BC stage 2 Chemo first

Hello

just recently diagnosed 10th Sept. with stage 2 E+ P+ her2+  Small pea shaped tumour close to lymph nodes +1 or more lypmph nodes.

Its all happening very fast. Have had to stop working ( I work in a school) and now have a start date 8th October for 6 rounds of new adjuvant chemo( doing chemo first). So phew... some days I have to remind myself of what has happened. It’s funny but at 52 - I feel a bit young to be facing this.... But apart from those sort of circulating questions.I’m Mainly calm and pragmatic With the odd weepy episode for good measure.   They want to see how the chemo goes ...and then we will see how extensive the surgery will have to be. Hoping for lumpectomy - quite like my breasts  and don’t really fancy having them messed about with if I’m honest. Just pray it melts it down.  Also doing Herceptin and another antibody. So menopause here I come!

have fasted before so thinking of doing that as there is now recent research to support its efficacy. Think there was recently an article also in the oncology nursing mag. So hope I won’t meet with any objections. And looking for any other tips re chemo-

 

a friend said to wear layers and wrap up warm. I read something also about ice chips in the mouth during chemo to help protect the mouth. Do they delay chemo if you catch a cold? Just my son is already full of cold from school and I can see it’s going to be difficult to avoid some contagions. Oh and  Can you drive afterwards? And do you have to take steroids and anti nausea drugs. Don’t like the sound of that really. Sorry full of questions!

Thanks all for taking the time to reading my post

x

  • Hi Beautiful life

    Im sorry for your diagnosis - I too am almost 2 years since my TNBC diagnosis and mastectomy followed by chemo and radiotherapy- do let your team know what your doing - they truly are amazing people and will help you through this - I had ice lollies during my first 3 rounds of chemo and yes it does help to protect your mouth - it worked for me anyway - I wish you well and hope everything goes well for you - this forum was a great place to come when I was going through my treatment - ask anything - there's always someone who will offer advise and share their experiences- take care x

  • Thank you

    ice lollies got it.

    And wishing you well - and Hope life is going well for you post all this trauma!

  • Ah thank you - can’t  wait to be 2 years past this...but trying to believe that there is a life lesson somewhere in this new situation that I find myself in. 

    Hoping life is going really well for you now!!

  • Wow..very wise words Lorraine

    i guess there is no real getting beyond this...it’s a game changer

    and as the oncologist said - breast cancer doesn’t kill-  its if it moves around...so yes

    getting free of it - for now - is the best you can ask for

    and then learning to  live along side that uncertainty

    thank you

  • Hi Beautiful.Life

     

    I'm a few weeks behind you - diagnosed with BC 21 Sep. Like you my treatment will be chemo first -  then surgery. My oncology appt is 5 Oct so waiting to hear how many cycles etc.

     

    Have dropped you a friend request so we can private message if you'd like. 

     

    Thinking of you this week in the lead up to it starting.

     

    Ali x

  • Hi, 

    sorry to hear of your diagnosis , I was diagnosed with grade 2 HER+ Brest cancer in June and am now halfway through 8 cycles of neoadjuvent chemo (actually at chemo now ).

    i understand with the feeling too young as I’m 33 so not really what was expecting (2020 best year ever hey!) but your attitude so far seems positive which will take you a long way. We all have our down moments but most the time I survive on sarcasm and playing the cancer card at inopportune moments to the horror of my mother lol.

     

    It depends what chemo you are having I think but I have had to have steroids for EC and now for docetaxel , sorry . Chemo is ok again has it’s ups and downs having the treatment itself I’ve found fine it’s more peaceful than being at home with 2 kids during lockdown was and the nurses are all lovely.

    i too will have herceptin and pertuzumab which I’m starting today so see what hormonal fun ensues.

    I quite like my breast too but as dcis was found on now I have to have mastectomy so hoping I won’t look wonky with reconstruction .

    worst part so far for me was when my hair was falling out I had to shave it off as the malting was more depressing than it not being there.

