Historic Election Changes Everything

I know, the title of this post reads like a newspaper headline, but it’s truly how I feel about last night. Canada is different place this morning and for a number of reasons.   When this election started I was very much of the opinion that it was unneeded and would turn out to be a waste of time. I, like many people, felt we would likely just get more of the same, a Conservative minority government.

However; as you have likely noticed even if you didn’t stay up till 2 am to see the final results as I did, the face of the nation underwent a significant facelift last night.

The Conservatives have their majority mandate, largely centred in the west but with significant presence in Ontario. Harper’s place in history is secured with three Conservative victories in a row.

Jack Layton’s place in history is confirmed as well, leading the NDP to it’s most prominent place in Parliament ever – Her Majesty’s Loyal Opposition. He has good reason to feel proud this morning. With its base in Quebec it is a historic accomplishment. It will be interesting to see how he performs in this situation.

Micheal Ignatieff is more than just a footnote as well. He must wear forever the mantle of being the leader who took the Liberal party to the back benches for the first time in its long history. I’ve read two of his books and was impressed with his writing. I wonder what the title of his next book will be.

Giles Duceppe likely has the most to answer for. He not only lost the election but the Bloc has lost official party status. We will not be hearing from them in Parliament any time soon. The question now is will the voters of Quebec compensate for this massive turn by putting the Parti Québécois back in power provincially.

And for the fifth change in a single election, unprecedented in any previous election at any level of government, Elizabeth May has won the Green Party’s first seat in Parliament, earning her party a limited voice and a seat at the debates four years from now, provided the media types don’t change the rules in the meantime.

But there is one more change that took place last night that cannot be seen in the popular vote, the number of seats, or who does or does not have official party status. In previous elections, as the night wore on, I would find myself sitting in front of the TV set watching the results come in essentially by myself as Roberta dosed off on the couch beside me. But last night I had company.

Sarah, and Carlo, and Darby, and Brian and a host of others were watching right along with me. We commented and cajoled, lamented and wept, cheered and boasted back and forth without even being in the same room together. Through the medium of Twitter, Facebook, Skype and Messenger I was able to watch the results and converse about them with over a dozen friends and strangers from all across Ontario, from Guelph to Ottawa; across the nation from New Brunswick to B.C.; and even heard from friends in the United States and as far away as the British Isles in real times, only a few key clicks away.

It will change the face of Canadian elections forever, as it has done in other jurisdictions. Last night the major broadcasters followed the rules and refrained from sending out results across the nation until the polls were closed, but Canadians did not. From the beginning Tweeters and Facebookers sent out the word 140 characters at a time. As soon as the first ballot box was counted in Goose Bay, people in Vancouver knew the result.

Broadcasters, pollsters, political parties, Elections Canada even everyday Canadians are all going to have to spend the next four years figuring out how to conduct an election under this new reality. This new level of connectivity has the potential to make strategic voting a tactic that will skew and slant election results even more than our antiquated first-past-the-post Westminster model of government does already.

The results last night do, I believe, demonstrate the need for electoral reform. An 8% increase in the popular vote garnered the Conservatives and additional 13% of the seats in Parliament. An 11% drop in the popular vote in the GTA cost the Liberals nearly half the seats in Toronto. There does seem to be a valid reason to seriously consider proportional representation.

But what isn’t known yet, and won’t be known until the statistical analysts have had time to crunch all the numbers, is how much did Tweeted results from Charlottetown affect voter response in Burnaby. How much was the slight increase in voter turnout from 2008 inspired by the Social Voting movement and how much was due to Frank in Kingston screaming on Facebook, “Harper’s winning! Get your ass out there and VOTE!”

The pundits will pontificate for months on why we have the results we do. Did Harper get his majority because Canadians care more about the economy than they do about honesty and transparency? Or did he get it because we hate elections and punished Ignatieff for forcing one? Did Jack gain in Quebec because his attack on Micheal’s attendance record hit home? Or because he bloom has fallen off the Separatist rose? I’m not certain we’ll ever truly know for sure.

