Top 10 Reasons to Think You Might Have Diabetes Insipidus

4 up

10. You don’t bother putting the toilet seat down after peeing because you’re certain you’ll be the next person using it.

9. You fill up a blue bag with recyclables from the backseat of your car.

8. You plan every trip by noting the destination’s access to clean public washrooms. If there isn’t a place to pee nearby, you don’t go. The corrollary: When choosing a movie at the multiplex, the movie’s Rotten Tomato ranking is less important than the film’s proximity to the restrooms.

7. When the attendant gives you one of those enormous 64 oz glasses of pop (soda), you know that it won’t be nearly enough, so you get one for your partner, and leave it by your feet.

6. You’re on a first name basis with the young woman who lets you back into the theatre. When you leave, she asks you if you enjoyed the movie, and you realize you don’t have a clue what it was about.

5. Over two hours, you visit the bathroom five times more often than the combined total of your wife’s eight-member book club.

4. You dream about being a cocker spaniel in a lamp post factory.

3. You find your former wine-writer self creating tasting notes for soft drinks, so you start a new blog with a beer-loving friend called Hops and Pops.

2. You pee outdoors so often it’s like you’re five years old again.

1. You start thinking about your time in the hospital with a catheter as the “good old days.”

Posted in Humor, Life, Wall-E—The Neuroendocrine Tumor | 8 Comments

21 Days in April

Hospital

It’s frightfully amusing to watch people checking me out — and by that, I mean the folks who know that I’ve just had major neurosurgery to remove a huge pituitary tumor. They invariably search my face for scars, for swollen bits, for black eyes.

Anything that might suggest trauma.

Yet I look just the same as I did three weeks ago. Truth to tell, I looked fine one day after surgery.

Thank God for endoscopy. Twenty years ago, this operation would have involved cutting away chunks of my forehead or temple to get to Wall-E, the pesky bugger who came for a visit in the early 1990s and never left. Today, neurosurgeons just widen and scrape each patient’s sinuses, and then cut the important holes internally. So just 60 minutes after my five-hour operation, I looked fine, apart from one seriously bloody nose and, under my hair, two nasty goose egg wounds inflicted by the vice that held my head tightly during the procedure.

Otherwise, I looked unscathed.

An Odd Week

The irony is that even though I look pretty good, I haven’t had an easy time of it. I spent four days in the neurosurgery step-down unit and, apart from one brave and seriously-ill grandmother with a shunt draining blood from her cranium, my roommates changed several times. My cronies were men, shaved bald, with Frankenstein stitches from having half their skulls cut away, yet they were shuffled off to ward beds after 18 hours, and released a few days later. The guy who looked like he was still waiting for his day in the OR had to be kept under close observation.

It was an odd week, by any measure. I had but 12 hours notice that I’d be going under the knife. Thursday morning was frantic, as I called in sick to work, sent off a few messages to friends, and then rushed out to fill the car with gas, to purchase a few prescriptions I’d need in the hospital, and to buy a new robe (at half price!) because my old one, circa 1981, was disintegrating.

I arrived at the Halifax Infirmary at 11:30, was processed over the next hour (they lost my file temporarily), and left to wait in the holding area, wearing a sexy johnny shirt and a warm blanket. I have great legs. I could tell all the nurses were checking me out.*

I spoke quietly with Kristina and with my sister when she arrived. Although I hadn’t really slept the night before, I wasn’t nervous, and my blood pressure was only slightly elevated. The truth was that I’ve been so sick over the last eight months, I just wanted to put the bloody thing behind me.

The Long, Dark Tunnel

The neurosurgery operating room is seriously impressive — it’s huge and crammed with a CT scanner and rows of electronics. When I climbed up on the table, a dozen doctors and nurses swarmed, and we chatted warmly for five minutes. Then I felt the cool drip of anesthetic… and oblivion.

After a time, I entered a long, dark tunnel, though mine was decidedly prosaic. I came back to the land of a living by walking down a dimly lit corridor lined with Smart Technology projectors and whiteboards.

