I was diagnosed on 7th Nov with T3 N2 OC, and then went on 2 cycles of 21 days of CX.
on the 25th Jan I've had a scan to see the effectiveness... the aim was that it would shrink the tumour... I had been told back in Nov by two surgeons that they were confident they could operate and the chemo would make it 'even more' successful.
Wednesday I got initial CT scan results and annoyingly the primary cancer has not shrunk, its got larger... and it's spread to my ribs.
I get more info on Monday afternoon.
I feel totally devastated and all my positivism has drained away.
Since a few days before the last chemo tablets on the 24th Jan I have had difficulties with swallowing... to be fair, up until then, I had pretty much been okay within reason.
I am now anxious to hear what the next options, if there are options will be.
I just wish they had removed it initially, but i don't recall getting the option that it was 'optional' to have the chemo. I have subsequently read that some people are more involved in their treatment plan... admittedly I would have probably said yes because I think/thought the MDT team know best.
Its going to be a long weekend...