Scared for next steps
Hello. This emotional roller coaster I am on, along with web surfing has landed me here.
I have very dense breasts. Last year I chose to have an ultrasound completed. They found cluster of cysts and do focused imaging on every 6 months.
This month I had my annual mammogram, and the Radiologist found a focal grouping of calcifications with a BIRAD of 4 - suspicious.
I have my stereotactic biopsy this week. I am on an emotional roller coaster and I guess I am looking for something. What, I am not quite sure.
Maybe someone has had the same thing and can tell me that they have done well. I am scared and just want to breathe.
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@bkfx2
How did your biopsy turn out? I hope it’s benign. 🤗
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2 ReactionsI’m glad you got through it with flying colors! I pray for your good results. You definitely get stronger and more resilient! We are all here for you.🤗
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2 ReactionsSame here so I opted to skip it. I did the rest—CT, bone scan, petscan (took 1/2 Xanax and practiced with board over my face for weeks). I do know at some point as a regular check I may have to do it but I have found places that do the rapid MRI, which is half the time. Honestly I will fly to another state to do the sitting MRI if available for breasts..otherwise I’m going to ask for the new mammogram where they use contrast for dense breast + ultrasound. I did mri one time and never doing it again if I can avoid it. Petscan is golden so opted to bypass MRI for this go around.
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2 ReactionsDear CMDW,
What are they waiting and monitoring for? Something to happen before they take action? I had a single mastectomy on the right side followed by a recurrence 2 weeks later. Then two lumpectomy surgeries to get clear margins on the right chest wall recurrence. Because of all this trouble and anxiety with the right side I knew that I wanted the left side off too. I had to engage in a massive lobbying campaign l. However, the opportunity of calcifications gave me the opening for the mastectomy on the left. It helped that I agreed to a double reconstruction at the same time. I am relieved it’s gone. My surgeon told me that the chance of BC on the mat side is now 5% as opposed to 17-20%
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3 ReactionsI think the waiting is the worse. I, too, am newly diagnosed. I had to wait about three weeks to see the team. Those three weeks were bad and this is my 5th cancer! I finally figured out the other 4 times I was working so I had something to occupy my mind. Now I’m waiting on surgery. If you meditate it can really help as well as deep breathing. Thinking of you
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5 ReactionsHi! @shelbym
I am so sorry for all you've been through... It broke my heart upon learning that this is your 5th cancer:(
Thanks for sharing your experience to help us! Have you done Genetic Testing for inherited cancer Risk before? Perhaps talk to your care team on this matter - if you haven't; for early detection always is the key for successful cancer treatment, and it is important information for your blood relatives to know if there's any abnormal mutations.
My heart and prayers go for you all, my friends. Wishing you all a better journey ahead with faith, hope and love enjoying your loved ones!
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4 ReactionsTake it one moment at a time and just breathe. I was diagnosed 5 years ago with triple negative, metaplastic BC and I seriously thought I was dying. Here I am., still breathing. We are all here and we do not fight alone. Listen to your team and take it one step at a time. I know it is scary but you got this.
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3 ReactionsThank you so much for the encouragement! I was DMX with bc, stage 1, grade 2, yet I couldn’t help but worry about metastasis! I’m brca2 and recently had bilateral mastectomy. Still, the thought of metastasis is never far from my mind. Your message helps a lot! 🤗
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