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Majellablue's avatar
Majellablue
Member
5 years ago

What do bone Mets feel like?

Hi Gals
I was diagnosed almost a year ago with stage 3C DCIS - (Beryl for those in the know!) Beryl was pretty busy and managed to have 13 not so darling babies (lymph nodes). So a mastectomy was on the table and as I was awaiting test results for BRAC gene I decided to go for gold and do two for the price of one - I do love a bargain!
Results of the test came through the day after my surgery and I was indeed positive for BRAC2 gene.
So Beryl and her kids had been rendered homeless and I had the usual chemo, rads and AI’s to ensure they did not come back. All was good until about 3 weeks ago when I started to feel persistent pain in my rib (same side that Beryl and the kids popped up on). I have a CT scan on Friday but just wondered if anyone could describe the pain. I have pain that comes and goes (mostly there) and goes from a sharp pain to a dull ache. I am hoping the Beryl has not decided to return! 
Any advice?

pain
scans

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  • Hankster's avatar
    Hankster
    Member
    5 years ago
    Hi I have bone Mets . The first pain I got was muscular, I now know it was my body protecting the area of my spine that had disease .  It was severe and persistent nothing would stop it physio was a waste of time.  I then got really bad spasms in my neck.  The bone pain started once I had been diagnosed.  It is hard to explain except to say it was different to any pain I had ever experienced.  It took 6 months for mine to be diagnosed,  I was 10 years cancer free. My advice is if any pain is persistent insist on an X-ray of the spot.  That is what I ended up doing. My doctor was devastated that she did not pick it up earlier. 
  • arpie's avatar
    arpie
    Member
    5 years ago
    Welcome to the blog, @Majellablue - SO sorry to see you here, but it is the best place to be to ask any questions of the group & get honest answers - as we 'get it'.  

    I was checked late last year for persistent pain in my pelvis - and got the all clear - but am very aware of any new persistent pains as they present.  :(  Sadly, it is all a part of this bloody disease & a side effect of the AIs we are on.

    I actually asked  my Onc about the 'pain that could indicate Mets' - and she said that it is a deep seated persistent 'different' pain to 'general aches & pains' that we get from AIs ..... but advised to get anything investigated if it lasts longer than 1-2  months.

    All the best for your CT on Friday - fingers & toes crossed for a good result.  xx
  • ddon's avatar
    ddon
    Member
    5 years ago
    I can’t answer your question but I have my fingers and toes crossed for you that there is nothing nasty going on xx