Just diagnosed and still in shock
Just recieved the news that I have IDC. Two lumps were palpated in left breast, (both under 1.5 cm.) and biopsied. I am scheduled for an MRI next week and a first meeting with the oncologist. The plan is for chemotherapy first, followed by segmental/partial mastectomy and sentinel lymph node biopsy, followed by radiation. I was told I was Her-2/neu negative and I was not a candidate for anti-hormonal therapy. I am overwhelmed with the terminology and what it all means. Is there anyone out there with a similar diagnosis that has gone through this or is going through this?
Comments
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Hi JoLynn712,
Mine is not exactly like yours but I'm writing to say I'm so sorry about to hear about your diagnosis. It is terribly overwhelming and I so wish you didn't have to go through this. Little by little you will gain the knowledge you need so you'll be comfortable with your treatment plan. There's a ton of information and just keep asking questions and getting opinions until you know you're doing the right thing for you.
BCO has a lot of information and there is a list of terminology. I also received a booklet from the American Cancer Society (800) ACS-2345 (www.cancer.org).
BTW, I'm from California but have been in Washington for about 5 years. I wish you all the best.
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Hey there - I wanted to take a minute to welcome you but let you know how sorry I am that you have to be here. This is a wonderful place but also a place nobody wants to have to be.
I was a candidate for hormonal treatment but at the recommendation of the docs at MD Anderson elected to try chemo first hoping the more agressive approach might yield a better outcome. So far I have had 4 chemo treatments and have been very lucky so far and have had minimal side effects. They have very good drugs to help with the nausea issues and while I have some nausea and am very tired for a few days after treament I have never actually thrown up and am getting through it. Granted it isn't a pleasant thing to have to go through but it is doable.
Once you get through the initial diagnosis part of this nightmare and come up with a treatment plan you will find yourself starting to feel a little better emotionally.
I wish you the best possible outcome and please keep us posted.
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Thank you Beanius for your encouraging words. I will keep asking questions. Right now, there seems to be so much information to be processed and understood and it is very overwhelming. I am so glad that there are websites like these where people can connect with one another and share their experiences. I know that this will make this journey much easier. I keep seeing the term "triple negative" and wonder if that applies to me. Does it refer to the Her-2, ER/PR results?
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Welcome
Triple Negative is ER-/PR- and Her2 negative..there is alot of information about that
but first are you sure of your ER/PR status?? At any rate, I know you are trying to
get a PHD in breast cancer in a couple of weeks, and it is a frustrating time. You
have alot of information on this site info part...discussions are good too...I see you are
in S. Cal also...where are you going for treatment? Just for what it is worth, how about
a second opinion just to help you ...I did...
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Hi Lorrha,
Thank you for your kind words. It is encouraging to hear that you have had minimal side effects after four treatments! My surgeon also recommended the chemo first for a better outcome. I will have many of my questions answered when I finally meet with the oncologist, but I know I will be visiting this website often for support. I feel like such a zombie right now! My brain is in overload.
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JoLynn - For at least 48 hrs after my initial diagnosis I did practically nothing but sit and tremble. I'm not too sure about the triple negative, and wouldn't want to tell you the wrong thing. I sat down with my breast surgeon and he explained my pathology report in detail. At that time I was still in bad shock. Then I sat down with my radiologist and he went through it all again and he drew a lot of pictures that were helpful. Slowly it started sinking in more and I've been reading a lot here on BCO. You are in the right place to find answers to your questions. It will definitely get better as you are probably in the worst phase of shock right now. Take care and keep taking a lot of deep breaths, also drink a lot of water. All the best to you!!!!
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Hi SoCalLisa,
Pretty sure about the ER/PR negative. Thank goodness my daughter came to the appointment with me and took notes! I was told that I was not a candidate for anti-hormone therapy because the tumor would not respond to estrogen or progesterone. I understood that to mean I was ER/PR negative. I definitely am Her-2/neu negative. My surgical pathology report indicates both tumors are Elston-Ellis Modified Scarff-Bloom-Richardson Histologic Grade 3. No lymphatic or vascular space invasion identified. I was told these are very stubborn and aggressive. I read somewhere that triple negative responds very well to chemo. Where can I get more info about that?
