Told cancer free after bilateral mastectomy but...

dlittkemann
dlittkemann Member Posts: 234
edited January 2019 in Pain

I'm getting pain in back... kind of ribs. Does everyone worry about every pain now? Or is it just me. Yes I got great news in Nov but I have a pain and had it all during chemo. Dr said not to worry buthow do u deal w the worry of every pain? I assume gets easier with time?

Comments

  • WC3
    WC3 Member Posts: 1,540
    edited January 2019

    As far as breast cancer goes, I would be wary of any doctor who proclaims someone is cancer free as opposed to having no evidence of disease. "Cancer free" just seems like a claim that we can't really substantiate yet being breast cancer has a history of going dormant and popping up again years or decades later.

  • dlittkemann
    dlittkemann Member Posts: 234
    edited January 2019

    well wow. Didn't need to hear that right now. Maybe she did say no evidence of disease??? I guess I like to think of it as being free.

  • dlittkemann
    dlittkemann Member Posts: 234
    edited January 2019

    I'm well aware of recurrence being an issue. I was asking about the pain part. That's my question.

  • edwards750
    edwards750 Member Posts: 3,761
    edited January 2019

    Since I didn’t have chemo I don’t know whether back pain is the norm. Hopefully someone who has had that treatment can address your concerns.

    I can say with absolute certainty that you do worry about every ache and pain once you’ve been DX. Let me rephrase that - I do however, I bet a lot of others do as well. It’s hard if not impossible to manage that fear factor when you have been branded with the C word. Goes with the territory/DX.

    Mincing words like NED or cancer-free is just rhetoric. To me it doesn’t matter which term they use because the end result is the same for now. Cured is another story. There is no cure - if only. We all just manage our disease.

    We have all heard horror stories about the beast coming back after multiple years. That’s not the norm but it does happen. Time does help. Btw I was 7 years out last August and I still go into anxiety mode before my annual mammogram.

    If the pain persists I would get checked. Despite your doctor assurances not to worry do it for your ownpeace of mind.

    Good luck.

    Diane

  • jo6359
    jo6359 Member Posts: 2,279
    edited January 2019

    dlitt- during chemo I did experience occasional pain in my back. My oncologist was not concerned at all. I did speak to several other women receiving chemo and a few of them did experienced a significant amount of pain during and several months upon the completion of chemo. If you are really concerned can you request a scan? I was told by my MO bone pain was quite common with t + C.

  • Meow13
    Meow13 Member Posts: 4,859
    edited January 2019

    Don't you love it, oncologist never seems to concerned about side effects. So focused on killing the cancer.

  • jo6359
    jo6359 Member Posts: 2,279
    edited January 2019

    Meow13- at one point my hands and forearms were covered in blisters. My Oncologist looked at the blisters and said, "hmmm". and " you heal quickly". He was mostly concerned about diarrhea, extremely low wbc's and weight.

  • wallycat
    wallycat Member Posts: 3,227
    edited January 2019

    I don't think WC3 was trying to scare you, just wanting to make sure you have a good doctor. Some say things to make us feel better and obfuscate facts so we don't stress. I wish I could tell you the worrying stops. Maybe for some gals but I'm going to start year 12 in April and anything unusual still brings me to the ugly place. Breast cancer is one of those incurable ones. It isn't to say we all will get a recurrence; many gals end up growing old and dying of something else/natural, but the reality is what it is. I think that is why the concerns and worries seem to persist. I hope you can find some doc that can reassure you the pain is just from treatment. And I hope you are amongst the lucky ones that never deals with this again.

    On a brighter note, there are new and better and more targeted treatments cropping up all the time. Maybe those of us that fret will find some comfort in that and it will help our concerns. Best to you.

  • AliceBastable
    AliceBastable Member Posts: 3,461
    edited January 2019

    Re: cured vs. NED vs. cancer-free: I was fortunate not to need chemo, but my attitude is that they removed the cancer surgically and mopped up with radiation. Unless and until I have proof that it's popped up again somewhere, I HAD cancer, past tense. This goes for all the cancers I've had. If something seems worrisome, I'll check with a doctor, but I just don't want to spend time or energy on "what if."

  • dlittkemann
    dlittkemann Member Posts: 234
    edited January 2019

    thank you so much. I appreciate the words of encouragement x

  • dlittkemann
    dlittkemann Member Posts: 234
    edited January 2019

    Thank u all. I am sure the worrying will subside a bit as time goes on. The last part of my journey for treatment is radiation so I'm still in the process. Probably normal to worry right now. Thank u to all who left encouraging posts.

