Stage 3c - triple negative

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shereejoy
shereejoy Member Posts: 25
edited June 2014 in Stage III Breast Cancer

I live in Australia and would love to hear from anyone currently going through treatment or any survivors out there with the Triple Negative Breast Cancer. 

I had 3 tumours in my right breast hence a mastectomy (multifocal disease).  My biggest tumour was 5cm.

I had all lymph nodes removed and 13 of my 26 were infected with cancer.

I am 36 with 2 young children (boys aged 3 and 5).\

My chemo treatment is 3 x FEC and 3 x TAXATERE (every 3 weeks).  Will be up to my 4th on the 9th of June.  Been terribly sick!

Also will more then likely have 6 weeks of radiation.

Would love to hear from anyone. xo

Comments

  • shereejoy
    shereejoy Member Posts: 25
    edited May 2011

    Oh and also mine was the Invasive Ductal Carcinoma.

  • KerryMac
    KerryMac Member Posts: 3,529
    edited May 2011

    I'm not TN, but just want to welcome you! I am originally from NZ, but have lived in Canada now for about 15 years. I also have small kids (were 2 and 4 when Dx) and did FEC-T Chemo. If you have any questions, fire away!

    Glad you have joind, you'll get loads of support here! 

  • littletower
    littletower Member Posts: 333
    edited May 2011

    Also not triple neg, but high node count also and wanted to say hello. So sorry you're here, but this is a great group of women and its a good place to come to get the support you need. Hugs from the Stateside sisters!

  • kathleen1966
    kathleen1966 Member Posts: 793
    edited May 2011

    I'm also not triple negative, but stage III with smallish children (though I had them "older", just turned 45), a nine year old and a five year old. Welcome to the stage III forum and to the breast Cancer forum in general!  Hang in there.  There are other women on here with a lot of nodes and large tumors who are doing well.

  • AgentMo
    AgentMo Member Posts: 72
    edited May 2011

    Dear shereejoy,

    I am not triple negative, but given that you have a lot of nodes and are triple negative, I would push for a more aggressive chemo. Have your doctor explain why you are not eligible for double dose-dense chemo, which is known to work better than the one you are currently about to get if the node count is high. You are so young (as am I by the way) and since you are triple negative chemo is your only weapon, so make sure you give it the hardest shot you can get. Double dose-dense chemo  (means every two weeks and higher dosage of meds) may be hard on your body, but you are young and you can bear it. Ask for a second opinion, too, if possible, because you only have once to do things right.

    All the best and hugs AgentMo

  • Anonymous
    Anonymous Member Posts: 1,376
    edited August 2012

    I'm not 3-, but saw your post on the Active List. There is a Triple Negative Foundation in New Jersey, USA , and you'll find a great deal of information on their website:http://www.tnbcfoundation.org/

     Also, because you are so young, the Young Survival Coalition, http://www.youngsurvival.org/ will have information you might find valuable.  They have many groups in the States, and I wold expect they might also be able to connect you with women in Australia.

    There is a Triple Negative Forum on BC.org too.  I hope you find all the support and information you need.  Al the best to you.

  • JacquelineG
    JacquelineG Member Posts: 282
    edited May 2011

    Hi sheerejoy,

     I too got 3 FEC and 3 taxotere. I was staged 3c and my onc thought this regimen was among the most agressive, if not the most agressive. Dose dense is a bit different but not necessarily more agressive than the regimen you are on (according to my onc).

    Best of luck and hope you're feeling better soon!

    Jackie

  • alexanjb
    alexanjb Member Posts: 304
    edited May 2011
    hi Shereejoy-I am 3c TN.  And my name is Joy Laughing.  I am older though and my kids are grown up.  I had a uni mx on the right, dense dose AC and Taxol followed by radiation.  As far as we know I am cancer free.  I don't have experience with the type of chemo you are having, but I found that if I didn't try to be conservative with the anti nausea meds I did OK.  Hydrate and then hyddrate some more.  Don't go to chemo on an empty stomach, treat it like morning sickness, have crackers and ginger ale during treatment.  Eat several small meals instead of 3 large ones.  Rest as much as you can...with little ones that is very hard, I know.
  • jennyboog
    jennyboog Member Posts: 1,322
    edited May 2011

    Just wanted to welcome you, I'm not triple - but several on here are and I believe there is a triple - forum you might find helpful.  I was 34 at dx and have 2 small kids (2/4), I also did taxotere (that was a rough one) so I know what you're going through.  Had 2 tumors, did BMX in Jan. finished rads in April.  Rads will be so much easier than what you're going through right now.  Take it one day at a time....you're reaching the top of that big mountain, come here often, we understand.

