Is this going to get worse??
Posted , 6 users are following.
Hi everyone
Im fairly new to my diagnosis of fm, in my case it is secondary to 2 autoimmune disorders. I feel shattered all the time and sometimes I can't lift my head off the pillow for days. Im 33 and had a disc removed when I was 27 and so have struggled with chronic pain for years anyway. Im on immunosuppressive medication and also medication to tKe the edge off the pain plus I can take tramadol or dihydracodeine. All of my joints and muscles hurt everyday but I am still more mobile than most on here, it seems. What id like to grasp, is how can I expect this to progress as I get older, in others experiences? It is possible I will remain as mobile as I am currently or is it more likely to get more and more difficult? I only use a walking aid when my lower back goes but it does effect my neck and shoulders to the point where I cant turn my head properly or lift my arms, but this isnt every day or even every week. I am still clearly less able than 'non sufferers' but I would just like some idea of what I can expect for my future? Any advice or to learn of others experiences-although I appreciate everyone is different- would be really appreciated. Im feel like im gradually going downhill and its effecting my career and life overall. I know im not dying but I dont feel like im living much fibrat the moment either.
0 likes, 18 replies
alison37384 kate288a
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hugh07153 kate288a
Posted
kate288a hugh07153
Posted
I'm at work at the moment but will try and have a read this evening. In relation to my back surgery, I was lucky enough to be working for a health insurance company who provided health care to their employees. I basically got fed up with my GO fobbing me off and telling me I was too young to have problems that I 'told' them to refer me to a private orthopaedic surgeon. Once referred my surgeon sent me for an mi which concluded I had a prolapsed disc with an annular tear..They tried 2 epidurals in the space of year but these failed to give any long term relief so surgery was the only option.
Hope this helps
Kate