Just diagnosed-feeling a little overwhelmed

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  • TikkasMom
    TikkasMom Member Posts: 83
    edited November 2015

    Orlmagic,

    Welcome and good luck. Know that you're not alone.

    You have lots of tough decisions ahead but if you're comfortable with a decision you've made; then it's the right decision for you.

    After careful consideration and talking with friends about their Mom's decision to take the holistic approach, and failed, I have scheduled my mastectomy for November 19. My family cancer history is very extensive. I am at peace with my decision.

    Thank you all for your input, very much appreciated. Good luck to all here.

  • Mayor007
    Mayor007 Member Posts: 2
    edited November 2015

    I am a breast cancer survivor (6 years ago). Don't remember type other than it was agressive and in stage 3 when discovered.

    Suggest you check credential of physicians before proceeding. If you need help with this, Let me know. I have three MD's in my family.

    Think positive and proceed.

  • BTJ
    BTJ Member Posts: 17
    edited November 2015

    I'm so sorry to hear about your diagnosis, but you are going to get through this! This is a time to take care of yourself, allow others to show their love. I had Invasive DCIS, stage 2, estrogen +. I am coming up on my 5 year cancer free on Dec 30th. I had a lumpectomy with planned targeted radiation. Pathology found a tumor outside the ducts so I had a mastectomy on my right side and a lift on my left. I was offered, and accepted nipple sparing mastectomy with immediate reconstruction. It was a 6 month process. I took anti estrogen therapy for as long as I could tolerate and then, with my oncologist's hesitant agreement, stopped it.

    It really helped me to use this chat room. The support and care of women who have or are going through the same thing is very powerful. I also found that guided meditation helped immensely in slowing down the constant chatter in my brain, and the fear of the unknown. Meditation and music in nature saved me. I would walk for as long as I could in the woods letting the music fill me, lift me, allow my mind to become unfocused....always bringing it back to my breath or the music.

    As a woman and a mother, I already know you are a warrior woman. You will rise to this challenge. You will have days when you crumble and your loved ones hold you up, then you will find your strength again.

    Your surgical team will likely include a survivalist that will have free access to the guided meditation I mentioned, but there are lots of free ones online. I am holding space for you in my heart, surrounding you with healing light, asking your guardians to protect and heal you. Blessings of love and light...


  • orlmagic
    orlmagic Member Posts: 7
    edited November 2015

    Thank you so much. I wanted to ask everyone about the "perforator free flap" reconstructive breast surgery, since I have chosen to have a mastectomy. My surgeon referred me to UF Health Cancer Center here in Orlando, FL to a reconstructive plastic surgeon that specializes in it and I am hoping someone can share their experience with me. This site truly helped me prepare for my diagnosis...of IDC. Thank you all.

  • Granann2
    Granann2 Member Posts: 3
    edited November 2015

    I am so sorry about your diagnosis, but you & your family will get through this. Waiting for test results was very hard for me. There are other tests for HER2 so hang in there, & you will know more after your surgery. My lumpectomy & Sentinel node surgery went very well. I felt better when I had a plan. Just 1 step at a time. Prayers for you and your family

  • Moderators
    Moderators Member Posts: 25,912
    edited November 2015

    Mayor007, welcome to BCO and thank you for sharing with everyone!

    Granann2, we are with you on one step at a time! Hang in there, Everyone!


  • mesharon1959
    mesharon1959 Member Posts: 16
    edited November 2015

    So I had an MRI on Tuesday to see if the rest of my breasts are clear of suspicious lumps, etc. Today I got the report that I need additional imaging due to a nodule in the lower outer area of my right breast...I will be going in for an ultrasound on it tomorrow morning. If the nodule is any kind of cancer, my surgeon says I might lose my right breast to mastectomy. The area where my DCIS is located is directly across on the upper inner part of the same breast... The surgeon told me it's medically irresponsible to have two lumpectomies on opposite sides of the same breast performed at the same time. She has to go back in to take a larger margin where she did my first lumpectomy, and then she'd have to open me up on the opposite side for the other one, so it'll be like doing both at once. Now I've had to push out my surgery scheduling and my radiology oncology consult for yet another week.....sigh....

