Forum Discussion
New to sharing
Hi all, first timer here I was first diagnosed May 2013, 6 rounds of chemo, 30 radiation treatments, then Tamoxifen til 31st Oct 2017 when my world fell apart, bone , lung, and a few other places mets, nail inserted on 24th Nov, lucky to get a place on the ribociclib compassionate access program, combined with letrizole and denusomab, mixed results so far. I am still trying to get my head around this. I am so tired most days and pain is my new normal. Anyhow, just wanted to say hi, I usually keep pretty much to myself but it's good to know I'm not alone.
15 Replies
- Hi Kattykit,
Do you have a hopes and hurdles kit ? https://www.bcna.org.au/resource/kits/hope-hurdles/
feel happy to vent with us ask for support and share and read the posts .... Yes unfortunately we are not alone..... but this forum is a great supportive environment for anyone going through BC - Welcome @kattykit. Share away whenever you need to.
- Welcome @Kattykit, and wishing you all the best. This disease totally sucks.
XO - Big hugs and welcome @Kattykit xoxoxo
- Hi @KattyKit. I am sorry you have found yourself here, but having said that, it's a wonderfully supportive, warm and helpful place to be.
You are having a mo fo of a tough time but you are definitely not alone. There are lots of women here who are experiencing the same as you, and even thriving from what I gather. Keep sharing, and hang in there. Big hugs. K xox
