Waiting on breast biopsy results - heads a mess

Hello everyone.

Ive never really posted on anything like this before but I just feel so lost and scared right now I thought Id see if there is anyone else out there feeling the same. 
Im 36, beautiful son and hubby. Couple of weeks ago was doing my fake tan, noticed just the slightest of dips in my left breast (bottom outer corner). I was due on my cycle so left it a few days encase it was something related and when it didnt go I made an appointment with my GP. They couldn't feel anything but made a referral to the breast clinic based on asymmetrical breasts. 
So I head to the clinic, consultant has a feel and agrees on the dip and can feel a lump underneath it. This then leads them to book me in as urgent for the following day but for a biopsy, mammograms and so on. So I have the mammograms done, they take multiple images. Wait again to head into the consultation room with 2 student nurses, the consultant, a Ultrasound tech and a nurse. They start talking about the lump and identify another one but at this point Im a bit numb and not really taking it all in. I have the biopsies done and then the consultant speaks to me, here is where Im upset at myself as I cant remember the exact wording (my head was and is a mess) but something along the lines of “Concerned” or “Suspecting” malignancy. It was all so fast though. I had titanium chips popped in over the two lumps tested then sent back out for another mammogram to confirm their placement and booking me in for an MRI. During the last mammogram I felt so stupid, I was almost literally frozen as every muscle was so tense and I just couldn't stop trembling. The poor technician was trying to get me to relax but I just couldn’t 
I feel so lost, so scared and to be honest completely blindsided and I don't know if Im just being a big baby or if this is a normal reaction to it all. Has anyone experienced something similar and its come back as benign? Im praying it comes back benign but their reaction and way they are speaking has made me feel like they already know it’s cancer. Then I spiral thinking oh god what if its spread already? And the littlest pain anywhere is making me so paranoid.
Im so grateful to my GP and hospital for moving so quickly, the other half just feels terrified. 
Sorry for the long rambly post and thank you for reading, I just feel like Im free falling right now x

Parents
  • Hey everyone, 

    Hope your all okay. 

    Struggling to sleep right now. 
    Had my meeting with Oncology today, lovely person and talked me through everything. I just feel like it was such a different conversation compared to my post ops. 
    Post ops was so positive and it all felt very “you can go for chemo if you want” radiotherapy wasn't even discussed. I was told to check over Predict with the sentiments that my cancer was removed with surgery and due to its stage/grade and as a luminal A its less aggressive/likely to return and if I wanted I could just take my tamoxifen and go but I opted to go for chemo to mop up any strays and for my own piece of mind.

    Cut to today’s appointment and its now being referred to by the Onco as “more aggressive” and although in terms of treatment Im HER - it did have HER cells but its still negative and it wont change treatment at all. Il be doing 4 sessions of EC and 4 of Paclitaxel over 4 months. Il also be having some sort of injection for my bones once every 6months for 3 years and being put forward for ovarian suppression now. 
    The Oncologist felt Oncotype would just be wasting time as due to my age and it having been multifocal it would likely have scored in the intermediate to high risk bracket and have just merely delayed chemo. He then throws in radiotherapy due to my age even though I had a Mx I should discuss RT. I had to ask if what I was told about it all after surgery was still the case as it just felt like such a different conversation. 

    I feel like what positive sentiments I took from my post ops have been shaken a bit. I know its silly to but a part of me clung on to the fact my predict score was good (98% for 5years and 90% for 15 years) for comfort but I was told by my onco to “take Predict with a pinch of salt” although he did go through it with me and got the same result as me but said where as on predict it gave me a between 1.5 - 3% benefit to chemo he felt it would be closer to 10% benefit in reality. A pretty huge difference in my eyes!

    I suppose I just feel a bit more scared again which is weird as apart from the bit about HER2 I knew the rest, just felt a bit like today had a more threatening tone to it all. Has anyone else had this kind of difference between their surgeon to their oncologist? Id rather go belts and braces with it but post ops just felt so much more hopeful, reassuring and less threatening than today. 

    Sorry for the long vent its just all playing on my mind. 

    xxx

  • Hi Rambleon. Yes I had the same experience between my surgeons and my oncologist. I haven't been given my Predict scores but did do it myself. I am now very sceptical about my surgery and I'm now even wondering if I was given the right advice about that too.  It doesn't help our piece of mind at all. I go back to the oncologist tomorrow for the first cycle review. Xx

  • Thank you so much, appreciated. Hope your doing OK....x

  • Early days for me in my journey and currently waiting for results from pathology. Just trying to deal with one thing at a time otherwise my mind would be like a runaway train.x

  • Just wanted to say thank you ladies, I have found this chat so helpful. I felt something not right at the end of August and was diagnosed with grade 2 IDC & 4 lesions last week. Mastectomy and sentinel node removal booked in for late November and then, if they think they’ve removed all the cancer and the lymph node is clear (bit nervous about that as it’s swollen but looked ok on the ultrasound) 5 years of tamoxifen ahead. Waiting for the biopsy results has been by far the worst bit so far, no tears since the actual diagnosis (didn’t need the emergency toilet roll I brought to hospital for eye mopping/nose blowing). My aunt also had breast cancer in her 40s and died of it so I was very scared.

