Hello Cruel World
Friday, November 13, 2009
Contemplating yesterday
Don't really like that word "palliative", when it's used in my direction. "Curative" or "healing" would be much nicer. Doctors say most important thing is to make my quality of life as good on possible for as long as possible.
OTOH, not having something to "make me more comfortable" is an even worse thought. Much medical treatment is a lot like torture with good intentions (even with pain management). I've definitely learnt cowardice, like the burnt child fears the fire.
Should really get on with photo books & "arranging affairs" (@#!&*%*#@!! paperwork). Probably in some kind of denial/ultimate procrastination. Don't appear to have learnt anything important from the last 10 years of "teaching experiences". The stupid must go right to the bone: Cue one of Pris' better-known quotes. Still, market for inspirational books (Above It All: My Spiritual Journey from Cancer to Climbing Mt Everest in a Wheelchair*) must surely be glutted now. So many people are getting to ages of more illness, there'll be more authors than readers.
Feel better after blood for anaemia yesterday (Vampire Mez. Practicing accent: Wampyr.). Charcoal tablets seem to be working, too, unless some other thing is helping reduce gas explosions. Will add to stock for trip. Another landmark: got Nelune car lift to hospital because was scared if I walked same gas blow-out would happen as the other day when I tried to go to pay bill, shops.
Was going to discuss "palliative" with friends — being up at hospital with them, back in Rehab (separate room, with openable window, own toilet, relative peace and quiet), after treatment and appointments — but got distracted talking and dealing with odd problems that popped up.
Hope your Black Friday went well.
* Note: Not entirely a joke. There's a new one out about a couple of Aboriginal(?) footballers(?) travelling out in the desert, one of whom is in chemo/radio therapy at the time. (So either it's a short trip or they've spaced out treatments longer round the trip or it's actually just after treatment.)
[UPDATE] Kurt Fearnley, who normally uses a wheelchair because he was born with the lower part of his spine missing, went back to his childhood form of locomotion — pulling himself along by his arms while his much-shrunken legs trail along after his body — to crawl along the entire Kokoda Track because the steep slopes & muddy ground made using a wheelchair impractical. (Up & Down Stories – Kokoda & Me) While I have to drop my shopping and lay down for quite some time just after going around the block and climbing the 57 steps back to my flat, and he's an athlete. (See news.smh.com.au/ breaking-news-world/ exhausted-fearnley-finishes-kokoda-crawl-20091118-ilga.html.)
Labels: cancer, medical, medicine, quotidian, stroke, thoughts, treatment, words
Friday, October 16, 2009
Chemotherapy + Gripe
NOTE: Skip this to avoid whinging, complaining & yukkiness.
Think I've washed most of the cytotoxins and their accompanying protective drugs out, as far as possible, so started on the new drug from specialist.
Eating as healthily as I can manage, with fresh fruit & juices, vegies, fish, organic meats & milk, nice bread, etc. Have the best emergency low-prep foods I can manage — low-processed frozen food, parboiled rice, dried pasta from different grains. There's a few made-up "boil in the bag" meals that don't need freezing & some canned stuff in case of times when I just can't manage anything more.
Near low-immune part of cycle, so I'm doing things like throwing out any slightly-suss food, rinsing plates & utensils in boiling water, cleaning surfaces, using different sets of rubber gloves for handling different stuff, washing gloves in disinfectant, washing my hands with sanitizing stuff before eating, or after toilet. Being extra careful not to get nicked or bruised, staying away from crowds.
So WHY am I exploding hydrogen sulphide gas from both ends like a locomotive blowing steam!?!?!? Diarrhoea for about 24 hours. Now this morning, without more food today than some ginger to try and settle stomach, brought up half a litre or so of bright yellow bile. Bleurgh.
Is it new drug? Did I pick bug up in Rehabilitation Unit, where they had gastro going round erlier? Was food more suspicious than I suspected? Or what? How?
Just what I need when I'm already weak & tired & really low & washed out. Bleah.
And I definitely don't want to take this in to sick friend, or his partner. Will try some peppermint tea soon. Maybe barley sugar to keep up energy.
Labels: chemotherapy, medical, medicine, personal
Wednesday, October 14, 2009
Friend's Stroke: some wonderful news
I haven't been too well, so haven't written much, and, worse, haven't been to see my friend as much. So it was great first to see him with a new tracheotomy that meant he could put a finger over the tube and speak, and in a separate room.
