Newly diagnosed with grade 2 IDC, grade 3 post surgery

I am a 57 year old lady who Found a lump in my right breast around middle of August 2021. I was due my mammogram on 1st September so wasn't overly concerned as had cysts drained in the past.  Attended my mammogram and pointed out to the radiographer I thought I could feel a lump so advised to see Gp as mammogram results would be another 3 weeks. Attended Gp appointment on 3 rd September referred to breast team,  appointment for 5 th September arranged, very prompt I have to say. 

Had ultrasound and biopsies taken on 5 th September then went on holiday. Came back to appointment for biopsy results on 27 th September but had also received my mammogram results which basically said everything ok see you in 3 years!

Attended for biopsy results which shown grade 2 IDC lump 1.9 cm to right breast.  Referred for MRI to confirm size only to get results that something was showing on my thyroid, second lump in the same breast and something in my armpit! Absolutely gutted and a nervous wreck! 
Following an MDT made up of different professions overseeing and discussing my case they advised second look ultrasound. I attended  for separate ultrasounds. The  Thyroid ultrasound shown  nothing of concern, the breast ultrasound shown the second lump as a cyst  therefore drained to dryness and the armpit lump didn't show anything of concern too, how relieved was I !

Fnally I had a lumpectomy and sentinel node biopsies done on 27 th November  2021 and from the tissue removed and  sent for testing it shows a grade 3 IDC not grade 2 and a 2.2 cm lump, fortunately the 3 sentinel nodes removed are all negative.

I am now waiting the oncotype DX results to see if I need chemo. I have tried looking to see if there is anybody else on here with the same cancer that has not had chemo for this. As highlighted I know everybodies treatment plan is different.

I am also told that my cancer is ER positive and HER negaive and that I will need radiotherapy and hormone therapy too.

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  • Hi, I was initially told my IDC was grade one but after my lumpectomy it was regraded to 3 . To say I was horrified is putting it mildly . They got clear margins and no lymph nodes involved so I was given 5 days of radiotherapy and tamoxifen . I finished the radio in July . My oncotype eas 18 so eas tons no chemo necessary. I'm 54 . 

  • Hi Terry just a little update. Oncotype came back as 35 but the oncologist was more concerned the the tumour has eroded some vascular vessels. I am now due to start chemo next week, gutted I have to say!

    I will have FEC once every 3 week for 6 cycles so 18 week process. I am praying it goes well and the side effects are minimal.

     

    love Kiera

  • Hi Donna, no I didn't cold cap. I'm not convinced it works brilliantly for lots of people but I know sone do benefit from it. I think it has to be individual choice based on the information   they give to you.

    I hope you get your treatment plan soon as it does help when you know exactly what's going on.

    take care, here to help if I can

    love Kiera x

  • Hi Donna 

    I am having Chemo, 3rd FEC next week and then 3 Docetaxel, I'm using the Cold Cap, happy to share my experience so far.

    If you can go to the Hospital before maybe when you first go for your first bloods to get it fitted, I did this which was better as they had my size before my treatment.

    It is crucial it fits correctly unfortunately my doesn't as I have a tiny head so have lost my hair at the crown. 
     
    The Nurses will wet your hair and apply conditioner, take your own with you, I use Simple Shampoo and Conditioner Pax also do one. Take a hairband to protect your forehead, I also put a cotton ball on my temple inside the hairband.  I take a paracetamol 2 hours before then 4 hours later. The first 20 minutes is tough but after that it's a doddle, it does make the whole process a lot longer but it's worth it. You do get cold , they will have blankets but I take a hot wattle bottle with me, keep your neck and shoulders warm if you can, my hospital put heat packs on my shoulders. I also put a little bit of soft material under the chin strap as it' can be tight. It's so important it fits properly so they need too make sure you have the correct size. 

    paxmanscalpcooling.com/  make sure you read this it has all the info, I wash my hair once a week, I use a  wide Combe but I also do brush it. You will have a big shed around 14 days in but it does slow down, my hair has gone thin but I still have lots, I am not sure how it will be at the end, the thing is for me I have (had) thick big long blonde hair, I'm 38 and it's actually the only thing I like about me, I wasn't willing to let it go without a fight, my Cancer isn't taking that aswel, Even if I lose most of it, it is very gradual which has reallly helped. 
     
    Hope this has helped, I wish you well xxx 

  • Thank you for that. I really appreciate the information.  I'm definitely going to try the cold cap, nothing to lose!! I'll watch the video later. Any help during this time is good as it's a minefield!! Xx hope you're fairing well xx

  • No problem,

    it's a link too the Website, this is the machine my hospital use but the Information will probably be the Same, Chemo is Managable, take all the Sickness they give you. The key is too drink lots and flush it out. 
     

    love Sarah 

  • Hi Kiera

    Any better with the different anti sickness drug ? Yes I am bored , thinking of doing some online courses to keep my brian ticking over.

    Turns out I have a blood clot in my arm which is why it felt tight.Now have more stomach injections and will be on warfarin for up to six months.Bloods Monday and Tuesday so I hope 2nd chemo can go ahead on Thursday.

    The nurses were lovely , but I do think they should make people more aware of blood clot symptons when putting the picc in 

    Hope your not feeling too rough x

  • Hello my dear. It's a bit early to tell as I have only taken 2 last night and 2 this morning but I there has been no light headedness or wobbling as yet so hopefully gonna be better.

    oh gid do you, your the third person that has told me that, 2 ladies where I live.

    oh I hope it goes ahead for you, poor you I feel for you, as if you havnt enough going on. Yes I agree the should make you more aware, I thought it was a rare occurrence but obviously not .

    im doing ok, just cant wait till I've had the 6 th and it's done.

    you look after yrself, let me know how yr treatment goes xxx

  • Hi Caroline how are you doing? I've been loads better this time. Starting 2 days working from home this week. I can't believe what a difference the new sickness tablet has made xx

  • Hi Kiera

     

    Thats good news , glad the new anti sickness worked well.It makes such a difference and each one is one step closer to the end.I have been better with second chemo too, I think just worked out when best to take the meds, drank loads of water and put on anti nausea travel bands.

    They have sorted my blood thinners so just on warfarin not stomach injections yeh ! 

    Glad your'e working , i think keeping an active mind and body also helps.

    Speak soon x

  • Hi Caroline, that's better then. How long did you have yr Picc in before you got the clot?

    when is yr next chemo? Mines on 25 th that will be number 3, half way xxx

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