But what we do know is this, for better or for worse the people have spoken and we are going to have to live with it for the next four years. And I am fairly certain that last night’s results will change the way elections are conducted in this country, one way or another.

Unexplored Territory

Yesterday I went down to the Juravinski Cancer Centre for the first check-up since the end of my radiation treatments. My radiation oncologist Dr. Wright and his resident poked, prodded, peered and perused every corner of my throat, inside and out. The tissues are healing nicely, slightly ahead of the average curve apparently, there’s no swelling anywhere there shouldn’t be, and everything is returning to a colour vaguely resembling the colour it was before it all began. The conclusion: he is willing to go out on the proverbial limb and declare me to be 100% cancer free – with 95% certainty.  The 5% is reserved until after I have a high-contrast CT scan performed in the next few weeks in case it reveals something completely unexpected. Failing that though, I’m done. To quote the good doctor, “Just keep doing what you’re doing and we’ll see you in six weeks”. In two weeks we’ll see if my surgeon is willing to make the same bold declaration.

If he does, it’s a declaration that has me facing some previously unexplored territory – the future.

Let me explain…

I was 14 in 1967 when my Dad decided to explore the family genealogy as part of the whole ‘Centennial Year’ thing. What we discovered was that the males in the Gray family are pretty short-lived. On average we tend to kick off in the mid-Fifties, with the overall average being a ripe old 56. In the dozen or so generations he was able to track down nobody survived past the age of 60. My father did not buck the trend, passing away from colon cancer at that very same Gray family average.

So over the next few years I thought about that from time to time and by the time I reached my twenties I had pretty much resigned myself to the idea that 55-60 years was the best I could hope for. Planning for retirement was pretty much set aside and I started living life with little more than your basic 5-year plan.

But now, it looks like I have to re-jig my thinking. It would seem that there is a new paradigm on the horizon; for the first time in my life I have to seriously consider the prospect of growing old!

I know, to you it sounds strange, but the reality is that I truly had fully resigned myself to dying of cancer sometime in my Fifties. In fact, in some respects I was actually looking forward to it; you know, seeing Jesus and all. When Dr. Wellman revealed that cancer had been found in my cyst back in November there was no shock, no dismay, no fear, because I had been expecting it all along. The diagnosis arrived exactly on schedule just as it did with my father. There were no surprises at all.

However, one thing has changed – medical science. Unlike all the preceding generations, when the inevitable struck me, no one was saying, “This is it I’m afraid. You have x months to live.”  No, instead, there was a very confident team of specialists saying, “Here’s how we’re going to get you out of this.” They laid out a very convincing plan of action and all that they planned has gone exactly as planned, maybe even a little bit better.

There was another difference as well. While my family has always been of the church going variety, faith in God to change the future was never a part of the religious dynamic. Faith was something that carried you through the hard times and gave you the strength to face certain doom with the traditional British stiff upper lip. Disease, misfortune and death were not things to pray your way out of, they were part of God’s mysterious ways and no one seriously expected anything to change.

I however, have been blessed to be part of a praying and more importantly believing faith community. Dozens of people have contacted me to tell me they are praying for my successful recovery; there have been dinners brought to the door, rides to treatment offered and a variety of other expressions of love and support that have, quite frankly, left Roberta and I feeling slightly over-whelmed. And it would seem that all that prayerful support have borne fruit. The cancer has come and gone and I’m still here. Praise God!

Now, before I get a minor flood of emails taking exception to my crediting God in this I will answer your objection right now. I have absolutely no idea why everyone who is prayed for as I was doesn’t get healed. I have no doctorate in theology, no inside track on the details of God’s plans for the Universe, and no pretensions for being anything other than the simple believer that I am. However, I am a believer, and I believe that the prayers of my friends at Kortright and elsewhere have had just as much a bearing on this outcome as the ministrations of the doctors, nurses and technicians at the Juravinski and St. Joseph’s in Hamilton.

And I am immensely grateful to each and every one of those who prayed, cooked, drove, hugged, filled in for, and gave of their time and resources to support Roberta and I over the last 5 months.  You people are amazing!  God bless each and every one of you!

