Best Of
Re: Birads 5 with calcification
@maggie15 I completely agree with you about the imaging and I'm actually okay with the idea of repeating some of it if needed. However, I’m leaning toward declining the MRI-guided biopsy.
During my appointment, the radiation oncologist mentioned seeing something on the mammogram of my right breast (I had imaging done on both sides) that looked questionable. She wanted to make sure it wasn't pre-cancerous even though they didn’t see anything on the MRI or Pet scan. But both the oncologist and the breast surgeon who came in afterward said it wouldn’t be necessary to pursue further if I’m already planning on a double mastectomy, which I am so I was surprised when scheduling called today to still schedule me for it.
They were actually really intrigued by the location and feel of my tumor. While it’s not unheard of, invasion into the pectoral muscle is somewhat uncommon, and they all agreed it was a great catch something they definitely would have missed if they were relying solely on a physical exam.
That said, while I know UAB has some of the best doctors, more advanced imaging, and access to more clinical trials, it is also a teaching hospital. With my case being a little unique, I’m sure they would love to use me for teaching purposes. I can tell, just by seeing how fascinated they were with my tumor placement. I just don’t want to go through another biopsy unless it’s absolutely necessary
@scaredme The nurse actually called me that afternoon to set my start date for chemo, and I was given the option to begin on the same day as my next appointment, which is the 13th. So it’s officially set, I’ll be starting treatment that day.
Since I’m doing chemo first, the only information they can go by right now is what showed on the ultrasound, MRI, and PET scan, which thankfully didn’t indicate any lymph node involvement. But I completely understand that staging can still change later on, especially after surgery, and I’ll be sure to keep that in mind moving forward.
For now, I’m just thankful to finally have some answers and feel like there’s a little light at the end of the tunnel. I really appreciate your support, it means a lot.
Re: how about drinking?
Today would have been my Daddy's birthday. Went to his grave for a birthday visit and also to say Happy Birthday to my late maternal grandma for her birthday which would have been Mondaynext week. I miss both of them so much.
Re: CRAZY TOWN WAITING ROOM - TESTS coming up? All Stages Welcome.
So Feb.'s ocular scans showed no change, maybe a bit of shrinkage. Hoping this August's will be similarly stable—in which case I can opt for annual surveillance. There's a chance the stability means the tumor is dead (knock wood, kinahurra, scutta malocchio).
My annual full-body skin check (actually, 18 months because my regular derm quit just before the one I was supposed to have in Jan. and this was the earliest appointment I could get) was similarly uneventful. Just a small sebaceous cyst on my back—and the new derm said "if it doesn't bother you, we won't bother it." So I'm cool for another 6 months (rather than a year, due to having a squamous cell ca excised a year ago).
And the echocardiogram that followed up my stress test was normal, too: great ejection fraction, no change since 2013 (when I weighed 217).
Re: Newly Diagnosed Post Biopsy 50 years old
@rockrma - Suzie, we are sorry that your recent diagnosis has brought you here but glad that you found us. A helpful place to begin is our Just Diagnosed? Start here thread. You’ll find clear information to help you understand pathology reports, consider treatment options, and navigate the stress that often comes with a breast cancer diagnosis.
We look forward to keeping in touch with you as you begin this journey. Use this community for support and encouragement. We're all here for you!
Sincerely,
The Mods
Newly Diagnosed Post Biopsy 50 years old
Hello everyone!
I found this page on my own after I was given my biopsy results today. A nurse called and asked if I wanted results over the phone or come in. I opted for over the phone - but it seemed she could only share partial information: that the biopsy showed cancer in the fluid that was aspirated as well as the tissue sample taken last Wednesday (7/30). She mentioned a lumpectomy would be performed but my surgeon would be able to provide a full explanation from pathology report at my consult (soonest they could get me in is 8/21). It's been a roller coaster of emotions today, even though it seems like it is very early stages due to the small size of the lesion. I appreciate any words of comfort as I learn how to navigate this news - my family is wonderful and will be a big support but I want to hear from others like me. I went in thinking it would be a benign outcome since BC doesn't run in my family. I wasn't really prepared for this news. I am a Grandma of 2 adorable kiddos and right now, they are my best medicine when it comes to keeping me busy and mind grounded. Thank you, in advance… and for those who are getting ready to fight their own battles with this disease, I pray for successful treatments in the months to come.
Suzie