Doc recommends spinal fusion from T12 - S1.

Posted by sassytwo @sassytwo, Dec 2, 2023

66 year old female Considering spinal fusion from T12 - S1 for pain standing and walking. Has anyone had this full lumbar fusion? I am concerned for permanent restrictions or loss of mobility post surgery.

I am active and very social. Looking for what I can expect for future life mobility restrictions as I weigh whether to move forward with this surgery. I would like to hear about your post surgery experiences as I weigh my decision, understanding healing is a very individual experience.

I believe I am at the tipping point and am moving towards surgery, if I can live with the restrictions and if I will be able to acclimate to my body new abilities and be active WITHOUT pain.

Prior Micro discectomy L2 - L3 in 2015.

Pain again about 2018 and has progressed to not being able to stand more than 20-30 minutes nor walk more than a mile. Significant pain when I do either of these things....cooking....walking to an event....putting on make up.

Once I sit, fortunately the pain lessens and eventually goes away. I can sit hours mostly pain free and laying down and sleep without pain.

I had to use a wheel chair to tour a museum with friends and find I am not doing things I want to do to avoid hurting which indicated to me that I should stop kicking the can down the road and consider more surgery.

I was surprised with this full lumbar fusion recommendation and did not realize how restrictive my life will be permanently. I am confident in my surgeon and do not feel pressure to move forward with surgery.

I bicycle 60 miles a week pain free (sitting) and it is my go to escape and exercise. I will be most unhappy if I am not able to bike. Anyone a biker

I am a massage therapist and I have stepped away from work except one worksite client. I golf and exercise and am social. Travel and site seeing is painful, but I do it anyway.

Any new treatments on the horizon? Concerns if I wait to have surgery?

My MRI reports.
1. Progressive moderate levorotoscscoliosis centered at L2, which measures 30 degrees and previously 18 degrees in 2015.
2. Progressive degenerative disc disease in the right half of L2/L3 disc space.
3.At L2/L3, previously noted right parcentral/posterolateral disc herniation has been relaced with moderate-sized osteophytic bone ridge which narrows the right lateral recess and results in mild to moderate right foraminals stenosis.
4. At L4/L5 and L5-S1 mild to moderate broad-based left paracentral and Posterolateral disc bulge/herniation relusts in progressive moderate to advanced left foraminal stenosis.
5. L3-L4, mild multifactional central spinal canal stenosis due to posterior disc bulge/herniation, bilateral facet arthropathy, and ligamentum flavum thickening. Mild-to-moderate right foraminal stenosis. This has progressed.

Thanks in advance for any information you are able to share. Tamra

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Thank You for your reply I am not working with a endocrinologist as I did not know there was such a person ! ! ! However now that you enlightened me I will get a referral to a endocrinologist Thank You again ! ! ! I am waiting for the results from my Dexa scan I'm hoping the bone density is sufficient to move forward with the procedure that was suggested to me. So happy for you I hope the C5/C6 fusion fixed your pain Great that you are doing well.

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I am a 74 year old male faced with nearly the exact same symptoms, spine issues, and my neurosurgeon wanting to fuse the same T12 through S1 section of my spine. I am in considerable pain and would like to hear what other group members have to say about this, or similar surgeries. I am extremely reluctant to have so much of the most flexible and much needed to be flexible portion of my spine surgically made immobile. I can only imagine the impact upon my life from here forward if I go through with it. Yet, what are my choices when the pain becomes intolerable???

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@hel73

I am a 74 year old male faced with nearly the exact same symptoms, spine issues, and my neurosurgeon wanting to fuse the same T12 through S1 section of my spine. I am in considerable pain and would like to hear what other group members have to say about this, or similar surgeries. I am extremely reluctant to have so much of the most flexible and much needed to be flexible portion of my spine surgically made immobile. I can only imagine the impact upon my life from here forward if I go through with it. Yet, what are my choices when the pain becomes intolerable???

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Hi, so it has been almost a year since the post you responded to. I hear you ...it is daunting to consider a lifestyle with significant mobility restrictions. Even more so, because I am quite active, social, still work part time. For myself, I have continued to deteriorate in abilities and pain is now restricting my life to the tipping point. I am scheduling a fusion from T 12 - S2.

I have been trying diagnostic nerve blocks and epidurals ( no more steroids...do not work and cause significant hair shedding). I did not find any temporary relief.

