Spine conditions: Told I would not walk without surgery
I have severe lumbar stenosis and Spondylolisthesis as well as a bulging disc. My main symptoms are throbbing in my calf muscles. I was told by a pain management Dr that he thought if I didn't have surgery I would not be able to walk in a few years ! it would be fusion. I would like people's feedback. I don't have pain in my Back, all in my legs.
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Just wondering, how you know that Mayo is not for profit ? I didn't think any hospital in the US was not for profit. I don't have loss of bladder or bowel control luckily, but my other symptoms seem to be getting worse, the throbbing and cramping.
@annie1 I know from watching the documentary about the history of Mayo, that the Mayo brothers donated their property and wealth from their early success to form the Mayo Clinic Medical Foundation (not sure of the exact name). They did that instead of leaving their wealth to their heirs. At that time in history, medicine was in its infancy, and the success the brothers built attracted more medical talent to the organization, and this was the beginning of what Mayo is today. Mayo does fund raise as all medical centers do, and they put the money right back into research and expanding facilities for patients and operating costs including expanding into other regions. All patients are welcome here on Connect, and you don't have to be a Mayo patient to participate. It is meant to provide connection and sharing of experiences and Mayo funds this forum and created it for the good of all of us.
The doctors while I was there as a patient told me about being salaried employees and not getting paid more to do surgery thus giving a more objective opinion. The Mayo model is completely different from most hospitals as most are run for profit. No one owns Mayo, it is run by a foundation. It feels completely different to be there from anywhere else where I have been as a patient. I volunteer here because of how good Mayo has been for me, and I am not paid for what I do here. I didn't know this existed before I came to Mayo.
Are you considering requesting an appointment at Mayo?
Here is more info about my diagnosis according to a Rehab Dr I saw yesterday. The following issues were addressed: Spinal stenosis of lumbar region with neurogenic claudication and Facet arthropathy.
I just read that neurogenic claudication can lead to permanent nerve damage. I am worried that I have it already.
Hi @annie1, I thought I'd jump in to provide more information about Mayo Clinic's nonprofit status. Mayo Clinic is a nonprofit organization committed to innovation in clinical practice, education and research, and to providing compassion, expertise and answers to everyone who needs healing.
"As a nonprofit organization, Mayo Clinic reinvests all earnings into giving patients high-quality care, finding answers to the toughest medical cases, and training the next generation of doctors and researchers. Reinvestment lays the foundation for everything we do, ..." Read more here: https://www.mayoclinic.org/giving-to-mayo-clinic/contact-us/frequently-asked-questions
@annie1 I just found this post and didn't know you had been turned down by Mayo. I know that is hard to be turned down because I was turned down 5 times before I came to Mayo because the surgeons just didn't understand my case. My gait had also changed because when muscle spasms were shifting my cervical vertebrae around, it put pressure on the spinal cord and affected my legs. When my PT realigned my neck, I could walk normally again and she was also correcting my pelvis alignment.
If you wanted to try again in the future, first, I would check if you have insurance they accept because that is a reason for denial. Here is the Insurance and billing page for Mayo.
https://www.mayoclinic.org/patient-visitor-guide/billing-insurance
Sometimes patients apply again or apply with the recommendation of their doctor. You may be successful at another time. It may be that the department you are applying to has no more capacity to accept patients at this time. You may be more successful applying to another department. I do hear that neurology gets many more requests than they can handle because of so many patients with neuropathy.
I can appreciate what you say about dance and how you know your body. There are pelvic dysfunctions that mimic spine issues casing similar symptoms. My pelvis gets out of alignment and I have worked with my PT on this with her doing myofascial release. It does cause back pain when it is out of whack and I know some things to do to help myself when I can't see my PT. Having my pelvis go out of alignment does also send sciatic pain down my legs, and that resolves when I get it straightened out.
This article has a lot of good information:
https://mskneurology.com/identify-treat-lumbar-plexus-compression-syndrome-lpcs/
This is our discussion on Myofascial Release and it has helped me a lot.
Neuroapthy - "Myofascial Release Therapy (MFR) for treating compression and pain"
https://connect.mayoclinic.org/discussion/myofascial-release-therapy-mfr-for-treating-compression-and-pain/
You can search for an MFR therapists at this link. Forgive me if I've mentioned this before as recommend this a lot. http://mfrtherapists.com/
My PT is in northern IL and does take insurance like Blue Cross and Medicare and she has a traditional training plus the myofascial release certifications. She knows how to code the visit so insurance will accept it. She may use neuromuscular reeducation, I don't really know, but she knows what to do to keep insurance happy.
I don't work in the medical field, but I did consider medicine as a career and earned a pre-med biology degree. I then worked in university research for a neuroanatomist who was publishing research in journals. When I became a spine patient, I was able to understand medical literature from my background and read a lot as well as watching online spine surgeons presentations at spine conferences. I struggled for 2 years trying to get a surgeon to help me and in that time, I learned a lot. I got all my medical records and looked up everything, so I knew how the doctors were getting side tracked and missing the correct diagnosis. I found my correct diagnosis in medical literature right after being dismissed the 5th time, so when I requested an appointment at Mayo, I sent that literature in with my request asking if my case was like this, and I was accepted at Mayo, and right about my diagnosis because surgery fixed the problem.
If you can find a good MFR provider, they may be able to help resolve some of the physical issues. Surgery is a very big step, and I knew I was there because I was loosing muscle mass and coordination in my arms and shoulders and was so weak that after pushing a shopping cart at the store, I had to take a nap in the car before I could drive myself home. Driving was also exhausting. My MR imaging showed spinal cord compression from stenosis with a ruptured C5/C6 disc that had grown bone spurs in the spinal canal that was pressing on the spinal cord.
Jennifer
@annie1 I'm glad you are working with a rehab doctor. I know you are worried about nerve damage and I was too with bone spurs pressing into my spinal cord for 2 years, and I did fine. We are all different of course and the best one to advise you about when nerve damage would begin would be your providers. I found this information from the National Library of Medicine that may be of interest.
Spinal Stenosis and Neurogenic Claudication
https://www.ncbi.nlm.nih.gov/books/NBK430872/
You mentioned getting cramps and throbbing pain your calves. Cramps and spasms happen when nerves are irritated and sending signals to a muscle. In biology class, we did some experiments with sending electric shocks to see when the responses changed from a twitch response to a sustained contraction (as in a cramp) and found the frequency and speed of signals that made that happen.
I wouldn't worry that permanent nerve damage has already set in, just do the best you can at rehab. You would probably notice something like that if a function just disappeared and stopped working, but do ask your rehab doctor that question.
Jennifer
So much conflicting information. The Rehab Dr told me I need surgery. So I went to one surgeon, who said I could make out ok with just a laminotomy, then another surgeon said that could make my spine more unstable ! Don't know who to believe and what to do.
@annie1 Perhaps this article may explain a bit of the risks after laminectomy involving weakness and uneven functioning of spinal muscles. Scar tissue affects things a lot too. You may need to consult another surgeon. You may want to ask about how many different procedures could address your condition and what the drawbacks are for each of them.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941765/
I can't remember from your original post, were you trying to avoid fusion? Would an artificial disc be an option?
Actually the surgeon said he would do a laminotomy not laminectomy, which is a little less invasive and the recovery. Seems to be much shorter. Also I am trying to avoid fusion because I have osteoporosis in some areas and as you may know with fusion they have to put hardware on your bones so your bones have to be strong enough to support them. There is a way they can put some kind of cement into the hardware which also could lead to some complications. I am trying to avoid fusion. I'm waiting to hear back from the surgeon about the question I asked about the safety of the laminotomy.