Oct 242004
 

cu.jpg

Here’s a funny little story that has taken a few months to unfold.

Back when I was newly diagnosed, I got an e-mail from a dyke I don’t really know. I mean, we have been on a bunch of e-mail lists together over the years and we certainly know folks who have seen each of us in the flesh, but we have never met.
Anyway, said dyke e-mailed me and she said she felt awful that I was sick and she offered to buy me a t-shirt.
Now, having never met, there was no way for her to know how much I like a good t-shirt or what a push-over I am when it comes to certain marketing.
It was the perfect thing to offer. I was delighted and more than a bit touched, particularly since we didn’t really know each other.
I spent a chunk of time amusing myself at some of my favorite websites, looking at what I might like, narrowing my selection… it was great.
Ultimately, I picked a t-shirt that I had seen a friend of mine wear. It is a black t-shirt that says “Cowboy Up”, just like that logo at the top of this entry.
The term “cowboy up” means to suck it up in times of adversity.
After all my long hours of figuring and searching, it seemed like the perfect choice for the current situation. So, I e-mailed my friend and told her and she put the wheels in motion.
Or she tried, but when she went to order the shirt, it turns out that the distributor that I had connected her up with didn’t have a secure site for their credit card orders so she had to arrange to order the t-shirt over the phone.
It’s bizarre to me that they wouldn’t have a secure site, but it’s true.
So, the order was placed and then it was just a matter of time and I would be all stylishly dressed for my next chemo treatment.

Oh… an important detail in the story telling here… I had arranged to have the package shipped to Seattle, to my friend H’s place, because the last time I had something shipped from America, there was an extra $40 brokerage fee on top of the regular fee and the shipping and the duty, so the package I received, a t-shirt as a matter of fact, was extremely expensive by the time I got it on my body. Hoping to avoid that situation, I arranged to have the t-shirt shipped to H’s place and then another old friend who is travelling back and forth to Seattle a whole bunch said she would bring it up for me.
It should all have been extremely easy.

A bunch of time passed and no t-shirt, no t-shirt, no t-shirt, and then I hear that there is a package on the way, and I am pretty happy about that.
L drops by my place on her way home from work, she is looking a bit concerned and a bit amused and says she hopes I am not disappointed.
Off she tears and when I open the package there is no t-shirt, but there are 2 cowboy hats, from the Coor’s Rodeo, and 2 Coor’s belt buckles.
Oh… that’s odd.
I have no idea why I have these cowboy hats and belt buckles, but they do seem to fit the g-f and I and that part is okay.
I send an e-mail to V and let her know that a strange thing has happened, and I have no idea whether it is related to the t-shirt shipment or not, but…. well, I just don’t know. I wasn’t expecting any other packages, so I think perhaps there may have been a mistake somewhere along the way.
V gets on the phone and it turns out that, yes, the cowboy hats and belt buckles have been sent in error. It seems that they got the packing labels mixed up on my package. Someone hoping for a couple of cowboy hats got my t-shirt and vice versa.
V gives them a good blast and tells them they have to correct the problem and no, we will not be shipping the hats back because it is a total hassle with borders and duty and all that so they can just fix it and take the loss.
I was impressed.
And settled back to waiting.
So, a week or so ago I got the word that a package had arrived in Seattle for me.
I was doing some mental calculations about when I might take possesion of my long anticipated shirt.
L went down to Seattle and did the weekend thing and came home.
I got some e-mail from all the key players in the drama asking ‘well, was it worth the wait?’ but I hadn’t yet received the t-shirt.
And then I got an e-mail from L.
The e-mail said her car had been broken into the night before and, along with a bunch of her stuff, my t-shirt had been stolen.

So, that’s the story of the t-shirt so far.

I am thinking of getting a new shirt to celebrate the end of chemo.

I think it should look like this:
super-man_distressed_ringer_logo_link.jpg

I may just do the old fashioned retail approach to getting that shirt.
That may be how I do it.

That said, I do want to thank everyone who has tried so hard to get me that damn t-shirt.
Could it get more complicated?
Damn.
Thanks for trying, everyone.

And for folks following this saga from the beginning, you may recall that in one of our early episodes, the door of my truck suffered a compound fracture because of an unfortunate impact from Elaine’s (then) van.
This would be auto trouble #1 of 04, followed shortly by the pinching of the van (auto trouble #2 of 04).
Anyway, I am delighted to say that my truck door has been fixed up by my mechanic and former co-worker, Brain and I no longer have to squeeze past my gear shift like a Dukes of Hazzard loser.

Hooray!

 Posted by at 10:56 pm
Oct 232004
 

You know, since I got sick, I have spent more time thinking about how many of us in North America spent the bulk of our energy consuming things.

Here’s a piece from the CBC website about how well that is working out.

http://www.cbc.ca/story/science/national/2004/10/21/world_enviro041021.html

GENEVA – People are consuming the planet’s resources at a rate that outstrips its capacity to support life, a global conservation group said Thursday.

The World Wildlife Fund report, called The Living Planet 2004, shows humans use 20 per cent more natural resources than Earth can produce.

Report’s authors recommend switching away from fossil fuels.
Between 1970 and 2000, populations of land, freshwater and marine species fell about 40 per cent, according to the report.

The destruction of habitat is the greatest threat to wild species.

“Forests are being cleared to plant crops or to graze animals,” said Jonathan Loh, one of the report’s authors.

Other threats include:

River dams.
Pollution.
Climate change.
Overexploitation of species like fish.

Invasive species such as cats, birds and rats that are not native to a particular country can also threaten indigenous species, the report said.

Earth’s ecological footprint ? the amount of productive land needed on average worldwide to sustain one person ? is now 2.2 hectares.

Based on the amount of productive land and sea on Earth and the total population of 6.1 billion people, the planet has only 1.8 hectares available.

