Scared

ScaredSoBad
ScaredSoBad Member Posts: 4
edited July 2015 in Just Diagnosed

Hi everyone!! Well it all started 8 months ago I had some fluids coming from breast and horrible pain scheduled a mammogram. They told me there was nothing. Eight months later here I am trying to make sense of all of because now I'm told I have stage 2. I worry so much for my kids who don't know yet, my husband who never shows emotion

Comments

  • Molly50
    Molly50 Member Posts: 3,773
    edited July 2015

    scaredsobad,


    Sorry you find yourself here. Do you have a copy of your pathology report? Are you scheduled to see a surgeon? I understand you are scared, it is scary to hear you have cancer. I have my lumpectomy next week. It seems like forever since I was diagnosed in early June.

    Do you have a good friend or relative who can be supportive and go with you to appointments? My sister has been really helpful and supportive to me.

    Hugs,

  • queenmomcat
    queenmomcat Member Posts: 3,039
    edited July 2015

    Nothing specific to add at the moment, but coming over from your husband's thread to wave hello, and send sympathies for starting down this fraught path. Many lovely ladies, with experience and compassion, here on the boards who'll help with questions, fears, suggesting where you might go from here. Just ask..

  • ScaredSoBad
    ScaredSoBad Member Posts: 4
    edited July 2015

    Molly50,

    Sorry to hear about you. I actually never got any papers or anything. I sure am learning a lot of what they should have done though. I'm hoping this new doctor will do everything that is needed. I appreciate you talking with me also.

    Hugs back



  • ElaineTherese
    ElaineTherese Member Posts: 3,328
    edited July 2015

    Hi Scared!

    Hope things work out with your new doctor. I didn't tell my kids about my cancer until I had a plan in place. Then, I could tell them that Mommy was sick and would need to go to lots of doctors' appointments and have surgery to get better. My 16 year old DD probably was the most worried because she's known teachers who died of cancer. By the way, there are actually children's books for the little ones that explain breast cancer to them.

    Prayers your way and best of luck!


  • Leighrh
    Leighrh Member Posts: 317
    edited July 2015

    Just poping in to say, I know these first cpl of weeks are rough but once you see a good doc and get a plan in place you will feel a little better! As far as kids go, I have young boys, 8 and 10. I have never said the "C" word. They don't need to hear that because they know my dad passed away from it. They know I had to have surgery to remove a bad spot, they know that I have to take medicine for a little while to make sure the bad spot doesn't come back. They are totally clueless and I prefer it that way. They are happily going about their daily lives. Just my experience :)

  • ScaredSoBad
    ScaredSoBad Member Posts: 4
    edited July 2015

    Leighrh,

    Thank you, I think that's a good plan to wait until we know. II'm sure it's harder on older kids because they know everything lol I never thought about books that's a great idea!! Thank you. I'll be thinking about you also.

  • rainnyc
    rainnyc Member Posts: 1,289
    edited July 2015

    I saw your husband's post yesterday and just wanted to say good luck with everything. Don't be afraid to ask a lot of questions. And don't be afraid to ask for help.

    As for children, I have a 15-year-old. I didn't see any reason not to tell him what was going on from the start--but leaving out some of the nitty-gritty details. He knows it's breast cancer, that I'm having chemo, that the oncologist says--and I can see for myself--that it's working. If I had younger children, I might choose to withhold more of the details.

    But....good luck, and I hope if goes well for you from here on in!

  • ScaredSoBad
    ScaredSoBad Member Posts: 4
    edited July 2015

    queenmomcat,

    Thank you! I am worried about him he's a very tough guy but I don't know how to get his feelings. And the more I learn on the more upset I get that the doctor was just lazy pretty much

    Best wishes

  • queenmomcat
    queenmomcat Member Posts: 3,039
    edited July 2015

    All this is hard on husbands--you're the one with the cancer but he's the one who has to watch you undergo treatment. (Mine is a bit better at expressing his feelings, but it's still hard on him.) There are a lot of practical things he can do, but "stop the treatment, take away the cancer" isn't one of them. Alas! All we can do is make sure we've got an accurate diagnosis and an appropriate treatment plan, and it sounds like you've at least made a start on that.

    I didn't have to face the "how do I tell my kids?" issue, but had just enough of a brush with "how do I find a doctor I can work with if I live in a sparsely populated area?".that your problems with that resonated with me. At least there's a solid though basic cancer program in my community now--there wasn't when I first moved here--so I'll be getting radiation five minutes from where I live.

  • Maureen813
    Maureen813 Member Posts: 2,893
    edited July 2015

    hi scaredsobad and welcome to this site. Many women will provide valuable information and questions you need to ask your doctors. I'm angry for the treatment the medical community did not provide you. I'm so glad you've found a doctor you can work with for the long haul. I communicated with your husband yesterday and he seems like he wants to fix it immediately. I understand that however this disease doesn't work that way. I'm sorry you find yourself in this position but so happy you reached out for help.

  • msphil
    msphil Member Posts: 1,536
    edited July 2015

    yes sweetie, husbands do go thru this with us, we were making wedding plans when i found my lump in shower, he was right there for me, thought me having breast removed would make a difference to him but it didn,t, i am a 21 yr Survivor, and been married 21 yrs also, after chemo was done and before rads we were married, you and us ALL our daily in my prayers. msphil(idc, stage2, 0/3 nodes, L mast chemo and rads and 5 yrs on tamoxifen)

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