Fibromyalgia, what are the signs?

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Mary-Lou
Mary-Lou Member Posts: 2,230
edited June 2014 in Life After Breast Cancer
Fibromyalgia, what are the signs?

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  • Mary-Lou
    Mary-Lou Member Posts: 2,230
    edited May 2008

    I have some really bad pain in both my legs. It was getting on my nerves, but I thought that the pain was from being on my feet at work all day.

    Well I have been off my feet recouping from my reconstruction, so they hurt just as much , if not worse.

    My hands are stiff and hurt. My inter elbows hurts to the touch, and my shoulders.

    I really believe something is wrong. Then I also wonder about bone mets.

  • Isabella4
    Isabella4 Member Posts: 2,166
    edited May 2008

    Hi Mary. I have Fibromyalgia, but I don't think its as bad as some get it, but its still pretty painful.

    I started out about 20 yrs ago,I was the middle car in a three car smash, so got it from front and back. Got a bad whiplash, this pain then progressed down my arm, just felt like siatica does when it runs down your leg. B-A-D.

    Then I progressed to pains in my 'long ' bones, thighs and upper arms, the muscles were on fire, really sharp throbbing pains.

    Then I got  Glandular Fever, which was very prolonged, I  was jaundiced for about a month, and then it was diagnosed as  M.E., which then changed its name to Chronic Fatigue Syndrome, and as I kept on and on at my GP I kept getting re- evaluations, and some wise chap said it was now Fibromyalgia.

    To get to this diagnoses I had to have blood tests and x rays to eliminate most other things they could think of, and a curious test where he pressed various 'pressure points' mainly on my head, neck and back. I think they have to press 18 places, and if 10 make you yelp then hey presto! its Fibromyalgia.

    I think  all these 3 diseases are one and the same thing, its just everyone seems to get it in different forms, and at different levels. Some people are pretty much bed ridden, and some, like me, CAN work thru it, it just bloody well hurts all the time !!! (when you come in from work you just go to sleep)

    It  feels a very muscle-y type pain, all the time, you also feel flu-y and fatigue-y quite a lot of the time, and the 'brain fog' drives you mad. I take pain killers most days, I do try and cut them down, if I can, and put up with it, just because I don't want to be constantly stuffing painkillers down my throat.

    I know there are a lot much worse off than me, and there isn't really an answer at all. Quite often in the tests they kept on doing they kept sort of suggesting it could be 'all in the mind' If I could have passed it on to them for just a day they wouldn't have said that!!

    Its quite a long job to get a diagnosis, but its been worth it for me. Without the consultants say-so I wouldn't be able to get an easy parking badge, and a 25% reduction in my local taxes....every little helps !!

    I must say I have noticed on this board quite a fair number of us  saying they have Fibromyalgia, can't see a link with bc, but anything is possible with this disease !! Hope you find an answer. 

    Isabella.

  • Mary-Lou
    Mary-Lou Member Posts: 2,230
    edited June 2008

    Thank you so much Isabella! I will talk to my Doctor and get to the bottom of this. I feel so much older than my age of 52.

    I know what you mean about the going to bed as soon as you come home from work...I work 2 days maybe 3 and I can just make it through 6 hours. Which is spent on my feet.

    I can remember working 16 hour days at the hospital, ER was my dept, double shift pulled on the floors if they were short . Man I know that would kill me now....Cry

  • footprintsangel
    footprintsangel Member Posts: 43,890
    edited June 2008

    Dear Friend, I was told my pain in my legs are lymphedema from all the surgerys I have had and now I have to wrap them. I hope you are able to find out and get the pain under control. Also I a on a hormone that makes me hurt worse. (But if it help my fight, Ill take it)  Good luck to you, I will be praying for you. Luv, Debbie

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2008

    Mary, oh, boy, you're talking to the right person...I just got off the "Fibroymalgia" yahoo group!  I have been  diagnosed with Fibro and post polio.   Just finished breast cancer treatment, hormonal type so they think it is all gone,wish I could say the same for fibro.  It is hard for me to tell where the pain is coming from fibro or pps, but think majority of pain from fibro.  The more I walk, the more pain I have, so am mostly in power wheelchair.  I'm  65.  Onset after c-section when i was forty...also just two years before that in car accident..so figure these main triggers.

    Pain is 24/7 and I eat pain pills.  Retired on disability.  With PPS I suspect that I get double dosed, so don't want you to  lose hope.  GoogleFibromyalgia Network symptoms.  There are pressure points that the doctorcan use to idenity diagnosis. 

  • Mary-Lou
    Mary-Lou Member Posts: 2,230
    edited June 2008

    Oh Lori, such helpful info.....I will have to look that site up.

    Thank You

    ML

  • Anonymous
    Anonymous Member Posts: 1,376
    edited June 2008

    Mary Lou, do you have constant pain?  It seems so different for each person.  Getting your doctor's support is so important.  That all-over, hit by a Mac truck feeling and the enigma that every day is a different level can be frustrating.  Hang in there...and don't hesitate to keep in touch..

  • Mary-Lou
    Mary-Lou Member Posts: 2,230
    edited June 2008

    Lori- Thanks for all the advice. My Doctor checked me and said that is wasn't that. I was glad. I had to go early because my Inner-ear made me feel like the room was spinning. Never had that happen when I was sober. LOL

    I have a good work up on Thursday.....fasting after 12....

  • Harley44
    Harley44 Member Posts: 5,446
    edited June 2008

    Good luck Mary, with your blood work on Thursday...

    BTW, I have read that having ANY auto immune conditions puts us at increased risk for getting ANY kinds of cancer, so it makes perfect sense to me that there are LOTS of women here who suffer from Fibromyalgia, which is an auto immune condition.  I have Hashimotos/Hypothyroidism, and it is also auto immune.  You see, the body sees my thyroid as a 'foreign invader', so I feel 'run down' alot, and my body is constantly trying to fight this attacker, my own thyroid... DUH... I guess my body is stupid, huh? 
    YET, it let in the bc...  it's like, while your body is busy fighting off something that really belongs there, the nasty invader sneaks in....

    That is jmho, fwiw.

    Good Luck!  Let us know how your tests go, and what the results are.  I'll be thinking about you, and praying that all goes well.

    Hugs

    Harley

  • Mary-Lou
    Mary-Lou Member Posts: 2,230
    edited June 2008

    Thanks Harley , I

    will try to keep you

    all updated....

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