People in the developed world consume resources at an unsustainable level, the report concluded.

An average North American consumes twice as much as a European and seven times more than the average Asian or African, according to the report.

To stem the tide, Loh suggested governments, businesses and consumers switch to energy-efficient technology, such as solar power.

Written by CBC News Online staff

 Posted by at 10:20 am
Oct 222004
 

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Just a reminder to those of you who like to play the odds and collect the fancy prizes, the time is coming to a close to get in on the B.C. Lifestyle Lottery.
The tickets are expensive. On the other hand, it’s probably the only way anyone I know will ever live in the British Properties, so that alone makes it worthwhile.
More info can be found here.

More local goings-on…
If you live in Vancouver and you like to read, you have to go to this.

We went to the library book sale yesterday. It wasn’t a planned thing, but before you knew it, the E’s and I were heading downtown to the booksale.
It’s a great, great sale. I didn’t really expect to be able to go this year, what with being sick and all, but it worked out and the big E and I were much more moderate than normal.
See, the library fills a whole room with books they have taken out of circulation and the most they charge for any book is 2 bucks.
And historically, the g-f and I show up with rolling luggage and load up.
We were really quite conservative for us.
But you should go and check it yourself.

Other news around town, well, I decided after how hard the last round of chemo was that I would try accupuncture this time.
The guy I am seeing comes highly recommended and I already knew he was a nice guy because we used to live in the same co-op together.
At this point, I can say that *something* seems different, though it is still a little early to tell.
The accupuncture may be a big chunk of it.
I am also getting way more fussy about the meds I am willing to take and how long I am willing to take them for after each round.
And the other thing is, I am resting more this time than I did last round.
I think last time I just became aware of how easily I get worn out and now that it’s 4 weeks later and the weather is crappier, I am less tempted to go for a walk. Maybe in December, but right now, I don’t want to get stuck in the rain without enough steam in the engine to get myself home.

On other fronts, my waist continues to blossom.
I know there are some folks who think it’s kind of funny that my formerly svelte self is now squishing myself into sweatpants and whatever else I can find that fits today.
Me, I am kind of hating it.
Basically, I look like a shoe box on top of two spindley little legs.
Oh, and don’t forget the great bald head on top of the shoe box.
That’s a pretty hot image, no?
Anyway, I know my body is taking on water, just like a little row boat, and I know that in a couple of months I will have my life back and I will be able to go to the gym again and get myself feeling like myself again, but right now, it’s kind of annoying.
Any locals with old 34″ waist jeans that they can lend out for a month or two, do give me a shout.

The other thing that has been going on lately is I am having some strange feelings about the chemo actually ending.
Okay, I don’t actually mean I am apprehensive about the chemo ending.
I am nervous that I have to make the decisions now about how I live my life and how to make sure I don’t have a recurrence.

See, I guess you have to start with a basic willingness to believe that the doctors and their poison have actually done the job and wiped the bad cancer shite away.
Then the question becomes, “What do I need to do to keep it away?”, because I am here to tell you, if I can avoid the encore in this performance, I would be more happy than you could know.
And, clearly if I have been doing all these organic modifications to my diet, then I believe that diet matters.
So… what kind of diet is going to do the trick here?
On one hand, I could be macrobiotic.
Okay, I probably couldn’t, but one could make a good argument for a macrobiotic diet being a good idea to rebound after this treatment.
On the other hand, I could make a significant reduction in the fat I have in my diet.
I am kind of keen on that.
Not like I eat a lot of greasy foods, but I eat a lot of cheese and other dairy foods, and I could cut down on the meat as well.
My acupunturist says I should stay away from spicy foods because they make my body run ‘too hot’.
Oh, okay…

Then someone told me I need to figure out how I want to eat in a way that makes sense to me and in a way I will enjoy and then just forget the rest of it, because otherwise I will be miserable and I will make myself nuts.
So, I can’t see having any Hastings Steak for the remainder of this lifetime, but I don’t have to exist on wild yams and kombu.
Whew!

Aside from that, I have been spending the day teaching myself how to make carrot bisque.
It’s quite nice, actually. I am on my 3rd pot.
It was sort of an accident how I came to make so much soup, but it will keep really well and soup is a nice comfort on a rainy day like today.

I am sure I have lots more to tell you. In fact, I probably owe you an e-mail, that seems to be the current trend.
If I am behind on answering you, please be patient. I will probably answer soon, and if I don’t, feel free to nudge me.

I want to say thanks to everyone again.
This has been awfully weird and hard and awful, but I know some spectacular people who have made it so much better.
There are also those spectacular people who I don’t know who have made it way better too. To all those kind strangers from Alberta, thanks so much.

All right, it’s late, it’s cold, and it’s time for a fire in the fireplace and some Buffy reruns.

Keep the faith.

 Posted by at 6:41 pm
Oct 162004
 

Well, who knew that the chemo floor was open on the weekend?
Not me.
But on Thursday they were still scrambling, trying to find me a time to do chemo on Friday. Then they called and said my appointment was on Saturday.
Well, okay.

And now I have gone to the appointment and I am home.
Today I am feeling pretty okay and in pretty good spirits.
Elaine points out that this has a lot to do with all the drugs they have pumped into me and that it gets a bit different.
That’s a bit of a bummer, eh?

Today’s treatment was kind of interesting for me.
I won’t mention the part about opening my eyes as the woman sitting directly opposite me almost barfed.
I think it was homophobia.
heh..
Okay, I don’t think that.
I think it was really unfortunate timing on my part and really an unfortunate situation for her.
Luckily her treatment was over really quickly. I only came close to seeing her barf one more time.

Anyway, today felt different.
For one thing, I was one of the very few bald people doing a treatment today.
There were maybe two other bald people, and everyone else was new enough that they still had their hair or they were coming back for follow-up treatments and their hair had grown back.
So, that part was different.

