TRIPLE POSITIVE GROUP

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Comments

  • ElaineTherese
    ElaineTherese Member Posts: 3,328
    edited January 2017

    Well, that's better than waiting and worrying for the six months! Hope she can bring you some reassurance. Ha ha -- at this point, haven't we all been felt up by all kinds of medical personnel?

  • momallthetime
    momallthetime Member Posts: 1,575
    edited January 2017

    Fluffqueen0 wish you the best. Of course this 6mos business is so nerve wrecking. Deep breaths!

  • mkmarty93
    mkmarty93 Member Posts: 1
    edited January 2017

    I was diagnosed Triple Positive (Stage 2A) in September 2016. I have completed 3 of 6 rounds of TCH and will have radiation after chemotherapy is complete.

  • ElaineTherese
    ElaineTherese Member Posts: 3,328
    edited January 2017

    Half-way through, mkmarty! Good for you! Just keep thinking, "Only three more to go. Only three more to go." Hope the rest of your chemo goes OK!

  • Anonymous
    Anonymous Member Posts: 1,376
    edited January 2017

    Yes, apparently they think the whole thing is due to the new machine they have. I remember asking about that xray machine when I was diagnosed. It was state of the art then. She said she wished she had one.

    At least if it does turn into something, we are watching it early.

  • ElaineTherese
    ElaineTherese Member Posts: 3,328
    edited January 2017

    fluffqueen, something similar happened to me when my local clinic switched from mammogram to 3-D mammogram. At my August 2016 follow-up, there was some concern expressed about my scar area. The radiologist had them perform an ultrasound right there, and said that it was probably an artifact of switching machinery. Yes, it's good that you're watching the suspicious area carefully.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited January 2017

    I met with my breast specialist yesterday. She did a thorough exam, didn't feel a thing, pulled everything up on the screen to show to me. She had talked to the radiologist in the meantime also. They still both feel it is related to the scarring, but she did say she wants another MRI in 6 months, and told me to check the area often to make sure there aren't any changes. So, that's the plan.

    I think I am going to restart Arimidex after my 3 month break. That made me a little nervous

  • ElaineTherese
    ElaineTherese Member Posts: 3,328
    edited January 2017

    Good news, fluffqueen!

    Hopefully, nothing will have changed in six months. It's nice to hear of a medical professional spending so much time with a patient.

  • momallthetime
    momallthetime Member Posts: 1,575
    edited January 2017

    Terrific news Fluffqueen. MRI sounds perfectly reasonable. Take good care.

  • Anonymous
    Anonymous Member Posts: 1,376
    edited January 2017

    Yesterday was the official day! Can't believe I forgot. Guess it's a good thing. Hate knowing I still have to be watchful, but better that than the other.

    image

  • SpecialK
    SpecialK Member Posts: 16,486
    edited January 2017

    fluff - yay! Welcome to 6-yearhood, it's a good place to be!

  • amylsp
    amylsp Member Posts: 188
    edited January 2017
  • Mommato3
    Mommato3 Member Posts: 633
    edited January 2017

    Congrats Fluff!!

  • ang7894
    ang7894 Member Posts: 540
    edited February 2017

    Great news Congrats Fluff

    Winking

  • kae_md99
    kae_md99 Member Posts: 621
    edited February 2017

    hi all!


    this is what i know so far, IDC,right, 2.5 cm by UTS, 3cm by MRI. DCIS, both breasts. ER,PR, Her2 all positive.MRI, no nodal, no chest wall, no nipple involvement.chest x-ray negative, CBC,BMP normal. i am 44 y/o. oh i have endometriosis and i will need tamoxifen later on so the uterus and ovaries might need to go away at some point?meeting with my OS and MO this friday. i know i wont get the whole picture until after surgery but with these info, what are my options? what have you done? i would like to be prepared and i am taking the advice of some sisters here and will be writing questions in a notepad when i meet my team. i am a mother of 8y/0 twins and i would like to give this cancer my best shot, i would like to see my kids grow up, go to college . thank you ladies for keeping my sanity since i got diagnosed. i need to get a 2 d echo right? i will request for a pet/ct and bone scan also, hopefully my insurance will pay.God bless us all.oh i live in the US.


    kae

  • debiann
    debiann Member Posts: 1,200
    edited February 2017

    So sorry you have to be here kae. My best advice is to not spend too much time googling HER2 + because you will get a lot of grim statistics that do not apply today. The targeted therapies available now, hercepton and perjeta, have been game changers for her2+ gals. Yes you will need to have a few 2d echos or mugs scans to keep an eye on your heart during treatment.

