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Fusion spineys- Do you ever get to the stage

AnonymousUserAAnonymousUser Posts: 49,578
edited 06/11/2012 - 7:23 AM in Back Surgery and Neck Surgery
I was just wondering if you ever get o the stage where you are not aware of having a fusion.
If you have experienced this how long did it take you and how many levels did you have done, what was the procedure etc.
I am so waiting for that day. I still need my raised toilet seat in the mornings though could do without it as the day goes on. Not a big deal but with other things I feel I am constantly aware that I have had back surgery and would like to move on.

I would love to read your stories.

Blessings Sara O:)
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1

Comments

  • Sara, thanks for starting this thread for I am also curious if I will ever feel "normal" or close to it. I'm 5 months post op S1-L4 fusion and not doing well at all.

    Carrie
  • yeah, I know what you mean. Still need the raised toilet seat, use my cane, walker is on standby. I'm so glad I didn't give them away after my first surgery.
    I still have problems and am always getting on and off steroids and Toradol for the back pain and sciatica that just won't quit. Now my other leg wants to act up. Oh well. I feel like I did prior to surgery, but I know I have to be patient.
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  • Being patient is the hardest thing to do some times. I know I'm getting sick of hearing that word. I feel worse now then before my surgery. The only good news I've had is that I finally started to fuse. Sorry to be so crabby. I'm just so frustrated.
  • so looking forward to the day when I am unaware of having any surgery. I know it will come. ;)

    O:)
  • hi all-
    im a year past 2 surgeries L4/5 plif and at 6 weeks post op a removal of screw inpinging on the l5 nerve root.
    i am still waiting for that time when i dont feel like ive had back surgery - i dont think its ever going to happen. i do feel that i will never feel normal - lets face it it is a massive surgery - i do feel better pain wise tho. and as the months go by there is still improvement. i go to the gym now - every other day i do a 10 minuite fast walk, 5KM on the multi strider in 21 mins, followed by 4KM in 10 mins on the recumbant bike, followed by climbing 15 floors on a stair machine, followed by 6 minutes on the versa climber, then i get my swimming costume on and swim 30 lengths in the pool. i would never have been able to manage that before my op - so i think im doing pretty much ok.
    i wanted to give people here a positive outlook because although i still have some nerve damage caused by the screw - i am trying to get on with my life, and only have to take maybe 1 lot of painkillers every couple of days or so.
    patience is the key - i dont have much of it, but neither do most.
    have a reasonable day
    love AJ x
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  • That is great you are doing so much.
    I have been going to the physio- gym. A gym set up and supervised by the physios and then hyrotherapy. I only have 3 sessions left and am sure hoping that I can go to the gym after that.
    I would prefer the gym to just walking and as summer is nearing it is also air conditioned :))(

    But I really am impressed and will think of you every time I get on the walking machine.

    Sara O:)
  • Sara,

    I am 17 months post op from a multi level fusion and I can honestly say most of the time I am aware of my fusion. There is that stiffness or twinge when I turn or twist. Occasionally, if I am doing something which absorbs my attention, I'll forget about my back.

    Dick
    Emergency surgery in March of 2006 for spinal infection of L 2 and L 3. During surgery, discovered I had Cauda Equina Syndrome. Spine became unstable after surgery and had 360 fusion with 10 pedicle screws, plates and rods in April of 2007.
  • I am 7 weeks post op tomorrow-honestly, if I did not have to wear this stipid brace, I think it would be easy for me to forget I had the surgery! I am just a little sore. I am so thankful that my recovery has been so quick. I pray that yours only gets better!
    btw-I walk, walk, walk,.........MIN. 1 hour a day-up to 2 hours a day. Walk and rest. that is it!
  • I'm glad to read this post. It gives me an idea of what to expect. I am looking at a three-level fusion, L3/4-S1 soon. I am still working, sitting on a very strange looking cushion and getting up to walk (more like shuffle) every now and then. I am wondering what it will feel like when those three discs are fused. I suppose I won't be that hot on the dance-floor anymore, right? :D As if I am now! I'm figuring I'm always going to have some level of pain and stiffness, but I'm praying I'll get to a place where I can get rid of these Fentanyl patches and just occasionally take something for pain. I do have times when things feel fairly calm, but other times when I am so frantic with the pain I cannot even imagine what it would feel like if I weren't on the patch with percocets to back me up. I also now have a TENS unit that seems to help a bit.

    Linda
    3 level spinal fusion, L3/4, L4/5, L5/S1, November 2008. Stiff, but I can walk.
  • Sara, I had exactly the same three-level fusion as you, but my surgery was a week earlier than yours. I actually feel quite normal, that is, I am not aware of the hardware in my body, and I observe the BLT rule because I was told to do so, but I think I could actually move quite well (sometimes I have to reprimand myself because I realize I exceeded my allowed range of motion). A few days after surgery my lumber area felt a bit tight, also when I began walking. But it is OK now. The only indication I have that I am still recovering is that I tire rather easily. But I only need a few minutes rest to recover. I am walking 1 1/2 hours on the average day, sometimes a bit less, sometimes more. My Os does not want me to walk more than 1 hour at any one time. My pre-surgery symptoms are gone (leg pain and numbness) and even the "rusty" feelings in the morning or when I got up after sitting for a while, when it took several minutes before I could straighten up and move with ease I discovered that was not due to getting old, because I no longer experience it.

    This was my first spinal surgery, so maybe I didn't have so much scar tissues as some people with multiple surgeries. Also, after my problems began within seven months I had my fusion, so probably there was no permanent nerve damage.

    Kin
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