And I think it’s just kind of different because it’s a weekend and so it feels less busy around there.
A bit less crazed.

But I also think on one level, I am sort of mentally packing my bags and getting ready to say adios to my pals on the chemo floor.
And I have to be careful with that.
It can be really hard for me to just stay in the moment and not rush ahead. I find myself making a lot of future plans in my head, way more than I did before I got sick. I hope I follow through on quite a few of them when I get better.

It’s that fine line between optimism/determination and denial.

When I started the treatments and I would be feeling really confident about making it through everything, I would wonder about that and whether that was just some elaborate denial thing.
If it is, I seem to be able to inspire it in others, because quite a few people have said they are confident I am going to make it through all this. I agree and appreciate the feedback.
And anyone with a dissenting opinion could keep that opinion to themselves, okay?
Anyway, over the last few months I have struggled with ‘what *is* the difference between optimism and denial?’
I don’t think I am in denial because I get so goddamn cranky about all my aches and pains and pokes and jabs and general inconveniences.
I don’t think I am dealing with a little thing.
I think I am in the middle of the most important battle I will experience in my life and it’s a dogfight.
But I plan on winning. And I have a great team of people helping me get there. With Elaine in the coxswain position.
I have had a lot of love and support along the way in this weird ride and I feel really lucky.

And, even with that, I was sitting there at chemo today and there was a woman sitting across from me. She had a bit of a dykey feel to her, and so did the woman who was there giving her morbid support, so I may have paid a bit more attention to them than I normally do.
Anyway, the woman who was the patient seemed to be getting her first chemo treatment; she was one of the hirsute ones there today. Her partner/support system was asking all kinds of questions about her meds and that was smart.
And then the woman who was the patient started having a bit of a rough time.
You could tell she was feeling dreadful by looking at her. Her face became blotchy and flushed and her shoulders were slumped down a bit and it looked like no fun at all.
And I looked at her and I remembered my first treatment and how I crashed and it made me realize, in some ways, how far I have come since then.
I don’t think you can do this much chemo and not become a bit of a natural with the whole system they have down. And, all things considered, I kept my contact level with the BCCA at a minimum. There are lots of supportive things they want to do for me, and mostly I just come home and get my support from my own people.
But still, I remembered how freaked out I was the first time and how sick I got, first in the chemo room and then when I got home. And how I spent an entire week on the couch and thought that was how I would be spending my life for the next 6 months and being pretty sad about that.
And then we changed some of the meds and added a bunch and it’s different now. It’s no party by a long shot, but it is so much better than the first time.
But when I saw that woman feeling like crap and being afraid and being at the beginning of the process, I also caught a glimpse of this wild ride I have been on and how long it’s been like this.

As a f’erinstance, my normal oncologist is at a conference right now, so I had last week’s appointment with a different oncologist. And it’s really interesting to see the different approaches and the different things people see as important.
Anyway, last week’s doctor, Dr. Pike, says that it is common for people to have an emotional crash after they finish up their chemo.
She said after months of being in the system and doing all the stuff you do, all of a sudden it ends and you have time to think about everything you have been through and you crash. And you can crash extra hard because you have been waiting and hoping and living for the day when you can stop chemo, and it arrives and then so does all that baggage.
So, I need to be careful to watch out for that.
For sure I have been dealing with this like I was walking a tightrope and I know that if I look down, I may stumble. So, I just keep looking straight ahead.

Anyway, it’s late and it’s time for me to take some more chemo day medication. I don’t have enough to share with the whole class, so I better log off and go do that alone.

More as it happens.

 Posted by at 10:17 pm
Oct 132004
 

okay… so there have been some really generous people who have come out of the woodwork since I got diagnosed a few months ago, and I want to say that that has been a huge help for me and for us on a lot of levels.

Late last week, we got some ‘spike-aid’ help from some folks in Alberta, most of whom we don’t know.
That is just so over-the-top sweet and kind, I don’t know what to say, except thank you, virtual strangers.
That is so amazingly kind.
Thanks.
You all made this weird trip a whole lot easier.

 Posted by at 12:07 am
Oct 122004
 

I’m sure this isn’t the last time I will end up having to wait for something in this whole great, long, draw-out cancer episode, but anyone who knows me, knows that I am, sometimes, a very patient person, until I’m not.

So, the current deal is, my red blood cell count is/was too low to do my 7th chemo treatment and I got told to go home and get better or something.
I’ve been at home for almost a week now, and it turns out that I am now ‘on the waiting list’ for chemo for this week and hopefully they can squish me in later this week, probably Friday, but hey, who knows?

I think I may personify the expression ‘mixed feelings’ right now.

On one hand I am so tired of feeling crappy and I am kind of delighted that I am not in my predictable downward spiral right now (since I should have had chemo last week.)
On the other hand, I am so close to the finish line and I just want to be done so I can get on with my life and with growing back my eyebrows (yes, my eyebrows… and my eyelashes and all the hair on my pointy little head.)
But on the other hand, which doesn’t exist on mere mortals, I don’t really have the jam to get knocked down again right now.
But I sure would like to be done…

Anyway, it seems that the chemo floor has turned into its own equivalent to a 5 star restaurant and I have to wait for them to call me and say when they will have my table by the window, overlooking the roof-top garden.
And so I wait.

 Posted by at 11:09 pm
Oct 072004
 

Well, I went for my bloodwork and my regularly scheduled visit with the oncologist and it seems one of the counts on my blood cells is off and they want me to wait an extra week before I do my next chemo.
So, no chemo this week, instead we will do it some time next week.
And apparently they will have me wait 4 weeks between round 7 and round 8.
I didn’t actually hear that part but my g-f did, so I reckon it’s true.

And while it’s sort of a relief to have that extra chunk of time to bounce back, I confess I was really looking forward to being done at the beginning of November. Now that will be the last treatment in the middle of November and a few weeks to recover after that.

