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Here's the local newspaper's report about the Childer Award Presentation at the Town Hall last week. Jaime received a medal and is in the middle of the group photo.
"All sorrows can be borne if you put them in a story or tell a story about them."
(…and apologies to anyone (a) under 40 and/or (b) not a Brit as that cultural reference will have gone over your head without parting your hair. Yes I am over 40. I realise that is a shock. I should break these things to you more gently, I know.)
I’m into the final furlong of my week at the Christie, the end is hopefully in sight, and I get out tonight. (Sweet Bird of Space, hurrah!!)
It’s been a mixed week – mostly the choice being which meal shall I barf up next?
In addition, I had a ‘fabulous’ Friday wherein I hurled myself out of a bath and nutted the (very sharp) edge of a hazardous waste bin. Yup, a drama queen to the last, huh? Clearly I wasn’t getting enough attention throwing up, so I decided to throw a faint for a change. One moment I was towelling myself off, the next minute I was flat on my back with my heels in the air (if anyone dares say ‘no change there, then’ I swear I shall SUE your asses), surrounded by nurses asking me how many fingers I could count.
I am now sporting a fine scar, picture attached (only if you have email – sorry Myspace friends, I’m so not posting it). I think the dopey grin is sheer relief that I didn’t faint while I was IN the bath… hmmm.
But my week has improved dramatically since then (could it get worse?) when I discovered that I could order halal meals – yes, CURRY!!!!
For some bizarre reason I thought the halal menu was for Muslims only, but no, not at all. Since then I have been stuffing myself cheerfully with real food. Rice! Veggies! Biriani! Wheee!
.. And I’ll be honest, I think one of the reasons I’ve been so bloody queasy is that the hospital food, though ‘nice’, is nothing like the food I eat at home. And it has been difficult for me to digest anyway… even without chemo to help it on its way.
So my lovelies, take care out there, and Nil Illegitimi Carborundum.
Rosie xxxx
IV Bag Lady
Or evening, or middle of the night depending on which time zone you’re in… yes, that would be me showing off at how far flung my friends are. Ahem… Hamburg, Rotterdam, Amsterdam, Stockholm, Dallas, San Francisco, NYC, Buenos Aires, Sao Tome (look it up, you lazy lot), Winterville GA (honest, not making this one up), wonderful wonderful Copenhagen – not to mention glamorous Widnes and even more glamorous Salford!
Right, showing off completed – for now (he he he).Yes, I’m checked back into my glamorous boutique hotel – er, ok, the Christie.
And for anyone wanting to visit me this week, I’m on WARD 11!
A whole different part of the hospital too, so lots of exciting new opportunities to get lost while you’re trying to find me. Although this Ward does seem to be better signposted…
Anyhow, it’s Day 1 of my treatment and naturally I am pretty perky after two weeks respite. I managed to wean myself off Buffy eventually (thank god) as my brain cells returned. You’ll be pleased to know that she did manage to slay all those pesky demons – I know you’ve been holding your breath over that one.
I even did some gardening yesterday! I find ripping up weeds and hacking at things with shears most therapeutic…
I thought I’d send an update now before the drugs kick in and I start feeling GHASTLY. I’ve just poked down a big plateful of veg moussaka with rice followed by chocolate sponge with chocolate custard (delightfully reminiscent of school dinners). I might as well stuff myself while the going’s good.
…and bizarrely, I have lost weight over the past 2 weeks – it hardly seems possible, considering the way I’ve been eating for England. I dunno, maybe chemo/cancer shifts one’s metabolism into a higher gear?
So, nothing profound or zen today folks – just sending love to you all.
Keep rubbing those lucky pebbles & sending Rudie Vibes (you know who you are), lighting candles, or crossing all crossable body parts – whatever it is you are doing, it’s working!
Rosie x
(Aka Barfy the Cancer Slayer)
Then they locked up the social democrats
I remained silent;
I was not a social democrat.
Then they came for the trade unionists
I did not protest;
I was not a trade unionist.
Then they came for the Jews,
I did not speak out;
I was not a Jew.
When they came for me,
there was no one left to speak out for me.
Hello darling friends,
And welcome new friends who have just joined this list!
Needless to say, if anyone is fatigued by / bored with these updates, or if they just aren’t your bag, do say and I’ll take you orf.
Right! It’s a week since I got out of The Christie following the second round of chemo – and oh GAWD have I been knackered…
So apologies if you’ve emailed me and I haven’t responded, or have drooled inarticulately at you (something I do very well, apparently).
The drugs were ‘fun’ - the first one (Taxotere – you can look it up if you’re that way inclined, I am still not going anywhere near t’interweb) I don’t really notice because it’s only pumped into me for an hour. The second one (Cisplatin) is shoved into me for 6 hours, and that’s when the amusement starts. Has the dual effect of making me barf AND sleep! Luckily not at the same time… Just when I’ve got over that I get the third drug for days and days (called 5FU because no-one can pronounce it. But it does sound something like an Aztec god) which stops the barfing, but turns me into an insomniac!
Wheeee!
So, cue inspirational power chords on guitar and Alice Cooper yodelling Poison… runnin’ though ma veins…
It was also quite a Zen week. I shared a bay with two women, who were very similar in some ways – both in their seventies, both pipecleaner thin, both with completely ruined lungs and spent most of the day on oxygen / nebulisers.
However.
D. was sparky, cheerful, delighted to see her visitors, enjoyed little pleasures that came her way like one of the nurses taking the time to blow dry & comb her hair, or wheeling her and her oxygen tank into the garden. She told me how she used to be a real worrier. ‘But I don’t worry about anything now. I just enjoy life.’
Then there was L, for whom nothing was enough. In the week I was there she saw more doctors, health care workers, occupational therapists, masseurs, nutritionists, family and other visitors etc etc .. and yet she still said ‘no-one ever comes to see me.’
She moaned about no-one caring about her food – despite having a special diet menu made for her. She was fully mobile (unlike D.) yet, when asked if she’d like to go and sit outside in the garden in the astonishing sunshine, her immediate response was ‘I’d never find my way there.’ When reassured someone would take her, she responded ‘I’d never find my way back.’
The joys of hospital life.
Anyhow, I am back home, and am just about vertical. Have spent much of the week watching Buffy for the umpteenth time as my brain hasn’t been capable of much else… Run, Buffy, Run!
Love and gorgeousness to you,
And here’s to lumps buggering off completely,
Rosie xxxxxxxxx
Recycling Radioactive Waste So You Don’t Have To
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