Then they removed the trachie and the nasogastric tube altogether! Talking! Started him on fluids; soup, yoghurt, etc; then puree/mashed meals. Now he's out of the hospital building, over in Rehabilitation Unit — same building where I was in hospice care, on floor above. So back to shared ward.
If you've seen 2001: A Space Odyssey, the mashed meals remind me of the coloured goo in squares on a white rectangular divided plate that Poole and Bowman ate on the Jupiter. Except they are served out by what may be an icecream scoop and the plates are round.
Labels: friends, medical, medicine, personal, treatment
Monday, June 02, 2008
Xeloda (Capecitabine) - Side Effects of Chemotherapy
Xeloda and Capecitabine - Side Effects of Xeloda - Chemotherapy Drugs: "Xeloda �
Generic Name:�Capecitabine"
www.chemocare.com/ bio/ xeloda.asp
Hand-Foot Syndrome


Xeloda (Capecitabine) cancer treatment, side-effect: Hand-foot syndrome (Palmar-plantar erythrodysesthesia or PPE) Skin rash, swelling, redness, pain and/or peeling of the skin on the palms of hands and soles of feet.
(see also www.chemocare.com/ bio/ xeloda.asp)
A mild version, the reddness doesn't show up very well. On the hands it is on the last joint of the fingers and thumb, with another patch where the thumb joins the palm. On the feet, it's on the bottom of toes and mostly the ball and non-arch middle section of the soles. Skin is peeling on some of the left (lymphodeomic) hand, the balls of both feet and some toes.
Xeloda belongs to the category of chemotherapy drugs called antimetabolites, subcategory "Pyrimidine antagonist". It is prescribed to treat Metastatic breast, colon or rectal cancer.
Labels: health, medical, medicine, pix
Monday, November 12, 2007
Boyer Lectures online
Apropos mainly just people finding something interesting, I'm alerting y'all to the start of the 2007 Boyer Lectures. This series (the 48th) is called Restoring The Senses. It's available streaming, or as a podcast or transcript from www.abc.net.au/rn/boyerlectures (don't be put off by the short excursion into philosophy/theology near the beginning). Their summary:
"Professor Graeme Clark, creator of the bionic ear, is ABC Radio National's Boyer lecturer for 2007. In this series of six lectures … Professor Clark draws on decades of experience as a clinician, surgeon and researcher to celebrate our senses. He also tells the compelling story of how the bionic ear was created, and provides an insight into the extraordinary future of bionics."Archives, either as transcripts or audio recordings, back as far as 1997 are also available on the ABC site.
Labels: audio, biology, health, medicine, science
Wednesday, May 10, 2006
Health Hiatus
Major medical personal upheavals still going on. Might be able to fill in when I have the time & energy.
Chemotherapy starts on Friday, 12th May, 2006 and will continue for quite a few months, followed by radiotherapy and hormone treatment too. Fun, fun, fun...
[EDITED LATER TO ADD:]
Though drugs are more intense than last time, and more side-effects, OTOH the dose regimen is shorter, one day rather than a whole week. I'm considering finding a small flat to operate from for the next few months, it could help me organise cleaning out Mother's and be safer than staying at Pyrmont while I'm sick. Finances might be able to take it, especially if I can manage to stay on working.
In short:
Chemotherapy - Adjuvant FEC
- Starts Friday 12th May
One dripfeed every three weeks, for six cycles. Picked Friday so can recover over weekend.
This, if we've calculated right, would end on August 25th.
Many people are able to keep working part-time.
Hair will go; drugs to help with nausea & diarrhoea, other side-effects possible but rarer - can mean a pause while you recover.
Radiotherapy
Would start at end of chemotherapy - not sure if after 3-week gap.
Daily (weekdays) a 20-minute dose for five weeks.
This would take to mid-October or early November, depending on gap, also any pauses.
Not sure how practical working would be through this. Apart from how serious any effect of the therapy would be, trying to fit in the travel to the hospital & time of the treatment as well as work & commuting to it seems very awkward. Doing all that while not feeling too good might work against healing well too.
Hormone therapy
Foggier on this - happens after chemotherapy, but not sure if it overlaps with radiotherapy.
Tablets, don't know more details.
Until I'm able to put up information here, search for "Adjuvant FEC" or "fluorouracil, epirubicin and cyclophosphamide" if you want to find out some details.
Labels: cancer, medical, medicine
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