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.
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I live in california. Where is Sloan? I had breast cancer 13mm in left breast. 92% chance will not come back had lumpectomy. Margins clear. Lymph nodes clear. Did not show up on mammo. Ì felt lump and had ultrsound and showed up on mri. Did not show up on ultrasound til I pointed out felt lump. Opted not to have radiation nor hormone blocker. Will only have mris from now on and ultrasound. Mammo did not show cancer.
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4 ReactionsI went to Sloan Kettering after my doctors watched a lump I has in my breast turn into cancer. If you have cancer go to Sloan.
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4 ReactionsThanks. All good points to consider. I live in S. Florida and since Lobular Carcinoma is at the bottom of the research list, I am looking to consult someone who might be more on the edge of the research.
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1 Reactioncasbc | @casbc
All of us want to have the best and there are many excellent doctors. Luckily I live in Rochester, MN so my choice was easy.
If I had to pick someone at different locations, here are few things I would consider:
1. It is not just one doctor, you want to go to a clinic that provides a team that coordinates your care; oncologist, surgeon, radiologist, etc…
2. Location, though you may be willing to go anywhere for care, think about logistics. If just starting treatment it is many appoints and follow up. Want to go somewhere that is convenient.
3. Insurance, once select a few to follow up on, make sure they take your insurance.
4. Wait time for first appointment, some places are very busy.
5. It is OK to get 2 opinion.. If see one doctor and want to get 2nd opinion, it is OK.
American cancer society web site has article that might help:
https://www.cancer.org/cancer/managing-cancer/finding-care/where-to-find-cancer-care/choosing-a-cancer-doctor.html#:~:text=Choose%20a%20doctor%20who%20has,or%20accepts%20your%20health%20insurance.
Laurie
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1 ReactionHow does one find the top Invasive Lobular Carcinoma Doctor in the USA?
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1 ReactionMy cancer was invasive lobular, HER2 positive, hormone negative. My oncologist told me that women are happy -with their decision once they make it. I'm not so sure. I opted for a single mastectomy and reconstruction. I re-thought this decision occasionally but once everything was done, I wondered If I really needed the reconstruction. I did not have the option of a lumpectomy though. I was 75 when I had to make my decision. That was 2 years ago. We all have decisions to make everyday. Think about where you are in your live. Once you make your decision, embrace it as the best one you could make.
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3 ReactionsSue Ellen, My scenario is same as yours, but I don't want radiation. I also don't want to have to go through with this again, if I can do everything in my power up front. I am not good with "wait and see" as it relates to this topic. I know it's not a guarantee to have mastectomy, but in my mind/emotionally, getting rid of the breast tissue in its largest portion, goes a long way toward decreasing my anxiety about recurrence...lurking masses that previously never showed up on any imaging, despite having 3D mammos every year for several years. The MRI report stated the tumor in the right breast, large clump of cysts in proximity ("probably benign") and left breast with several oval masses "probably benign, recommend MRI again in 6 months". The word "probably" leaves me no consolation. I suppose many might think I am looking at this as overkill, but the reasons for me are many, including having watched a very good friend die a miserable and painful death from peritoneal cancer and know that ILC has a propensity for the peritoneum, bones, along with GI tract if it decides to show up and live elsewhere. Some people are willing to roll the dice. I am not. Now, might the plastics guy talk me into a single? Maybe. I won't close my mind to it, but my inclination/spidey-senses are telling me to do the double.
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6 ReactionsHas anyone had experience is asking for liquid biopsy or contract enhanced mammo. I was disappointed as at my one year out ILC (lumpectomy , 19 radiation, letrozole) appt with onco, she couldn't be bothered to answer either of these questions and this is at Dana Farber, Boston. In Boston I do know that Beth Israel offers CEM and while MRI the goldstandard especially for use dense breasters but CEM is a cheaper, often more approved by insurance option. I believe Signatera is good for liquid biopsy but not sure how to find out more! Any thoughts? xo
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3 ReactionsWhat did your MRI report? I'm also 58yrs old and one year out from stage 1A, grade 2 ILC in right breast (easier in terms of radiation) - just shy of 2cm - prob misssed due to very dense breasts. I chose Lumpectomy (at MGH and Dana Farber) as studies showed no upside in masctemomy and a mastectomy seemed overkill at this point. I'm very happy with my decision and I will advocate for alternating mammo and MRI - ILC if mets it usually not within 5 yrs and typically not contrabreast. Good luck!
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3 ReactionsRegarding your aversion to radiation, my question is whether you have investigated the possibility of proton radiation. I have ILC, I had a lumpectomy , and spoke to my radiation oncologist. The photon oncologist recommended 4 to 5 weeks of daily radiation. I then scheduled an appointment with a proton radiation oncologist who suggested that two weeks of radiation was all that was needed. I elected to do that. I also used Mepitel film to cut down on any potential radiation dermatitis. Radiation was the easiest part of this journey. I also elected to do the radiation because I Wasn’t sure if I would be able to handle the aromatase inhibitors for a number of different personal reasons. I ultimately decided not to use the AI and having the radiation cut down my risk of recurrence by the same 50% that aromatase inhibitors would do. I hope this helps.
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