However, that still leaves me facing a future I never thought I’d face.  And though the prospect is actually a little scary, I’m looking forward to it. I now have to actually ponder what I might do with my twilight years. Any suggestions?

Till next time… Shalom.

Once More with Feeling

Today I am headed down to the Juravinski Cancer Clinic in Hamilton for the LAST of my 35 radiation treatments.

In recognition of this momentous event, I present to you dear Reader a poem I have been working on for ahile now. I feel it only right to recognize the person responsible for my experience of the last 7 weeks.

Of course this will not be my last trip to Juravinski. I’ll be back for a check up in 4-5 weeks, and then a CT scan 4-5 weeks after that. But, as they say, the worst is over. Now I can start to heal.

Until next time, enjoy the poem… or not.

Shalom.

On Madame Marie Curie (by Dennis Gray)

Madame Marie Curie
It’s all her fault you know,
The pain I’m feeling now.
The constant scratching in my throat,
The taste buds that no longer work,
Spit glands producing at under 10%,
Energy levels of a man twice my age,
Leathery skin that flakes so easily.
It’s all part of her legacy.

She started it you know, she and her radium, polonium.
It didn’t take long for the crackpots to follow;
Radium water, The Cosmos Bag, Radithur
Fiesta Ware, eat your meals from uranium dishes
That will cure your ills.
All because of her and those Nobel prizes.
Cures worse than the disease.

But “time marches on” as the newsreels say
And soon the quackery falls by the wayside,
And Marie’s science remains still.
Isotopes collide, neoplasms fall,
30, 40, 60 Gy (gray) and counting,
The tumours can only take so much.
The Cancer succumbs to the onslaught.
Pain is temporary, moisture will return,
The colours in the CT scan will realign,
The “South” will rise again,
And there is new hope for tomorrow.

Yes, it’s her fault alright!
Marie Curie and her little glowing saucers.

Merci Madame. Merci.


Addendum: For those of you who may not know; Marie Curie and her husband were the first to experiment with radium and other radioactive materials (a term she coined).  Among those experiments was the use of radio isotopes to destroy neoplasms, that is, cancers.  She won Nobel prizes in both physics and chemistry for her ground breaking work.

Image courtesy Wikipedia Commons.

Marie Curie - wkipedia commons

Marie Skłodowska–Curie

Side effects may include…

It’s a strange thing when you are doing well means you aren’t doing any worse than average. I had my third review with the radio-oncologist the other day and he tells me he’s pleased with my progress. I suppose I have to take that at face value, but it’s hard when you realize that his standard is based on how bad most cancer patients feel at this stage. Since most people feel the same as I do or worse, he’s pleased because I’m not feeling worse than I am. My pain levels are increasing “pretty much on schedule” and he’s content to continue “farting around with various meds” until we find the combination that manages my pain the best.

I know that it’s my frustration talking but it really is hard to endure some days. I never truly appreciated how small changes in my life could make such a big difference.  I haven’t talked much about about the side-effects of the radiation treatment, so now seems like as good a time as any.

The primary target of the radiation treatment is my throat, since that’s where the tumor was located in what was my right tonsil. However, since the cancer cells that originally blew the whistle were in a cyst attached to a lymph node basically everything from the Adam’s apple up to my earlobes is being bombarded to one degree or another.

Most noticeable is the area at the back of my throat, the traditional ‘I have a sore throat due to cold’ location; although in what can only be described as the biggest pain in the neck since  the guillotine, nothing that would traditionally sooth a sore throat can be used in this case, as all of the traditional remedies will actually aggravate the condition. So no cough syrups, lozenges, citrus based juices, or dairy (yes that means ice cream).

What this all boils down to is swallowing hurts – all the time. Imagine the mother of all strep throat cases and there’s nothing to take for it except Tylenol3, in liquid form no less as liquids are a little easier to swallow than solids. However, the Tylenol elixir stopped working about a week ago and now I’m on another liquid cocktail of various pain medications. Fortunately, it can be mixed with juice so it tastes a little better (I’m using mango) but that’s really a moot point because….

Everything tastes like crap!