    Things you can start thinking about are mastectomy vs. lumpectomy. I'm guessing you are leaning toward mx because it is in both breasts. You may possibly be able to skip radiation too, if you have an mx. Also, you will need to do either tamoxifen or you can have the ovaries removed or suppressed with drugs and then take an aromatase inhibitor. If you do mx, there are lots of options for reconstruction like implants or tissue transfers like DIEP or you may want to go flat. If you need to spend time googling, these are the things to investigate. This forum is a great source of information on these topics.

    For now, try not to think about the future, your prognosis is good. Try to focus and the treatment decisions you need to make right now. Once you have a treatment plan in place that you are comfortable with things get easier.

    Prayers for you,

    Debi

  • kae_md99
    kae_md99 Member Posts: 621
    edited February 2017

    Thanks Debi,

    yes i am thinking about BMX since both breasts are involved. i wonder if neoadjuvant chemo will be suggested for me.....yes, i am really scared about being her2 positive.


    kae

  • coachvicky
    coachvicky Member Posts: 1,057
    edited February 2017

    kae

    If I had ever thought I would be this happy with beast implants, I would have had my breasts removed years ago! My prayer for you is not to be scared and know that a cancer journey can bring joy, peace, and health. Best wishes as you make your decisions.

    Coach Vicky

  • Tunegrrl
    Tunegrrl Member Posts: 196
    edited February 2017

    Kae, our stats are somewhat similar, but i was diagnosed last July. What i can tell you is the first few weeks after diagnosis are truly horrifying. But you caught this early, and there is every reason to believe you will have an excellent prognosis. Clear nodes, small tumours, no skin or nipple involvement. Excellent. Even being triple-positive is a pretty decent roll of the dice. Since Herceptin arrived on the scene, our stats are on par with HER- sisters.

    Chemo sucks, but not as badly as you might think. A few days of being unwell interspersed with mostly ordinary days. Radiation is a walk in the park (for me, so far).

    Mastectomy probably sucks but reconstruction options are good and since you have no nodal involvement, you might be a candidate for nipple-sparing mastectomies with immediate reconstruction, no radiation therapy. Waking up with new boobies, none of this tissue expander business that drags on.

    If you do decide to go with a lumpectomy, recovery is easy. I was on just ibuprofen after the first day. If your rack is big enough you might even have the option of a breast lift during your lumpectomy surgery. Honestly, mine turned out so well it almost (*almost*) makes breast cancer seem like a nice idea.

    Best of all, you found your way here. It is awesome to have access to this 24/7 support forum, with lots of thoughtful, kind, insightful women encouraging each other through this.

    After my diagnosis i felt like i was in free-fall, not knowing whether i would die from this. The two biggest things that helped me get a grip were

    1) the Predict breast cancer online calculator giving me solid stats on my prognosis, and

    2) getting a treatment plan in place. (Like the Paul Simon song where he says, "breakdowns come and breakdowns go, so: what are you going to do about it? That's what i'd like to know".)

    There has never been a better time to have breast cancer. You are probably going to do great. Sorry you have to experience all this. But you *can* be the hero of your story, not a victim of this. Choose for yourself what you want. Navigate as a protagonist. Good luck!!!!

  • kae_md99
    kae_md99 Member Posts: 621
    edited February 2017

    thanks Tunegrrl. i will ask my PS about the possibility of immediate reconstruction when i meet him next week.

  • debiann
    debiann Member Posts: 1,200
    edited February 2017

    Kae, I think it is likely that you will have neo-adjunctive chemo with heceptin and perjeta. I had adjunctive and just Herceptin, but things have changed since then. I had a DIEP recon (tummy tissue used to make new breast mounds). The outcome was great, but its an involved process with more than one surgery.

    When selecting a Plastic Surgeon know that they will usually only tell you about the types of recon that they themselves do. Before seeing a PS, you may want to learn about the types of recon possible, then find a PS who does the procedure you are interested in. My first PS gave me the option of implants or tram flap. I didn't like the tram flap idea, so I considered implants, thinking that was my only other choice. But from this forum I learned about DIEP flaps and I looked for a micro-surgeon who did that type of recon - and found it way my PS's partner. Even with implants, there are different options. You'll have plenty of time during chemo to figure out what you want to do regarding surgery.

    If you are choosing no recon, you will want to talk to your Breast surgeon about not leaving extra skin behind and you may want to seek the opinion of a plastic surgeon to "clean up" the area after you've healed or want to get some fat transferred to fill the divot.

    The roller coaster starts moving real fast after dx . Ask your questions here, there are so many knowledgeable people, They helped me tremendously.

  • kae_md99
    kae_md99 Member Posts: 621
    edited February 2017

    thanks debiann, yes i think i might be getting neoadjuvant chemo also.. i will keep you guys updated.

