Dear BCN community
A warm thank you to everyone in the community. I’m new to BC and also to the forum, but have found the personal experiences & information shared here so helpful.
I was diagnosed with Grade 2 IDC, no sign of lymph node involvement in ultrasound, ER+, PR+ and HER2 negative last month. An MRI was done due to dense breast tissue, now awaiting the biopsy result of a 2mm dot that was observed in the MRI. The SLNB and wire-guided WLE that was originally scheduled to happen this week was rescheduled to allow time for the latest result. My surgeon explained that if it turns out to be positive that will mean two WLE’s. I now have some unrelated questions.
- Do you normally get a copy of your biopsy pathology result before surgery? Or is this best left until post-op pathology results are in?
- Has anyone been through anything similar in terms of two lumpectomies on the same side? While I await the second result, I was wondering whether it’s usual practice for the surgeon to make the decision about the type of procedure (lumpectomy vs. mastectomy) in such cases? When I briefly asked about the decision between 2 lumpectomies vs mastectomy, the surgeon mentioned that where possible they would always go with breast conserving surgery, which I do get but still wonder if I should be asking any other questions? I’m trying my best to reduce the number of questions I ask as my natural tendency is to want to understand the reason/background rather than just being told this is how it is. But have found that getting the how/why answers to questions is not as easy as I thought it would be, partially because this is all so new to me and I expect that they must be trying to limit what they share for some logical reason that I haven’t quite figured out yet. On reflection I am thinking it may be their way of trying to reduce information overload, trying to share information in a staggered manner, or that they probably don’t have the answers themselves, even though I’m looking to understand the broader picture, a professional/personality trait.
- I have sensitive skin & have also had allergic reactions to the adhesive in plasters, which has then taken many weeks to heal. So I’m trying to figure out how I can avoid this happening post-op. My most recent allergy was to the adhesive in the dressing that was used to cover my biopsy site (only kept on for 24 hours). I keep repeating this allergy when asked about allergies but don’t feel it’s necessarily high up on the priority list when it comes to types of allergies/problems. Perhaps irrationally, at the moment I’m more worried about the adhesive in the dressings that will be applied & kept on for many days post-op, than the actual op itself. When I asked my BC nurse about this, she said that would be a question for the surgery team nurses. But wouldn’t it be too late to just mention it on the day of my op? And on top of that I am now wondering if they use glue instead of stiches post-op and what if I’m allergic to that too! Does anyone know if they use glue or stiches for a lumpectomy? And is there such a thing as hypo-allergenic stitches/glue & dressings that they have in hospitals that I can request? I may be worrying over something trivial but was wondering if anyone had any information or advice that would help.