Guess I'm moving on

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lanagraves
lanagraves Member Posts: 596

I had hoped for at least a few blissful months (or years) after TX before having to face this again. I guess it is not to be so. :(

Comments

  • Momof2inME
    Momof2inME Member Posts: 683
    edited September 2012

    Lana,

    I have followed your posts and I am so sorry about your progression. I will be thinking of you and hoping the Tamoxifen blasts that little bugger away.Smile Stay strong!

  • lanagraves
    lanagraves Member Posts: 596
    edited September 2012

    Thank momof2. I'm visualizing the Tamoxifen in terms of one of the little Dragon Ball people on my son's favorite tv show blasting away at the cancer cells every time I take one. Lol. Can you tell I live in a house full of boys?

  • bak94
    bak94 Member Posts: 1,846
    edited September 2012

    Aww, I am sorry to hear that. Yep, blast those little buggers away! Will you do radiation also?

  • lanagraves
    lanagraves Member Posts: 596
    edited September 2012

    No more radiation just yet. He said if I was in a lot of pain, or if it was a weight bearing bone, they would do rads, but since it's a rib, and I'm not hurting, they won't.

  • ck55
    ck55 Member Posts: 346
    edited September 2012

    Lana, So sorry to read this. F*#king cancer!!!!!

    Cyndi

  • MandalaB
    MandalaB Member Posts: 111
    edited September 2012

    I'm sorry Lana.

    xo

  • TectonicShift
    TectonicShift Member Posts: 752
    edited July 2020
  • Kay_G
    Kay_G Member Posts: 3,345
    edited September 2012

    I am sorry to hear that. (((hugs)))

  • Bugs
    Bugs Member Posts: 1,719
    edited September 2012

    Oh Lana, WTH?!  I'm so sorry about this.  Keep us posted on the treatment plan and how you are feeling.  Damn right those dragon balls are going to blast that sucker away!

  • Elizabeth1959
    Elizabeth1959 Member Posts: 346
    edited September 2012

    I am sorry to learn of your progression. I hope treatment will keep you NED for a long time. I'm so sorry you have to deal with this

  • mamabee
    mamabee Member Posts: 546
    edited September 2012

    I'm so sorry to hear this. I hope the tamoxifen gets you to NED right away. (((hugs)))

  • NancyD
    NancyD Member Posts: 3,562
    edited September 2012

    Do what you have to do. Stay strong. I hope you are dancing with NED very soon.

  • Alicethecat
    Alicethecat Member Posts: 535
    edited September 2012

    Hi Lana

    It's Alicethecat here from the chemo marchers thread. I was so sorry to hear your news. However...

    My oncologist told me that a single bone met is not the end of the world and he can keep people going for many years.

    Best wishes 

    Alice

  • 116
    116 Member Posts: 108
    edited October 2012

    Alicethecat............ I am sure your oncologist meant well, and was maybe he was just trying to reassure you, (Did he say this in response to your bone mets?) but it seems kind of like kind of an insensitive thing for him to say to someone that just discovered that their BC has metastasized to the bone......just a thought.........

  • lanagraves
    lanagraves Member Posts: 596
    edited October 2012

    Thanks Alice. My onc is very optimistic and believes that Tamoxifen will knock it back quickly. I feel great physically and my energy has come back after chemo and rads. He told me the same thing - that we can manage this for many years.

  • kathleen1966
    kathleen1966 Member Posts: 793
    edited October 2012

    Lanagraves, I am soo sorry you are having to face this but I think there is much hope for you to live a very, very long life.  And the longer the time you WILL get, the more time there will be for newer, better and more effective treatments to be discovered. I sat next to a woman in the chemo room who was going on 16 years with just bone mets.  She was not there for chemo, but for some hormone treatment.  Other than her sleeve, you would never have known she was in treatment by her appearance. Full head of hair, etc....I hope you continue to feel hopeful!  It sounds like you have a wonderful oncologist who will be there for you.

  • lanagraves
    lanagraves Member Posts: 596
    edited October 2012

    Thanks Kathleen. I do have a wonderful medical team - MO, RO, research nurse, breast cancer navigator, etc., they're all great. I'm really not taking it as hard as I thought I would. And my friend at the office who has been by my side throughout this told me this morning that she has been Stage IV with two bone mets to vertebrae since 1998. I asked why she didn't tell me before and she said because she didn't want to scare me and make me start wondering even more if that's what was going on with me. She's a very private person anyway. But she is doing great. You can't tell she has anything wrong at all. She has had two bouts with cancer in her breast and has another spot now that they are about to begin treating. The bone mets are stable, and have been since 1998. She was diagnosed with MS earlier this year and is more concerned about that than the BC. She is truly an amazing woman.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited October 2012

    Lana - what symptoms did you notice this second time around?  I'm scared as heck that I won't have any real symptoms to tell me something's recurred.  Was it by elevated tumor markers in your bloodwork?  I also had BMX, and didn't have a clue when dx'd.  And only through ultrasound did my cancer actually show itself.  I hope and pray you stay strong --you can do this!

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