    At what point do I tell my adult kids? Any pointers?

  • Emily4me
    Emily4me Member Posts: 5
    edited November 2015

    I just went in to have a diagnostic mammogram because I have swelling and tenderness under my right arm pit. I was shocked to hear I have two masses in my breast on the right side.One is near the nipple and the other is in the chest wall.I have 4 lymph nodes that are involved,two under my right clavicle.They started with me at 9:30 in the morning and finished with an ultrasound around 3:00pm. They were very thorough.Afterwards the DR SAT ME DOWN AND TOLD ME SHE WAS VERY CONERNED WITH THE FINDING AND SHE TOLD ME THIS LOOKS VERY MUCH LIKE CANCER.I was so stunned I couldn't even think of one question to ask.I have biopsies scheduled in one week.It took another 24 hours to wrap it around my brain.I even called the office to make sure I heard her right.I asked them how could she use the cancer word without a biopsy?I was told sometimes the dr can tell by looking.My question is this,does this mean I have cancer?Can they sometimes tell by looking and is it being caught late because it is involving my lymph nodes?Waiting a week  seems brutal!I have a high risk of breast cancer due to my family history.I am 56 years old.Any opinions will be welcomed!

  • LisaAlissa
    LisaAlissa Member Posts: 1,092
    edited November 2015

    Hi Emily4me,

    I'm so sorry to hear you had such a "terrible, horrible, no-good, very bad day."

    And while the doc told you it "looked like cancer," and I hope she wouldn't have said that if she didn't think she was right, it won't be definitive until you have the biopsies. Consider starting your own thread here.

    Did you get a copy of the imaging reports? There will be separate ones for each test you had. From what you say, at least two of them (the Diagnostic Mammogram and the Ultrasound), but there may be more. You want a copy of each of them. You should be able to get copies. When you do, put them in order (from the first test to the last), then read them through. Don't get caught up on them the first read through. Some of them will say things like "more studies in order (ultrasound or biopsies)." Look for BIRAD scores.

    Note that you won't find a BIRADs score of "6" (cancer confirmed by biopsy) because you haven't had a biopsy. Cancer has not yet been confirmed!!! There is still a chance that it won't be. Even BIRAD scores of "5" can turn out (once there's a biopsy) not to have been cancer.

    Hang in there!

    LisaAlissa

  • Smurfette26
    Smurfette26 Member Posts: 730
    edited November 2015

    So very sorry you have found yourself here Emily4me. Only a few weeks ago I was in a very similar situation.

    I got a call back after a routine screening mammogram.

    Had a diagnostic mammo, followed by an ultrasound. I was told then and there that it didn't look good.

    My biopsy was at the same clinic on the same afternoon. The Dr's told me to expect it to come back as malignant.

    In fact the Dr said he was so certain; that if it come back negative, he would re-biopsy. Three days later he called me with confirmation.

    Really hoping for better news for you. This is really such a difficult time. It is the hardest time and there is so much waiting.

    Keep busy and surround yourself with those you love. There is a wealth of information on these forums (Avoid Google) and the strength and support you will find here is amazing.

    Keep us updated. Will be thinking of you. Hugs Donna.



  • Emily4me
    Emily4me Member Posts: 5
    edited November 2015

    Thank you guys for taking the time to address my concerns.I am a little more calm today and LisaAlissa your'r right,I haven't been diagnosed yet.So I am going to try to enjoy not knowing this week before I find out for sure because if my life changes forever after a positive diagnosis I will miss out on this time of ignorant bliss and if it turns out to be negative then I would have been freaking out for nothing.I tend to not want to know the bad things in life for self preservation..lol.

    Smurfette26 I'm sorry to hear of your diagnosis.Thank you for sharing your experience with me

  • mesharon1959
    mesharon1959 Member Posts: 16
    edited November 2015

    I got lucky - the ultrasound Friday revealed the cyst they spotted was B9! I seriously dodged a bullet there. So for now at least, I will be having surgery to widen the margin from my previous lumpectomy, a round of radiation and an estrogen blocker. I haven't met with a medical oncologist yet so I don't know what my options are going to be....However I'm keeping a positive attitude about it. I finally told 3 of my 4 grown kids - the oldest didn't answer or return my call yet. I'll try to reach him today.