Other news…
there are a couple of events dealing with ovarian cancer coming up.

For the local folks, there is a workshop on Oct 27, details below:

“Listen to the Whispers, An Evening of video, Q&A and discussion on Ovarian
Cancer for Lesbian & Bisexual Women. October 27th, 7 – 9pm at North Health
Unit, A&D Lounge , 2nd Floor, 1561 Commercial Drive (First & Commercial) A
free event. Registration requested. To Register call 604-684-5307.
Presented by Pride Health Services, a partnership of 3 Bridges Community
Health Centre, The Centre, AIDS Vancouver”

also, there is a one day symposium in Victoria in late November.
Here are the details for that.
Unfortunately, it’s unlikely that I can make it to Victoria that day but it does look interesting.

*****

British Columbia Ovarian Cancer Symposium

An educational program for healthcare professionals, survivors, friends
and family members

Please join us in Victoria on November 20th for an informative and
inspiring day. The purpose of the symposium is to learn more about
ovarian cancer and also to address some of the issues relating to coping
with a diagnosis of cancer, including genetics, palliative care and
communication. One of the highlights of the day will be an inspiring
presentation by Dr Annie Smith, an art historian, author as well as
breast and ovarian cancer survivor.

Other speakers Dr Elissa McMurtrie, Gynecological Oncologist, Shelley
Gordon, a counselor on finding “Balance and Hope” and Dr Brad Nelson, an
internationally renowned expert in cancer research.

*****

That’s all for now.

 Posted by at 8:01 pm
Oct 062004
 

Tomorrow I do bloodwork and talk to the doctor.
Friday I do the 7th chemo treatment.

This is gonna be quick and dirty and may not make much sense.
But here’s the thing.
I am exhausted, more physically than mentally or emotionally, but probably in those ways as well.
I’m going to take a wild guess and speculate that the same is true for my g-f right now. I don’t know why, call it a hunch.
And I never really bounced back this round, not like in the past. That leads me to think that this next round may be even worse than the last, and frankly that is a little troubling.
So, if you have been thinking of getting in touch with us to give us a hand somehow, we are more likely to accept that than in the past.
On the other hand, we may not need anything right away or we may not know what we need today.
But if you were thinking of offering, I wouldn’t want to discourage that at all right now.

And on that note, I think I will go to bed so I can get up and get poked and all that jazz tomorrow.
Stay tuned.

 Posted by at 11:14 pm
Oct 012004
 

well, yesterday, I did the first of the two bloodwork episodes for round 7 of my chemo.
This chemo next week is 7 of 8.

And, I know we are all in agreement that this round of chemo will be the beginning and the end of my cancer treatment, the alpha and the omega… the ‘let’s not wear out our welcome here at the BCCA’.
Anyway, the folks at the BCCA send me the paperwork that I have to take to the lab for the bloodwork. In the envelope I found the paperwork for yesterday’s appt and also for one for the 8th round.
It was such a relief to look at that and realize that it stands as the last of its kind in the series.
And with any luck, I will have smashed all the cancer to bits and it will be too scared to come back.
That’s my hope.

On other fronts, I am really worn down.
I think the chemo is really starting to take its toll on my body and not just the weight gain and the lack of hair.
The gal at the lab had a hard time finding my vein, I could tell.
Now, if you know me fairly well, you’ll know I am a bit of a sissy when it comes to blood being extracted from my arm, or any big ass needle going in my arm.
I look away and I get really tense.
So, there I am, looking away and being really tense, and my g-f is holding my hand on the non-pokey side… and it’s taking quite awhile.
And the scene in the waiting room had been completely overwhelming, with babies screaching and people spitting up their lungs and such, so I was already a little tense.
And, I could tell she was having some trouble finding the vein.
And that’s new.
I have never had that problem before, and I do have 2 more rounds of chemo to do, plus all the accompanying bloodwork.
So, I don’t know what will happen next.

I have a feeling I will end up getting some sort of shot or new pill to supplement my blood counts, because I have been so run down this time.

I am finding it hard to keep up with people when I go out for a walk lately. And that’s pretty strange. I just do my little walking thing and I chat with whoever I am walking with, and all of a sudden I wonder why they are going so very very fast. And then I realize it’s me who is going slow. That’s pretty weird because I really like walking and all of a sudden I am having trouble holding my own on a walk.
It’s weird.
And, I suspect it will continue to get bad for a couple more months and then it will start to improve around December 1.
And then hopefully I can start going to the gym again and get things back on track.

The other thing that happened yesterday is, a package arrived that contained 2 cowboy hats.
I am not really sure where it came from, or who it came from.
That may be because it’s a secret or it may be because someone had a conversation with me and I forgot about it because of the chemo drugs (yeah, they really do wipe whole conversations from my memory).
Anyway, I have a new cowboy hat and Elaine, who was very enthusiastic about the package, also has a new cowboy hat.
From the Coor’s rodeo, no less.
And 2 Coor’s belt buckles.
Holy screaming homosexual!
Good one, that’s all I can say.

Anyway, that’s me.

It’s another beautiful day here in Vancouver and I think I will try to wash the scuzz off my truck, because I can.

 Posted by at 10:03 am
Sep 272004
 

galiano bw.jpg

Do you know me?
Many people don’t. That’s why I carry the American Excess card.

Err… well, anyway…
It seems that the extra 30 pounds I have put on in the last few months, coupled with the lack of hair, eyebrows and eye lashes all add up to a confusing visual image for a few folks.
Today I had 2 different people, both of whom I have known for years in a casual kind of way, not recognize me.
I think that means I look different.
What do you think? You think I look different?

