Newbie & scared

Posted by simone1 @simone1, Jul 25, 2023

Hello,

I just found out I have breast cancer ( stage 1) first I was in shock,
next came depression and crying. I'm just scared and need someone to talk to in this group, thank you

Interested in more discussions like this? Go to the Breast Cancer Support Group.

@jmc7003211953

I am a newbie x 2 weeks. It is invasive lobular carcinoma. My surgery for a lumpectomy with a larger margin is in 5 days. I am a RN who worked as an outpatient and my latest employment was a nurse in a inhouse hospice facility so I have seen and know more than I want so yes, I am not so scared of the diagnosis but it is the "Invasive" portion that I am scared about. I have read up on my diagnosis which probably is not be a good thing to do but I did it anyway. My surgeon oncologist said I will need radiation of unknown length of time and a anti-estrogen receptive oral therapy and I read for 5 to 10 years duration. How prone is metastasis disease with this oral medication route? Does anyone know the answer to my question.
I don't need an exact answer but I would like to see if one could tell me what they think.

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Hi @jmc7003211953, I think you question about the likelihood of recurrence with or without anti-estrogen receptive oral therapy is a reasonable question. As an RN, you know that the answers are never complete guarantees. There are so many variables.

I think these 2 resources may be helpful for you:
- About Oncotype DX https://breastcancernow.org/about-breast-cancer/diagnosis/oncotype-dx/
- Is There a Role for Oncotype Dx Testing in Invasive Lobular Carcinoma? https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995885/

Has Oncotype been discussed with you? Is it appropriate for your decision making? How are you doing?

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@grandmabecky

Hi...brand new to the club no one wants to join - just received my diagnosis on Friday of last week and spent the weekend in shock and tears, of course. Waiting to hear from the surgeon about what she feels the best plan of action will be in my case.

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@grandmabecky, I thought I'd check in. Did you get more information about your diagnosis and treatment plan? How are you doing?

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@windyshores

Sorry you are dealing with this suddenly. Many of us have been there and are fine now!

You will meet with a surgeon and oncologist. Your biopsy will provide some information but the pathology after surgery provides more.

I bought the Mayo Clinic breast cancer book which I found helpful. But too much googling is not helpful! These days, for certain cancers, a test called the Oncotype is used to determine treatment and many of us avoid chemo as a result.

Keep us posted! The first days of waiting are the hardest. Once you have a plan you just do it. It has been 8 1/2 years for me now since my diagnosis.

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I am a newbie x 2 weeks. It is invasive lobular carcinoma. My surgery for a lumpectomy with a larger margin is in 5 days. I am a RN who worked as an outpatient and my latest employment was a nurse in a inhouse hospice facility so I have seen and know more than I want so yes, I am not so scared of the diagnosis but it is the "Invasive" portion that I am scared about. I have read up on my diagnosis which probably is not be a good thing to do but I did it anyway. My surgeon oncologist said I will need radiation of unknown length of time and a anti-estrogen receptive oral therapy and I read for 5 to 10 years duration. How prone is metastasis disease with this oral medication route? Does anyone know the answer to my question.
I don't need an exact answer but I would like to see if one could tell me what they think.

REPLY
@grandmabecky

Hi...brand new to the club no one wants to join - just received my diagnosis on Friday of last week and spent the weekend in shock and tears, of course. Waiting to hear from the surgeon about what she feels the best plan of action will be in my case.

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Welcome to connect. I am glad you found us. This is such a shocking and scary time. I remember it like it was yesterday.
Connect is a pretty great place to get information and support.
When you got your diagnosis, do want to share more of that diagnosis?

REPLY

Hello!
I had an aesthetic breast reduction last June 2023. The pathologist detected DCIS. Has anyone had the same problem?

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@grandmabecky

Hi...brand new to the club no one wants to join - just received my diagnosis on Friday of last week and spent the weekend in shock and tears, of course. Waiting to hear from the surgeon about what she feels the best plan of action will be in my case.

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Hoping all goes well for you! Everyone who posts on this forum will be rooting for you to receive the best care possible. Please post often, to keep us up to date with your progress!

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Hi...brand new to the club no one wants to join - just received my diagnosis on Friday of last week and spent the weekend in shock and tears, of course. Waiting to hear from the surgeon about what she feels the best plan of action will be in my case.

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@auntieoakley

Welcome to the club no one wanted to join, but we are all in this together, even if we aren’t together. 😁 some of us are newbies, but I lurk on this page just to attempt to bring comfort where I can. I am 20 years from my initial diagnosis. I have had a few hiccups along the way, but I am living life like someone left the gate open most of the time. My wish is for my journey to bring hope and encouragement to others.
I know waiting for results is hard and the day before surgery is an anxious kind of day, but I am waiting with you. You got this❣️
Will you come back and here and let me know how you are doing after surgery?

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Hi Chris, yes I will surely come back and I appreciate your response. Thank you!!!

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We are all warriors here!!!!! Fight on!!

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@jfhpink

Hi everyone, Also new to this group. I recently posted about my lumpectomy which was on Aug 21st and tomorrow I have my reduction. I am 64 and was diagnosed on June 30th. E+ P+ HER2-. Stage 2 (in one node) Waiting for my oncotype score which should be here in about 8 days to determine whether or not I need chemo. Reading your comments has been a comforting support and I am grateful for all you "Club" members. Wishing you all happy days ahead.

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Welcome to the club no one wanted to join, but we are all in this together, even if we aren’t together. 😁 some of us are newbies, but I lurk on this page just to attempt to bring comfort where I can. I am 20 years from my initial diagnosis. I have had a few hiccups along the way, but I am living life like someone left the gate open most of the time. My wish is for my journey to bring hope and encouragement to others.
I know waiting for results is hard and the day before surgery is an anxious kind of day, but I am waiting with you. You got this❣️
Will you come back and here and let me know how you are doing after surgery?

REPLY
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