Partner diagnosed with recurrent breast cancer this week - so afraid right now

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Hi all, my partner was told she has had a recurrence of the breast cancer she had in 2018 which she was previously given the all clear for. Though she hasn't had a full diagnosis yet or seen an oncology team (because the hospital she first went to doesn't have a cancer unit) she was told that it had returned and there was evidence that it had metastasised into a build up of fluid around her heart and lungs (this has now been drained and the fluid has been sent off to be analysed to see if it actually does contain cancer cells). She was also told there was evidence of growth in the bones around her spine also. From her first diagnosis in 2018 there was never any evidence that her cancer had gone beyond her breast and some lymph node involvement. 

We're both utterly shocked and devastated by this because she's been in such exceptional health of recent times, has had zero symptoms or concerns before 10 days ago when she felt poorly because pain in her abdomen (which we thought at first was and on a par with a bad stomach upset) and as recently as August and mid September had completely clear breast scans (breast checks and bloods all fine too, her treatment team very happy with how she's been). She's also been so fit and active lately, she's fairly young (in her 40s) and even just the day before she started feeling unwell she'd done a very long 15-mile hike with me (and 10 miles the day before that) and had been feeling absolutely fine, no issues whatsoever and then literally overnight she felt unwell. We're utterly incredulous that she can have gone from no evidence of disease, with no symptoms and fit and healthy, to this awful situation in the space of 4-5 weeks since her last scans.

She had pericardial window surgery earlier this week and the operation was a success. She is regaining her strength after a very stressful week and is still in hospital before she's going to soon be received by the oncology team to see what happens next. We have so many questions about what has happened and how this could have happened, and until she's had a full diagnosis (the hospital team that did her first scans this week are not cancer specialists so a lot of things still haven't been done and there are big gaps in our knowledge) but it seems like there's so much information missing before we can know truly what this all means for her. 

Because of tight covid restrictions in the hospitals in the city where we live, we've struggled as a family to be able to see her. One visitor per day if we're very lucky, sometimes not even that. She isn't getting the emotional support she needs and her anxiety levels are pretty high. She's doing incredibly well but I know she's so fearful of what she might next be told. And so am I. 

When people hear the word 'Metastatic' of course they immediately fear the absolute worst outcome of imminent death, and right now we don't know what her options or prognosis will be. The oncology team have used the words "treatment plan" though and the assumption is that she will be given one - but after such a terrible week I take nothing for granted any more. Just doing all we can to keep our heads above water. So many of our friends and family don't know right now, we didn't want to say anything until we knew everything but we don't know when that will be. 

It's such a scary situation to be in, isn't it!

  • Hi

    Sorry to read about your partner, like you say the diagnostic process is scary - then waiting for a treatment plan - then .. and then...

    Often when people first hear even the work cancer it can seem the end of the world - often we hear of this described on here as a form or pre-grief, that life we imagined has gone and it is so easy to be reminded we are all mortal.

    My wife's cancer (Leiomyosarcoma) was metastatic from diagnosis - the doctors think the origin was in her womb but it was only discovered some months after a hysterectomy when her lymph nodes did not return to normal. She had two different chemotherapies and the second seems to have put her cancer to sleep - six years of that so far and we now are living with cancer rather than anything else.

    It seemed to me in some ways my wife was coping better than me - I was imagining all sorts of things going wrong but then I did a living with less stress course that really helped me. The key thing is to try and deal with events when they arise rather than letting our imagination run riot - and most important of all remember to make some time to be nice to ourselves.

    <<hugs>>

    Steve

    Community Champion Badge

  • Thank you so much Steve for your kind and useful words. I wish your wife every success in her continued health and wellbeing. 

    I am doing all I can (since the original shock) to be a support to my partner and reassure her that there’s a lot we still don’t know and that the options for her are not yet known but there will be some. She was supposed to be coming home yesterday after her pericardial surgery but she’s been having mobility issues and was sent for an MRI late yesterday as they were concerned about her spine. I know that fatigue is the most likely cause right now for her being shaky on her legs but it’s shocking to see someone who was so active literally two weeks ago be in her current situation. It’s beyond words and we’re just at a loss to explain how this has happened. 

    Am doing all I can to keep calm and exude optimism though I’m also wary of false hope. We have been here before too, it brings back a lot of bad memories. Right now it feels like cancer is pulling all the strings and we’re utterly powerless. 

    I will look at the coping with stress suggestion, thank you. I normally have my own pillars of support but they’ve largely gone out the window this week. 

    Thank you for responding, it’s greatly appreciated. 

    There is a light and it never goes out. 

  • FormerMember
    FormerMember

    This is identical to me first a lump xx surgery was supposed to be 3 weeks it was put back 7 due to COVID x I went from 3 inch tumour one enlarged lymph node to 6 inch tumour 16 lymph nodes removed by the time they did the op x I had no idea x it’s spreAd to my spine now and lungs and liver xxx I was feeling fine until. A week before op when I broke down could feel my body deteriorating.  Nhs said they weeks didn’t make a difference x I’m on treatment radiotherapy for back just couple sessions and metastatic is a scary word xx I left doctors in shock my parents are in denial my kids don’t know cxx it’s all pma one day at a time that’s all we can do cx hopefully like me your wife’s will be hormone based which means can be treated by tablets n jags show shrinkage hopefully cccc first time on forum and it was like I was reading my own post xxx please take care and feel free to contact me your wife I mea x I’m 40 feeling fit even now.and ready to fight for my life x doctors can be abrupt but plz fight it all the way.  COVID is causing ops to be pushed back further and I wish u all the luck in the world Fiona 

  • FormerMember
    FormerMember in reply to James UK

    I know exactly wot u mean a balance of hope but reality I’ve found can only be take one day at a time x enjoy your life I enjoy my kids and do not let the dark thoughts come now xxx my friend is in same position 3 times she’s had the all clear in 3 years fighting fourth time round and she had to fight for scans and treatment all the way xx we know our bodies x sorry for ranting just your post touched me as we are my family and I in same boat x I’ve told everyone no tears don’t u dare cry I’m here now and staying ccxx

  • Dear Fiona, thank you so much for your kind words. I too wish you all the very best with your ongoing treatment and for you and your family. There's a lot we still don't understand about her diagnosis. As her surgeon said to us yesterday, metastatic is "one word with many different meanings". Simply don't know enough right now to know what this ultimately means for her, but we do know the oncology team are talking about a treatment plan and we have a call with the oncologist we had the first time she was diagnosed back in 2018, 

    She has been in really good health, super active and she eats very healthily. (always has done the entire time I've known her) The fact she had no symptoms at all prior to late October also mystifies us - living with a serious illness but not so serious that there's anything for us to notice or be concerned about. 

    Despite the covid situation, they've dealt with her case rapidly and we hope that continues to be the case. Until we know more it is going to feel scary but we're doing all we can to be positive. She's recovering well from last week's surgery. 

    I hope treatment continues to work for you and you can stay in good health. 

    There is a light and it never goes out.Â