Actually everything tastes like tofu on wet cardboard. You see, the radiation has shut down both of my saliva glands, which means I suffer from a very dry mouth. Your taste buds require saliva to function properly, so now, due to that and the radiation thing nothing, and I mean NOTHING tastes the way it used to. Ice cream and all other dairy taste like paste, bread tastes like tofu, potatoes taste kinda like sucking on a wool blanket, you get the idea.  The only thing that tastes normal are a few spices so right now I’m loading up on cumin and oregano just so there is a flavour of some kind.

Dr. Wright assures me that after the radiation treatments stop my saliva glands will heal and return to function, but never back to 100% so while flavour will return things will never taste quite the same. I will admit to a certain curiosity as to just what this implies. Will I suddenly like lentils? Will chocolate lose it’s appeal? Who knows?  A friend who had this same situation had to have most of his tongue removed, taste buds included, and now just eats to refuel as there are no tastes left to him at all.

The dry mouth also has affected other things. I’m drinking a ton of fluids (4 liters + a day) to compensate and there is a special mouthwash that is a concoction of the good doctor himself that helps a great deal, but no fluid except saliva can replace saliva and so there are still things with which one must deal.

My dentures not fitting or tasting right is one. A few weeks ago they felt okay and tasted of nothing. Now they float a lot more and have a definite flavour that occasionally triggers my gag reflex. Lots of fun.

Spontaneous coughing is another one. Although that could be a virus that I’ve picked up on top of everything else, because the radiation has also compromised my immune system. My boss called me and told me to stay away from work today because he has something I don’t need to catch. I wasn’t about to argue.

The dry mouth, non functioning taste buds, and the hurts-to-swallow thing have left me with little or no enthusiasm for eating; which is bad because the radiation is burning up my energy levels which come from the good calories not the fat ones so actually I should be eating more than usual. I’ve lost 10 lbs since I started and that’s about the limit. They tell me I must gain some weight this week. Cue the protein supplements.

The extra fluids are of course giving my kidneys and bladder more exercise than they’ve seen since my college days. (Actually I didn’t go to college but my girl friends did so I went to a lot of parties.) This means a change in habits as I must now never, ever, bypass the opportunity to visit the loo.  Even more fun I must say.

Finally; dry mouth, spontaneous coughing, perpetual sore throat and a tripling of the need to pee do not combine to make sleeping an easy thing to do. Especially since I need to sleep more to compensate for the radiation sapping my energy levels. Cue to sub-lingual lorazopam 1 mg. under the tongue before bed and while I do wake up three times a night to visit the room next door, I do sleep between visits. Thank You!

So, if I seem a little agitated from time to time folks, you now know the reasons why. Like most guys, I’m pushing myself too much and d0 need to rest more, but for the most part I seem to be handling things fairly well.  But that’s only because I’m getting a ton of support. At church, at work, on the Internet and of course from my own dear wife Roberta, the emotional, spiritual, and physical support has been amazing. I can’t begin to express my gratitude.

When I feel my lowest in the midst of all this even just knowing how many people are out there praying for me makes a world of difference. I feel like I need to see this through just for them. And believe me I will see this through. I have every intention of participating in the 2011 Ride to Conquer Cancer with a yellow flag attached to my bike designating me a cancer survivor.

Oh wait… there’s one more thing. The radiation has also killed numerous hair follicles on the sides of my face, so the beard that I have traditionally worn for the last 20 years is now toast. Guess I’m going to have to get used to looking at this face… and so will the rest of you.

So thanks everyone! Until next time …  Shalom!

What’s Up Doc?

Monday was the first of 5 Review Clinic sessions I’ll have with Dr. James Wright, my radiation oncologist. Every Monday for the next 5 weeks (the last 5 weeks of my treatment cycle) I’ll meet with the good doctor and one of the nurses in the Review Clinic to take a look at how my regimen is progressing.

We started off yesterday with a look the CT pictures they took as part of the planing session. They are a series of cross sections of my head inside the mask used in the linear accelerator. Imposed on this in a number of colours, are bands that define which areas of my head will receive what levels of radiation exposure.