  • Lillo57
    Lillo57 Member Posts: 16
    edited January 2019

    alicebastable, well said. I wish there was a like button on this site👍🏻

  • jo6359
    jo6359 Member Posts: 2,279
    edited January 2019

    Alice- I like your way of thinking. I'm not there yet. Neither do I dwell on having cancer. I have one more treatment left. I don't feel comfortable saying I had cancer instead I usually state I'm receiving treatment for my cancer.

  • leftduetostupidmods
    leftduetostupidmods Member Posts: 620
    edited January 2019

    Chemo has its own set of side effects and a lot of those are various pains. I know that at the end of it I was walking like a penguin because my lower back/hips were hurting so bad - kind of a mix between birth pain and a broken tailbone.

    You also didn't mention if you had reconstruction or if you started taking AIs - those also contribute to pain.

    Please don't get defensive when someone tells it as it is. As the sister who posted above, I'm 9+ years out and still any new pain brings me in that dark place. Because this IS the harsh truth: we're never cured. It's never gone. With the imaging technology they have right now they can't give us any 100% assurance. You will have to learn to live with the fear and not let it control your life. It took me more than 3 years before the first thought in my mind at waking up in the morning was not about BC.

    This being said, there are two rules of thumb: if a pain lasts more than two weeks, get to your doctor. Second, if something really really worries you, get it checked. Because for one, nobody knows your body better than you, and because worrying is not good for you.

    This being said, one of the known side effects of BMX is costochondritis, inflammation of the connective tissue over the ribs. Normally that appears only in young athletes after physical effort, but in our case it's because of all the trauma our torso went through with the mastectomy. I've had it since the mastectomy back in October 2009.

  • dtad
    dtad Member Posts: 2,323
    edited January 2019

    seachain...I had costochondritis last year for about 3 months. Thankfully it went away the same way it came. The pain was debilitating. Just want to put it out there so others are aware of it. My pain was on the right side so I wasn't worried about my heart. However I was worried about a recurrence. My doc poo pooed it like so many do. We have to be our own advocates and be aware of side effects from the drugs and the treatments. Good luck to all.

  • nash
    nash Member Posts: 2,600
    edited January 2019

    If the pain persists for months or gets markedly worse, ask for a bone scan. If nothing else, it will put your mind at ease.

    As far as the worrying goes, I know it's hard not to. But take it from me, try to not worry, b/c things are just going to go the way they are going to go. You don't want to waste good years with fear in your head constantly.

    I had my first primary in 2007, a local recurrence in 2015, a new primary in 2018, then brain mets in 2018.

    I spent several years after the first primary in 2007 worrying. A lot. Then after awhile, things faded into the background and I had a nice stretch of several years where cancer was not on my mind. Then the local recurrence hit in 2015, and things have been a constant nightmare ever since. So I'm grateful for the years I had where I just lived my life as normally as possible, and the only things I had to do were to pop my Tamoxifen and get my yearly breast MRI. Now, with the brain mets, I have more worry than I know what to do with.


  • jo6359
    jo6359 Member Posts: 2,279
    edited January 2019

    nash- how overwhelming this must be for you. Is your treatment regime stopping the progression of the brain Mets? Physically how do you feel?

  • nash
    nash Member Posts: 2,600
    edited January 2019

    Hi jo6359. I had cyberknife on the brain lesion June 2018 and that knocked it down. I haven’t had any new lesions since then, but I’m having brain MRIs every three months to check.

    I’m on Ibrance/Faslodex/Zolodex. None of that passes through to the brain, but it seems to be holding things below the neck steady for now.

    I’m very tired, but overall feel pretty well everything considered


  • jo6359
    jo6359 Member Posts: 2,279
    edited January 2019

    Im glad you are doing okay. I'm especially glad you haven't developed any new lesions. Fatigue seems to be a common side effect. Hang in there.

  • Zupozi99
    Zupozi99 Member Posts: 3
    edited January 2019

    hi Nash,

    Do you still have tamoxifen as your hormonal therapy or use AI drugs instead?


  • nash
    nash Member Posts: 2,600
    edited January 2019

    Hi, Zupozi99. I had a recurrence while on Tamoxifen. I'm on Ibrance/Faslodex/Zolodex now.

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