My 30 year old daughter just had a core biopsy
A lump had come up on my oldest daughter's left breast. At the time she was with her boyfriend and I made 2 appts at the breast center to get it checked out. He didn't get her to me so I could take her. Finally after her coming back home my husband and I got her in to have a ultrasound and mammogram done.
She had the mammogram then the NP wanted to get a few more positions so she got a few more mammogram pics taken. The NP did a ultrasound and told me that we needed to get her in for the surgeon to do a core biopsy because she didn't feel a fine needle biopsy would be as good as the core. There were some microcalcifications in and scattered around the left breast only as well.
We took her in Tuesday for the core biopsy and I had been reading about some things and breast cancer and asked the doctor what the BIRAD was, she said 4-5, which tells me it's most likely malignant.
The waiting is tough. She scheduled an office visit for July 5, but said if it comes back she'll at least call us with results so we don't have to wait the entire weekend.
We just buried 2 family members just 2 months ago the same week from lung cancer. My uncle and my husband's stepmom. Then my mother was just diagnosed with small cell lung cancer 4 weeks ago today. Because the size of her mass and it's position pressing on her trachea they admitted her and started treatment immediately. I'm still trying to accept my mom's diagnosis and wrap my head around it. She's 77 but doing really well so far.
My fear is my daughter is being diagnosed so young. She's not had children yet. I'm afraid it's going to be one of the more aggressive types. I'm scared to death at this point and the days are dragging by.
Every morning I wake up, I pray all this is just a bad dream. It's just too much to deal with at one time. I know everything happens for a reason but just feel lost right now.
Thanks for reading and any input you can give me. HealLove & Light 🙏🏼🙌🏼❤️
Comments
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I'm sorry SimolySammi. The waiting is the worst. I had my the results of my biopsies pretty quick. I know it must be so hard as a Mom to have a major health issue with a child. Don't over google your research just yet. You will always find yourself going to the grimmest places and worst case scenario pages. There are many successful treatment options should it become necessary and this is a great community to help answer questions and explain things. Stay as positive as you can and I'll keep you in my prayers. Hopefully you will hear something soon. I'm sorry about the recent loss of family members and your moms troubles. .
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SimplySammi, If the NP said BIRADS "4-5" then you didn't get a score. They are given as either "BIRADS 4" OR "BIRADS 5". They are clear and based on the characteristics of the area or lump upon imaging. The difference between the 2 categories is pretty significant, so you shouldn't jump to the conclusion that it's malignant. BIRADS 4 biopsies turn out 70-80% of the time to be b9. "After biopsy the average rate of carcinoma in category 5 biopsies is about 75-97%." Read more about BIRADS here: http://breast-cancer.ca/bi-rads/ So as hard as it is, waiting and remaining calm (you being anxious will certainly not help your daughter) is the best course of action right now. I am hoping that (B9) results come back quickly so that you can all relax. Your family has been through enough. ((hugs))
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Lego and MTwoman thanks for your replies and support. I thought today the surgeon would call for sure but she didn't.
I looked at the link and it was helpful although I can't say completely takes away my anxiety. Around my daughter I'm pretty calm and have said no matter what we'll get through this.
I let my anxiety out by posting and brief cries when I can let it go. My husband is especially concerned and I've found him crying as well. He lost his first wife to BC in 1981 and he raised his 2 boys alone. I know that's a long time ago and the medical field has made leaps and bounds since then, but I am sure it brings back very sad memories for him.
I'm especially concerned because when the doctor came in after mom's Ct-scan he came out and said it was cancer. I argued that he can't say that until the biopsy was done and it was confirmed. I was very upset that he said that and then so disappointed when it turned out to be true.
So, although we don't have the "biopsy" back, knowing the surgeon didn't like the mammogram or the ultrasound results makes me a little more nervous had we not just been through what we have.
I'm trying to keep my thoughts positive but, need this outlet and am grateful for the input.
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Results
It's IDC mass 5cm and through out her left breast. I'm speechless but haven't broke down in front of her yet. More test start tomorrow & Friday. Appointment with oncologist on the 20th.
Chemo then surgery due to the size the surgeon believes.
That's all I have right now
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I am so sorry to hear these results. Your daughter can get through this! I will keep her and your family in my thoughts and prayers. (Hugs)
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Hi!
