Number 3 …. Half way there… Sort of! They have added an extra FEC cycle. Reason: I didn’t get enough of the Epirubicin, as it leaked into my hand In round 2 (sounds like a boxing match when I say it like that) and then what I had was counteracted by the antidote.
So I just had a full round and then next time I am having a smaller FEC Cycle (full 100ml each time but 75ml instead ….I think… Don’t quote me).
Today went well! Which is good I am now just lay in bed chilling, trying to rest and then fall asleep after I have written this knowing me!
I caused mayhem again! As ever! You honestly wouldn’t believe me when I say the male nurse in there has now told me and Cass He is booking my next FEC treatment off! 😂
I told Cass to make me a tea and herself a coffee as I did yesterday when I was in the waiting room to see my onchologist after my minor surgery – not sure I can really say it’s surgery but an insertion. No that sounds bad we will stick with surgery and I’ll explain that later! But anyway, I digress, she got told off, she’s not meant to touch it. And the man (really nice guy – they all are in there to be honest) said she cant touch that laughing and I was like I did yesterday, I’m not telling you who told me I could though 😂😂). That is probably funnier in my head than in writing and reading. Any which way I got my cup of tea!
This time instead of spending a small fortune on food and drinks we had the provided tea and coffee rather than Costa. And brought our own homemade chicken, avocado, salad (mine in a wrap… Cass no wrap… I know I was naughty having a wrap but it tasted so good!)
So chemo went well, as ever I had a sneezing fit at Epirubicin, which is completely wrong… Everyone else sneezes (if they react) to a different drug of the 3 but not me! So my wee is now red already and my mouth tastes of iron and I’m just hoping all the anti sickness drugs work on the full dose of chemo I had as well as they did on the slightly less one last time!
I tortured the ward with my selfie stick everyone laughing at me, but I tell you there were a few converts that want one now I reckon. I even used it as a devise to poke my anti-sickness drip to see what it was (I can’t remember, already!)
Anyway, as you can see my chemo now goes through my upper arm and not my hand. I have a brightly coloured contraption sticking out me, but it is all wrapped up so no scaring any small children and I opted to wear a tube grip over it so its just not so unsitely, I know I talk all these selfies and post them on this blog and Facebook, Twitter,….. Ok and Instagram 🙈😂 but I’m quite a paranoid person so have real … ‘Are they staring at me?’ Issues! I like to be in control of what people see, I guess, who knows how my subconscious psyche works!
So to have the pic line put in I had to have a local anthestic, I get laid on a bed and they guide a pic line to your heart by ultrasound then check it with an X-ray then push and pull it around a bit more and then off you pop all done. It is quite strange feeling all the pulling and pushing. But I had a really nicer radiographer who was chatting to me (distraction technique) about holidays. And as those close to me know I’m always happy to talk sunshine and tanning (and food).
So it’s in, it’s gross and I dread it coming out, but true to the many people who said it to me… Chemo through that was easier.
So that picture above is what is looks like inside me and this is what I have.
Then below is how it looks after the chemo nurses bandage it up a bit further and I just Pop a bit of tube grip over it. Happy days.
Well I’m off for a sleep now! 😴