Diagnosed in April, going through the process...
Hi Community... new here.
Back in April I started discharging "milk" from my right breast. After 2 week of this still happening, I figured I must have an infected duct, and went to my PCP for antibiotics. To my surprise, that was not what happened. Since the discharge was milky looking, with no blood or brownness to it, I was sent to get blood work done. This was to check my hormone levels and rule out a brain tumor that affects the pituitary gland. She also noted the fibrous area of my right breast, but I've always been fibrous, so I really didn't think much about that.
I had my blood work done, every thing came back A OK, but now I needed an Ultra Sound to see what was going on with the fibrous area. This came back ok, nothing lit up enough to cause concern, but since there was the fibrous area, they recommended I see a surgeon. I had my appointment with him and he gave me my options after the exam... he recommended a biopsy, so that's what we did. This was the Friday, and he told me he'd get the results in 3 (working) days. Wednesday came around and I received the call that I had breast cancer. I went numb. Somewhere in the conversation, he asked me to come to his office later that day so we could discuss everything.
My husband and I went, and he informed me that I had stage 0 DCIS. He ordered an MRI for me, and I had that later in the week. This showed the same, DCIS, nothing more. (side note, I had my first mammogram in Sept '16, it was clear) My husband and I met back up with my Oncology Surgeon later that week to figure out my action plan. With the amount of affected tissue with the DCIS, a lumpectomy wasn't an option. With my age (44) I decided I wanted to have a bylateral mastectomy. I didn't want the next 40 years to be waiting for the hammer to fall when it came back on the other side.
So that was the plan... I had surgery on June 5th. The pathology came back on the 9th. the mass of DCIS removed was 8.5cm, and hiding very well inside it all was a 1.2cm of invasive cancer. The pathology came back that it was ER+ PR+ & HER2+. Of the 3 lymph nodes tested, 1 came back with cancer cells. All this from a little discharge !!!
I also had the genetic testing done and everything came back negative. I have NO family history, but had to know for my daughter.
So now I am preparing for chemotherapy to begin on 7/14. I am really glad I found this resource, to be able to "chat" among others that are going through the same as me.
I had the expanders placed during surgery, and have my first "filling" next Tuesday... I'm not sure how this will feel, my chest is so sore and tight as it is... but I'm told that it's normal, the deflated expanders will loose the hard ripples as they are filled up. (I think of them a deflated balloons)
I have to say the hardest thing so far since surgery is the horrible feeling of fabric on my breast skin... where the feeling is partially gone, fabric touching it feels like daggers, so if anyone has any advice on this, it would greatly be appreciated!
Again, glad to have found you all...
Anna from So Cal.
xox
Comments
-
Hi Buuzbee, and welcome to Breastcancer.org,
We're so sorry you find yourself here, but we're really glad you found us. You're sure to find our incredible Community an awesome source of information, advice, and support. You're sure to get some posts soon from others here who are always happy to help!
We also wanted to point out to you the July 2017 Chemo forum, where you can feel free to join in with others who are going through chemo next month too, and you can compare experiences, ask questions, and have some virtual chemo buddies.
We hope this helps and we look forward to hearing more from you throughout the boards!
--The Mods
-
Buuzbee, I am so sorry you've found yourself a member of our club! This site is full of wonderful women who are generous with their experience and support. I could be wrong, but with 1.2 cm of IDC, I don't believe that is called a micro-invasion. I would think that you would be classified as IDC triple positive in addition to DCIS. There is a HER2+ forum that may provide some good support and information, as well as the IDC forum.
I remember my TEs and how strange they looked until my exchange surgery! Btw, I had numbness across my chest and up under my arm for quite awhile, but it has mostly gone away. My underarm and the skin across my foob have complete feeling again, so it is possible!
Sending you warm thoughts and gentle ((Hugs))
-
Thank you MTwoman... so many names & terms for all the cancers!
Please, if a mod can move the topic to the correct forum, it would appreciate it
-
they did it, buuzbee. It is a steep learning curve, but you can do it!
-
Buuzbee - go to the left side and click all 'all topics". That will get you stared with abbreviations, surgery threads, chemo threads, HER2+ threads, etc. Sorry you've had to join us.
-
Hi Anna
I was diagnosed in April too. I am 39. Just a "routine " mammogram to get a baseline was done. I had a Grade 3, ER and PR + and HER2- tumor. DCIS plus invasive ductal carcinoma (4.2 cm ) with an oncotype of 18.
I live in Northern California. Had my double mastectomy on May 25th with immediate reconstruction with expander.
Will be starting chemo in July too. Are you looking into Penguin cold caps to prevent complete hair loss?
I will be thinking of you.
Maria
-
Welcome Buuzbee,
Sorry about your diagnosis. Mine also came as a shock. I opted for the recommended lumpectomy. At 62 I would not bother with reconstruction. Mind you I pray I never have to go through this again. I had surgery in April and just finished my 2nd round of chemo. I'm sporting the bald look. Chemo side effects are harsh but manageable if you follow the plan. I have found Claritin and Tylenol 3 helpful. The best tip "Claritin" was from this site. Took 3 days before and after infusion the 2nd time. What a difference
Good luck!
-
The process is something, isn't it? I went to the doctor on June 19th for a lump I felt in my armpit. GP found a lump in my breast. Mammogram and ultrasound was performed on June 22nd and they were fairly certain it was cancer. Biopsy of both the breast and the lymph node on June 28th. Diagnosis of IDC June 29th. Had genetic testing yesterday, July 7th. Tonight I'm having a chest MRI.
I was told yesterday I wouldn't meet with the surgeon until July 24th because they need to wait two weeks for the genetic testing results to come back and the MRI may lead to additional scans.
I just thought that once I found out I had cancer they'd want to do something about it sooner. We already know it's in my lymph nodes and my breast tumor is bigger than 5cm. So now I'm just trying to watch my diet really carefully so it feels like at least *I'm* treating it.
-
ElleElle - while you aren't "ready" for surgery yet, you can start interviewing surgeons while you wait. My GYN agreed. I used my waiting time deciding on which docs I wanted for surgery & plastic surgery. I also met with an oncologist in case chemo was determined to be necessary. I felt empowered by taking some kind of control.
-
Buuzbee - Want to give you hope -- I was Triple Positive - diagnosed 5.5 years ago -- huge tumor - lots of nodes -
I am doing well and going strong!!
Sending all my best wishes!
-
@MinusTwo, I'm already on the best breast surgeon's docket in the area. All of the local survivors I've met agreed. Not sure I want to spend the money on appointments that don't get anything done, but I'm glad that worked for you. My nurse navigator offered to set me up with appointments with additional doctors, but she did warn me of the cost. I'd rather use my resources proactively. Wouldn't mind finding a dietician or naturalist to supplement my care though...
-
Elleellebee
Sorry you're here with us. So much of cancer treatment initially feels like hurry up and wait. It is frustrating but try to find ways to do other things! After surgery and treatment I was laid up for a bit. I'm glad I spent the time beforehand doing things I loved to do!! Hugs to you. -
Anna,
I found that I could only tolerate cotton fabric. You may want to try GABA, a supplement. It helped me tremendously with nerve pain, which may be causing the "dagger" feeling you are experiencing.
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