I was also diagnosed with a 5 cm lump of IDC and had chemo first. At first, I was annoyed that I would have to wait six months for surgery. However, I'm happy that we did neoadjuvant (before surgery) chemo. Every week, I could feel my lump getting smaller. By the time I'd finished five months of chemo, a PET scan and an MRI showed that all the active cancer in my breast and compromised lymph node was gone. As a result, I was able to get a lumpectomy rather than a mastectomy.
Remember that breast cancer is one of the most treatable cancers out there. Even with my big lump and compromised node, my chances of living for years are quite high (over 80%).
Your daughter is lucky to have a Mom like you who can help out and be there for her. ((Hugs))
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I was diagnosed stage IV from the beginning just 7 months ago at age 41 and while it initially feels devastating, it does get better once you have a plan and some control back. This can turn out pretty well in the lower stages and even not so bad as MBC depending on the location of mets. There are threads here for younger ladies and those in their 30's specifically, I would recommend this site to you and your daughter, the support and information here are so valuable.
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Hey there. It will be ok. It breaks my heart to hear your fear and distress because I know that is exactly what my Mom and Dad went thru when I was diagnosed at 33. Guess what? I am 36 almost 37 now and plan to be an old lady some day. Best advice for you, get a therapist where you can vent. You need to have a safe place. Lots of love. 💘
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Thank you all for your encouraging replies. Yes, I believe once everything is done there's a plan in place I will feel much better. The unknown is the worst part. At least we know it's the most common type. Blessings to you all!! You're such Warriors and I am so glad to have this support system.
I'm a level 2 Reiki practitioner and believe in healing through diet as well.
Thanks again. Love & Light 🙏🏼❤️
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simplysammi11, speaking of eating, my oncologist told me 2 things, rather firmly at our first meeting.
1. Eat an at least 80% plant based diet
2. Do not microwave food in plastic (containers, bags)
And I personally believe that exercise is crucial to a good mental state and reduces some treatment related side effects. Not necessarily "workouts", I just really enjoy a couple of 20-30 minute walks per day.
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SimplySammi, - I can imagine how difficult this is for you, as well as your daughter, - but she WILL get through this and be ok!!
My daughter has a 32 year old friend who is also dealing with BC. She, too, is single and was able to harvest her eggs before beginning treatment. She had a dbx, and has only one chemo treatment left. She used cold caps so she kept enough of her hair to avoid needing a wig. Her friends all pitched in to help with the caps on chemo days. She stayed with her parents for 2-3 days after each treatment, but then returned to her own apartment, and to work, and social events. She was able to join a group for young BC patients, - perhaps your daughter can find one, too!
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Hi Sammi. I'm just a little older than your daughter. My mass was also large but it turned out to be not very aggressive.
I know you are in shock. I'm sorry you are both going through this but you will get through it.
I have found a lot of help, answers to questions, and support, within the Young Survival Coalition Facebook group. There are hundreds of young women on there with BC. She will find a lot of help and good advice about treatment, fertility, surgery, etc. Please encourage her to join when she is ready.
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Oh Sammi, I am so very sorry to hear about your daughters bc! We are here to help her and you. Please let us know what you both need. There are forums full of different threads about IDC, chemo, surgery (discussing various types of surgery and reconstruction). If you are looking for something and can't find it, just let us know. The wealth of experience and support here is immense. Sending you both warm thoughts and gentle ((hugs))
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Thank you all for your kindness and support. My daughter had her chest x-ray and bloodwork on Thursday and a Breast MRI w/ contrast on Friday. We go Tuesday for BRCA 1/2 saliva test and meet with surgeon right after for the results of the tests so far. Hopefully by the time she meets with her oncologist on the 20th we'll have results for everything. Again, thanks for the support.
She's up and down right now as expected I'm sure. Her mind always races from one thing to another so she's actually not thinking about all this BC stuff right now as much as I am.
She's already met with her psychiatrist that's really supportive and is starting back with therapy which will help her I'm sure. I'm praying for you all as well. Attitude is so important. Love & Light ❤️🙏🏼
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simplysammi, do you think it would be helpful for your daughter to join the forums here so she can start to get information that will let her make treatment decisions with her team?
