← Return to ACDF and recovery post-op?
DiscussionComment receiving replies
Replies to "I have posted before that my ACDF surgery had not helped my symptoms at all. About..."
Jennifer, thanks for replying. Yes it is a bummer. I went through a complete NCS and EMG before with a separate neurologist, but he did not explain any of his findings to me, just saying "you need to see a neurosurgeon". My overall situation probably looked bad given the several different places (including myelopathy with my spinal cord) that needed fixing. And I have no doubt, based on the 2nd opinion of a different neurosurgeon, that I needed to have my ACDF.
But it now seems like one of those 3 might have been able to say to me "You need this surgery but you have other severe issues that may prevent a complete fix for your pain and numbness".
I definitely do not want to consider *more* surgery if not needed. That is why I phrased my request as "is there anything else I could do in parallel with waiting a year?".
My new followup after the CT-scan and EMG is Apr 23. I will report on what happens....
Mitch
Yesterday, I saw my neurosurgeon for my 3 mos. post-surgery checkup. My C5 palsy is resolving itself such that I can use my right arm more but the doctor said it could take a full year for the nerve and muscles to completely recover. He is otherwise disappointed that I have not had more progress with my other neurological issues, like the arm pain, numbness in my hands and my "unsteady" gait. My most recent cervical CT Scan does show that there are no issues with the areas that the surgery "cleaned up".
The results of the recent scans and neurological testing show that I have significant damage coming from the C5-C6 nerve root area. He wants to wait one year before looking at other ways to possibly address this (like nerve blocks or further surgery, but from the back). He believes my issues may be congenital, his diagnosis is Myelopathy with cervical radiculopathy and that I may now have "dead" spots on my spinal cord, but that can only be proven through an MRI.
He said he supports the idea of me getting an MRI compatible pacemaker when it is replaced this year and is willing to talk to the cardiologist and insurance company, if needed.
So really it is still "wait and see". I feel fortunate that I still have mostly the use of my right hand, although numb and sometimes painful.
I have some difficulty managing my thumb and index finger, and have to be careful picking things up. I cannot button my shirts.
But things could be worse.
@birdman518 Mitch, I agree. That sounds important. I was curious, so I searched for some info about MRI compatible pacemakers. If you are on Medicare, it may take a lot of paperwork from your specialist to get it done and that may take awhile.
https://www.mayoclinic.org/medical-professionals/cardiovascular-diseases/news/new-protocols-allow-for-mri-in-selected-pacemaker-patients/mac-20430571
https://www.health.harvard.edu/heart-health/mri-is-safe-for-most-people-with-pacemakers-and-defibrillators
Connect

@birdman518 Mitch, I'm glad you got some answers about the cause of your pain. I am wondering why.... I would have expected all of the issues to have been addressed in your surgery unless there was a medical reason it couldn't be done at the same time. Was the foraminal stenosis discussed before your surgery? How does this report compare to the imaging report before your surgery? This also says that your spinal canal is smaller congenitally. I'm sorry you are in this situation. I hope you find a resolution to get your pain under control.
This link explains some of these issues. https://www.spineuniverse.com/conditions/spinal-stenosis
Thanks for checking in.
Jennifer