45 year old mom & just diagnosed

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Jennifer522
Jennifer522 Member Posts: 254
edited September 2017 in Just Diagnosed

I am 45 with a 5 year girl (who is my whole world) and I just got the call the biopsy tested positive for breast cancer.

I found the lump myself on Labor Day weekend. I could see it in the mirror when I undressed to take a shower. It's always been a lumpy part of my breast but it was different. I had a clean 3D mammogram on this side at the end of January. I do have some stable microcalcifications in the other breast. No family history and don't meet any other risk factors except having a child after 30, that I breastfed for 17 months.

MRI and oncology appointment next week

Comments

  • Jojo0529
    Jojo0529 Member Posts: 193
    edited September 2017

    Sorry you find yourself here, but you will find a ton of support. Did the biopsy state the type? DCIS? IDC?

  • Jennifer522
    Jennifer522 Member Posts: 254
    edited September 2017

    IDC they won't stage until after other tests. But it measured 6cm on the ultrasound. I couldn't believe it measured that big. If I feel it, it's feels half that size. I did know when I saw the ultrasound it didn't look good, irregular borders but you still kinda hope it's not what you think

  • Falconer
    Falconer Member Posts: 1,192
    edited September 2017
    Jennifer,
    I'm so sorry you find yourself here. The community is wonderful, and you'll get a lot of support. I, too, was dx'd at 45, when my youngest was 3. It's been a hard road, and it breaks my heart that he knows his mom was sick. I hope you have support from family and friends as you go through the stages of treatment and recovery.
  • Jojo0529
    Jojo0529 Member Posts: 193
    edited September 2017

    try not to fret about the size. In my opinion is not as important as tumor biology. There are many big lazy tumors.

  • Meshell5324
    Meshell5324 Member Posts: 54
    edited September 2017

    I'm pretty new to this having been diagnosed on the 7th. But I too have a fairy large tumor at 4.6 cm. My primary physician and the 1st surgeon I saw were kind of freaking me out about the size issue. But my oncologist said "I don't care about the size, you can have a little angry tumor that's going places or a big lazy tumor that's not going anywhere " there are many tests that they can do on the pathology. I'm still waiting for my mamaprint results. So far, he doesn't think I'll need chemo. Surgery, possible radiation and them hormone therapy. Everyone is different, have you seen a Breast surgeon or oncologist yet?

  • Mojojennijo
    Mojojennijo Member Posts: 173
    edited September 2017

    as jojo said, try not to worry about size! I just finished clinical staging and we were all very happily surprised that the cancer is only in my Breast! I haven't had node biopsy yet as I have chemo before surgery (her2+) but size doesn't always mean spread. I have a primary 7.3 cm tumor and a satellite that is about 1cm. Same Breast.

    There are some things that tumor size effects as far as treatment plan but doesn't always effect your prognosis. And that To me is most important. Try to Keep your cart behind your horse and hang in there for the waiting! MRI is a good tool to use in getting more info as is the complete biopsy info.

    We are all here for you 😊❤️ I am 41 and also have a 5 year old (our surprise son) and two teenage daughters.

    This site is such a wealth of information. You will find it a great benefit!

  • PauletteK
    PauletteK Member Posts: 2,205
    edited September 2017

    Don't stress out about the size, do what your MO suggests and one step at a time. It is hard to wait for all the tests and this journey is not easy but doable. You found a great support group and we will reach to the end of the rainbow.

  • Jennifer522
    Jennifer522 Member Posts: 254
    edited September 2017

    Sometimes I wonder how I am going to get through this. But what choice do I have? Put one foot forward and take it a step at a time

  • EastcoastTS
    EastcoastTS Member Posts: 864
    edited September 2017

    Jennifer:

    That is about how it will go for a bit. One foot in front of the other...

    You will get through this. Research each step on this site. That's what I did -- and it helped tremendously. I was prepared and well informed, at the very least. Ask anything you need to and come here to vent. Unfortunately, we get it.

    Hugs to you.

  • Jennifer522
    Jennifer522 Member Posts: 254
    edited September 2017

    I had my MRI today. I was pretty nervous. Not for the procedure but the road ahead of me. I went to the local hospital, checked in and paid. Oh yeah a $2500 bill because we haven't met our deductable for the year yet.

    I was there with 4 other newly dx women (as I saw on the sheet of the check in desk), all with somber looks on our faces. I can see us looking at each, probably wondering if we were all here for the same reasons. Or thinking, she is older than me, she is younger than me, she is smaller than me, she is larger than me. We all wonder why us....

