Lobular Breast Cancer: Let's share and support each other
Since lobular breast cancer is only 10-15% of all breast cancer diagnoses and now understood to be a unique subset of breast cancer as a whole with different characteristics than ductal breast cancer necessitating different treatments and inherently different risks, I would like to see a separate category under the breast cancer forum so that the most appropriate info is being disseminated for this specific subset of BC. Just a thought.
Interested in more discussions like this? Go to the Breast Cancer Support Group.
Hi @trishc, how are you doing? Don't forget that everyone reacts differently to medications and that people who do not experience challenging side effects likely do not report on a forum like this one. So it can give a biased view. Forums like this one help women cope with managing side effects and discussing options.
Your oncologist will review the various options available for you, and the pros and cons of each. Ultimately, the decision is yours. You are in control. Did you have the consult with the oncologist to discuss hormone treatment?
Thank you-so glad to have found this discussion. I have a super supportive hub and fam and friends but its just not the same. Its a road you dont know or understand until you are on it. Of course stopping all HRT in december has thrown me right into terrible night sweats and insomnia, not helping, and also makes me dread the hormone blocking meds. I will be following this group/posts and wish everyone well. ❤️
Hi - Hang in there and so understand where your "are" - I finished my 19 radiation treatments last week and my onco likes to wait two weeks post radiation to start anti hormone meds. I'm 57 and will start on letrozole which I've very anxious about but taking one day at a time. I think your plan for re-excision sounds very similar to what my plan would have been had my margins not been clear. Once you get your oncotype results you will have a better roadmap in terms regarding if chemo would be part of the plan. I also was anxious about lumpectomy vs mastectomy but I am now very comfortable with lumpectomy decision as the science really does say in our cases the mastectomy doesn't impact the rate of re-occurrence. Don't look back on HRT treatment as who knows whether that had any impact. Keep us posted and hang in there!!
Hi..I am getting results of my biopsy tomorrow.
Diagnostic mammogram classified mass as highly suspicious. I am 72 and with no family history, this has devastated me.
I have had a knot 🪢 n my stomach since the biopsy last Thursday.
I writing this because I know all of you have been where I am tonight.
I am so scared.
Thanks for listening.
Hi there
New here. I was diagnosed in dec with ILC 2.1 cm. Had lumpectomy and sentinal node removal last week and found out 1 node had "rare isolated tomor cells". My margins weren't clear so I have to go in for re-excision. I am feeling very anxious about lumpectomy decision bc possibly mastectomy could be done. But Ive been advised that outcomes were same for both options and conserving breats more ideal for me? I am small chested and feel like if it doesnt help outcome why go thru all surgeries/spacers and implants? The plan is radiation starting about 4 weeks after final re excision and unsure about chemo, then the hormone blocking meds for post menopausal. You seem to be in similar situation and to everyone reading does this seem on par with your plans if similar? Were you recommended same plan? Any input so welcome. This all is just brutal. Oh and FYI I had been on HRT for 5 years bc menopause was so rough (i am 55) and MD said I was a good candidate bc no history of breast cancer.
Newly diagnosed with invasive lobular cancer as well as DCIS. I am very interested in all information I can get. Thanks for starting this thread.
I agree, push for a PET scan. It will show everything you have. When you go to your appointments be armed with all your questions and write down the answers or record the session on your phone or have someone with you to be the designated recorder. When you schedule your tests scans or otherwise if they aren’t soon enough ask them to call you if they have a cancellation. Or call
Every day if you have to. Everyone of us are unique so advocate for you, ask questions and get answers. This is not a one size fits all disease. All of us here have been through or are going through what you are going thru. You will get great support here and anything you need to know pretty much someone has an answer. I pray you have the support at home to see you through this difficult journey.
I highly recommend you be your own advocate. Demand a two week turn around for your biopsy. Push your DR., one who schedules your mammogram, to get your appointment moved up. It's critic for both your physical and mental health. Or tell your DR. you are open to traveling a reasonable distance to get the biopsy. DRs sometimes forget that they signed up to help their patients get the care they deserve. They focus on the immediate need of the current day...they need to be as concerned and helpful and motivated to get you that appt and then continue to push the follow up.
Ask for an MRI. Do you have dense breasts? If so, that's the only way to see thru all the strata that dense breast have. Take control of your situation. I urge you to be
your own advocate.
Either an MRI or a pet scan. Mine showed up on a pet scan