  • fightergirl711
    fightergirl711 Member Posts: 300
    edited February 2017

    I'm a nervous wreck - last Herceptin tomorrow, as well as my first mammogram since dx last year. I think I would be a little more emotionally stable if it weren't for my dad passing on Sunday, his birthday is today and the funeral is Saturday. Of course, it was from a cancer diagnosis. <deep breath>

  • SpecialK
    SpecialK Member Posts: 16,486
    edited February 2017

    Oh fighter - that is a lot. I lost my dad and only sib to stage IV cancer as well, but I was thankful it was prior to my diagnosis, during my own treatment it would have been so hard - hugs to you. Let your last Herceptin be the least of your worries, and just breathe through the mammo - you can do this. We are there with you holding your hand.

  • sportsmom16
    sportsmom16 Member Posts: 25
    edited February 2017

    Hi-- I am finishing up my last chemo and then have to have an MRI mid Feb. to see if the tumor shrunk and they saw something on the right side that they may need to biopsy but since I had already started chemo they decided to let that move forward and said if the mass in the right shrunk, they would know if it was cancer.

    Read the post and it looked like some folks knew it had not spread to the lymph-- I was told that it doesn't appear to have spread but there is no way to know until they are in surgery and they can biopsy them. One doc said lumpectomy- one said mastectomy but both are saying have to wait for final MRI? Then plastic surgeon said that if the lumpectomy is too large or they need to go back in - the ship has sailed for reconstruction. Feel like I am buying a used car-- have no idea what to believe-- also am so unbelievably depressed-- is this the chemo or just how life with this disease is going to be? Having a hard time finding hope--- I am grateful it is not worse and I tell my self that constantly but today is a rough day and I cant stop crying -

  • ElaineTherese
    ElaineTherese Member Posts: 3,328
    edited February 2017

    Hi sportsmom!

    I'm sorry to hear you had such a rough day yesterday. I'm also sorry to hear that you are unbelievably depressed. I hear ya; it's par for the course with this disease. That doesn't mean you should just accept it, though. Do you have a nurse navigator at your breast care center? She might be able to recommend a counselor who is experienced in working with BC patients. There's also the medication route; I myself am on Celexa because aromasin was making me moody. In any case, if this depression is ongoing, I would strongly urge you to find some help.

    I also had neoadjuvant chemo and had an MRI after chemo ended. It showed that chemo had wiped out all of the active cancer in my breast and node. So, I felt comfortable getting a lumpectomy. However, if I had tested positive for BRCA, I would have had a mastectomy.

    Happy to hear that you're finishing chemo! That's a big accomplishment right there! Take care of yourself and ((Hugs)).

  • coachvicky
    coachvicky Member Posts: 1,057
    edited February 2017

    Hi SportsMom16,

    I too am sorry this all has been so upsetting. Maybe you could ask for something to take to calm you down for a few days while you make some decisions.

    Crying can be a good thing. It is a cleansing process.

    If it is any help, I too listened about "saving the breasts" versus the double mastectomies. I decided on the double mastectomies with immediate tissue expanders inserted. Once I made the decision as to what I wanted, I felt in charge. I did not ever want to revisit this issue again. I have no regrets. Like you I cried for what seemed forever but today I dance on my eyelashes (well, the few I have LOL) when I look at my new breasts!

    Best wishes.

    Coach Vicky

  • sportsmom16
    sportsmom16 Member Posts: 25
    edited February 2017

    Thanks for responding-- sometimes feel like such a rookie-- what is BRCA? sorry to be a dummy

  • kae_md99
    kae_md99 Member Posts: 621
    edited February 2017

    hi all,

    so i went to my oncologic surgeon today. i really like him,he is old with 50 years of experience and i am happy i have him. according to him i will have neoadjuvant chemo with herceptin and perjeta. he said that in his practice ( he is the head of 2big hospitals where i live) everybody who got the neoadjuvant chemo all responded except for one so far. i pray that i will have the same response. i asked about SNb and he said that we could do it prior to chemo but it will not actuallyy change anything.he ordered brca testing and ultrasound of my nodes.he said that he could do lumpectomy on me if i respond to chemo but he also said that since i am young and i have 3 cancers in both breasts i might want to do Bmx, with immediate recon. he said immediate recon has the best cosmetic effects. i will see my Ps and onco next week. he said he said he will already talk to my MO regarding his findings. he did a very thorough exam on me ,felt my breasts,chest wall,lymph nodes,armpits amd even my organs. he said he does not think pet/ bone scan but he will leave it tomy MO.. i forgot to ask him about radiation and how long is my neoadjuvant chemo will be. to those who have had it,how lomg did it tke you to complete it?thanks y'all




  • kae_md99
    kae_md99 Member Posts: 621
    edited February 2017

    oh i know i could ask my MO about how long the chemo will be bu my husband is asking me because he is looking how much pto he has just in case he needs to take some time off from work. we have 8y/0 twins with disabilities. thank you

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