pre-surgery jitters ?
I have finished chemo (4 ACs and 12 T) and will have a lumpectomy along with lymph node dissection on Monday (tomorrow). I am really worry with lymphedema. My surgeon also confirmed that I am at high risk. At this point, I even questioned whether I really have breast cancer. I looked back at the whole process, I am not sure whether anyone even read the biopsy report. (I changed oncologist before treatment and it was a long story). Isn't it true that the biopsy report was the ONLY piece of information positively determine whether we have cancer?
I read many posts where many of you talked about the size of the tumor, the stage/grade level etc. I did not know. I asked my oncologist, she did not really know, but pulled out the report and read the first number she saw to me, she did not give me a direct answer on what stage I am on. Are we supposed to know how many lymph nodes will be removed? I read some of your doctor discussed whether there is a need for radiation etc, but it was never given to me as an option and when I raised the question to my surgeon and my oncologist, I was told it was based on clinical experience, chemo -> surgery -> radiation.
I plan to have the surgeon answered me those questions tomorrow. Am I crazy?
Comments
-
fac03, I’m so sorry you are not feeling confident in your team. This is hard enough without the added burden of wondering if your team is on board with you. What they have apparently neglected to tell you is that the final size of the tumor and staging are done at surgery. However, it takes about a week to get the final pathology report. My initial biopsy report indicated approximately 3mm tumor but final pathology report was 7mm. Grading is done at biopsy as well as ER/PR/HER2 status and type of bc. Typically they don’t know how many lymph nodes will be removed until they get into surgery.....they inject radioactive fluid to find sentinel nodes (nodes where bc is likely to go to) and remove those nodes for biopsy and maybe a few more for safe measure. As for lymphedema, the most important thing is to follow post-op directions to a T!! Trying to do too much too soon puts you at great risk, so follow directions. Of course, with your team you may have to research this on your own. You may develop lymphedema regardless and there are some good threads here that you may find helpful. Good luck with surgery and recovery. Let us know how you are doing.
-
Yogatyme, thank you.
When you wrote "Grading is done at biopsy as well as ER/PR/HER2 status and type of bc", you meant the initial biopsy, right? I heard from the other doctor that I am ER+. I asked my oncologist, I had the impression that she was not sure or did not know, I didn't push further, what did you mean by the type of bc? I asked for the biopsy report which my oncologist gave me, but I just do not understand it.
I met a PT ceritifed for lymphedema, she made some measurements and gave me some suggestions on exercise, but when I asked her when should I begin the exercises, she told me I had to ask the doctor and the doctor will have to write another script.
-
Im sorry that your doctors have not been more informative with you. Thats the only way I can cope. My surgeon sat down with me for 1/2 hour and drew everything out and explained all aspects of my pathology report.
Wishing you much success tomorrow with your surgery.. -
fac03, yes, I meant initial biopsy. As you will learn if you stay on this forum, breast cancer is not one disease. I had no idea either until coming here. There are hormone receptive positive and negative breast cancers, HER2 positive and negative bc’s, triple positive, triple negative, and a number of less common types. The type determines the treatment. I so hope things take a turn for the positive for you. Stay on this forum.....it is a treasure trove of info. Read all posts by Beesie, she’s the bomb!! Loads of info.
-
Yogatyme, thanks. I am ER+/PR+. I was on this forum for a while, but after an infection and hospitalized during chemo. I became tired easily.
Does anyone know whether the percentage of ER+/PR+ mean anything?
In my report, it stated ER Positive 95% / Strong
PR Positive 20% /week to moderate
-
I found some more articles that may explain the result.
https://www.breastcancer.org/symptoms/diagnosis/ho...
https://www.breastcancer.org/symptoms/diagnosis/pa...
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team