I am hoping that I have now turned the corner on feeling crappy from this last treatment.
This round has been brutal.
I *think* I am starting to rebound, but I can tell that rebound means something really different than it did a couple of months ago.
Mostly, without wanting to whine too much, I feel like I have been dipped in a light coating of wax every day for the last few months. Each layer is sort of insignificant on its own, but its cumulative effect is a bit much. And taken as a whole, the overall effect is that my entire sense of touch is wonky.
I also feel like I have had the flu for about the last 4 months, which, of course, isn’t true… but I feel worn out and just so tired of feeling crappy.
But hey… 2 more treatments and then, fingers crossed, I will be done.
That’s the big hope.

The end of all this treatment is close enough that I start to pine for feeling regular and I find myself making little activity to-do lists in my head.
I have been wanting a particular tattoo and I need to get my ear re-pierced and I can’t do either of those things till I get my immune system back, so I toss that around in my head.
But most of all, I am just looking forward to feeling sort of regular again and acting regular and going to work and all that jazz.
I realize most people I know wouldn’t miss going to work, and may think I am nuts to miss it, but I think lots of people would miss going to work too.
I mean, if I had been at Club Med for the last few months, then maybe I wouldn’t miss work, but I think I probably would.

So, this will be a short and sweet entry.

Apparently, I look different.
I suspect I am going to be looking a whole lot of different ways for the next while. I am really looking forward to growing my hair back when I can, so that will look different.
I suspect I am actually not done putting weight on, since I seem to put on about 5-10 lbs per treatment and I have 2 treatments left.
I am really looking forward to getting my body and my immune system back on track and heading back to the gym just as soon as I can, probably in the New Year.
Also, I saw a stationary bike at a second hand store the other day and I the more I think about it, the more tempted I am to go buy it, though I have no idea how much it costs. But the thing is, I have tons of time on my hands, and I can’t use my gym membership now, and I imagine sitting in front of the tv and pedalling and sweating out some of these toxins.
Now, some days I wouldn’t have the strength for much, but other times I think it would be really good.

I guess I should go see how much money they want for it.

 Posted by at 9:18 pm
Sep 232004
 

My girlfriend deserves a great big medal.
Have I said that before?

I hope so, but there is the whoppingly good chance that I have spent all my time going ‘ga-blah, ga-blah, ga-blah, poor little Spike, poor Spike…’ and not mentioning how she loves me and pats me on the head even when I am a cranky ass bastard and I am so sick of being sick.
Which is pretty much how I have been the last couple of days. And it also follows the course that has been established by the whole chemo scheme since we started this exercise.

In case you missed it in one of my previous posts, at about this point in the process, right now, about a week after the treatment, is when I start to come pretty unhinged.
Cole’s notes for those joining the story late…
they give me a whap of drugs, mostly steroids and shit, so I can function better and do at least some basic life things.
Now is when I am either off or tapering off most of those drugs, so I am detoxing at the same time I am feeling all the lousy feelings inside my body.
It sucks.
How many times have I written that in the last few months?
Shit.
If you want to know how I feel, think of it like this…
You know in elementary school and you learned that at this time of year the jolly Quebecois people put on their little snow shoes and go out and tap into their trees and extract the yummy sirop de ?rable? And you know how the sirop de ?rable is yummy and tasty and good for you?
Well, not to be too dark about it, kids, but I feel like if they took that same spigot and rammed it in my arm (and don’t think they haven’t been at labs all over my fair town) it would be the anti-thesis of yummy goodness that would pour into the pail. It would be the opposite of organic.
And hey, that’s actually okay. It’s there, it did its job and now it’s time for me to get it out of my body, one way or the other (thank you, great big bottles of distilled water.)
But it is not all that different than those scenes in Alien when it makes its way out, and I am just about as happy as any of the crew members when they realize they aren’t travelling solo.
Ga-blah ga-blah poor me.

Anyway, you, gentle reader, have probably been spared a whole lot of the detail because, really, who can understand what it really is unless you are in it. And if you were in it, why would you want to read about it?

I know, you think, “look at how long this gawd awful post is, how could I possibly have been spared anything?”
Well, tonight, I ain’t sparing you much. I need to vent some and if you came here to see what’s up, I am gonna give you the full meal deal tonight.
Well, actually, even this is abridged but you are getting more of what the locals enjoy than what I serve up here normally. You lucky bastard.

Tonight I was laying in my bed, trying to sleep, succeeding at that for a few minutes and then waking up again.
I gotta tell you, I am kind of cranky these days.
Not at anyone in particular, except say, Gordon Campbell and all the healthcare budget cutting bastards of the world.
On a human level, I have been spectacularly lucky and try to be grateful, even when I am crabby.
But I feel a little rant coming on, so if you are having a sad day and you thought you’d look here for some sunny encouragement, well, first you are terribly misguided, but secondly, you should hop on over somewhere else.
Here is a short list of stuff that is pissing me off.
Bear in mind that I know that in a big picture kind of way, I have sweet fuck all to be pissed off about. I have lots of people who love me and care for me and do what they can to make it better.
And still, I find myself pissed off…
Go figure.

And here, in no particular order, is a short list of some of the stuff I am pissed off about right this second.
If you pass me on the street in two days, don’t think you need to check in with me about any of it, because mostly I just need to blow off steam *or* it’s a big and complicated thing that I probably don’t even want to talk about and I wouldn’t if I wasn’t so full of fucking chemicals.

I am so pissed off about time.
I am pissed off that before I got sick, I had such big plans in my head about what a great summer this was going to be. I planted my sure-to-be-bumper-crop of tomatoes and the rats ate every single one of them.
Oh, yeah, my punk-mod-goth friends think I am kidding, but no, I am not. My totally loved to death, organic to the max tomatoes… not one did I get.
Which is not to say that I haven’t eaten my fair share of tomatoes this summer, but one thing I like about summer is eating the tomatoes that *I* grew… not someone else.
So, I am pissed about that.
And that’s about thinking things will go a certain way and then they don’t.
And guess what? That’s life, buckeroo.