I saw the face of Dr. Clarke. He told me the surgery went well. Then I saw my sisters, Lorraine and Linda, and Kristina. I knew pain, could feel where parts of me had been carved away, but the pain was bearable. I learned that my tumor was massive, much bigger than expected. Dr. Massoud, the ENT specialist who assisted on my surgery, told me that it went everywhere and, if it had grown upwards as most of these do, I wouldn’t be posting to my blog now because I would be blind or dead.

The good news is that they successfully removed all the tumor they could see, though it is expected to return. The bad news is that the tumor had completely encased my delicate pituitary gland, and the surgery proved too traumatic for my little buddy.

One Lost Little Buddy

At the moment, my pituitary has decided he needs to take some time off. He’s headed south for a little R&R at an all-inclusive resort in the Dominican Republic. Odds are about 50/50 that he will spend the rest of its his days there, and I’ll have to do with out him.

Despite his pint size, the pituitary is the lord of all glands, so this leaves me in a bit of a pickle: My body isn’t producing hormones, so I must rely on pills and injections to my body functioning. With some, missing a dose here and there is no biggie. Skipping hydrocortisone, however, would quickly prove lethal.

Interesting, then, that I miss vasopressin the most. It’s the hormone that regulates our kidneys, so mine have become marathon runners. They never stop pumping. I drink, I pee. I don’t drink, I pee. I am forever chasing my thirst, always feeling like I’ve just crossed Death Valley with a leaky water bottle.

DI Infraction

The condition is called diabetes insipidis, though it has nothing in common with the better-know diabetes mellitus. In the hospital, despite IV lines and and an attempt to drown myself by drinking a litre of water an hour, I was often too parched to sleep. As a result, I felt progressively worse every day after my surgery, and my doctors — I’m at the fulcrum of three medical specialties — told me to put my feet up and stay awhile.

They administered vasopressin to turn off my kidneys at regular intervals, but overshot the mark. Suddenly, my urine became too concentrated, and sodium poured out of my body in a torrent. I felt like a ton of bricks had fallen on me, suffered excruciating migraines that I could not control, and threw up painfully.

It was pretty fucking horrible. I had a brief, passionate love affair with Zofran. Eventually, through saline drips, salt tablets, and fluid restrictions, I remembered what it was to be human again.

I was released, eight days after surgery, feeling much the worst for wear, and mostly impressed by the care I had received. I continue to suffer the vagaries of diabetes insipidus, and the migraines have been constant and brutal since surgery, which doesn’t surprise me. Every nerve in my face feels inflamed from Wall-E’s extraction, so it’s painfully easy to fall into a two-sided migraine, the worst I suffer.

I need to heal.

But it isn’t quite my time. Bad karma, I guess. Two weeks after surgery, I had stitches and a silicon shunt removed from my sinuses, along with a plug of blood as big as my thumb. Within a day or two, I had raging infection that lit up my face like a lightening storm. My face swelled, and I aged about 15 years.

I’ve spent most of the last week at the limit of my pain threshold. Finally, today, I feel like the antibiotics might prevail. Maybe.

I have love for all god’s creatures, but not these little fuckers.

Sorry, did I just write that? That really doesn’t sound like me. Perhaps I am not quite myself. But maybe, in another week or two, I will be.

The truth is that I’m cranky because I think it’s amusing, but I remain grateful. I’m here. I have another chance. I can afford the chemicals I need to stay alive.

I have people who love me.

Yeah. I’m good.

_________

* Not really. One nurse did have a crush, but it came when I was at my worst, and I needed her help. The Lord works in mysterious ways.

Posted in Life, Wall-E—The Neuroendocrine Tumor | 8 Comments

Blessedness

Blessedness

A few hours after my operation, I wept.

Yes, I was a simmering kettle of emotion. My neurosurgeon had recently informed me that my pituitary adenoma was massive, much bigger than expected, but he quickly added that the operation had gone well, so I was relieved. A few minutes later, I looked upon the faces of Kristina and two sisters, happy that my eyesight had been preserved.

As the grogginess evaporated, it seemed like I could taste and smell blood, so I imagined those vital senses would deepen with time and healing.

I took a few minutes to ensure that I could remember my life, and the lovely people in it.