I have consulted other orthopedic surgeons and neurosurgeons and looked into lesser remedies. I wish I was a candidate for lesser fusions, disc replacement etc., but have decided that the long healing time, a chance of other nearby segments being destabilized from surgery (I will face more surgery in the future), I am scheduling this fusion for hopefully December if we can secure a surgical room or in January.

I am finding good advice on what to expect and how to set up my home to function best with the "new me"! I have gone through my home room by room, drawer by drawer. NO ONE pretends this is a cake walk and will require patience and persistence for a year or more. I have decided when one door closes another can open. I am finally going to spend time with painting classes and other pursuits.

I am finding very specific advice for how to set up my home, what to take to hospital, on a facebook spine group. Most are having surgery soon or have recently had surgery.

Please feel free to reach out to inquiry on my progress. I will try to post down the road as well.
What I know for sure, if I am not alone in this journey and am grateful each and every post I read here! Tamra

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@sassytwo

Hi, so it has been almost a year since the post you responded to. I hear you ...it is daunting to consider a lifestyle with significant mobility restrictions. Even more so, because I am quite active, social, still work part time. For myself, I have continued to deteriorate in abilities and pain is now restricting my life to the tipping point. I am scheduling a fusion from T 12 - S2.

I have been trying diagnostic nerve blocks and epidurals ( no more steroids...do not work and cause significant hair shedding). I did not find any temporary relief.

I have consulted other orthopedic surgeons and neurosurgeons and looked into lesser remedies. I wish I was a candidate for lesser fusions, disc replacement etc., but have decided that the long healing time, a chance of other nearby segments being destabilized from surgery (I will face more surgery in the future), I am scheduling this fusion for hopefully December if we can secure a surgical room or in January.

I am finding good advice on what to expect and how to set up my home to function best with the "new me"! I have gone through my home room by room, drawer by drawer. NO ONE pretends this is a cake walk and will require patience and persistence for a year or more. I have decided when one door closes another can open. I am finally going to spend time with painting classes and other pursuits.

I am finding very specific advice for how to set up my home, what to take to hospital, on a facebook spine group. Most are having surgery soon or have recently had surgery.

Please feel free to reach out to inquiry on my progress. I will try to post down the road as well.
What I know for sure, if I am not alone in this journey and am grateful each and every post I read here! Tamra

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@sassytwo Hi Tamra! My surgery is scheduled for December 11 so I will definitely be checking on your progress.

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@sherrym25

@sassytwo Hi Tamra! My surgery is scheduled for December 11 so I will definitely be checking on your progress.

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If possible mine will be December 10th! :). However it is looking more like mid January now.
Wishing you the best -- keep the faith and please reach out. Tamra

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@sassytwo

If possible mine will be December 10th! :). However it is looking more like mid January now.
Wishing you the best -- keep the faith and please reach out. Tamra

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Wow!!! Please let me know when you schedule it!
I prayed and put it into God‘s hands, and that is how my journey to surgery has been led.
All my preop’s are scheduled for the 10th and surgery on the 11th.
Faith is what keeps me where I am today🙏❤️
Thank you so much for your message!!
I will definitely be checking in on you!
Sherry

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@gliebisch01

@sassytwo @jenniferhunter
Earlier in this thread I discussed my similarity to the @sassytwo case. I have had a significant change in my condition, and have seen two surgeons since then. My spine surgeon who did my L5-S1 19 months ago, now recommends an L5-T11 decompression and fusion to replace the original surgery. I sought out a second opinion from a well known and respected spine surgeon in our area, whom I shared my MRI with. He said "you don't want that surgery." He himself is 50 yrs old and has already had two back surgeries. He suggested I get back to my prior exercise and stretching routine, and lose some weight (I am slightly overweight but by no means obese). How could two surgeons have completely opposite recommendations? Are there approaches to surgery in the spine medical community that are that divergent? I could have been left in a quandary with these opposite recommendations, EXCEPT that, at about the same time, my pain was receding, and within the span of about 48 hours was easily down to a pain level of zero to 1. This was after about 8 weeks of pain (levels up to about a 7), with relief only when sitting down. I came to the conclusion that I would be a fool to subject myself to surgery with all its risks and possible complications at this point. Of course I know it could return at any time, and there is no guarantee on how long my relief will last. Had I not gotten the unexpected relief, no doubt I'd be going for a THIRD opinion. For all I know, maybe there is regular debate in neurological medical circles on when to pull the trigger on surgery.

