Forum Discussion
Emotions and costs of BC
Since the initial shock of diagnosis I have had so many emotions and many new ones and unfortunately many old ones. Something that has bothered me from Day one is the feeling that we, newly diagnosed...
When I first got diagnosed in October 2015, I was told go public even if you do have health insurance. All my scans and surgery back then was no out of pocket expense which was good since neither my hubby or I were working and we aren't old enough for an aged pension. We used to buy and renovate and rent out houses but no way I can physically or mentally do that now. I just had a follow up ultrasound, thru the public hospital who works in with the private hospital and the ultrasound was free for me. Not sure how we'd cope if we had to pay for any tests. Heres something to bolster up your depression. We all care for you. <3 http://https//www.youtube.com/watch?v=rOr38bGCZto&feature=youtu.be&utm_source=ThePianoGuys&utm_campaign=1b48ff75f8-celloopa&utm_medium=email&utm_term=0_005ec3cc31-1b48ff75f8-15139069&goal=0_005ec3cc31-1b48ff75f8-15139069&mc_cid=1b48ff75f8&mc_eid=3dff6cb11c