Severe Stenosis in Lumbar Region
I have an upcoming tele-med appointment with Mayo, Medical and Surgical teams. I am stressing over the recovery: how much pain to expect, and over what period of time; can I sit; can I sit on a plane to go home to NJ; what can i expect at home; do I need a cane; a walker; is there a special pillow to allow me to sleep; will I have to take opiods; other pain meds. I am so nervous. I have been told I do not need a spinal fusion (thank God); Please help with specifics. TIA.
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My first spine surgery, which included rods for L3 and L4 lasted 20years. But just this past year, when my overall health began to deteriorate, I was diagnosed with hypermobile Ehlers- Danlos Syndrome, a connective tissue disease. The old rods began to fail, and then my L5 deteriorated, setting my pain levels on fire until the day I simply could not get out of bed. Emergency surgery on L4-5 followed, with replacement of the old rods and a new one for L5. Recovery hasn’t been as easy as it was in my’50’s, but at least I can stand up and walk when I feel the need
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1 Reaction@sparkleberry Hello and welcome! I love that name, it sounds like a tasty sparkling fruit drink. I am a cervical spine surgery patient, and haven't had your specific experience. How far along are you with your recovery? Are there still some goals you are working toward?
Jennifer
Hello, Jennifer. I, too, have cervical issues, but PT and injections have helped there. My recovery from lower spine surgery with fusion has gone quite well considering the other issues that I deal with. I was in rehab for a month for some fairly intense Physical Therapy and Occupational Therapy and have continued the exercises at home
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1 ReactionI had the exact same surgery a year ago from last January and I'll tell you, in my case it almost seemed to make it worse! I'm taking 1200 mgs of gabapentin a day with not much relief. My knee joints always feel like they want to give out, my feet tingle and go numb. I still have lots of lower back pain. Not all cases are the same so maybe, hopefully, you'll have better luck!
Thank you for your acknowledgment and support. The time lapse since the spinal fusion of L5-S1 has been almost ten years. I am wondering when the rods will wear down. After the spinal cord stimulator was placed in last year, which has been successful, the neurosurgeon who placed it in, is very communicative and responsive when I contact him. He referred me to a scoliosis neuro at the Barrow in Phoenix, and he ordered imaging. Thank goodness he ordered a CT Scan and not a MRI, as with the SCS, it is a vey laborious process when in the "tunnel". I lightly freaked out the last time, as it was to be two 30 minute sessions, and I could only handle one session. I am looking forward to seeing the specialist next month, and go from there. My curiosity and interest is what the curvature is. I am extremely active, just turned 69, and cannot think of being on the sidelines.
Welcome to Mayo Clinic Connect. Thank you for sharing your experience.
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1 ReactionI love this platform I’ve learned to request mild sedation to help me relax enough to be able to endure the contortions some of those tests require. As for the rods, my neurosurgeon said the rods he put in are less likely to shift or break down due to newer materials
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1 Reaction@maxiandmary Hello and welcome to Connect. I'm sorry your surgery didn't give you better results. Have you followed up with your surgeon about this or sought a second opinion elsewhere? Have you had any recent imaging that could define the problem?
Jennifer
Thank you! Yes, I have followed up with my surgeon but unfortunately they don't seem to have an answer! I was told to try gabapentin which doesn't do much for the pain & it seems to make my legs feel numb. Due to a heart condition I'm unable to take any other kind of pain relievers. I'm just about at my wit's end!
I did. I had L2-L4 fusion two years ago with catastrophic results. I ended up a cripple with a permanent foot drop on my right foot and an unstable spine. It also didn't improve my back pain. At least two other surgeon told me, that revision surgery would be too dangerous and wouldn't help with neither the pain nor the foot drop. I wish I had never had spine surgery. I can no longer walk w/o a walker and I can no longer drive due to the lack of dorsiflexion of my right foot.
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