  • hello  

    Well done for listening to your instincts and getting checked!!! 
    Im so glad you have found it helpful lovely! Its a rollercoaster of an experience being diagnosed and that space in time between biopsy and results had me feeling like I was losing my mind its so tough. I had a mastectomy and have chosen to stay flat on that side. Its a shock initially but recovery was smooth and as a small busted lady I found the softie fine to use. Primark and matalan both sell really reasonable and comfy post surgical bras too. 

    Tears are super natural so if they do fall just know that we are here to chat you through it or just to be a digital shoulder who gets it.
    I was teary yesterday as after a successful pre-chemo assessment they raised that Id still not had my heart scan (booked for the 6th) but said as I was young this shouldn't delay it to then calling me 3 hours after Id left to say how I must have the heart scan first to its delayed. Emotions certainly can creep up, Ive found my pms so much worse since being diagnosed!

    Rubbish as it all is there are some awesome people out there, you arent alone lovely xxxx

  • Thank you! I was terrified of tears being triggered at work by people saying 'how are you' in the 10 days when I was waiting for those results (had my escape route to toilets/a meeting room planned). Will be back in the office on Friday but think it will be ok now. I am also not over-endowed with cleavage and going for the no reconstruction option. So glad to have a date for surgery even if I'm not looking forward to the after effects and then the fear before the next set of results. It is heart warming to see the kindness of strangers in this forum and a real comfort to know there are others going through the same thing. 

  • Oh hon, I think I spent about 3 weeks looking like one of the blues brothers as I just kept sunglasses on all the time to hide puffy teary eyes. By the sounds of it you have done a incredible job at keeping it together. If they fall like I said its totally natural, understandable and we are all here. 
    I can totally relate, having a surgery date is so helpful as its a step forwards again and another move to putting this behind you. Its a scary time but before you know it you will be the other side of surgery. Any questions you think I can answer around mastectomies and going flat please don't hesitate to ask I cant promise Il know but happy to help. 
    I hope Friday goes well lovely, I work remotely but will be back in work next week now as I cant afford not to work during chemo but grateful I can work from home. Xxx

  •     I'm sorry to hear you are going through this. I'm glad that you have found our chat helpful though. Certainly I found chats in this forum helpful.   The waiting  for news is the worst part and having a plan Certainly did help me focus and cope. 

    Keeping everything as normal as possible helped in the run up to the surgery.  

    I lost my mum to breast cancer in 2019 (her original diagnosis was in 2004 when she was 56 and we got the news it came back I  2016) so I understand your worries but treatments have changed a lot since these times. So please remain positive. A positive mindset makes such a difference psychologically and has actually proved to have a physical impact too! Xx

  • Thank you and I’m so sorry you lost your mum to this. You’re absolutely right about  treatment advancing all the time. Sending very best wishes.

  • Offline in reply to BF1

    Hi   ladies, sorry not been on lately, just had a *** week. BF1, we understand what your going through and crying well I still can't seem to stop. 

    I've got dates for Radiotherapy, starts Monday 11th Nov every day for 5 days...I had already booked Wednesday to Thursday off work months ago, so I decided to book the Monday and Tuesday off as well. As I've said before I don't get the support from work apart from about 3/4 colleagues so I thought you know what I'm using holidays for that week as there is no way I'm travelling to and from work in between Radiotherapy appointments...I'm giving the *** of a boss a two finger salute...I'm so fed up. Don't want wrapping in cotton wool but for **** sake a bit of genuine support would be nice. Just get treated like there's nothing wrong with me...rant over. How are you all doing? Rambleon88 aww hun, heart check? what is that for? Sorry I sound ignorant don't I, you know I'm not being ignorant, hope your OK lovely. 

    I've got my tattoo dots too ladies lol, hmm had to grit my teeth a little but I did find it ok. Apparently I did great holding my breath (the radiotherapy nurse practices the technique with you first). It was daunting being in the scanner but looking back it was ok. The nurses were amazing and understanding and talked me through it all. Still waiting for the blood results to come back to decide what tablets I'll be on...worried how long that's taken even though I've chased up....off to Wales at weekend, Paul Weller in concert, can't wait as it will be a fab little break. Sorry it's long post ladies....and it's late...chat soon lovelies and BF1, we are all here for hun....xxxx

  • Hi BFI,

    I'm glad to hear that you now have a date for surgery. I had a double mastectomy 14 years ago and stayed flat. If you want any information about that, feel free to ask.

    Kind regards,

    Jolamine xx

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