One thing that has been pissing me off for quite some time, but I have been too kind to say anything, is goths and stoopid fuckers who think Jim Morrison is cool.
Okay, this is your last chance to jump ship before I really hurt your feelings, because maybe you don’t know how easily I can do that.

Gone yet?
Okay, here’s the thing…
as someone who has put an enormous amount of energy into just putting one foot in front of the other and making it thru each fucking ‘today’ with the fervent hope that ‘tomorrow’ pans out to be better, watching a bunch of teenagers and overblown teenagers worship some doped up, nihilistic satanistic talentless middle class jackass misogynist just makes me want to puke.
There is absolutely nothing brave or courageous or artistic about deluded, straight, white middle class men self destructing.
Nothing.
There is nothing cool about it.
It does not require one single spec of bravery.
If you want to do something brave, do something that will both a) make the world a better place and b) challenge and scare you to try to accomplish it.
Getting famous for getting high doesn’t qualify.

If you want to do something cool or brave, then sit down and figure out what you want for your life and then… go do it.
And I really don’t give a red rat’s ass, assuming it doesn’t involve doing awful things to children or any other innocents, just go fucking do it.
Bungee jump, get your ear pierced at the equator, fall in love with someone and stick with it. Go to therapy, don’t go to therapy… pay your library fines.
Do something even if it scares you. Actually, do it specifically because it scares you.
If you want to do something supremely brave, go be a good parent to your kids.
Love your kids, be good parents and good examples and make sure they know you love them.
That’s brave.

But don’t sit around thinking that some morbid overgrown ooo-ga boo-ga mumbling from the dark side dude is where it’s at.
Because frankly, that’s for shit, in my opinion.
You wanna be here, then be here.
You don’t wanna be here, then figure out what you need to change you can maybe actually want to be here.
I am actually not saying that everyone in the world has such a ducky little life that they are obliged in some way to see it thru from beginning to end in whatever way the great cosmos stamped on your ear the day your momma spatted you out onto the linoleum floor.
I do believe that if you are sitting somewhere reading on your iMac while you sip a Latte Chai espresso, then maybe you have a bit more wiggle room about what can and can’t happen in your life and you maybe should think about what you want and try to go get it.
Just a thought.

Another thing that pisses me off and makes me nuts is feeling like being sick is a sand paper I have brought to my relationship with my g-f.
Now, like I said, I have no complaints about how super swell she has been.

They have those made for tv movies that explain what it’s like to be madlessly and hopelessly in love with someone and still fight that demon on your shoulder that says, “You know, if you two had never taken up with the dating, she’d be so much happier now… holy! She could get her work done and she wouldn’t have become a sharp-shooter with a pill splitter and she wouldn’t have impoverished herself and I think she’d get out more and I think she’d be happier.
Golly, I sure wish there was something I could do to pay her back for all this, but I have no idea if I can. I hope I get to get my strength back and take her to the beach for a couple of days and just relax and exhale… I hope it works out that way.”

And I am sure hoping it works out that we can get away, just us two, and relax and appreciate each other and everything we have been through.
Because she has made all the difference in the world. People have been really good and really kind, and my gf has been better than anyone.
So, if you all could give her a little hug, or a little non-contaminating smooch (assuming she agrees,) or a little e-mail greeting saying thanks for being swell to Spike, that would be great.
I think we are both getting a bit weary from it all these days and I am not sure she is getting enough support from folks out there.

And another thing that pisses me off these days is this bad rut I am in.
See… I am not feeling great, so I can’t do much.
It means if you ask me if I can do something with you, I really can’t tell till the day it’s supposed to happen and even then, I could get 30 minutes into something and realize I am in over my head and have to jam.
So, I am hard to make plans with.
Which means I spend a lot of time wandering around my house, wishing I could do something, wishing I could go bug my gf but she needs to work and make money and stuff and even see other people besides me sometimes.
And I wish I could sit and read, but the drugs mess with my vision for at least half the time of each cycle, so that’s not good.
And then there are videos and movies and shit, but it’s nicer to watch those with someone. And that gets to be a bit difficult to co-ordinate because, unlike me, regular people have jobs and lives and things to do.
And, inside all those regular people, there have been a handful of folks who have really been wonderfully attentive and engaging, and have made a point of taking me to appts and just running errands or even going for drives up the Sea to Sky Highway or camping or doing anything to break the monotony.
I can’t thank you guys enough.

The boredom has been one of the hardest things to wrestle with.
Sometimes just a wee field trip with no pressure has been so important for me.
And if after reading this, you are brave enough to think you might wanna come over and watch a movie, or maybe you wanna help me go search for firewood for my long, indoor, rainy winter, then drop me an e-mail or give me a call.
I know people have been trying to let us have our space to just be doing whatever we need to be doing, and also that folks have a life and families and jobs and all. But if you feel like it, it’s cool to ask and see what either of us is capable of.

E-mail is good too. I know I don’t always answer as fast as I should, especially if it arrives when I am really drugged or sleep deprived. But I do want people to know that I appreciate their e-mails, even if I don’t always respond.

And another thing I hate, in case anyone is still reading, is the fucking neuropathy in my arms and my legs.
At first, during the first chemo cycle, I couldn’t really bear weight on my legs very well, they were that unreliable.
Now, with the new, stronger, more all-encompassing drug regime I am doing, I can more or less walk around most of the time, though I do get a bit topply sometimes. Basically, I have needles and pins in my arms and my legs to some degree for the entirety of each 3 week cycle. It didn’t used to last so long, and the oncologist says it will almost certainly go away within 3 to 6 months after the end of the chemo, but maybe not.
But I tell ya, I feel like I am living my life in opera gloves.
At least I can be stylish in my illness.

And, along that theme…
Vanity of vanities, all is vanity
what about my fucking hair, eh?

