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In Memorium - sadiesservant
I wanted to let members know that our sweet, kind sadiesservant passed away on June 1, 2023. I only found out a couple days ago and got confirmation on it before I posted (thank you, chicagoan). I do not know any details, other than she’d been having some additional complications since about the beginning of the year.…
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Ibrance
I have been taken Ibrance with AI for over 2 years. I have bone only Mets when I first diagnosed as MBC. Ibrance worked very well in the first year and second and brought my CEA to 1-2 range. Since early this year, my CEA went up to 3, 4, and 5. My CEA lab yesterday is 7 and CA15-3 is 37. My CT/bone scan shows no changes…
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Operation in 4 stages
Hi all. I know that they don’t do surgery at stage 4, but I know cases when surgeons took it and performed the operation. I don't see similar threads on this forum and would like to hear from you.... Have any of you had stage 4 surgeries? Maybe someone knows such cases?
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Anyone else with just liver mets
is there anyone else on the board with stage IV only in liver? It seems everyone else has liver and….bone,brain,etc. I’m not complaining but at age 77 keep wondering what’s next or if we are missing something. I feel so sad for the young women and feel I’ve had a full life and I know where I’m going when I die. Not in a…
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Newly Diagnosed liver/bones LOOKING FOR LONG TERM SURVIVORS/HOPE!
Hello there, After 10 years of stage 2 breast cancer, 3 months ago I discovered it has returned stage4 to my bones/liver. I thought it was all behind me… I am finding it so hard to cope & terrified of my future, especially being a mother of a young child. I am hormone positive, Her2- I would love to hear from others with…
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Cognition issues
Hello First post, from UK. Stage IV with bone mets, diagnosed 2022, after first multifocal diagnosis in 2018, mastectomy and DIEP. Stable so far with abemaciclib, denosumab and letrozole. Just started on Serena6 trial. I've been so impressed by the ballsiness of this forum and the amount of knowledge and critical thinking.…
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Lymphangitic Carcinomatosis - Can anyone relate?
I was just diagnosed on Friday (7/7/23) with suspected lymphangitic spread (lymphangitic carcinomatosis?) to the lungs after being stable with bone only mets for 3.5 years. I'm a little devastated after meeting with my MO. I'm just wondering if there is anyone else out there living with this? At this point I have more…
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Is there anyone here on Margenza?
I have a friend who is about to start Margenza with the chemo Gemcitabine. She would like to know what she might expect with side effects and how this has worked for you. This is for mets to the liver. Thanks
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Morphine, Bone Pain, and Bone Loss in Metastatic Breast Cancer
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Bone Mets active again after 12 years
Hi all! Second treatment has now failed after 6 years (first lasted 6 years also) Ibrance/Faslodex/Zometa has done me right for quite awhile. Time to move on to the next option. Sad/scared/pissed/all of the rest of the emotions. Still planning on kicking it’s butt, but hate to have to restart.