Neuropathy and Cervical Stenosis?

Posted by Ray Kemble @ray666, Sep 29, 2023

I have been reading the evolving thread on neuropathy and lumbar stenosis with particular interest. I have idiopathic sensory-motor PN, giving me terrible balance and difficulty walking, even the shortest distances. In March 2022, I was diagnosed with cervical stenosis (“critical stenosis centrally at C4-C5, C5-C6 without cord signal change”: my neurosurgeon’s note). I had had no cervical-area symptoms then; I had been looking for an answer to my lower-body PN. That I had cervical stenosis came as a surprise. The neurosurgeon offered cervical surgery but cautioned that even a positive outcome might have no effect on my bad balance and walking difficulty. We decided on –– and are continuing with –– a wait-and-see approach to my cervical stenosis. Reading about others’ experiences with PN and lumbar surgeries has me wondering if any of you have ever had cervical stenosis surgery, only to be pleasantly surprised to find that it helped reduce or even eliminate your lower-body PN symptoms.

Interested in more discussions like this? Go to the Neuropathy Support Group.

@charts41

I have progressive Peripheral Neuropathy.... meaning it started in my feet/toes and hands/ fingers after femur replacement surgery and after twoyears of searching for a cause...I not only haven't found a cause,but the neuropathy has spread all through my body and into my face. Also had surgery to correct cervical stenosis which my neurologists thought might be
a cause of my condition,,.but it wasn't.
I am now still searching the internet for info on what this is that I'm dealing with ,but I'm more involved with working on trying to get on with my life in spite of my debilitating condition since it may be part of my daily life well nto the future!
Thanks for your interest, EB

Jump to this post

Mine started in my hands and feet in 2011. I am still fighting for an official diagnosis and cause. All symptoms point to small fiber neuropathy, autonomic neuropathy, and peripheral neuropathy because my sensory, autonomic, and large fiber nerves are all affected. I also have degenerative disc disease and spinal stenosis unrelated to the neuropathy and have had two cervical spine surgeries. I believe an immune deficiency and a virus caused mine. There are MANY causes of neuropathy, including but not limited to autoimmune issues, metabolic disorders, viruses, vaccinations, surgeries, and nutritional deficiencies. If your neurologist is not seeking a diagnosis with testing or seeking a cause, I highly recommend finding a new neurologist. I am seeing a new neuro next week because my current neuro only wants to focus on my chronic migraine. Everything I have learned about what is happening to me is from support groups and medical journals, not my doctors. Check out the Facebook group called Small Nerve Fiber Neuropathy. It is a good place to start since symptoms have spread to your face. Many people in the group, like me, have body-wide symptoms. The people are really helpful, and many are well-informed. Also, check out a video on YouTube, Small Fibers, Big Pain, and Radcliffe Institute, with Dr. Anne Louise Oaklander. I wish you the best.

REPLY

I too have stenosis between L4-5; I had a corticosteroid shot in my spine in that area & my back pain & PN pain went away for 3 months. You can get 3 shots a year paid for by Medicare. Surgery is not the only answer for stenosis or PN. Find a good pain doctor & explore this option. Hopefully, this is helpful.

REPLY

Been there and done it. Bad back and neuropathy are perfect mix for pain. Good luck and there are some people that shots work for them and get every 3 months. Good Luck on your treatment.

REPLY
@charts41

I have progressive Peripheral Neuropathy.... meaning it started in my feet/toes and hands/ fingers after femur replacement surgery and after twoyears of searching for a cause...I not only haven't found a cause,but the neuropathy has spread all through my body and into my face. Also had surgery to correct cervical stenosis which my neurologists thought might be
a cause of my condition,,.but it wasn't.
I am now still searching the internet for info on what this is that I'm dealing with ,but I'm more involved with working on trying to get on with my life in spite of my debilitating condition since it may be part of my daily life well nto the future!
Thanks for your interest, EB

Jump to this post

It's not fun. Good luck!

REPLY
@charts41

I have progressive Peripheral Neuropathy.... meaning it started in my feet/toes and hands/ fingers after femur replacement surgery and after twoyears of searching for a cause...I not only haven't found a cause,but the neuropathy has spread all through my body and into my face. Also had surgery to correct cervical stenosis which my neurologists thought might be
a cause of my condition,,.but it wasn't.
I am now still searching the internet for info on what this is that I'm dealing with ,but I'm more involved with working on trying to get on with my life in spite of my debilitating condition since it may be part of my daily life well nto the future!
Thanks for your interest, EB

Jump to this post

I wonder if it’s possible the femur replacement pinched or damaged a nerve? Might be worth get an mri if possible.

REPLY

@sshannan
I too have stenosis between L4-5 and have a spine that has slight curve near the bottom to the right. I am bein g told that I have sciatica. I had MRI of my lower back and the right neck. I went to two neurosurgeon to explore the need for surgery. The first one strongly recommended for a surgery. The second one stated that success of sciatica surgery is about 90%, but of spine 50%. I have not done surgery yet. I tolerate pain without any mediation. I am worse of when I sit too long on a couch or chair and after I wake up in the morning. I have been managing so far through exercises. I am confused. Is surgery the best way to improve? Any suggestions?

REPLY

With neuropathy and spinal stenosis, I have been to all doctors and did all tests. I was told my back would not be considered since it would take 15 hours and may be no results. I have not had surgery since I only hear bad results. I will live with it since there is no cure to this chronic adventure. Wish you the best and check out results of back surgery.

REPLY
Please sign in or register to post a reply.