Justin,
Thanks for posting this.
It is a good read and very timely for me.
I go for my second CT scan tomorrow and then two days after I have a dr appt.
I need to get all informed up as he and I are going to decide what my next step will be. It's interesting because after my first CT scan in September my dr and the radiologist thought I should be fused at L5/S1 and sent me off to the neuro. He,on the other hand looked over the scan and said "nope". He did not question me about my range of motion,nor my pain levels,nor how how my life is affected by the pain.....just no. My back is messed up on quite a few levels but the worst is L5/S1.He went on to explain that the disc is completely gone except for a very small smear....he also explained that I have quite a severe narrowing of the foramin..( thank you Katie)...plus my spine is pushed to the right. Add a bit of arthritis and some pretty prominent bone spurs .. that is the cause of my problem.However, according to him...fusion is not the answer and the artificial dics aren't long lasting enough to do that surgery as I am only 53 and so it would be best that I wait until I am older??? Go figure?? What kind of thought process is that?
This article clarifies things a bit.
This particular neurosurgeon said carry on with your life...just don't do any heavy lifting(over 20 lbs) don't lift and turn,don't stretch and lift,don't sit too long,don't stand too long,loose some weight ( that the 3 years of medicating my my "mysterious leg pains" with antidepressants packed on) and more recently the gaba,strengthen your core...but don't come to me for surgery! HELLOOO!!!! I did not ask for surgery I came with a CT scan that says I have a messed up back...I hurt badly and would like to know what can be done for me. I was told what wouldn't be done for me....by him anyhow.
I am wondering, Justin about the damage to the nerves?? You mentioned that in one of your posts....
I am medicated with gabapentin to keep the nerve pain to a level where I can function,then I have straight codeine for the pain ( it dulls it but does not take it away) also I have Valium and T3's when it gets real bad...which it does. If I was to take no meds the pain would have me almost stopped.
My question is, and I am not getting an answer from the drs; am I doing permanent damage to my nerves when I take the pain blockers/deadeners? and carry on.
I'd appreciate your input and the thoughts and opinions and/or experiences of any others on the site that might be able to give me some insight.
This is I think my biggest concern right now. Am I doing more damage that will be of a permanent nature?
I liken it to putting my hand on a burner but not being able to feel it burning because I have blocked the pain messages from reaching my brain!?
Does this make any sense?
mg



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