  • TiffanyF4
    TiffanyF4 Member Posts: 171
    edited May 2011
    come on over to the CALLING ALL TNS forum Cool
  • Octobergirl
    Octobergirl Member Posts: 334
    edited May 2011

    Hi Shereejoy,

    Welcome to the stage 3 group.  We are many and we are mighty....mighty supportive of each other. :)  I'm not TN nor have young children but I have done a difficult chemo regiment and am sending you positive energy as I write.  Having cancer is the bad part of being here; on the flipside, it's a gift to be able to meet women walking the same journey from all over the world!  I'm glad you found us.   Molly 

  • KerryMac
    KerryMac Member Posts: 3,529
    edited May 2011

    I just want to agree with Jackie about the FEC-T Chemo - it is a different thing than AC-T, and my Onc said it was the most aggressive treatment she could give me. They don't dose dense it (it is similar to TAC, which is also every 3 weeks)

    Please don't doubt your treatment, you are being as aggressive as you can!

  • kimber3006
    kimber3006 Member Posts: 586
    edited May 2011

    Also not TN, but wanted to chime in with another welcome.  I was 39 with a 4 year old when I was diagnosed.  It's only been a little over a year and a half, and he barely remembers it all now.  I'm sorry to hear you've been feeling so sick with the chemo.  As someone else said, be liberal with the anti-nausea meds.  The usual line up, which my onc said should completely wipe out any nausea, didn't work for me so we added some more!

  • lkc
    lkc Member Posts: 1,203
    edited May 2011

    Hi Sherree Joy, I WAS a STAGE IIIer, and thankfully am well.Please take heart , you have actually gone throught the hardest 4 tx. I had taxotere as well, and it was no party. However once done with it, I was thankful for this wonderful drug.

    Rads was on the whole was much easier on me.

     Come here often for support  and a wealth of great information and check out the TN group!

  • gillyone
    gillyone Member Posts: 1,727
    edited May 2011

    Hi there! I am not only stage IIIc but also TN. This weekend it is 2 years since I fould the lump that started all this. Hang in there and feel free to ask any questions.

  • shereejoy
    shereejoy Member Posts: 25
    edited May 2011

    Thankyou all for your responses :) . I am interested to know if any of you have changed your diet during and after chemo???

  • pupfoster1
    pupfoster1 Member Posts: 1,484
    edited May 2011

    Hi Hon,

    Glad you found us!  Although I am not triple- the rest of our dx is very similar.  I had multifocal disease as well with the largest tumor being 6.5cm.  13/15 positive nodes.  They threw everything at me.  Dose dense A/C every 2 weeks/4 cycles, then the same schedule w/Taxol.  Then had 30 sessions of radiation.  On Tamoxifen now.

    I wish I could say I've TOTALLY cleaned up my diet, but I must admit I still like my sweets.  I know sugar is bad, so I eliminated it from my coffee, tea, etc, try to eat low sugar cereals, but then I do indulge in ice cream or candy at night on ocassion.  I am also buying organic milk now, as well as other organic items if I can afford them.  There's a list they call "the dirty dozen" that if you can get organic you should try to.  Mostly b/c they come in direct contact w/pesticides, etc.  Like blueberries, lettuce, etc.  Google it and you'll get the whole list.  I also have pretty much given up drinking, but had already began that before my dx.

    While your in chemo though, my docs told me to eat whatever I felt like I could handle.  Some woman have a tough time eating through it.  I had moments of nausea but my worst side effect was severe mouth sores that even though I was hungry I couldn't eat or drink much at all.

    Keep checking with us and let us know how you are doing!

    (((Hugs)))

    Sharon

  • jennyboog
    jennyboog Member Posts: 1,322
    edited May 2011
    I changed my eating habits some but not as much as I probably should have.  I buy organic when I can, I eat alot more fruits and veggies, I try to eat well as much as I can so when I have a time that I can't I don't feel as bad for it.  Right after dx I was eating super good, only eating organic and stop drinking, etc.....that soon faded Smile    Good luck.
  • judylynn
    judylynn Member Posts: 28
    edited June 2011

    Sheree,

     I have triple negative, metaplastic breast cancer.  I had a mastectomy, chemo, and radiation.  I had surgery in September of '10 and my last radiation treatment was in March.  This is a scary disease but I'm managing pretty well right now. I really haven't changed my diet, but I think I need to after reading all the posts from others.  I will start an exercise program this month as well. 

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