Excruciating pain from cervical (C7/T1) radiculopathy

Posted by mlerin @mlerin, Nov 4, 2019

I've been in excruciating pain in the right shoulder and throughout the arm and hand for months. MRI diagnosis is C7/T1 and C6-C7 severe foraminal narrowing and stenosis. Had a cervical epidural injection last Thursday and so far no relief. Is prolotherapy or PRP a good option? Any other non-surgical treatments out there that actually work?

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Profile picture for birdman518 @birdman518

I recently posted about my experiences with realizing that I have (99% probability) cervical radiculopathy, plus possible ulnar nerve damage that causes pain and tingling from my neck down to my right hand. All fingers are affected, but mostly my thumb and index finger.

But the most pain I have is in my shoulder. I have assumed this was related to the neuropathy, but then I realized that the amount and intensity is almost the same as when I had a rotator cuff injury from playing tennis... probably at least 15 years ago. But I have not done anything like that to cause that problem to recur.

Does this sound to anyone here like it is part of the nerve issues? Has anyone with C6/7 nerve pain had shoulder pain?

Thanks,

Mitch

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Hi, I had a similar experience… I hurt myself at work manual handling heard and felt a pop in my shoulder/scapula area.. next day the right shoulder, arm and thoracic area throbbing and on fire burning, scan showed bursitis so 2 steroid injections and 4mths of physio still no relief, my physio wanted to mri both my shoulder and brachial plexis, both scans came back with nil issues, my shoulder was the main source of pain 2 months later dr decided to do cervical mri with shows severe disc prolapse and facet joint issues in the c5/6 and c6/7, I had no neck pain at all… neurosurgeon ordered a diagnostic c7 epidural injection with supposed instant relief, instead my neck became incredibly sore and stiff with severe loss of rom and pain radiated from my neck to shoulder and down into my hand, first and middle finger and thumb.
I found the injection aggravated what ever was going on.. fast forward another 3mths I had a c6/7 fusion… now 6mths after surgery my pain since the fusion has doubled, I now have that same burning throbbing frostbite feeling down my entire right side from neck to foot and have just been diagnosed with chronic regional pain syndrome.

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Profile picture for mlerin @mlerin

Thanks for the nicely detailed message. My main issue is foraminal narrowing which is most significant at C5-C6 on the left and at c7-T1, right. Interestingly enough, both areas have narrowing but my pain and all symptoms are on the right only, seem to be stemming from c7-t1. I’m 4 days out of an epidural injection and it’s not working making me think it didn’t take. I heard a lot about prolotherapy and PRP and prolo seems to be the next step I’ll pursue before considering surgery. I’m so glad you had such a positive outcome with surgery. I live in northern CA but am willing to go to Mayo Clinic to consult with good physicians. Do you mind sharing the name of your spine surgeon? Thanks again for the wealth of info. We should all live a life free of chronic pain.

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@mlerin
I have severe stenosis at that level along with severe disc space height loss at that level and the level above. Also, some severe to moderate stenosis in the two levels above.
I don't know where you are in Northern California, but I was a work comp adjuster for 30 years in Redding. If you're going to stay in Northern California, Stanford and UCSF are your best bets. I'm in Idaho now and having my surgical consult here on December 3rd. You're the only one I know that's had problems at the same level I have as my C7/8 T1 is the worst level. I'll be interested to see what you find out and what doctor you choose. It would be hard for me to travel as far as the Mayo for surgery. Wishing you the best of luck. Keep posting so I can see how you're doing, please.
Kathy

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Profile picture for Jennifer, Volunteer Mentor @jenniferhunter

@mlerin With stenosis, when it is bad enough and causing nerve compression, epidurals may not have an effect. An epidural works by reducing inflammation which takes a little bit of pressure off, but if it is too far advanced, the pressure will be caused by arthritic changes, abnormal bone growth or a ruptured disc. If there is any instability or a collapsed disc, it can put extra pressure on the compressed nerves. I had one epidural injection and it only stopped all the pain for 5 days, and then it slowly returned over the next few weeks. I can tell you that cervical spine surgery is not that bad at least in my experience. I had an ACDF or anterior procedure which is an easier recovery that a posterior approach that goes through muscle layers. If your issues are just in the foramen where the nerve roots exit, there are some procedures that just clean out the compression without removing a disc. If you have stenosis in the central canal, they access it by removing a disc. I had spinal cord compression in the central canal from a collapsed disc and bone spurs at C5/C6, and had a fusion. I had a great recovery and had a fusion without hardware, and only a bone graft. I stayed in a cervical collar until it fused. I took it easy during my recovery. You may want to get other surgical opinions before deciding. Ask your doctor about prolotherapy. I have heard about it, and it relies on an injection that causes some inflammation which is a step toward healing, but it will not fix any stenosis that exists. If you have muscle spasms causing mal-alignment, physical therapy may help realign your spine and could help if alignment or instability is adding to the problem. It will not fix stenosis either, but could buy some time.