When we first met with the oncologist, he wrote me a script for a wig and I smugly told him that I didn’t think there would be any need for one. And, I haven’t bought a wig.
But I certainly thought the bald thing would be way easier to deal with than it has been.
Luckily, some SF pals sent me a shit load of cool bandanas and that saved my baldheaded bacon, because I have simulataneously lost almost every single baseball hat I own, right as the autumn monsoon descends.
And I don’t like being bald and I don’t like being cold… so losing that stuff right now kind of sucks.
Anyway, unlike me, I digress…

I thought being a big old bad ass dyke, I would be ever so fine with the bald thing. Hell, I’d even considered doing it all on my own at various times in my life, how hard could it be?
And then, when bunches of my friends shaved their heads in solidarity, why, I thought I had been such a big baby and what was the problem.
Well, the problem is… maybe you should lean in cuz I am gonna have to whisper this.
I don’t want just anyone to know.
It’s a bit of a secret.

Okay…are you all scootched up close now?
Okay… here’s the problem.

It’s been said, and there may be some truth to it, that I am a bit of a control freak.
I would argue some of the details of that assessment, and I have certainly had my pot-kettle-black moments in those conversations, but the point stands.
I wish I had $10,000 for every time I have thought, “okay, I am ready to have my hair grow back now’, only to realize it’s not that simple.
See, cuz right now, I am not a regular person.
I confess, I woke up a couple of weeks ago, walked into the bathroom, looked in the mirror as I started to brush my teetn and I was surprised to find that I was still bald.
I don’t know why.
Maybe I had had a particularly hirsute dream in the night. I dunno.
Mostly what I hate, aside from how it symbolizes the lack of choice in my life right now, is that it announces me as a ‘sick person’ before I have even had a conversation with someone.
I guess being so dykey and cool that may not always be true because I bumped into an equally dykey and equally cool co-worker the other day who asked why I hadn’t been around work.
“Oh… I am doing chemo for some cancer,” says I.
She was aghast, in the sweetest possible way.
And here I thought my (straight boy) co-workers were gossip mongers.
What’s up boys?

My my… I do go on, don’t I?
I don’t post squat for weeks on end and then it all comes flying out like some Linda Blair roman shower. (go ahead, Google that, Jibsy.)

So, I miss my hair, more than I ever expected.
I am more vain than I ever knew, and I always knew I was super faggy vain.
I think my gf is almost a saint, and you may think so too but you probably really have no idea and that’s okay. Just believe me.

I’ve learned things being sick and I hope I don’t forget them soon.

I’ve learned most of all that you better figure out what you want and try to go get it, assuming it isn’t going to cause harm anywhere else to anyone else.

I’m still trying to grasp the fact that all those little moments are connected and they add up until one day you are sitting at your computer at 3 am thinking about the stupid little kid who couldn’t understand why the park ranger wouldn’t go retrieve her sandals from the bottom of the outhouse so many years ago.
I hope that man is enjoying his pension today.

So…
2 more treatments.
If you have been playing along at home since the beginning, you may have seen the pattern start to emerge here.
I’ll be crappy and feel like shit for a few more days and then I will try to post something again when I feel better.
By the time I go for the next treatment, I will have convinced myself that it won’t *really* get this bad. Even when it’s pretty hard to forget how totally crappy the crappy days are.
I’ll do the chemo and those 2 days will be druggy and weird, but not completely awful.
And then I will slide into all this again, and just as I sink towards the bottom of the deep mirky sea, I will bonk my head and remember to go back up for air, and then I will start all over again.
And then we will do number 8.

And then we wait and see what happens.

And don’t think that doesn’t weigh on my mind.

Have I mentioned my gf is almost a saint?
Maybe she is a saint.

And if you read this far, I guess you might one day be almost a saint as well.
Or else you need a library card.

Any questions?

 Posted by at 3:07 am
Sep 172004
 

I went and got poked again today. That would be the billionth time since we started this merry process a few months ago.
I actually tried to figure out how many times I have been poked or had blood drawn or had some fiendish goo poured into me in the last few months.
I was coming up with a fairly accurate estimate, and in the middle of my idle calculations, the nurse offered to put me in that drug trial to treat my anemia and said I would have to do bloodwork pretty much daily. I swear, at that moment, some internal support mechanism inside my brain collapsed and I just couldn’t maintain my light-hearted calculations any more.
But the bottom line is, I have been poked a lot.
I have a scar on a vein now. I find myself complaining about that a lot, which is sort of absurd since it doesn’t really hurt anymore and it isn’t that big.
I’m going to have to go thru all my notes from the training for my job and see if there is something I can do to pamper my veins for being so brave over the last few months.
If you are a medical type of person and know of something, do drop me a line.
Continue reading »

 Posted by at 2:18 am
Sep 152004
 

I bet you didn’t know that, did you?

I stumbled upon this site where you can find out what Google has to say about me or anyone else.

It’s kind of fun.
Go ahead, type in your own name.

Tomorrow is chemo day, number 6 of 8.
That means that I did bloodwork last week and again today.
Dr. Oncologist says that my CA 125 is at 4.7, which is still really, really good.
It’s up a smidge from last time, but he says that tiny little jump can be attributed to what time of day they took the blood.
Anyway, he continues to say that things are going really well, just as well as can be, and I will go along with that.

what else…

we went camping last weekend.
galiano.jpg
It was very, very, very wet and windy when we arrived on Friday.
Really, it was insanely windy and insanely rainy. Friday night was just basically insane.
Because the ferry arrived late and because the weather was so punishing, we set up our camp in the dark and in the rain.
We ate dinner at 11 pm, and then we started setting up the tents.
Friday night was kind of brutal.
And then we woke up Saturday morning, and it was sunny and lovely and it stayed that way thru Sunday.
And then we came home and it started to pour again, but that’s okay.
I had a great time getting out of town.
And, I am hoping to get out of town once or twice more in the next while, but I have to see what happens with me and my travelling companions and all that.

