Guest guest Posted December 13, 2007 Report Share Posted December 13, 2007 Deb, Great story...one I know we can all relate too. Sigh. When I look at where I am in my life right now it's kind of a " spoon " thing...but in a more " long perspective " kind of way. I am greatfully not dealing with the day to day chronic pain that just easts away at you. I do feel like I am dealing with a chronic condition...and I have to ration " my spoons " or I feel like I run the risk of having new problems develop related to this very fused spine. I do look at the world and see that most people as they age at some point must do this too...after all, no one gets out of this alive. I wonder if I am being overly cautious now, having probably been under cautious before. I just know that I do not want to go back to where I was the year before surgery...and if that means playing it safe and rationing my spoons....so be it! Looking forward to hearing how your vist in Chicago went. Take Care, Cam Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 13, 2007 Report Share Posted December 13, 2007 they other one i have heard combared to is diabetes... also that if either conditions are ignored and not properly managed they can be devasting... so a bit about myself... i'm 27 and live in indianapolis.. i work as a consultant for as a chemist for lilly actually (so i've been hearing quite a bit about cymbalta lately).. i was diagnosed with fibro and CFS when i was 23... last year i also was diagnosed with pernacius anemia (a rare disease causing maladpostion of b12) which untreated was causing the fibro to be worse.. unfortunately the anemia wasn't caught before i had some nerve damage done.. *sigh* over the years i've been a sponge in learning all i can about medication/coping methods/latest research/causes/etc on fibro...i finally found a combination of things that have given back my life and i can't be happier... i guess i'll mention as well that i'm also a animal lover with 3 dogs of my one.. 2 cocker spaniels (jake and pandora) and a bensji (maggie) that have been the only constant love and support during my struggles learning to cope with fibro on doctors... i have gotten extremely lucky to have a doctor that understood and was compasionate with all that i had gone through.. diagonsed fibro quickly compared to the norm and has been great finding a treatment method that worked... i also have had others that suck like we all now they can.. but there are good ones and i believe FM Aware has listing of fibro friendly doctors... to all, a wish to be pain free, full energy, and full of happiness and joy.. blessed be lizjeanniemalkiewicz <jmm127@...> wrote: >> Had anyone found a way to handle comments like this?There was a great article in the last issue of FM Aware that listed this as one of the top 10 worst things people say - and I think the author's comeback was "neither do people with heart disease, epilepsy, etc."> Be a better friend, newshound, and know-it-all with Mobile. Try it now. Quote Link to comment Share on other sites More sharing options...
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