I have cervical stenosis myelopathy c3 to c7 which seems to have stayed the same for a number of years, has anyone else had this, although the weakness in my right arm isn’t pleasant and the heavy pins and needles are awful I don’t feel that the risk in surgery is worth it.
cervical stenosis : I have cervical... - Fibromyalgia Acti...
cervical stenosis
Thank you for posting this, I have 4 nerve damage in my neck and spine, I wasn’t able to have surgery because I’m so claustrophobic I can’t do the MRI scan, so now you have said it makes no difference, and you still have pain and pins and needles, I may think twice about it??. Sorry it hasn’t worked for you.
Hi Blue, I may have read the post wrong. But I got the impression the poster was saying. Even though they have the problems. They did not feel going down the surgery route was for them. Not that they have had the surgery?
Apologies if I've read that wrong. Not sure if the poster was maybe replying to another post has it was not fibro related xx
Momo
sorry you mis-read my post, I haven’t had the operation that they say is needed and hope that I don’t need to. The mri is not the best experience,I failed my first one , but had one on April 1st and still waiting for results, hopefully it will show no deterioration.
I have cervical spinal stenosis have had since the pandemic not much the docs can do apart from injections and they can operate but they told me only if I started getting numbness so I still manage it with conservative treatments like warm showers and painkillers