Secondary Breast cancer

I finished radiotherapy on Monday after a mammoplasty lumpectomy and full lymph node surgery - it was in 1 of the 18 nodes removed. I am in total shock as yesterday I was advised the breast cancer is o my lung and my back!

i had a Ct scan before Christmas because a indeterminate nodule was found on my lung at initial diagnosis.  The doctor had said it was most probably mucus - but obviously the cancer had spread before the initial diagnosis.

i have a full Ct scan booked on Tuesday but my fight has gone!  On Tuesday I thought I had reached the end with finishing radiotherapy and starting on hormone therapy but instead I have limited time left !  

  • Hi Staypositive,

    I can understand how devastating this must feel, just as you finished your radiotherapy. Unfortunately, this is the rollercoaster that is cancer. Let's wait and see what your CT on Tuesday brings. There are many people on this site, who have had similar diagnoses, yet continue to overturn the course of their prognoses. Do you know whether or not chemo, or immunotherapy are treatment options?

    Please keep in touch and let us know how you get on. We are always here for you.

    Kind regards,

    Jolamine xx

  • Thank you for your support and reply.  The consultant mentioned the following treatment but obviously until the scan results I can’t be sure.

    Abemaciclib

    Letrozole ( currently started in November on Tamoxifen)

    Ovary suppression

    Bone strengthening injections

    He did say that there were different options available along the journey. Just waiting for Tuesday.

  • Hi,

    It sounds as if there are still plenty of treatments for this, so don't give up hope yet. I shall be thinking of you on Tuesday.


    Kind regards,


    Jolamine xx

  • Hey Staypositive 

    im leanne and was diagnosed secondary breast cancer back in November with mets to spine rib and pelvis! My primary diagnosis was back in April!!  

    it’s defo a shock for u and I know exactly how u feel as I was going through chemo when I discovered I had this! Very bitter sweet to get to 7 out of 7 chemo and told this!!!

    u don’t have limited time none of us know how much time but you can’t give up your fight!!! We are strong women  and are bosses of our journey!! Keep the head up and keep busy!! Obviously it’s difficult and there are days that it gets on too but the minute the head is down then it’s won!! It’s not easy but we can’t let this ugly disease take over our life!! 

    always hear if you need a chat xx

  • Hi Staypositive,

    I have been thinking of you today and I hope that your CT went well. Did they say when you would get the results?

    Kind regards,


    Jolamine xx

  • Hi Leanne,

    I am so sorry to hear that you are in this position too. This news must have come as a real kick in the teeth, when you had got to 7 of your 7 chemo. I completely agree that we cannot let cancer take over our lives. We've got to fight it with all that we've got. I sincerely hope that you continue to fight it for many years to come.

    Please keep in touch and let us know how you get on. We are always here for you.

    Kind regards,

    Jolamine xx

  • Thank you Leanne for your encouragement/ positivity.  My initial scan was rearranged so the not knowing is currently not helping and my back has definitely got worse since being told 2 weeks ago.  I assume if my spine scan is particularly bad they will telephone.  Have a consultation next Wednesday.

    Has starting medication for your mets helped?

    Good luck with your fight against cancer - you deserve to keep winning.

  • Thank you Jolamine for checking in on me - very appreciated.

    My initial CT scan was postponed but have now had Pet/CT and CT scans.  Pain in my back has definitely increased since being told about mets to spine - need results to know full picture.  Consultation appointment next Thursday and starting on ovary suppression and bone strengthening then too.  1 further week to wait.  Assume if spine particularly bad on scans they will ring?  

    Thank you again

  • Hi Staypositive,

    I am sorry to hear that your initial CT was postponed, but glad to hear that you have now had Pet & CT scans. They are usually fairly accurate with the length of time that they say it takes to get your results, and it tends to stay the same, irrespective of what the results are. I shall be thinking of you on Thursday week and hope that the cancer hasn't spread far.

    Kind regards,

    Jolamine xx

  • Hello sorry for late reply! Didn’t notice the reply

    So after I was told about the met to the rib I constantly thought that the pain was intesifying but when I was busy I did not feel the pain only when not doing anything which I now know was psychosomatic pain or probably just anxiety!! 

    the not knowing is awful and waiting is just not needed!! 

    im on phesgo jag but not had this since beginning of December as my heart function has reduced due to this medication lol so Got a 6 week break and due back on 14th feb (how romantic); my treatment is phesgo and tamoxifen! I’m also taking a lot of supplements and back at gym so keeping busy is helping! I’m very fortunate I don’t have any new back pain! The back pain I have has been the same for years (basically since my epidural) - I sometimes wish they didn’t find mine so quick and that I at least had some time to be “cancer free” or believe I was but I didn’t and everything happens for a reason 

    keep positive, keep busy, keep being you and never give up!! Like I say if you need to chat always here xx