bad pain

Posted , 8 users are following.

Woke up this morning in terrible pain in my hips and legs so bad

1 like, 30 replies

30 Replies

Next
  • Posted

    I have had the same thing for weeks. Yesterday particularly down the left side. My leg was giving way.
    • Posted

      Its getting worse i dont know what to do im taking a lot of tablets for it at mo sad
    • Posted

      There is a good article on the Facebook Fibromyalgia Network group specifically on hip pain. I have tried to post a link but that has gone to moderation. If you google 'pain in left hip fibromyalgia' mit is the top answer. In case you don't 'do' Facebook, the text is as follows:

      The following question was answered by Allan L. Metzger, M.D., a Rheumatologist in Los Angeles, CA.

      Hip pain in fibromyalgia is usually a right and left side phenomenon. It's a very diffuse type of pain, unlike the hip pain of arthritis that is more localized or centralized to the front groin. Non-centralized hip pain is often related to structural problems in the back that refer to the hip, inflammation at the back of the hip (bursitis), or myofascial trigger points in the hip region.

      However, if there is a change in character or a worsening of pain, especially in older fibro patients, with groin pain and referred pain traveling down to the knee, then I must exclude an incidental or isolated osteoarthritis for the hip joint. Most "hip" pain in fibromyalgia is really not due to the hip joint, but rather the soft tissue structures supporting the hip and buttocks regions. Muscles in these areas may have painful myofascial trigger points. Whether your hip pain is due to trigger points or arthritis, it should be evaluated by your doctor so that the appropriate treatments can be applied.

      To remain unbiased, we do not accept endorsements, advertisements, or money from the pharmaceutical industry. Articles are for informational purposes only. Consult your physician for treatment.

    • Posted

      Cheers for the info i will have alook now wish there wasmore info at hand for fibromyglia ypu r very thpughtful thankssmile
    • Posted

      Yes they do, I follow a couple they are very very informative...:-) xx
    • Posted

      There is tons of stuff on the internet but as with everything you have to be careful and selective in what advice you believe.

       

  • Posted

    sadO' no, poor you HOTpicks..really feeling for you right now., very gentle hugs from across the seas..be blessed...:-) xx
    • Posted

      Thank you for your wishes im really down at mo being in so much pain wish i could just stay in bed its that badsad hugs to youx
  • Posted

    I've had it for weeks too, wakes me up through the night, this morning I was up at 2:30, took painkillers then slept, occasionally, on the sofa. I saw the Rheumatoligst last week, I said I thought I needed a new hip, she touched the sore bit exactly, it's one of the fibro hotspots. I'm glad I don't need a new hip but I'm stuck with the pain. She's referred me to the pain clinic and for nerve conduction tests as my spine is bad too. Have you seen anyone about your back? Sometimes we put everything down to Fibro when it might be something else.

    take care

    enjoy the sunshine 

    Shelagh xxx

    • Posted

      I havent seen anyone about my back cos its a fight to see anyone sooo tired and in pain really fed up with it all thanks for your reply really appreciate it hope they can sort you out hugsx
  • Posted

    you just have to grit your teeth and wait for it to pass 

    thats what i do ,its just a bloody misery 

    i dont take any meds from gp 

    simply because i am very sensistive to meds 

    so theres no option but for me just to get oin with it 

    i use magneisum oil when i ache and it keeps me awake 

    iv brought a new gel to try for around the joints havnt tried it yet

    called flexiseq i havent tried it yet.

    because i am finishing up another one at the moment .

    iv got a feeling that as several people on here have said the same at the same time about increased pain . it may be linked to the weather 

    my pain changes with the weather . if its biting cold i get a aching bone pain ,with contracting clawing muscles and tendons , when its humid like it has been the last few weeks ,i get tenderness pain  i seem to feel swollen but with no signs of swelling and fatigue is also worse when the weather is warm .

    • Posted

      Hi tiswas; yes this is something that I have tried telling docs too....that the weather plays a Very big part in my symptoms....when Hot as we had here in Australia in  November....a Heat Wave....my muscles were Screaming in pain...and in winter, my fingers (and other body parts), also play up....I find it even extremely difficult to type (have found special Osteo gloves/mittens...with fingertips removed, that help my hands).....I'm pleased I have read your piece, as you are the first that I have read who also feels the weather has a big part to play....Bron
    • Posted

      oh god bron the weather really does play apart in this condition and others

      i did have one gp say to me in october one year when it was cool but damp

      for a long period this weather must be driving you mad when theres a lot of moistier in the air i have much more pain and diffitculty getting about 

       

      dry heat no problem ,heat /humidity  or cold/ damp absolutly cripples me 

      i wish i could live somewhere dry and warm all year round some where like madrid .  

    • Posted

      biggrin  you keep thinking re where we should go....and just maybe we can meet up there....I've still got a few years left....maybe Portugal....I hear that's nice and laid back???   You take care and receive my hug in the meantime.....Bron
    • Posted

      Hiya Bronwyn...what part of Australia are you in...or have you already told me..mm...brain fog..I know that there are two people on here from. Oz, .who write fairly regularly..I too use those special gloves with fingertip cut out mine also have lots of little magnets in them...soo good for OA in winter...the heat/ summer is quite fine for me as I'm in Tassie and it's cooler than the mainland..but it's those wonderful hot water bottles that really help me..winter or summer..be blessed..:-) xxx

Report or request deletion

Thanks for your help!

We want the community to be a useful resource for our users but it is important to remember that the community are not moderated or reviewed by doctors and so you should not rely on opinions or advice given by other users in respect of any healthcare matters. Always speak to your doctor before acting and in cases of emergency seek appropriate medical assistance immediately. Use of the community is subject to our Terms of Use and Privacy Policy and steps will be taken to remove posts identified as being in breach of those terms.