The hot zone, not surprisingly, is the location of my former right tonsil, where they found the tumour. They did cut the tumour out when they took my tonsil, but there are an unknown number of microscopic “roots” that are left behind and need to be destroyed by the radiation. This area of my anatomy is a bright yellow colour in all the various scans.

In the red and blue zones are the various lymph nodes located in and around my throat; down each side of the neck, along the upper edge of the clavicle. Since the cyst that disclosed the presence of P16 was in a lymph node, radiating the lymph system makes sense and gets the next highest does based on distance from “ground zero.”

There’s a green line (I think – I have colour blindness issues) that delineates the outer most reach of the treatment. No radiation above the level of my nostrils. Don’t want to irradiate the grey cells at this point. But then in my case, every cell is a Gray cell! lol… (All right. I’ll be good.)

The clavicle forms the lower border. No radiation below that level. Everything in the middle will receive one of about 11 varying degrees of exposure that were detailed on the CT scans.  I was impressed that they could discern all the exposure levels in such detail. Gives you a real feeling that they truly knew what they were doing. That is, until Dr. James Robert Wright made this encouraging, and inspirational statement.

“Yeah…    So…  there it is.  We’ll keep fartin’ around like this for the next five weeks and when it’s all over hopefully we’ll get the results we were looking for.”

Excuse me! You describe this supposedly high-tech, targeted procedure on which I am betting my continued future existence as “farting around” ?? Nice choice of vernacular Doc!

Flatulence references aside however, the good doctor is mostly correct in his assessment. The fact remains that as far as we have come and as much as survival rates have increased, cancer therapy still remains, to varying degrees, something of a crap shoot.

They can take a guy like me, mid-fifties, slightly over-weight, average health, clean removal of the tumour, a ‘species’ of cancer that has the best response rate there is to radiation therapy, and 8 or 9 times everything will work well and you get the results you were hoping for. Then there’s the 10 or 11th guy in the list; all the same parameters, all the same drugs and treatments, and for reasons you and your $100 million cancer clinic have yet to work out, it all goes to hell, the cancer remains firmly entrenched, and the guy dies.

I don’t know if Jim Wright had one of those days last week or not (I was his first appointment on Monday), but I can imagine that after a man like him, who has invested his life in this work, has a case go sour on him it can feel like all he’s doing is “farting around.” We are all prone to feeling ‘useless’ when we do everything right and it still doesn’t work.

However, focusing on the 10th or 11th guy isn’t going to help any unless you’re a research pathologist. For the rest of us we… I need to focus on the other 8 or 9 guys who make it. It’s like Paul says in Philippians:

Finally, brothers, whatever is true, whatever is honorable, whatever is just, whatever is pure, whatever is lovely, whatever is commendable, if there is any excellence, if there is anything worthy of praise, think about these things. Philippians 4:8 (ESV)

So we continue on. Supported by Dr. Wright (whom I still have complete confidence in) and his amazing medical staff and volunteers at the Juravinski Centre, and by the many of you who are out there praying for Roberta and I. If you are inclined to do so add Dr. James  Robert Wright and his staff to your prayers; they work hard, care much, and need all the support they can get. Besides, he gave me these lovely lorazepam tables that make sleeping through this a hundred times easier.

I know, but before all you amateur pharmacists (and professionals for that matter – Joan) start emailing me the Wikipedia entries, telling me how highly addictive a drug it is, and regale me with all the side effects associated with benzodiazepines (I can Google it too), I am taking it under my doctor’s care and I’m real good at following instructions. So Chill!

But pondering the doctor’s choice of words aside, I seem to be in good shape; tat is, the treatments seem to be progressing as expected. The sore throat, treated with liquid pain killers, the sleeping aids, the general lack of energy and loss of appetite are all textbook symptoms and appear to be right on schedule. So I am hopeful.

Actually today, I am more concerned for my friend Darby than for me. At 10am today (Wed. Dec. 12) she goes in for a hysterectomy to remove a large fibroid she’s been carrying around for some time now. If you’re praying for me, pray for her too, please!

Till next time … Shalom.