Just diagnosed 3 hours ago with IDC
I have a "My Journey" notebook and everything to go along with the diagnosis. My husband said that he thought the radiologist and nurse navigator expected us to be a bit more emotional. I think coming on here (we both have) helped tremendously. The nurse navigator is setting up an appointment with the surgeon my primary care doctor suggested.
I feel really different and yet the same at the same time.
Comments
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sorry to hear that the diagnosis ended up being this
I hope you get your treatment plan organized quickly. Many people find the time between dx and treatment start to be a difficult time - but I think you sound well prepared and strong.
best wishes
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So sorry for the diagnosis you received. So glad your center has a nurse navigator. I don’t know what I would have done without mine! I wish you the best as you get more information on your diagnosis and begin a treatment plan.
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I never did meet a nurse navigator, although I saw one listed at the breast center. Got through everything just fine without one. I didn't get emotional about any of it, either. Well, I got cranky at the radiologist once, but that was it.
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Sorry to hear about your diagnosis. Sometimes it can take a bit for the news to really hit home. For some of us it is when we hear the news, when we go into surgery, starting treatments, or even ending treatments. Each of us handlesit all differently. My hope is that you keep a positive outlook (it makes all the difference in the world) and yell, cry, or scream when the need arises. This site is a great place to go to vent or just read other’s stories. Best wishes to you moving forward!
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Thank you everyone. My nurse navigator called yesterday with an appointment for next week with the surgeon. She is worth her weight in gold.
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Got to see the preliminary report today.
Addendum: Preliminary pathology report left breast mass, twelve position, core biopsy states invasive high-grade carcinoma consistent with mammary ductal primary. Focal ductal carcinoma in situ, nuclear grade 3. Breast tumor markers as follows: ER negative (less than 1%),progesterone: Negative (less than 1%) and HER-2/neu: Equivocal (2+,weak to moderate, indeterminate). Results are concordant with expected results.
So does this mean that the HER-2 is negative or that they need to retest? I will be seeing the surgeon on Friday so I guess I can ask then
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Hmm, usually if the HER results are equivocal with the ImmunoHistoChemistry, or IHC test, the sample is sent out for the FISH test. My cancer was equivocal with the IHC test, but I tested positive with the FISH test.
In your situation, it might be better off to be HER2+ because that offers more treatment options than triple negative. (ER-/PR-/HER2-). Good luck!
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Thanks Elaine - my surgeon gave me the final report yeaterdaywhich came back as HER-2 positive. It made me feel better to know that I am not as limited in my treatments.
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We HER2+ patients are blessed with a growing number of treatment options -- Herceptin, Perjeta, Kadycla, etc.. What was once seen as an aggressive cancer with poor outcomes is now very treatable. Unfortunately, treating HER2+ cancer is a marathon, not a sprint. Surgery, chemo + targeted therapy, radiation, a year of Herceptin..... Sometimes, treatment seems like it never ends. But, I found that if I took it one step at a time that it was doable. Have you met with an oncologist yet? That is the person who will help you with chemo and targeted therapy. I ended up doing Adriamycin + Cytoxin (X 4) and then Taxol (X 12) with Herceptin and Perjeta. However, many HER2+ breast cancer patients get Taxotere + Carboplatin + Herceptin + Perjeta. If your tumor is on the small side, you may be able to get just Taxol + Herceptin + Perjeta. Best wishes!
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I meet with the MO this week with a tentative appointment for the 10th to get a port put in. The surgeon said likely chemo, surgery and then radiation. If the MO says surgery first then that's what will happen. My tumor is 1.3 cm
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I did chemo first; it is encouraging to watch the cancer disappear (if it's visible). But, my lump was big (5 cm. with a satellite), so my MO could actually measure (with a ruler!) my lump as I went through chemo. By the end of chemo, an MRI and PET scan showed no active cancer left in my breast and compromised lymph node. Surgery confirmed this outcome, though my surgeon did remove a tiny pocket of high grade DCIS.
Of course, not everyone's cancer disappears during chemo. But, neoadjuvant chemo does tell us whether or not chemo was effective for our particular kind of cancer.
Your lump is fairly small but probably not small enough just to do the Taxol only regimen. (You could ask your oncologist about it -- Taxol only is gentler than the AC+T or TC chemos.) Also, you may or may not be getting Perjeta -- when I was treated four years ago, the guidelines held that the lump should be at least 2 cm. to qualify for Perjeta. But, more women with smaller lumps have been able to get Perjeta since then, so that may still be an option for you.
Good luck with your port surgery! I love my port, but my oncologist thinks I'm crazy for keeping it, as I'm almost 5 years out. I guess I'm just superstitious!
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DogMom--
Be encouraged! My tumor was growing like crazy right at the time of my diagnosis. My Colombian MO with beautiful olive skin lost all the color in his face the second time I saw him after my MRI, which he requested so I would qualify for Perjeta because the tumor needed to be 2 cm (see what happened in my stats below). I found this site and read about women with tumors larger than mine melting away, even after the first treatment--not uncommon with HER2+ because you receive Herceptin, (Perjeta if it's big enough), and chemo. Mine did not melt away after the first treatment, but I kept feeling something the entire time of treatment, as if a war was going on inside my breast. It didn't hurt per se, but it was a definite sensation, and would even wake me at times. I even felt it at 4:30 in the morning on the way to the hospital for surgery, which made me think there was still live tumor there (imaging six weeks before surgery showed it as "tiny.") My post surgery pathology report said there were no cancer cells in the breast or the sentinel node--just the clip placed there at biopsy. I still have cancer hanging over my head--but when things were looking so bad I couldn't imagine being where I am now.
Twenty-five years ago, our diagnosis was a death sentence, but as my MO told me on my first appointment, now we have some of the best outcomes. I read the book about the development of Herceptin while in treatment---we HER2+ ladies owe our lives to Dr. Dennis Slamon. Here's a speech he gave sometime back that is sort of like a Cliffs Notes version of the book if you want a distraction: Slamon Speech on Development of Herceptin and Future Treatments
None of us here would have chosen this, but you can do it!
Beesy
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Thank you Elaine and Beesy for the encouraging words. I will have to look up that book. Gives me something to do during treatments!
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