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i am new on here, but have had cs for around 4yrs, when i was diagnosed the dr didnt tell me what to expect, i now get pain in legs, they feel stiff, and my hands as well, thats on top of neck pain and headaches please could someone advise me if this is part of the cs, im 43yrs old by the way many thanks in advance traceyx
0 likes, 9 replies
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Gerry_the_neck tracey64776
Posted
It is notoriously difficult to make any future predictions about C/S outcomes....and the professionals are usually reluctant to spell out the details of prospects, or speculate, for any individual patient. Some cases settle down, some continue in phases, and some require surgery. Almost impossible to predict ! The symptoms you mention are all usual for C/S, but any changes in symptoms should be reported to GP, in case there's a need for further testing to assess severity. C/S is considered a 'degenerative' condition, and it requires a continuous assessing to determine what treatments might be required. A Physiotherapist is usually more qualified than a GP to assess progress of the condition, and with more severe cases there is a need for assessment by a Neurosurgeon. An MRI scan can help determine what level of attention is appropriate.
tracey64776 Gerry_the_neck
Posted
Gerry_the_neck tracey64776
Posted
Yes, I've had C/S since I was first diagnosed 30 years ago, and probably had it before that for several years. My C/S is injury-based, rather than OA-based(osteo-arthritis), so it has developed more slowly than most who post here. At the same time, it's given me a lot of insight into the dynamics of the condition, and I tend more towards self management , rather than the medicated or surgical route. There are many 'dodgy' treatments out there for C/S, so I like to explore my skepticism to restore some balance to how I deal with it. We all get like that after treatments don't match expectations, I suppose.
tracey64776 Gerry_the_neck
Posted
Gerry_the_neck tracey64776
Posted
Agreed. I try to explore other methods for managing day to day. I think there's an obvious shortage of good advice available to C/S patients on this issue. Have a look at this link on cervical spondylosis guidance....might be some things you van relate to : http://www.physiobob.com/forum/musculoskeletal-outpatients/30602-cervical-spondylosis-self-management-advice.html. It might take a day or two for the moderators on this site to allow this link to be posted. If they don't, I will send it by private message. It's mostly about some tips for self management I've collected over the years. Always room for improvement and new ideas !
Gerry_the_neck tracey64776
Posted
Because I included a 'link' in my response, it may take a day or two for it to be moderated and posted. If it's refused, I'll send link by private message. It's just some tips on self management I put together a few years ago. Feel free to judge, or comment.
maria39241 tracey64776
Posted
I have had cs for a few years now but am currently in a flare which is far worae than before. My rt side neck is painful and I have pain rt temple and over eye nearly 10 days straight. My last x ray a while back confirmed cs and a bone spurand narrowing at c5 c6
I just wondered does anyone else get pain at temple and eye it can make me feel nauseous.
Cannot tolerate pain meds well so am struggling. Would appreciate it if anyone else has had same symptoms if they could reply
Maria
Gerry_the_neck maria39241
Posted
I think it would be quite unusual for any pain at temple, or in eye, with C/S. Never heard about similar. Sounds more like Myalgia, or Neuralgia, which can can be an after effect from shingles (chicken pox). Sometimes it doesn't show for many years. Just guessing, but I think it's worth mentioning to your GP, rather than thinking it might be tjhe C/S. Could be from getting run down with the C/S, and the neuralgia kicking in. Headaches with C/S are usually at rear/base/top of head.
tracey64776
Posted