     

    ive enjoyed ice lolly’s at home haven’t found any need need to have them during treatment but I haven’t suffered too bad with ulcers , I’ve worn just a hoody or cardigan and a vest top to chemo and have been fine.

    iv got 2 young kids at home and have to be careful for risk of infection but iv avoids any so far even with them returning to school. 

    I think most people would be able to drive themselves home depending what chemo you have s how far, it hits everyone different so might be worth getting loff for your first one .

     

    coudlnt tell you about fasting as I love food too much can’t imagine .

     

    sorry for loonnngg reply, that’s how exciting chemo is  

    good luck with your treatment x

     

     

  • Hi Ali

    have sent you a message!!!

    x lee

  • Thank you for all the deets- it helps with that fear of the unknown. And I’m sorry to hear of your diagnosis - ️suddenly my 52 doesn’t sound quite so young!! I’ve got 20 years on you of eating cheese and onion crisps and far too much Prosecco! 

    Glad your halfway through and you make it sound bearable - I need reminding of that.

     Hopefully your be done for Xmas - if you know what I mean. That M word around the surgery frightens me and you must now be thinking lots about that...phew... another big step forward. 

    Yes the hair..( do you know by the second session that you are loosing it?) I hate the thought of son being frightened by my appearance and partner seeing me looking like... a marine.

     

    Since the oncologist mentioned a voucher towards a vinyl wig- We have been joking about getting two for the price of one at the party shop -I fancy  the red haired Scotsman with the tartan beret and the platinum girls world barbie wig for special nights out. ( I have Scottish ancestry)

     

    did you you have a PICC line? I have had it suggested to me by the IV nurses.

     

    hoping this chemo round leaves you fit and strong.

     

    thanks 

    lee

  • Don’t worry I’ve fitted in my fair share or eating crisps and drinking and still am well the crisps mostly :) there’ll be plenty of catching up on celebrations after and yes chemo should be finished before Xmas thankfully.

    Not sure when will have surgery haven’t had my consultation for that yet.  I’m looking at the positive that at least it will all be gone and I hopefully won’t have to have radio after with the mastectomy which I would have done with lumpectomy so that will be a bonus.

     

    And it is bearable, some days it’s JUST bearable but most days it’s ok and luckily we’re women as god help us if was our other halves lol.

     

    i had longhair so cut it off too long pixie cut before first chemo but yeah once min started falling out it just seemed to get everywhere , I could tell at first when touched it was in my hands and brushing etc then it went to just falling everywhere, was in my food all over my clothes that was defo worse than shaving it off but I know some people don’t want to and I would still have hair as I look like a sprouting spud so defo still got some but I didn’t want to go down the patchy route trying to cover it either , basically I’m just lazy haha. I have a 9 and 3 year and although the oldest wasn’t too pleased for his street cred he soon got over it and my youngest used to still play with my hair when going sleep or having cuddles so I was worried how he would react but he was actually fine , now he just strokes my head :) 

    and I keep telling other half I look like Gollum but he says not I’m not so convinced .

     

    i haven’t got any wigs as was told they weren’t doing referrals cus of covid and tbf I wasn’t going out during lockdown so weren’t a problem but am thinking of looking into it soon....might avoid my Scottish heritage on this one tho .

     

    iv got a port in , so it’s in my chest straight into vein so don’t have to cannulate every time and it’s fine now but was painful straight after having it in but I think worth it   As I didn’t realise that one of the targeted therapies for 12 months have to go have at chemo suite so will get its ‘moneys worth’.

     

    Thanks chemo all done now for another 3 weeks so feel ok for now usually be pretty rough for about a week starting from tonight then pick back up , assuming it’s same pattern as the EC was .

     

    im going to blame the drugs for me chatting so much as im proper wittering on but hope some of it helps put your mind at rest and into reality for you .

    I hope your first chemo goes well 

    vikki x