It’s late and I have to get my stuff put together to go for chemo tomorrow.
Wish me luck, comrades.
It’s a bugger of a process and I am getting more than a little tired of doing it and really really tired of not being able to do a whole lot of other things. But I think in a big picture kind of way, I have very little to complain about.

Okay… more when it happens and I simultaneously remember to post something here.

Over and out.

 Posted by at 9:33 pm
Sep 042004
 

Welll…

it’s the Labour Day weekend, in case anyone had forgotten that. It’s been quite a summer here for me, and not the one I had planned.
And now it seems to be coming to a close.
It was blazingly hot this summer, and there was much whining about that at chez moi.
Then, in that classic Vancouver style, it just flipped to late October rain one day and it mostly hasn’t stopped yet.
And that’s good because the province was so terribly day, but I confess I was hoping for some sort of middle-ground.

We are supposed to go camping in a few days and it would be nice to have the perfect combo of

– quiet
– sunshine
– fun
– food

and all the other bits that I am looking forward to.

I guess I’ll just have to wait and see what I get.

But back to my point, it’s been a really wild summer.
You all know that, I suppose.
It’s been a summer of being blown away by the stuff people will do to help.
And it’s been a summer of tremendous frustration as the number of things I can do becomes less and less and my boredom and frustration escalate.

I think it might be my weirdest summer ever.

I started out doing pretty well, feeling pretty well, having pretty good energy levels, and it’s been a bit of a downward spiral over the last month or so.
3 more treatments and no real reason to expect that I will have an easier time, physically, with those treatments than I have with the last 2.

And, at the same time, my test results have been really really good.
Yeah, I have spent a lot of time feeling like crap, but I knew I was going to spend a lot of time feeling like crap.
It’s just differrent when you are in it and you can’t change the channel or wait a couple of hours to feel like crap again.
So, yeah, I have spent a lot of time feeling lousy and lousier this summer, and still, the test results are the most important thing right now and that’s coming back just as good as anyone could hope.
And I think, ‘why the hell am I whining and complaining? I have been on e-mail lists with women who had so much more to complain about and they went thru hell and did their chemo and then had a recurrence really fast.

So, let’s talk about that, because I don’t think I have, and if I have, it’s been a while.

Ovarian cancer at this stage has a freaky high incidence of recurrence.
I was on an e-mail list with a huge number of women and I had to unsubscribe because it was just so terribly depressing how many of them only had a couple of months of being cancer-free before they had to start up with the chemo drugs again.
The original numbers from my oncologist were ” I have a 50/50 chance of still being cancer free in 5 years.”
Because the 5 year mark is the important line in the sand.
And if you run the numbers through various websites, the 50/50 number could be seen as being kind of generous. I have seen it go as low as 30/70.
And all that depends on a bunch of things, like type and stage of cancer and overall health and age and luck and all kinds of things.

And, the latest word from the oncologist is that, with the rapid decrease in my CA 125 scores and having those scores well within the range of a regular person, I am ‘in the group they consider most optimistically’.
I think it’s funny how I have adapted to the medical model and I just accept that that is the best he can say.
Can’t say as I blame him.

Anyway, all that stuff is pretty good news.
You may not see it that way, but basically, everything is chugging along in a good direction,

It is my profound hope that I just do these next few chemo treatments and do a ton of bloodwork for the next 5 years, but we just skip the whole recurrence thing.
When I start feeling like I was hit by a bus, I try to think about it as doing one really big, long hard thing and if I just keep plugging along, maybe I get to just wrap up the cancer thing and get on with my life again.
That’s what I am hoping.

And, I need to say another big thank you to Elaine for being so sweet and loving and for looking after two lives and for running her ass off trying to keep it all together for both of us.
I am a very lucky bastard.

And I am lucky to have the love and support of the folks who have been pulling for me.

Thanks.

 Posted by at 11:23 pm
Aug 312004
 

Well, it’s about 5 days since my last chemo treatment and I thought I should say something.

I was just whining at Elaine that this chunk of time, this chunk 4 to 7 days after the chemo, is the worst.
The chemo itself isn’t all that bad, aside from being poked.

But right now, I am:

– bored out of my mind
– drugged out of my mind
– incapable of communicating much so I can’t generate dialogue with most anyone
– really easily worn out, which feeds right back into why I am bored out of my mind.
– completely absent-minded because of the drugs which makes me not much fun for a conversation which feeds into the boredom.

So, this is my main time to lay around and feel sorry for myself.
Unfortunately, I am bored with that too.

The other thing that is happening right now is the neuropathy in my hands and fingers. That’s annoying, though it does fit well with the way my brain feels. It’s interesting to have everything feel pretty much the same. Numb.

And… I know that it is a stage in the process.
And….. I also know that this stage of feeling crappy is starting to take up more and more time of each round of chemo, just because my body is getting more worn now and each time the sludge inside me gets built up a bit more and I have less and less resistance to all the shite in my system.
And just about the time the new cells start to grow again, we slam another needle in my arm and start the process again.
And, in spite of the whining, that’s okay.
I don’t like this process much, but I am not keen on the alternative.
Still, I am pissed off that my lovely summer of leisure is over and I never really got the sort of leisure I was hoping for.
And, it’s all for the greater good.
I do believe that.
I am just achy and whiny and watching summer evaporate before my eyes and I am grumbly about that.

Next year.
Watch out…. next year, I am going to be hedonism personified!

You know, in a big picture kind of way, I mean if you are going to have cancer and do chemo, well, things have actually been going pretty well for me.
In terms of what the test results say, my body has responded well to the chemo.
The people in my life have been wildly kind and supportive.
Things could be way worse.
I just get grumpy about some of the details.

But in a big picture kind of way, it’s going well.

 Posted by at 11:49 am