Hi Laramp
I am SO Sorry to see you join the club that no-one every thought they'd be joining 🙁
I only had lumpectomy, so whilst waiting for others to reply to your post, I'd suggest you join the Reconstruction group here as i think you'll get a more dedicated answer:
Group: Choosing breast reconstruction | BCNA Online Network
I'm glad you've found us tho - as you've found the right spot here for support & info from those who've 'been there, done that'! So hopefully we'll be able to smooth the way for your own story. Make sure you take a trusted friend or family member with you to your early appointments, as a 'backup set of ears', as it is difficult remembering everything that is said. Also, consider recording your sessions on your phone, so you can go over it again later, for the same reason. 😉
Mine was ILC - I was lucky to only have the one lumpectomy, rads & tablets .... and have recently finished with the tabs now!
Whack up ANY question - remember there are NO dumb questions!!! This diagnosis can really muck with your brain too - so if you feel sad, angry, distressed .... ask your GP (or your treating team) for a referral to see a counsellor .... or listen to Charlotte Tottman's podcast (link below).
She is a BC specialist counsellor who was diagnosed herself, also had a double mastectomy, so knows EXACTLY what we've all been thru, both emotionally and physically! Her own reaction to her diagnosis was also quite different to what she 'thought' it might be, given that she'd been counseling women's reactions for some years before, so thought she 'new' what to expect! She is VERY easy to listen to, too xx
http://www.drcharlottetottman.com.au/my-podcast.html.
There is HEAPS of info in the link below to help you navigate the blog and also some tools to evaluate your own physical and mental recovery thru your ongoing treatment! xx.
https://onlinenetwork.bcna.org.au/discussions/general-discussion/a-big-welcome-to-all-new-online-network-members-/222737
Take care & all the best for your surgery & ongoing treatment xx