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@gliebisch01 @sassytwo @jenniferhunter Survivors!
I've had the L1-5 fused & caged 13 mos back. Now the L5-S1 joint has deteriorated, so leg weaknesses, groin and low back muscles ALL constantly tight. One Ortho Surgeon says I should fuse the L5-S1.I think not as would greatly limit flexibility. Another thinks I should looķ into a permanently implanted Estim 'zapper'...
Qs
1) You agree do NOT fuse L5-S1 unless absolutely needed as will limit flexibility?
2) Anyone done the implanted Estim? Effectiveness and side-affects?
3) I'm on original Medicare, with a Supplemental plan F, not an Advantage. What's approx cost for an opinion from Mayo if Medicare won't pay?

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@gregda

@gliebisch01 @sassytwo @jenniferhunter Survivors!
I've had the L1-5 fused & caged 13 mos back. Now the L5-S1 joint has deteriorated, so leg weaknesses, groin and low back muscles ALL constantly tight. One Ortho Surgeon says I should fuse the L5-S1.I think not as would greatly limit flexibility. Another thinks I should looķ into a permanently implanted Estim 'zapper'...
Qs
1) You agree do NOT fuse L5-S1 unless absolutely needed as will limit flexibility?
2) Anyone done the implanted Estim? Effectiveness and side-affects?
3) I'm on original Medicare, with a Supplemental plan F, not an Advantage. What's approx cost for an opinion from Mayo if Medicare won't pay?

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@gregda I'm sorry to hear you have further spinal deterioration. The decision on procedures for your L5 S1 must be made only between you and your surgeon. This level must support most of your body weight on your spine and is extremely important. If you have vertebrae slipping at this level, it causes a lot of disability and mobility issues. I think you are beginning to experience some of that.

With Medicare coverage for surgery at Mayo, Mayo will need to answer about costs. Costs also depend on if there is any new imaging or testing required beyond what is current for you. I think that you would only be granted a consult at Mayo if you have insurance that they will accept, and that may be different at the different Mayo campuses. It's good that you have original Medicare. Mayo doesn't accept a lot of the "Advantage" plans, but they have to answer for what insurance they do accept. Your best bet is to call the Mayo department of Insurance and Billing and ask. Here is a link to their office.
https://www.mayoclinic.org/billing-insurance

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@jenniferhunter

@gregda I'm sorry to hear you have further spinal deterioration. The decision on procedures for your L5 S1 must be made only between you and your surgeon. This level must support most of your body weight on your spine and is extremely important. If you have vertebrae slipping at this level, it causes a lot of disability and mobility issues. I think you are beginning to experience some of that.

With Medicare coverage for surgery at Mayo, Mayo will need to answer about costs. Costs also depend on if there is any new imaging or testing required beyond what is current for you. I think that you would only be granted a consult at Mayo if you have insurance that they will accept, and that may be different at the different Mayo campuses. It's good that you have original Medicare. Mayo doesn't accept a lot of the "Advantage" plans, but they have to answer for what insurance they do accept. Your best bet is to call the Mayo department of Insurance and Billing and ask. Here is a link to their office.
https://www.mayoclinic.org/billing-insurance

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yikes... SAD to read that the diff Mayo campuses accept diff insurance. Would be GOOD if all accepted the same. - tho must say, I've talked w/ 2 St Pete Cardiologist who say they are NOT impressed with the 'quality' of opinions they've seen from Mayo-Jacksonville FL. They said they'e prefer opins from Vanderbilt or Duke, not Mayo-FL.

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@gregda

yikes... SAD to read that the diff Mayo campuses accept diff insurance. Would be GOOD if all accepted the same. - tho must say, I've talked w/ 2 St Pete Cardiologist who say they are NOT impressed with the 'quality' of opinions they've seen from Mayo-Jacksonville FL. They said they'e prefer opins from Vanderbilt or Duke, not Mayo-FL.

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@gregda There just isn't a one size fits all insurance plan. I always recommend to call and ask if insurance is accepted no matter where you go. There is also a list on the Mayo website for what insurance they accept. A lot of the so called "Advantage" plans only offer contracts for care that is limited to a particular state, and patients must live in that state. It's kind of like having an HMO insurance and they give you an approved list of doctors they will cover. It is a contract between a health insurance company and the doctors they recommend. I have also heard that Vanderbilt and Duke are good medical centers. I do know for cardiology, Vanderbilt has done some pioneering work. A friend of mine with a serious congenital heart issue received a heart pump there.

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