I want to puke...
Positive. Grade 2. Triple negative. In lymph nodes. Doctor indicated I will need a mastectomy, so I'm going to a hospital with a plastic surgeon, as I am only 43. I'm guessing because of the triple negative, chemo will happen too.
I'm scared, but don't feel alone. I just want it out of me. I have two school aged kids- 8 and 11. I'm scared for them and my husband. One of my childhood friends passed a couple of years ago and my neighbor a little longer ago than that.
Waiting for next steps is brutal. What if it spreads? What if I already have it in my bones or brain or somewhere? So many questions...
Comments
-
try to Sit tight as my mother used to say. It is very brutal waiting for the next steps to fall into place so that you can figure out what your plan will be. For me, and others who have posted, the anxiety seems to lessen once you know what steps you are going to have to take.
It is so scary, especially with young children. Try to hang in there and don't visualize the worst possible scenario.
Lots of younger women like yourself with the same diagnosis will be on board to help you through this. There is a lot of love on these boards to share with you.
Brenda E
-
You didn't mention what type of BC you are dealing with - DCIS, IDC, ILC, IBC. The TX (treatment) plan is varied for the different types.
Your TX plan should include not just a surgeon but also a Chemo Dr (MO) and a Rads Dr (RO) for the best TX plan. It is a Team Effort working together - not just different Drs going each in their own way without coordinating TX to be able to get the best results. Has your 'case' been taken to the Board at the Facility you are going to?
Surgery is not always the best option first option TX choice today. Neoadjuvant Chemo (Chemo pre-surgery) is one that is SOP for one type but is becoming more common with other types for the best outcome.
Bone scan, full body MRI and PET scans will probably be scheduled to check for possible mets to aid in getting the best TX plan for you.
Get a notebook and write down every question you come up with, make a second copy and hand it to your Dr(s) for answers.
-
Thanks, Kicks. I don't know what type. Getting the news was bad enough, so I didn't think to ask. I assume it's IDC, since it has spread to at least one lymph node.
Still waiting on the call back from the doctor on my appointments. The waiting is the hardest part.
-
Twaz - the waiting is the absolute hardest part. I am VERY sorry you have to deal with this at 43.
The best thing you can do for yourself is get the absolute best doctors in your area. Don't just settle
for anyone!!
It will all get better once you have a plan in place. Right now, it is just utter terror.
Sending my best to you and your family.
-
Twaz,
I'm sorry to hear that. I'm triple negative also, diagnosed 3 1/2 years ago at age 44. If you like, check out the "Calling All TNs" thread. https://community.breastcancer.org/forum/72/topics... I would echo the comment that your docs may well recommend chemo before surgery. That's common with TN. I don't know whether the grade 2 (rather than grade 3) changes anything. Are you going to a hospital/practice with docs who specialize in breast cancer
-
I echo what was said above. Couple things I would add. I am sure you have thought of this but take someone extra with you to appointments. When you do start getting so much information it can be easy to miss questions or information the doctors provide because at first there is so much to deal with. As hard as it will be, do NOT compare your situation to that of your friend and I am so sorry for you on that one. You are an individual. Please do not look to google for survival stats, they are usually out of date and do not take you and your individual health into account. There will be many more people along to give suggestions. Kicks above is correct, when you do get your pathology, have the doctor explain clearly what it is, what it means, not just medical but layman's terms as well. One day at a time. It will be a long process to get through but it will get mapped out for you. I am sorry you are having to join us here but you will get a lot of help from others on here.
-
Good idea on bringing a friend with you. If you are a reader, here are some reputable websites/sources about diagnosis/pathology. http://beltwaybreastcancer.blogspot.com/p/diagnosis.html
-
Twaz- I don't have a lot to add to what's already been said but wanted to say we are all in this together. Cancer stinks, no question, but here you are among amazing women who have been through it all. As hard as it is, breathe.
Hugs
Bet
-
Twaz,
Again, I am one day behind you. Received "the phone call" from the radiologist this a.m. All she said was it was positive and "sorry." Geez....so like my typical self, I asked questions and got a few answers. Mass and node positive. High grade IDC. I am seeing the surgeon and onc this afternoon.
I'm with you in this....we're tough....all of us here.
-
I am sorry. I have young kids, too. I know it's scary. Node involvement doesn't necessarily mean IDC. I had two positive nodes and had ILC. The treatment in my case wasn't any different. But ILC can be harder to detect, hence my decision to go with the BMX. I would strongly encourage you to join a chemo group. I couldn't have made it without the lovely ladies in my group. Best of luck to you. Please use BC.org for support. It is a great place to get answers.
-
Twaz - so sorry you've become part of a club that no one wants to join, but the benefit is that there are hundreds of sisters here who understand.
I wasn't triple negative, but my friend in quilting class was. When we met 5 years ago, she was a 15 year survivor. I guess that now makes it 20 years for her. She took things one day at a time, did what was recommended for her particular situation, dealt with family issues, and today is happy and healthy and enjoying being a grandma.
Try to keep busy, so your mind isn't consumed with the "what-if's".... and once you have a firm treatment plan, you will feel more in control.
Wishing you the best....
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