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arrow's avatar
arrow
Member
12 years ago

pathology results

Hi all,

thank you once again for the love and support that has been so freely and generously given.

I feel as though I haven't processesd, or responded properly to previous msgs - let alone offered any support to others - and now I've received results that make me feel a bit sick.

my surgeon is sick so I saw another one. The cancer was Grade 3. The scar is excellent even after one week. The margins were 30mm and it's not clear if they need to take more from one spot.

Oestrogen +, Progesterone weakly +, HER2 equivocal and I need to wait for the results of another test to become available. Next appt 25 August.

Even at this early stage I should have learned not to have definite expectations but .. I expected the cancer to not be very aggressive and to be oestrogen positive only. 'Only' - as if anything is 'only' with this freaking disease.

I have excellent family and friend support but keeping in touch, deciding how much to tell, dealing with the fuss, etc is already driving me crazy. God knows how much worse it will be if I need chemo - which I never EXPECTED!!!

I am 'convalescing' - her word - with my gorgeous Mum (80) and step-Dad (85) and they have been wonderful but I want to go home and rely and build my own coping skills, live by my own routine (which is no routine, and will poss lead to other bad habits of not eating well, drinking too much wine, smoking, etc.) FFS! I'm 58, I should be able to look after myself.

Anyway, thanks for the opportunity to let off steam. I'm going for a nap. Hugs and xx

 

8 Replies

  • Hey Arrow

    You are doing it a bit tough at present you poor luv.  Between yourself and your dad. 

    Making decisions are hard at any time but a lot harder at present for you I am sure.  I found I relied on my medical team to steer me in the right direction with regards what was right for my individual treatment etc. and they did a great job.

    I managed to do the majority of my treatment - surgery, chemo and rads on my own but I did find the few days after chemo my luv'd ones wanted to be there for me and I certainly didn't complain.  I did what I was capable of doing but didnt hesitate to ask if I needed it.

    Every single one of us will have a different road that we travel on our road to remove and destroy this horrible BC so you just take each day and even each hour as you come.  Do what feels right for you and remember if at any time in your BC travels you need to ask for help or assistance it is now. 

    Looking forward to catching up with you.  We are all here for you.

    Healing hugs coming your way, luv always, Mich xoxoxoxoxox

  • your support means a lot to me. I have a lot to be grateful for and positive about - small tumour size (22mm), no vascular or lymph node involvement. I feel very lucky to catch 'it' so early and between mammograms. And it's gone, there is nothing to fear. If its HER2 + - it is what it is. If I need more surgery for the positive DCIS margin, so be it. Feeling strong and very grateful for this group. Hope to see u on 6 Sept - will rsvp asap xoxoxo

  • ... as always, jessica for your info and support. Am doing well and will wait to see what info I get on the 25th. Take care, arrow

  • ... can't seem to make decisions at the moment but am doing pretty well - esp considering multiple dramas with my dad's advanced lung cancer over the past few days. At least it stopped me from thinking about myself! getting there and feeling more positive. Barracking for you and your 22 to go - that's my lucky number!!! Thanks for understanding the independence thing. Hope to catch up with you on 6/9 xoxoxo

  • Hi Arrow, Well done for making it this far. Sounds like the surgery went well, even if you were not expecting a possibility that you might be HER2+ I had the equivocal HER2, ie the reading was 2, so they have to do as ISH, FISH or SISH test determine whether is is HER2 receptor neg or pos. If you are HER2+, or even until you find out, there is a lovely on-line support group with an excellent forum at http://her2support.org/

    If your cancer is negative for HER2, you may well not have to have chemo, depending on whether the cancer was large and/or fast-growing, whether you had vascular involvement, and whether you are node-negative or node-positive, and if node-positive, how many nodes were positive out of how many taken.. Have they told you that yet? If not, it is probably all on your pathology report, which you should have been given a copy of.

    Oestrogen positive breast cancer is usually treated with either tamaxofen or Aromase Inhibiters which are medications you take at home to stop oestrogen reaching any remaining cancer cells and revving them up to grow again. So they cut you down to minimal oestrogen, and if you haven't been through menopause, you get related symptoms. Make sure you discuss any symptoms you have with your specialist, because many symptoms either have their own effectivet treatments, or indicate you need a change of medication, or will go away in time.

    HER2 positive cancer generally needs Herceptin or a Herceptin-related "targetted treatment" Since massive amounts of research via clinical trials of thousands of women, have been for Herceptin(or one of its cousins) plus chemotherapy, either with Paclitaxel, or with Docetaxel plus Carboplatin, and the treatment regimes using these combinations have been established as highly effective,  if you have herceptin, you usually are recommended to have one of the tested-out combinations of Chemo as well.

    If you do have chemo, be aware that while some people find it a breeze, others like me find they feel very fatigued, have severe digestive disturbances and problems with insomnia. It was a challenge, manageable and I would do it again if I needed to, but really no fun at all. And I was really, really grateful to have my adult daughter spend a lot of time looking after me on my bad weeks straight after treatment. My husband on the other hand had a lot to learn before he became the "chemo-companion asset" he ended up as. However fiercely independent you may normally be, it is possible that you will be really glad to have someone else manage shopping, cooking, washing your clothes and making you cups of tea etc during this difficult time. You may find it necessary to stay with your parents for at least the first week of each chemo cycle. Make sure they understand that while you are in that state, you need to be able to ask for something and have it provided with a smile, not an argument, and you may change your mind about what you can eat several times a day and that is just how it goes. Once you are through the chemo, moving back home can be part of the recovery process, something to look forward to. Alternatively, ask them to be on call to help you day and night if you need help, while you stay on at home. Don't be a martyr, ask for all the help you need and you can pay it forward when you get your time to help.

    Best wishes, you sound like you are in a pretty good space: hope that continues.

    Jessica

  • Hey Arriw

    Luvly to hear from you.  I know what you say when you have certain expectations and then they get blown away.  I remember the shock I got after my surgery and it ended up being nothing of what they said it was.  much larger size wise, not able to get a full clearance, lymph nodes active. There was just one shock after another.  I have made it, I survived the treatment and I am now cancer free.  I duplicate what Sarah says and that we are lucky.  It is hard to take it all in.  There is so much to absorb and then try and retain it. 

    As Sarah states she is here for you, I am here for you and you know all the Perth/WA girls are here for you at any time

    You have found a great online support group and hopefully we can get to catch up with you at the next Get Together coming up soon.

    Luv and healing hugs, Mich xoxoxoxo

  • Hey Arriw

    Luvly to hear from you.  I know what you say when you have certain expectations and then they get blown away.  I remember the shock I got after my surgery and it ended up being nothing of what they said it was.  much larger size wise, not able to get a full clearance, lymph nodes active. There was just one shock after another.  I have made it, I survived the treatment and I am now cancer free.  I duplicate what Sarah says and that we are lucky.  It is hard to take it all in.  There is so much to absorb and then try and retain it. 

    As Sarah states she is here for you, I am here for you and you know all the Perth/WA girls are here for you at any time

    You have found a great online support group and hopefully we can get to catch up with you at the next Get Together coming up soon.

    Luv and healing hugs, Mich xoxoxoxo

  • You're a gem and I appreciate your wise words and - especially - taking the time to sned them when you're in the middle of treatment. I will take it slowly and will remember what you said. Good wishes and healing hugs to you for the radiotherapy too xoxoxo