Diagnosed 4 days ago
Hello, I'm new to this site. It was highly recommended to me by two friends who survived BC. I still have a lot to learn regarding the terms. My path report says two things for the diagnosis:
Invasive ductal carcinoma, grade II, at least 0.25 cm (2.5 mm).
Ductal carcinoma in-situ (DCIS), intermediate nuclear grade, solid and cribiform types with comedonecrosis and micro calcification.
I had an MRI (with and without contrast) two days ago that showed no lymph node involvement. My lumpectomy is scheduled for Sept. 4.
I was told that I might not need chemo, which would be great! It depends on the outcome of the surgery, I'm told.
I'm hoping to meet others more experienced in this, and also to meet some that are going through this at the same time as I am.
Comments
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Hello Musiclady, Welcome! So sorry you have to be here, but very glad your friends directed you here. It is a great place to find support and to get advice if you want it.
It is a scary time and everyone here understands how you're feeling. ((((Hugs)))) to you!
There are many here, who have had the same Dx as you,They will be around soon. You may want to take a look at the September surgery thread, or even the information on the site about IDC.
I wish you all the very best and look forward to seeing you around the boards!
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Hi MusicLady,
I was also diagnosed with DCIS and IDC in May. I had my lumpectomy with oncoplastic reconstruction about three and half weeks ago. I was hoping for antihormone therapy and radiation, but my but my node was positive. So chemo is in my future.
Ariom gave you great information! The people on this forum are wonderful.
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music - for me, the news just kept getting worse. so basically you really don't know what you're dealing with until after the surgery, the full pathology report. the MRI will probably tell you more about the size of the tumor. i don't mean to be negative, both ultra sound and MRI didn't detect any of my node involvement until the SN biopsy.
i wish you the best....the surgery wasn't bad for me..it's the wait for the full path report that really stressed me out when i look back..
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To Ariom, PoppyK, and juneping: Thanks so much for dropping in to say hello! I really appreciate your messages because I'm brand new here.
I know that my cancer cannot be "staged" till after surgery.
PoppyK, did you have oncoplastic reconstruction because you lost too much breast tissue to look close to normal after surgery? Was that done right at the time of the cancer surgery?
Juneping, did you have your SN biopsy at the time of your surgery, or beforehand?
Thanks so much!
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The area the surgeon was planning on removing was about the size of a walnut. She said that because I have plenty of breast tissue, I would still have a good cosmetic result without reconstruction.
However, I am 5'3" and have back problems from carrying around 38G breasts. And there was an additional area of calcifications (which the doctors believed were B9) in a different quadrant of the same breast. I chose to have both areas of concern removed. Long story, the BS removed the sentinel node, BC and area of calcifications on the right side. The PS reduced and lifted the left side, then did the same on the right side. It was all done as one long operation. I woke up with the cancer removed and smaller, higher breasts.
Hope this helps!
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Thanks, PoppyK!
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You're welcome Music!
Although I had a Mx, not the Lx, the tracer was done for my SNB, in the morning, just before my surgery. The rest of the procedure, the blue dye and removal of the node, was done during my surgery.
I should say, there are differing views and experiences of the SNB tracer, but for me, and many others, it was absolutely painless!
I wish you all the very best with everything! (((Hugs)))
PoppyK That was a really interesting surgery, you had! Sounds just fantastic, as breast surgeries go, you know what I mean! lol To have had the problem removed and then to relieve that weight problem in the breasts and come out at the other end, with a great result, is so good! I am so pleased for you!
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Welcome MusicLady to the community. As you can see, the members here are kind, informed and can relate to what you are going through.
If you have any questions for us about the boards pop us a PM and we'll try to help.
Wishing you well.
The mods
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Hello MusicLady:
I had my bmx in January of this year. We are very similar. I had 2.5cm of DCIS and 2.6 mm of IDC - very close to your size. I am also ER+ and PR-. Are your HER negative as well? Some residual DCIS was found during surgery and a 1mm microinvasion, Fortunately no lymph node involvement. No chemo was recommended as the IDC was under 5mm - this is NCCN guidelines. I just finished my final phase of reconstruction 2 weeks ago. I am so pleased with my results. I do take tamoxifen. I refused to gain weight from it so I have changed my habits - eat only healthy foods, pretty much gave up my wine ( except on Sat. night
) and wake up at 5am and go the gym every morning. I have lost 30 pounds and feel fabulous.
this is a very scary time with all the unknowns until after surgery. However, there is beautiful light at the end of the tunnel so to say. I realize now what is important, I am kinder, more compassionate and I don't surround myself with negativity. I am definitely a different person after all of this and I truly like the person I now am. I wish you the very best and pray that all goes well for you during your surgery
Kathy
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