Generally, fixing this by decompressing the stenosis is best done before permanent nerve damage happens. Ask your surgeon's opinion on that and about how soon they think that should be done, and ask what will happen if you don't have surgery or wait too long. I had to make that choice too, and I didn't want to become disabled because of my spinal cord compression. I was also loosing the ability to use my arms and coordinate my movement. I lost about half my muscle in my arms and shoulders to atrophy. I tried to find surgical help for 2 years and was turned down by 5 surgeons, so I came to Mayo and had a wonderful gifted surgeon who gave me back my ability to do my artwork. I wish I had come there first and not wasted time with doctors who didn't want to help me. Epidural injections can also take a couple days to work, so time will tell. When I woke up from surgery, all of my pre-existing pain was gone, and I only had pain from the incision and surgical path. I also had a great physical therapist who did myofascial release before and after surgery. You need to trust your surgeon completely, so ask lots of questions and get as many opinions as you need. I'm glad that the others didn't want to help me because I had a better choice of fusion without hardware and probably would not have had that choice if one of the others had operated. I understand the anxiety, and I had a lot of that, but I learned to understand and control my fear and was able to be calm on my surgery day. I expected spine surgery to really hurt a lot, and it did not. Other patients who waited too long and have permanent damage talk about having pain that is not resolved by surgery. Doctors can't promise the surgery will take away pain, and they tell you it will keep it from getting worse. My surgery resolved all my pain and my range of motion is normal. Do your homework and research so you'll be able to make an informed decision. Here is my story on Sharing Mayo Clinic. https://sharing.mayoclinic.org/2019/01/09/using-the-art-of-medicine-to-overcome-fear-of-surgery/

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@jenniferhunter - did you have to wait quite a bit for the Mayo Clinic doctor? Many assume it is next to impossible to get in front of a doctor or surgeon there. Wondering if you can share how you ended up there? I had a spinal fusion and laminectomy of C2 to T1. That’s now been redone to T2. However, my first time- I woke up from surgery with no feeling in my arms and hands. It wasn’t just that I couldn’t feel them. They did not function either. So at 6 am - I had full use of both arms and hands. About 6 hours later- i woke up and I could not feel my arms or hands. No function either. I’ve gotten a little feeling bad but as a writer, journalist, and piano player - my hands make that nearly impossible. I had that surgery in 2022 and I still cannot write my own name today. Devastating.

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Profile picture for kdt @kdt

@jenniferhunter - did you have to wait quite a bit for the Mayo Clinic doctor? Many assume it is next to impossible to get in front of a doctor or surgeon there. Wondering if you can share how you ended up there? I had a spinal fusion and laminectomy of C2 to T1. That’s now been redone to T2. However, my first time- I woke up from surgery with no feeling in my arms and hands. It wasn’t just that I couldn’t feel them. They did not function either. So at 6 am - I had full use of both arms and hands. About 6 hours later- i woke up and I could not feel my arms or hands. No function either. I’ve gotten a little feeling bad but as a writer, journalist, and piano player - my hands make that nearly impossible. I had that surgery in 2022 and I still cannot write my own name today. Devastating.

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@kdt That is devastating. I am sorry that happened to you. I understand where you are coming from as I use my hands a lot as an artist. I was loosing coordination in my arms before my surgery, and I got it back.

As for your question about getting into Mayo, when I applied they said it was probably a 3 month wait. I had been seeing surgeons for 2 years and none would help. That probably helped me get in, and I had a condition that was misunderstood by a lot of surgeons called “funicular pain”. Because there was a cancellation, I got lucky and got an appointment 6 weeks after my request. It was because I read a paper authored by the Mayo surgeon that mentioned funicular pain that I found medical literature with similar cases. I knew I had found a surgeon who understood the problem that all the others missed. My issues were at one level and a lot less surgery than what you went through.

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