hi, i am new-need support
hello everyone,
i need a little support. please help. i had my lumpectomy..clear margins. however, one out of the three nodes taken was positive. therefore, i am now stage II. are they are any stage 2 + survivors out there who can help me through this?
at first i was very happy after my surgery last friday, b/c the doc was sure that the margins would be clear b/c of the position of the mass. i was more angry yesterday after getting my new results. i threw a few things around.
i am just so sick of the cycle...diagnosis, test, results, tests, more tests, results, wait, wait, surgery, tests, results,.....
now, i am looking a more surgery to check more nodes and most likely chemo. do you understand my pain, my fears? please help me!
i welcome any help, kind words..not just from stage II +. i would just like to know that i will be okay.
Comments
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So sorry you are going through this. I guarantee you that we all understand your feelings. I had a lumpectomy with clear nodes and rads last July. I thought I was done with this, but no...I am already dealing with a recurrence, so I get it. Your fears are totally normal but know that we all get through this with the help of each other, our family and friends, and our medical team. The waiting and not knowing is the worst of all. Once a treatment plan is in place, it's one foot in front of the other, one day at a time.
Hang in there, it will get better.
Hugs,
Michelle
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Determined, your story sounds a lot like mine. I started out with a lumpectomy that I was told right after surgery "got it all" and "no node involvement," only to be totally blindsided @ my follow up app't. 4 days later with news that my surgeon had not gotten it all, that I had a positive node with extracapsular extension, and that I needed a mastectomy. I honestly think I went into shock because I spent the next few days in kind of a twilight zone -- often wondering if I'd been in an accident en route to the surgeon's office and was unconscious, because surely I was going to awaken from what seemed like a nightmare. So I absolutely get what you're going through!
All I can tell you is, it does get better. You're in a bad spot right now -- a rollercoaster of emotions and events that seems out of control. But you WILL get through it and you will be okay.
One thing I did that may or may not apply to your situation is that I went to get a 2nd opinion because I wasn't sure I trusted my original team after the way things evolved. And I was so glad I did. I ended up changing medical teams, which turned out to be a real blessing, because where I went (UCLA) offered leading edge (DIEP) reconstruction, which was not done locally and never mentioned to me by my first surgeon. And there were some other differences, some of which are detailed on my bio page.
I'm so sorry you're going through this, but I'm glad you've found BCO. I'll be thinking of you. (((Hugs))) Deanna
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thank you both so very much for replying. support makes a world of difference. thank you. i will work really hard to stay encouraged...it is hard stuff. hard stuff!
also, if there is any additional info that you think that i should know or ask, please let me know. i see the bs and the onc tomorrow to discuss details. wish me luck for that too. ps, can i just tell you that i HATE seeing the hospital's number on my caller id? while i know that they are working for me, i am thinking"wtf now?" really. what now? calls are for bad news, decent news, confirming apts...you know the deal...grrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrr.
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Welcome to the roller coaster from hell....You will eventually get off of it. Hang in there all of us have thought it was over but its really NEVER over just different. You have changed to a stronger woman who WILL fight this. DLB is right get a second opinion and do things that will de-stress you. Yoga , massage, sauna anything . Dont feed the Cancer!!! You are not alone, you will get through this!!!
Yes your life is about your health and fighting the cancer you have. I had to go on disability just to get all my appointments and scans done as well as my treatments. Yes its unfair and not right what your going through but it is what it is and you just cant give up. Channel that anger and fight like a girl and 5 years from now you will be somewhere wonderful alive and healthy and stronger.
Hang in there girl!!! xoxoxox
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One of my two nodes had a small amount of cancer but the team of doctors decided not to take any more nodes out. When having radiation, they also gave it under the arm to kill off any stray cells. I didn't have chemo either because my OncoDx test was very good. I was 65 during treatment so that may change things slightly. My first doctor said chemo so got a second opinion and she didn't feel that I needed chemo. Hope that helps you some.
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thanks to everyone who responded to help with preserving my sanity...literally.
thank you!
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Hi Determined,
I originally had a lumpectomy with 17 nodes removed on the left side. Two came back positive. I had DCIS on the rt side and 3 nodes removed. All was negative. And now for the fun.. I decided I didnt want to have a reoccurance or more tests, mammos or biopsy's so I had my breasts removed. I had chemotherapy in between both surgeries. Having a double mastectomy was the best decision I have ever made and I am only 34 years old. It is not worth all the trouble just to save your breasts. I am now cancer free and living the good life.
You will be fine and you will make it.
