Hi, I’ve not been on here for about 4 years but here I am again. Just been told I hav bone mets in about 3 areas. Thankfully CT showed it’s no where else. I’m just after help and advice. I’m still waiting for appointment to discuss treatment. Thank you in advance, Pauline
Hi Pauline, sorry to hear about your mets, im quite new to the forum too.
Had primary 7yrs ago and found i had bone mets in March in my hip, spine and ribs, a real body blow!! Like you CT scan showed its no where else and im praying it stays that way.
My onc has put me on tamoxifen and also zoladex injections to shut down my ovaries, iv also just been started on Denosumab injections for my bones.
Hope this has helped a little, im sure you will get lots of help and advice from the other ladies on the forum, good luck, stay strong and let us know how you get on at your appt
Janette x x
Just wanted to say hello Pauline and sorry to hear you have bone mets. There is another thread "bone mets please join in that is very active at the moment but I’m sure others will spot you soon. I’m currently on Letrozole which may be one of your options depending on your hormone status, it’s an AI inhibitor others seem to be on bisphosphonates aswell to help with bone pain and strength. But my onc has decided so far not to give them to me. So it will be interesting to hear what they offer you but good luck hope you don’t have to wait long for your appointment. Look forward to chatting xxx