Metastatic breast cancer: Anyone else?
Hello...I am new to this site. I had BC originally in 1989 with lumpectomy, chemo and radiation. After 4 months of pains, thought to be muscular from lots of tennis, xrays revealed cracked vertebraes in the spine and led to MBC diagnosis, to the bones. I have been receiving xgeva and faslodex injections once a month since February 2015. One round of radiation in August to the hip eliminated that pain by reducing the tumor. Just wondering if there is anyone out there in a similar situation and how are you doing??
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Faslodex. It’s a once a month injection. Looking for a oncology clinic close to home to start my injections. I currently just gi to Mayo for everything and I’m in Tennessee
I am hoping you find a more local oncologist for your care. Have you asked your team at Mayo about helping you find local care?
I’ll be starting falsodex treatment soon. I was on Ibrance for 2 and a half years but it stopped working. Now we’re trying this.
Since I’m just getting shots they said I can go anywhere but I’ll still be going to Mayo for that oncologist and to get all my scans every few months.
I would go to Mayo for scans and checkups if I lived closer. They are so amazing. Crossing my fingers for you to find a local clinic for your injections, and for positive results with the new meds.
I'd like to welcome @mssewest to the MBC group.
Mssewest, would you mind re-posting your story here?
Please join us in the best group you never wanted to join. @mssewest
Sure, thank you Colleen
I would advocate for yourself and ask your doctor for a PET Scan.
They require intense unchanging pain that is localized. I advocate for myself, believe me. My point was that some of us are in pain a lot of the time so how to ever distinguish.