nervous about how painful it will be. I have heard that it can be bad but I think its pretty much based on personal experience. I am pretty much getting the botox front from everyone now. I received some more info on it but I havent read it since I have been working all weekend. It seems a little rediculous that it takes 3 weeks to take full effect but only lasts up to 12 weeks. So 9 weeks if it actually works? Sounds pretty expensive for a temporary fix. I am still saying no to the rhizotomy,
    Tracie C
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