Bi rad 4C on us/ biopsy today
Hey all. It's finally biopsy day. Iv been having chest pains all morning taking my xanex. Just wanna make a new post so I can fallow up on here with results in a few days and how things went. As well if anyone else with bi rad 4 score has their experience please share.
My biopsy was rated a 4C
Suspicious abnormality with angular indenstictive margins 1.3cm x 1.2 x 1.2
Now going in for biopsy! Best wishes for us all. Il keep updating. And again share your biopsy results with me!
Comments
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Curious on how yours goes, and hoping it turns out well!
I have a Birads 4 - suspicious abnormality but my appointment with BS isn't until Oct 11. They did not indicate if it was A, B or C.
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they didn't tell me either. I had to call my Drs office and ask them to read the hole report to me
. Il keep updates here now
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Biopsy is over. Nowwww Waiting on results if I don't get them Friday it will be Monday
I asked what makes it look cancerous they showed me the photo of how weird shaped it was and said begin is usually round/oval
Then at the end I said if it is something begin what do you think it would be he said fibroadenoma is most common in my age but that my Tumorfeatures don't look like the typical fibro cystic kind of tumor.
So just waiting now.
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(((((Hugs)))) Waiting is the hardest part, it's awful!
It's going to be difficult, but try to keep yourself as busy as you can, so you're not constantly dwelling on it. Our minds can go to some pretty dark and scary places, if we let it. When that starts to happen, come here! You'll receive a lot of support, which will help.
Most important.....stay off of Google! That's the worst thing you could do. If you want to look up info or have questions, once again, come here! This is one of the best places on the web for accurate and reliable info.
Lots of prayers headed your way for excellent results! Hang in there! -
Hi, I am new here (well I used to lurk for a friend) but I now have had my own biopsy Bi Rads 4 (no a b or c).
Sending you best wishes, prayers and warm thoughts for a B9 result! Please let us know the outcome. I will be watching for your update and keeping you in my thoughts because the waiting is difficult and I too agree, the internet is a scary place which is why I lurked here for my best friend who didn't want to look at the internet at all.
All the best,
KTF611
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sorry! Hope yours is good as well. When do you think your results will be in, i called yesterday nothing in yet. They said hopefully monday
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Hi - it is Monday by 3 pm.
No one wants to talk to me, i.e. hubby - he's a doer not a talker. I feel like I am going mad. Praying for best result for you on Monday too!
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Hi JXMom2 - good luck today at 1:45 PM!!!! You are in my thoughts, prayers and please come back and let us know how it went. There are so many here that can help you/me/us.
Much love and warm thoughts to you!
KTF M
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Hi everyone i have a long road.
So i got my diagonosis. Im 27 and have invasive ductal carsinma, grade 3. Her2 1+/neg est-/pro-
Awesome... Idk whats gonna happen im overwhelmed right now that dr got me an apt with a surgen in 3 days and he said from there il get an oncologis
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JX- So sorry to hear this! I can't imagine what you're going through! While I don't have much to offer as way of comfort, It seems like there are a lot of very experienced ladies here who have a wealth of knowledge that you can draw on!
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Sorry to read of your positive diagnosis JXmom2. It's all so overwhelming at the beginning but does get a little easier once a treatment plan is in place. Yes you have a long road ahead but you will get there. Grade 3 responds well to chemo. Am I reading this right - you are HER2 Pos, ER and PR neg??? Thinking of you. Hugs Donna.
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Thanks for support its gonna be a long road
her2 was neg but it says 1+/neg
And yes both others are neg. just grade 3 and the ki67 or somerhing says 90% high next to it.
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Thanks for the clarification. The ki67 refers to the cell proliferation rate.
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Hi JXMom2, i posted on my thread a response to your news and I am copying it here. As Smurfette26 and others have stated you will find a great deal of support and the most up-to-date knowledge here. You are in my thoughts and my prayers - for you are so young - exactly 50% of my age. I am stunned for you but I know that you will be ok and the right protocol will bring you to "NED" status (no evidence of disease). i will post my update separately. This is about YOU!.
From my thread: I am so, so, so, sorry. I am not well versed enough to tell you what your next steps will be. I am more well versed in stage IV cancer mets to brain due to my best friend but early stages, I am not yet educated enough to give you good information to help you along. I am going to search out your original thread and hopefully you have also updated there. Or start a new thread on this page and/or the page "JUST DIAGNOSED" and the women and men here who have been where are you are now will help you along with the medical terminology, your options, their stories, you can share your doctor's advice, listen to the feedback, keep track of all of your questions (start that process right now - find a spiral bound notebook and start writing down your questions in one section and your thoughts in another no matter how random they are. My daughter has a learning disability and this was the only way I could keep track of figuring out her diagnosis which took 4.5 years (narcolepsy).
I am at a loss for words to help clear the fog you must be feeling but to say you are in my thoughts and my prayers. Please bring someone with you to your very important upcoming appointments, be your own advocate (this is SO important which I learned via my best friend and being at HER appointments). You will be getting terms thrown at you which will make your head spin. Make the doctor stop and slow down until you understand each question/answer discussed. It is your RIGHT to understand the protocol and process' and if anyone gives you grief if you ask the question 80 times, let them know that they must stop and understand and respect your position/questions, etc., all politely but firmly of course!
Hang around HERE on these boards and read. Hard as that will be read and try to also write down items you pick up browsing these board which many be relevant to your situation. Ask for help. God helps those who help themselves; pride can be hurtful. Please remember that you are NOT an Island. As strong as all of us think we are everyone needs a soft place to fall - find that soft place and it may be a different place than where you have historically fallen. I wish I lived next door so that I could put on a pot of tea and just let you talk - about whatever you feel like talking about - the election, the stock market, your family, the diagnosis, your fears, all of it. Find that person -they are closer than you think. You are so young - 27 - do you have a family history of BC? You may be one of the youngest people I have "met" dealing with this God-awful mess.
All of my best wishes and kindest regards to you JXMom2 - you are a FIGHTER - you can do this!!!! I will be checking in!!!!
KTF Marie
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