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

  • Its so bizarre isnt it! 
    surgical were so positive but yesterday it just had a different tone to it all.

    My husband thinks Im reading too much into it as none of the information has really changed at all apart from the possibility of radiotherapy and reminds me I was still stage 2a and this is all preventative now. 
    I dont know how to describe it though, I know it maybe sounds a bit dramatic but I genuinely think Im a bit traumatized by it all as I really struggle the first few days after appointments, my brain is on hight alert.   what chemo are you on lovely? Im doing 4x EC and 4x Taxol over 4 months xx

  • I'm currently on 3x Ec and 3x Docetaxel. However I spent last week in hospital with neutropenic sepsis. My neutrophils went down to 0.06. Buy they couldn't find an infection as such. I rebounded well to treatment and was out of the 5th day.  I'm sure this will be discussed tomorrow. Xx

  • Oh hon!! How are you feeling now? Keep us posted on how you get on tomorrow lovely. Xx

  • Hope your meeting with Onco goes well lovely xx

Reply Children
  • Thank you. I hope your appointment on Monday goes well! Xx

  •    hiya...well this morning went OK apart from me just randomly breaking down in tears when the car park attendant asked if I was a patient or visitor. I was so overwhelmed with the drive there...anyhow all went well, explained what to expect etc. So I'll have 5 sessions of radiotherapy, one a day over 5 days. If for example it starts on a Wednesday then I get Saturday and Sunday off then just start again on a Monday. Prior to that I'll have a scan to measure me up and the famous tattoo dots a lot have told me about lol. Just a case of waiting for the appointment to come through. Should be anytime soon really. Drove to work after and took my time getting there lol. Hope you're OK xxx

  • Oh lovely, how are you feeling now? I dont see it as random at all hon, its very justified and understandable you’d feel emotional. Be as kind and lovely to yourself as you are to all of us, you have been through so so much and in the grand scheme all of us have gone/going through it all so very recently. Its all very raw and may be for a while yet. 

    Thats great news that your having the 5 sessions hon, it will fly by before you know it and then your out of the active treatment side and on to the road of putting this behind you!! 

    Have you looked into the Moving Forward courses? Ive never been one for sharing my feelings or counseling or therapy but have certainly had my fair share of experiences which may have benefited from doing so. Im definitely going to look to do the moving forward course as a way of starting to draw a line under it all as much as is possible.
    Im struggling at the moment with not worrying every time I have a ache or pain even though my CT and MRI were clear. Im also mid having my kitchen redone and every room is a state, plus Im smothering with a real sinusy cold at the moment too which isn't helping in the slightest as my house feels like a solid representation of my stressy psyche lol xxx

  • Hi hun, now I'm at home I'm OK, been a long day and been yawning like Bagpuss this afternoon lol. Your right it is still raw and all very new to us all. Going to a Cancer hospital was hard to, seeing everyone at their different stages...gosh you have got a lot going on, be lovely when the new kitchen is finished hun, oooohhh wish I could revamp mine, I've got a list of wha needs doing lol. I know what you mean about every ache or pain, it's like what's that, then you have to remind yourself we still just out of surgery and it's repairing now. My boyfriend keeps reminding me I've done the worse bit...I did spot the moving forward booklet today, annoyed with myself I didn't pick it up. I've got that Maggie's appointment on Thursday so maybe they will have one. Nurse today said it was great that I'm going as they get company's dropping off different moisturiser and skin cream and they hand it out so ill get a goody bag she said. I know it's a means to an end and that's what I'll have to focus on....xxx

  •      also look into the Someone Like Me service from Breast Cancer Now. I've found it really helpful. 

    I totally understand the fear of any new symptoms. I am living that right now. 

    I've got chemo cycle 2 on Wednesday. I went for blood tests today to confirm the cycle can go ahead and I've been and had my hair clippered short and now wearing my wig and caps. Quite a step, but my hair started falling out rapidly on Friday and throughout the weekend so it was necessary. Much better to take charge of it. 

    Keep on being strong ladies. You've got this!   Xx

  • Aww thanks lovely will definitely look into that as well. Sorry to hear about your hair loss so quickly. You sound quite strong and took charge of it, which is fantastic. Good luck for Wednesday, we've got this indeed and thank you all for the support it means so much...have a relaxing evening xx

  • OMG get all the goody bags you can hon! Ive heard this too about companies giving away products and lord knows we have all been/going through it so if there is a freebie silver lining to be found girls we have to lasso it!!

    Your exactly right hon, its a means to an end and as horrible as it all is as far as treatment goes your on the home stretch now and you have done so well :-)!! Xxx

  • You've made me proper giggle hun. Bless ya sweetheart and I'll definitely grab a bag, hugs xxx :-) 

  • Oh hon, how are you feeling now after cycle 1? Sending you a big hug, it really sucks not trusting our bodies right now. There is no innocent ache or pain anymore as my mind wanders to the “OMG but what if!?”. My right boob actually started aching so I emailed my bcn like “so I know left boob stole the show but just want to double check they took a real good look at righty because I just don't trust her!”.

    Hope your holding up okay with wigs and caps. Did you go for a wig like your own hair or trying something new? Ive got 2 blondes and a brown and may get myself something funky as I figure why the heck not! 

    Sending lots of love and hugs to you both ladies xxx

  • I coped with Cycle 1 better than I expected except for the neutropenia.  Due to this they are dropping the dose of the E part of the EC this time. 

    I went for one the same colour as my hair but a bit longer as the shorter style looked silly. I wore it for an hour yesterday and was glad to get it off to be honest. I'd had my hair clippered and didn't want to do the school run like that so I took the wig to the hairdresser and then on the school run. I'll just have to get used to it I think. 

    When do you start chemo? Xx