    Emily4me - sorry you are going through such a rough time, however enjoy your 'ignorance is bliss' breather and wait for a real diagnosis. You can do this and we are all here for you!!!

  • shorfi
    shorfi Member Posts: 791
    edited November 2015

     Citrinetiff ....It was a no-brainer for me because I was diagnosed twice, once in 2004 and then 2013.

    In 2004 it was on my left side...have never had any heart issues since that time. I was worried though.

  • orlmagic
    orlmagic Member Posts: 7
    edited November 2015

    tikkasmom...that you for welcoming me..I still am in shock I guess. But, here I go with my folder full of lab results and a calendar with Dr. appts I nevet thought I would have...can I ask you what kind, if any reconstructive surgery you will have? Is it good to be Hr Er positive and Her2 negative? And how do you know what stage you are at? I have my first Oncology visit Thurs. 12th. What can I expect. Sorry, for the questions...I just have so many....thank you for any help you can give me.....

  • Smurfette26
    Smurfette26 Member Posts: 730
    edited November 2015

    I'm only a couple of months into my breast cancer journey but can help with at least one of your questions orlmagic.

    HER2 positive breast cancer is more aggressive so hoping you are negative.

    Hormone receptive cancers respond better to hormone therapy I believe. The more receptive the better the response.

    I don't know much about staging but I'm sure there is information on here. From what I understand staging takes in the tumour size and node involvement among other things.

    I know cancers are graded from 1 to 3. One being low grade, three being the most aggressive.

    Have a list of questions written to ask your Oncologist.

    Is your cancer ductal or lobular?

    Good luck with it all. Hugs Donna.

  • TikkasMom
    TikkasMom Member Posts: 83
    edited November 2015

    Hello orlmagic, from everything I've read, ER+, PR+ & HER - are good . I'm new at this but hopefully someone else can explain it all.

    I am not having reconstruction surgery, I'm 63 and I am very lucky to have the Husband I have, who loves me for me.

    Good luck to you and if you're decision feels right to you, then it's the right decision for you.

  • TikkasMom
    TikkasMom Member Posts: 83
    edited November 2015

    Has anyone heard from cjafarm, she was scheduled for surgery last week?

  • Smurfette26
    Smurfette26 Member Posts: 730
    edited November 2015

    Oh no reconstruction for me either. I'm 51. Just don't want to contemplate more surgeries at this stage.

    Never say never but I'm not entertaining the idea at the moment.

    It's a very personal choice.

  • TikkasMom
    TikkasMom Member Posts: 83
    edited November 2015

    Good luck Smurfette26 hope your chemotherapy goes smoothly for you

  • orlmagic
    orlmagic Member Posts: 7
    edited November 2015

    Smurfette26..hi, thanks for responding...I have Invasive Ductal Carcinoma, IDC, my tumor is 1cm, ER and PR positive and Her2 negative...I have chosen a full mastectomy with immediate reconstructive surgery. Just waiting on a date. Don't think my lymph nodes are involved, seeing oncologist this thursday...I know I should be brave, but at 47 I am still a wimp about certain things and I am scared it will spread...truly, how bad is the surgery? Than you for helping me with your story...

  • orlmagic
    orlmagic Member Posts: 7
    edited November 2015

    Thank you tikkasmom...I am so scared of it spreading before I get to surgery.. .I appreciate your kind words...still can't believe this is my lifs now...ow do you know what stage you have?

  • marijen
    marijen Member Posts: 3,731
    edited November 2015

    orlmagic, if you have IDC I think they are going to have to sample a few nodes to be sure the cancer cells haven't spread.

  • TikkasMom
    TikkasMom Member Posts: 83
    edited November 2015

    I'm scared too orlmagic but being brave for my family. Be glad when this is behind me. Good luck to all the brave sisters here...

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