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determined - I had a similar thing happen to me. I started out Stage 1 and then had a lumpectomy. My BS said he was pretty confident no node involvement. Lo and behold the Path report comes back and there is a micromet in the SN. I understand it is not a perfect science and we all know drs are not perfect but like you I was blindsided. Welcome to tests, diagnosis, more tests, surgeries, treatments, etc...Like many of you I was pretty healthy so all these drs visits have been really tough especially when you dont know what they may find. Then the Path report came back saying I needed to have another surgery to even the margins....Good grief...Now I am scheduled for radiation starting April 28. It is hard but you will be fine. It is a process that seems to take forever but there is a light at the end of the tunnel. This forum is great...it has been my salvation....good luck...diane
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thanks again everyone for your help. i so appreciate it, as you must know.
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Hi determined3 !!
Right from the get go the BS & the Onco doctors said mastectomy (skin sparing) & chemo. Why??? it's so small & found it early. Answer.......b/c the biopsy showed BC to be very aggressive. Add to the fact I am small busted (B cup), a lumpectomy was never an option for me and have hearing some of the stories here about lumpectomy I am glad my docs were wiser than my fear.
I had 6 tx of TCH every third week with H on the off weeks. Lost my boob, lost my hair, and thought I would lose my mine. Of course I didn't lose my mind but I did drive the Onco nuts with questions. Now I am on triple dose of H every three weeks to finish my 52 week tx which really lightened the load. Once off the TC I finally found the energy I use to have..........that was a wonderful feeling !!! Painted all the trim on the outside of the house, planted all the flower beds and even carried 40# bags of mulch which I could not have done in a few mons. ago. I am telling you all of this to let you know that YES it is a rollercoaster ride and chemo is NOT a cake walk but at my age, if I can do it anyone can !!! I only have 5 more infusions of H. I am already on the aromatase inhibitors......starting with Arimadex but last week was switched to Femara (suppose to have less SE). I also saw a different doc in the group which is a lady and more forthcoming with info. I learned that the aromatase inhibitors were actually the most important factor of my recovery. She shared & clarified so many pieces that had been missing including my Oncotype scores. May just stay with her.
Hang in there, you will make it !! What kind of support do you have at home ?? Usually you can find BC support groups through the hospitals. Many of us feel like we want to stop the train & get off but we can't...........we have to fight if not for ourselves then for the ones we love. Hang on to hope, make sure you ask questions & someone who will take the time to answer them clearly. A good BS is a vital part in the very beginning (my OB-GYN recommended mine.)
Keeping in mind that I was not always a willing or eager patient, I still wanted more time with my one & only grandchild. TRY (although not always possible) to keep the stress level under control (this is my weak spot), rest when you feel tired regardless of what the time of day it is, eat well, and know that we all are here to try to answer any questions you may have.
In our thoughts & prayer,
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I am also stage 2a because of the size of my tumor. My advise to you is to get a second opinion or a third! I did and I am so happy a friend pushed me to do it. My first Doctor wanted to do everything, saying because I was so young (37) I needed to. Mastectomy, radiation, chemo, partial hystorectomy because i am premenapausal and ER+/HER2+. I was very overwhelmed by all of it. I found another Doctor who is more into modern reasearch and holistic med combined with the old standby standards. I did a large lumpectomy, HDR brachytherapy radiation, Tamox for 5yrs and Herceptin therapy alone without chemo. Make sure your docs are DNA testing your tumor, not all docs do and it is important in finding out if your specific BC will respond to chemo and which type.
And remember it gets better, not every day, but some days. Herceptin is no walk in the park, but I do believe I am doing better than if I had done chemo. And only 15 treatments to go!!!
Hang in there.
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I am new to this! After a mammogram on march 2 came back suspicious, ultra sound and needle biopsy later, I was diagnosed April 4 with stage zero non evasive DCIS in sutra . It was only in the duct. I did not even have a lump. After many long nights and talks with several doctors and people whom have been through this, i decided to have both breasts removed and get implants. So many cases the cancer comes back, more aggressive. I had a high-grade. I had my surgery April 21st, and have no regrets. After the pathology report came back, the lymph nodes are all clear, the cancer hadn't entered the breast yet, so no chemo or radiation is necessary. All of this from my yearly mammogram. Had I not gotten it, this would have grown into a tumor and much more evasive. Its a very personal decision, I am only 45 years old, and couldn't live with wondering if the cancer had returned or not. My BS confirmed after the surgery and path reports were back, I made the right decision, there was more cancer in the duct they had originally thought. Good luck with your decision, it was the hardest one I have ever had to make. I am married with 2 teenagers and couldn't bear the thought of not being in their lives.
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