Hi Sheila
youve dropped it of sight
how're things going?
Hi, I can really empathise with you not wanting to let go of something that is/was working, I hope you find out what's happening as that's the worst part, isn't it.
Hugs and love
XBlannaX
Thankyou Smelliedog...I'm sorry about the medical speak...I was exactly the same as you a year ago, and I spent a lot of time reading absolutely everything, on here and elsewhere, and I wrote down my questions before I went to see the oncologist. I think the biggie for me is that there never seems to be a definitive answer, as we are all so individual in our responses to cancer. The last registrar I saw before Christmas was delighted with my response, and said I could expect to be around for "a long, long time". I've had 9 months of being "clear" and thought this would continue for a couple of years at least (ever the optimist, lol) so I am now back to dreading the next clinic and having doubt. I think I was pretty calm at the start, almost resigned to my fate, but now a year later I am less so. It's ironic that I am less ready for bad news.
The one bright spark is that I have recently met someone, and may have some support at last. My son, 20yrs old, is ill prepared for anything negative so I sugar coat what I tell him. Meanwhile, I'm starting a notebook of things he needs to know how to do, and when!
I'm off to the Day Unit this afternoon for my regular treatment, Herceptin and Pertuzumab, wondering if it will be my last of these drugs.
Good luck with your consultation...be prepared!
Hi there - I think you are in a slightly similar quandry to me. After a lot of messing about which I won't bore you with, a week today, 1st June, I finally get to see my oncologist. At the moment I think I have cancer in neck and spine and these are secondaries.
Some of your message was in a foreign language to me - not your fault! I'm at the very start of a new journey when I see my oncologist and I don't know what questions I may need to ask! I too am on my own and don't have someone to chew the fat with! Perhaps we can support each other!
Smelliedog xx
Have they considered TDM1? kadcyla.
I think that this drug is appropriate for those who have had Herceptin.
my lumps under my breasts are just scar tissue.
Hi ladies, it's been last summer since I posted on BCC forum (I started a private fb page and have a lovely group of mixed primary and secondary ladies, very supportive). I feel today though that I can't really get the right help there and am hoping for your advice.
I was diagnosed double whammy last April, with secondary mets in liver. I went straight on to chemotherapy, having a course of docetaxol in conjunction with Herceptin and Perjeta as HER2+. My CT scan after Docetaxol and again in late November showed no signs of the disease, yippee!!. I have been having 3 weekly H&P, with one period where I went 4 weeks between (in February). I got CT scan results this morning at 12 weekly clinic appointment and have been told that although my liver mets are still nowhere to be seen, and my lungs/thorax is clear, I have a recurrence in left axilla (2 nodes, 14mm and 12mm). I had an exam, and the registrar couldn't find anything (deja vu, as I had no symptoms pre diagnosis). I have slight pain in both breasts, in the areas beneath the skin where my underwire bra sits, for the past month, but again on exam she couldn't find anything..Registrar was not sure how to progress, as there is a good chance they will stop giving me herceptin and perjeta (cost is too high if there is progression apparently) so she's seeking advice from a senior doctor and asked that I come back in 3 weeks. Meanwhile, continue with the H&P treatment.
Now, my point or question FINALLY?? What should I be asking for at this meeting? I don't know what to expect. I was reminded that there isn't a lot of different treatments; I can't remember what she said I might be moved on to. I'm scared that the H&P is "gold standard" and I will be on a downward path already, within a year...The last registrar I saw in December was delighted to tell me I would be around for a long time, and that I was responding very well to treatment.
So, can anyone else tell me what happens next? Should I ask for a more detailed scan, like an MRI to check the liver? Should I consider radiotherapy for the nodes?
Sorry about the length of this...I don't have a special someone to share the burden or help with the decisions. Thanks xx Sheila