  • msphil
    msphil Member Posts: 1,536
    edited September 2017

    hello sweetie I was diagnosed at 42 while planning our 2nd marriage I found lump in the shower I had my cry then decided to fight with Hope and Positive thinking thru my Faith I am now a 23 yr Survivor Praise God..msphil idc stage2 0\3 nodes chemo before and after surgery Lmast got married then 7wks rads. 5yrs on Tamoxifen have Hope.

  • FarAwayToo
    FarAwayToo Member Posts: 255
    edited September 2017

    Hi Jennifer, looks like you are doing all the right steps (MRI and oncologist appt). I was almost rushed into a lumpectomy, but decided to go to a multidisciplinary clinic at NCI-designated comprehensive cancer center, and so far I'm happy I did. I was told with my age, tumor size and Ki67 number (high), I will be a candidate for chemo anyway, and neoadjuvant was suggested. It makes a lot of sense to me, so I'm starting it on Friday (I hope).

    I also think about the fact how I never had any risk factors and now end up with BC at 40. I even had my children early and breastfed both (12 month and 24 month - so 3 years total). No family history either. Of all cancers, I was sure I would get melanoma, because I do have some strong family history there. Never worried about BC.

    Please trust us, when we are saying this is the hardest part - you were dealt a horrible blow, but you don't have all the info yet. Gradually, more information will come out and you and your medical team will put together a plan. Then you will concentrate on that, and it will become easier. I'm not very far down this road myself, but my mental state is so much better than it was when I was just diagnosed.

  • Jennifer522
    Jennifer522 Member Posts: 254
    edited September 2017

    The radiologist report from the mammo and US was finally posted online my chart and it seems the 6 cm I saw on the screen meant how far it was from my nipple and not the size of the tumor. So I am guessing that is good news.

    The palpable abnormality in the left breast corresponds to a 2.6 x 2.3 x 1.9 cm heterogeneous solid lesion at the 11 position 6 cm FN. Axilla is unremarkable. Biopsy is recommended.

    MRI was yesterday and Oncology doctor's tomorrow morning. So nervous about what my future holds.

    And thank you everyone for the positive words of encouragement. It does really help!

  • PerkyPeach
    PerkyPeach Member Posts: 2
    edited September 2017

    Hi Jennifer,

    I am originally from S.C. as well (the Upstate). Anyway, I was recently diagnosed as well. The news came to me on July 17th after a routine mammogram. I totally understand the nerves. I know this is easier said than done, but try not to worry until you have to. This may be a roller coaster of "wait and sees" for a little while. As someone who is nearing the end of the surgical recovery period, I can tell you that I made things a lot worse in my mind than they turned out to be! Sending hugs and positive thoughts to help you through those darker days.

    Also, I agree with the other advice you have been receiving here. You will have much more knowledge about the characteristics and behavior of your tumor when you get results back from your biopsy. Then you can plan what is right for you. However, speaking as someone who had a double nipple sparing mastectomy on Aug. 24th and is already heading back to work next week, it can turn out a lot better than our mind lets us think!

    Good luck! Thinking about you!!

  • lckaff
    lckaff Member Posts: 6
    edited September 2017

    Dear Jennifer:


    Sending positive thoughts your way! Those first few days are numbing, especially waiting for results, you just drive yourself nuts (hard not to). But take it a bit at a time, and hour at a time, and you´ll get through it. For me it helped when I finally had it clarified what I had, and a plan of attack. I had a mission. I realized there are so many people set to help me, so if I lose it a little, they can pick up the slack. Hug that 5 year old, its a hug from me!


    Good thoughts from Berlin

  • Jennifer522
    Jennifer522 Member Posts: 254
    edited September 2017

    Met with oncology today, what a lot to process.

    In the left breast I have the 2.6 cm tumor I found and MRI picked up another 2 cm behind it. My right I have stable mircocalcifications I have known about since my last mammogram in January. I was being watched and they are considered benign.

    The bad news is, I am triple negative. I have not done much reading on it, so I don't know exactly what that all means. The good news it, they don't think my lymph nodes are affected but won't know until surgery. Oh and I might have a heital hernia according to the MRI.

    Port going in tomorrow and chemo starting soon. Then I have chosen to get a bi-lateral mastectomy. What a hard decision to make. Even if my right has benign condition, I don't want to worry about it. Surgery is scary. Never had a surgery before. But truth is, this is all scary...

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