" Her mind always races from one thing to another so she's actually not thinking about all this BC stuff right now as much as I am." which is certainly fine, a respite from "all bc all day" is helpful. I just wonder if she is getting up to speed on the lingo and treatment options (pros and cons) so that she can make decisions for herself. It is a steep learning curve (as I'm sure you've experienced reading through these forums). At 30, she is certainly old enough to possibly have different opinions about what treatment she wants. While wanting her Mom to collect all the info and schedule the appointments etc is understandable, it is also important for her to begin to feel empowered in her own treatment by active decision making. Actually initiating treatment (after much testing, deliberation and planning) is a common turning point for many women in their mental road to recovery.
This post was meant to be helpful, not critical. Having a loved one with bc cannot be easy. ((hugs))
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@MTwoman ~ No offense taken at all. I wish she was able to research and understand all of this. She unfortunately suffers from various mental illnesses and hasn't been very stable for the past year.
I would love not to be in the position I am but, it is what it is and it is really sad. Also very hard on my entire family.
I definitely believe if she stabilizes and pray she does so sooner than later that she'll be more concerned and want to learn all she can. But, right now she's just not there so unfortunately I have to pick up the slack.
Her having a complete breakdown at 19 was devastating but to add a BC diagnosis to it is now almost unbearable and why the responsibility is too much, so I reach out all I can just to make sure I can at least try to explain everything I am learning from this site and others going through this.
I'm not an over the line mom at all and have 3 other adult children that fortunately are doing well. (2 married stepsons and another daughter that's 27) My daughter that's ill has experienced childhood trauma by her biological father and trauma since the diagnosis due to manic episodes.
This is a little more than I wanted to get into but, really wanted you to know and others that I'm researching and posting out of love, concern and necessity for my daughter. I pray she comes around and can help me help her. Nothing would please me more.
Praying for you all. Love & Light 🙏🏼❤️
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Oh my goodness Sammi, your concern and role as advocate are most certainly understandable, not to mention commendable. I completely heard the love and concern for your daughter, no question. And do know that no one can be pushed into doing research about a scary health diagnosis - not helpful, and even potentially harmful in her case. It sounds like her current treatment team (for mental health) will be invaluable as well as the new bc treatment team. Bless your heart. I am sorry for my intrusion, I just wanted to welcome your lovely daughter to join us, but totally understand that she will engage as much as and when she is ready. You are doing a great job in using these forums to get up to speed. I do hope that you have support of your own, it sounds like you're carrying quite a load. Sending you and your daughter warm thoughts and gentle ((hugs))
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Well my daughter, Heather, goes for genetic testing tomorrow and then we'll meet with the BS and get results from the MRI, Chest X-ray and her bloodwork. Praying it all goes well. Thanks again all for the support. Hopefully Heather will one day join this forum and research and learn. Blessings to all!❤️🙏🏼
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I'm so sorry she is having to go through this. It is hard enough on us older women. So not fair.
Take care of yourself too.
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Thank you Wrenn
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I'm sorry you find yourself here. I, too, found this website and found comfort here when i found a lump. I had the core biopsy as well. My tumor was a big black blob on the screen and was moderately suspicious. The results came back as a benign Phyllodes tumor. Benign was great to hear but when I visited my oncology surgeon he said... "well it says benign but they want it out because they just aren't really sure". Well that burst my bubble! I just had surgery and the whole thing is benign. I'm 44 years old. Mother of 3. This was my first surgery but it had a happy ending. I know I will never be immune to BC but I can breathe again. I am hoping the same for your daughter. My mother was a mess as we went through this. I just wanted to share my story with you. Hugs. Renee
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@reneeromer Thanyou for your story. I was so praying for an outcome such as yours and happy you did not have BC.
We're trying to take it one day at a time. My daughter has had her moments of disparity but, that's why I am here to fill in the space for her as she needs me. I'm also the researcher of the family so I read a lot although don't always post or reply.
This is a great place to learn things and to get support. I'm sure I will be on here more as we begin her journey and fight. I'm hoping she joins as well. Thanks again for sharing your story. I'm so glad there are those that have good outcomes and benign status. Light & love to you.
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We are all in her corner. Fighting for her. My thoughts and prayers will include her!
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