I am being treated in Palm Springs at the Desert Regional Medical Center - Comprehensive Cancer Center. This is after a misdiagnosis at another facility.
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Beanius ~ I can so relate! I still cannot believe this is happening to me. I see that you are about three months out from your diagnosis. How are you doing? Did you have chemo first?
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JoLynn
This is a good site, check it out...
http://nosurrenderbreastcancerhelp.org/breastcancer101/TNBC/TNBC.html
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Hi JoLynn...There is a website called Living Beyond Breast Cancer, lbbc.org that has a free download called The Guide to Understanding Triple-Negative Breast Cancer. It's very informative and worth checking out. If you decide to give it a try..look under LBBC Publications, under the heading Learn More..then under Books and Brochures and scroll down and you'll find it. I'm sorry you had to find us, but it will get better once you have a treatment plan.
I don't know if you are aware new members get 5 posts a day until you reach I think it's 25. You can send Private Messages. Best wishes.
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Hi, JoLynn ~ I see you're in So. CA, too. I know your dx is so new, you obviously haven't had time to sort things out. Before making any decisions about an acutal treatment plan, please be sure that your doctors are very experienced in treating TN breast cancer, because it is one of the rarer types, and not all doctors are as expert about it. I live near Palm Springs, and although I don't have TN bc, I did have some other oddities that made me turn to UCLA (after some treatment @ Desert Regional), and I was so glad I did. So I just wanted to say if you need a second opinion about anything, UCLA is top notch, and I know at least two of their oncologists specialize in TN bc.
I'm so sorry that you're joining the club that no one ever wants to be in, but I know you'll find great support on this site, including an entire forum (go to Forum Index above) with questions and information about TN bc. And, since I'm in the Palm Springs area, I'm going tol PM you my phone number, in case you possibly feel like talking. Click on Private Messages above when you see the message light. Deanna
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I am overwhelmed at all the information that is out there AND mostly by all the wonderful people on this site willing to give support and advice. I love this website and the fact they have a Discussion Forum! We're all in a Sisterhood that we really did not want to be.......but here we are and "Hello" to all of you!
I, like you JoLynn, joined this month, but was diagnosed in May. I too am Grade 3, just finding that out yesterday. I am disappointed that my surgeon did not go over the Pathology Report with me....but I do think he intentially left that for the Medical Oncologist since he/she is the one I will be discussing my treatment. The surgeon did tell me I was Stage 1a at the appointment two days after surgery, but that was all I knew until yesterday..
Speaking of treatment....right now I am waiting for an appointment and have NO IDEA what lies ahead. I was going to have the 5-day targeted MammoSite Radiation, but the surgeon had to cut out more tissue than he had first thought, leaving the surgery site too close to the surface of the skin. So, no Mammosite. I feel certain I'll still go through Radiation..........but wonder about Chemo. I am most anxious to have my first discussion with the Medical Oncologist. I wonder how long I will wait before I hear about my first appointment.
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Jolynn: My diagnosis was similar to yours. I had two IDC tumours in my left breast, 2.5 cm and 1.5 cm... both close enough together that I was a candidate for lumpectomy. I had surgery before chemo. My cancer was also triple negative - you will read and hear a lot of scary things about trip negative cancer, but there are some silver linings. One is, it responds well to chemo as it's fast-growing and chemo attacks fast-growing cells. Second, while the recurrence rate of trip neg is higher than for other BCs in first 3 years, it declines quite substantially after that. And, a low fat diet and exercise have been shown to reduce the risk of recurrence very subtantially in trip negative women.
There is another board here for triple negatives, so feel free to hop over there and ask your questions. There are many supportive ladies who have been through it...
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