Hi I’m 53, been diagnosed extensive bc mets to bones & liver. Diagnosis 3 weeks ago, 4 years on from original bc. HER2+ Stage 3, right breast mast.+recon(diep). Have had debilitating back pain for last 6 months - Doc eventually referred me for scans. Been non stop hosp appointments and phonecalls (due to Covid lot of info been given to me over the phone) so I only saw my scans yesterday with orthopedic specialist - they want to operate on left femur). Next week 5 sessions of radio to 2 spots (shoulder & hip) started on Let. already, Pal.+bone strengthening drug to follow week after. Pain has been level 10+ for weeks, they are finally getting a pain specialist from the local hospice to work with me. They’ve had 3 different oncologists speak to me - I’ve found them all cold & patronising. Today I was at radio planning & onc kept saying “you are going to die from this” & to majority of my questions “v good question but I don’t think it’s helpful to discuss now”. The mets are extensive in my spine, plus skull plus sternum. Told prognosis by oncs “1-2” “3-4” & today “3 months to 10 years”. I feel I can’t take it anymore. I’m completely shattered. I’m freelance so will prob lose my work. I feel a “number” with these consultants. I’m not an idiot & I don’t know why oncs are so cold. Already I’ve had friends say “I don’t know what to say” & then rush off the phone. It’s all been so fast. I live alone - keep thinking about a painful death because the pain has been so bad.
Best wishes, AlisonMac