Hip pain

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mmm5
mmm5 Member Posts: 1,470

Has anyone had hip pain from the Herceptin or Arimidex, how do you know the difference between SE and Bone mets?

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  • fightinhrd123
    fightinhrd123 Member Posts: 633
    edited February 2009

    Yep hip pain from herceptin - i think!!  Had xrays, no damage or anything, go for treatment number four (i think) tomorrow, so we'll see if it gets worse!  My onc said he's seen more and more of this lately.

    Laura

  • oma4
    oma4 Member Posts: 5
    edited February 2009

    Yes, I had hip pain while on the Arimidex. It was worse when I would sleep on my right side. Couldn't take anything for the pain because I was on Lovenox for blood clots. Once I switched to Femera the hip pain got a lot better. I stuck it out with the Arimidex for seven months but finally had to get off of it because of the joint pain. I hope that you will do much better on it or be able to find a remedy that works for your pain.

  • Maire67
    Maire67 Member Posts: 768
    edited July 2010
  • mmm5
    mmm5 Member Posts: 1,470
    edited February 2009

    Did you ladies have pain in one hip more than the other, what did it feel like?

    Mine comes and gos and feels like it is in the side of the hip by the joint.

  • AussieSheila
    AussieSheila Member Posts: 647
    edited February 2009

    I wondered about that too mmm5, I guess that the 3 monthly bone scans will show whether the pain is SE's  (Arimidex caused arthritis) or mets progression.  My Onc told me 2 weeks ago that the Arimidex was 'killing the cancer cells' in the bone mets, leaving me with the idea that I was being 'cured.'  Alas, she later explained that it was only temporary and that, although she didn't know how long it would be, eventually the Arimidex wouldn't work anymore.  Then she told me that I would get arthritis from the Arimidex. 

    I get the pain in my left hip and, although it has been gone since I started the Arimidex, Nov 08, it is now coming back in my hip, back, legs and ribs with a vengeance. I am finding it harder to climb the necessary steps into my house again. I find that I have to be very careful when standing up from a chair or when I need to change direction, when walking A to B. If I turn too sharply, I get a pain that makes me cry out, which can be frightening for me and those around me. I also find that lying in one spot in bed, on left side of course, can cause a quite heavy aching pain, but I also get it if I lie on my right side for too long.  Actually, I hate to say this, but I find what I call the 'coffin position' the most comfortable, ie - lying on back, legs straight, toes pointed up, hands folded on chest. At least it helps me get to sleep for a while.

    Sheila.

  • mmm5
    mmm5 Member Posts: 1,470
    edited February 2009

    Hi all am going to bump this again and ask if anyone can tell me the difference between hip pain from Arimidex and possible bone mets. My tumor markers are normal, I am node negative not even done with first year of Herceptin, how likely is it that I would have bone mets alread with my stats and Herceptin and normal tumor markers. The reason I am asking is I just can' t put myself through another scan right now (just went through a bad scare that proved to be nothing) please anwser if you have the time I am really suffering with intense anxiety!

  • JeninMichigan
    JeninMichigan Member Posts: 2,974
    edited February 2009

    I had bone mets to my left hip and along with other places.   They found the bone mets when they did my initial pet scan at time of diagnosis.  I didn't have any bone pain.  However, once I started Herceptin I did have alot of bone pain in my hips.  Riding in the car for long periods of time was difficult.   I take 1800 mg of calcium a day and it really helped.    I also am on Aredia every 6 weeks for bone met.  I have had two pet scans both completely clean...last one was two weeks ago.  So I know, for me, the bone pain had nothing to do with mets  but more with the herceptin.    Try upping your calcium intake and see if it helps.

    Jennifer

  • mmm5
    mmm5 Member Posts: 1,470
    edited February 2009

    Thanks so much Jennifer,It looks like you were on Zometa too, I am on the oral version of Zometa (clodranate) so that could be it too!. I also felt like if I had bone mets enough to cause pain my tumor markers would be up. I am glad the drugs are working for you, I sat in the chemo room yesterday with a lady that has been 4 1/2 years cancer free after mets dx, with Herceptin, Avasitin, and Zometa

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