Yet, inside, I was barely under control. My blood oxygen was low, and I struggled for air. With a silicon shunt in my sinuses to protect the wounds, my nose was so packed with blood that I could not breathe through it, and the very thought of lasting another two weeks so encumbered was daunting. The mental control I had to devote to this simple task was substantial, and I found myself frightened and frighteningly alone.

Perhaps all of that would be enough for tears.

But it was not.

My tears were not a sign of relief or fear, but of blessedness. They touched on revelation and unreserved happiness. They spoke of community and kindness. They reached to the heavens, but lived here with me on Earth.

They relieved me of a burden I did not know that I carried.

And they surprised the hell out of me.

What’s funny is that I knew Writers for Richard was coming. A few weeks before surgery, J.A. Zobair asked if I would mind if she worked with Steve Parrish and Wendy Russ to build a fundraising campaign to help us pay the bills during my two-month recovery. So I wasn’t surprised when many around me were. Yet when I visited the website, read the dedication, saw the dozens of editorial contributors and donors, I felt like untold years of cynicism and discouragement were lifted from my weary shoulders.

So, when my family left me to rest, I found that I could not. I wept with pure joy, for a gift that pulled one very tired soul back into the land of the living.

Over the next few days, I returned often to read the names of people I knew, and people who were strangers. I saw a few cherished names from real life, but most were online friends and kind people I haven’t yet met. I traced lines of connection from Dartmouth, Nova Scotia to other places in Canada, to the United States, to Europe, to Asia, and to Australia. I learned that I’m not alone, that people are beautiful.

I learned that love, actually, is everywhere.

So my words here are humble and heartfelt. Thank you. Each and every one of you. Thank you.

You’ve changed my life. You’ve turned a fortnight of challenges into fourteen days of blessedness that I will never forget.

Thank you.

Contributing writers to Facing the Sun: Erica OrloffJude HardinWendy RussJason EvansMichelle Hickman Sarah HinaAmy SaiaAerin Bender-StoneJohn KauffmanKate InglisAlissa GrossoNatasha FondrenTravis ErwinJennifer JosephJ.A. ZobairB. NagelNiki JabbourMark TerryCatherine VibertLaurel MontgomeryPeter DudleySandra CormierMelanie HooyengaMatt ShifelySarah LaurensonStacy ChambersAniket ThakkarStephen ParrishRobin BeckerNancy Bond

Posted in Author, Author, Life, Wall-E—The Neuroendocrine Tumor | 17 Comments

The Feasts of Lesser Men

Feasts

Stephen Parrish‘s The Feasts of Lesser Men is a spy novel based on the author’s real life experiences with the 8th Infantry Division (Mechanized) in Germany during the Cold War’s dark and dirty days. For most of this week, you can download it for free.

You don’t need a Kindle to read it; Amazon offers a variety of free reading apps, including Kindle for iPad. If you prefer a PDF file, simply let Steve know during the five-day free period and he’ll email one to you.

It’s one of the best way to market e-books. Write a terrific tale and let a couple of thousand readers become an army of promotion. Word-of-mouth has always been the most reliable way to grow a business or an idea and now, with the advent of Facebook, Twitter and the like, that army has the power to spread the message far and wide within a few hours.

Consider me one of the foot soldiers. You should march out and do the same.

Posted in Author, Author | 2 Comments

Writers For Richard

Facing

Three lovely friends — Wendy Russ, Stephen Parrish, and J.A. Zobair — have been running a wonderful fundraiser to help me manage the next two months of my recovery without having to worry about making rent or purchasing costly medications.

Their efforts have touched me more than I can say, and I’m usually quite good with words. In a nutshell, 29 writers have contributed stories to an incredible anthology — Facing the Sun — and you can receive a copy by making a donation. Any donation.

They had planned to turn it over to Telling Stories as soon as I was out of the hospital, and I was supposed to be released on Easter Saturday or Sunday. But then unwanted test results showed that I had developed diabetes insipidus, and needed more care.

So I really only arrived home late Thursday night, dry and weary, and I needed a couple of days recovery to feel ready to write again.

So, if you’d like to help, you can. The donate button is at the top of the sidebar. If you’d like to leave a comment, I’d love it. This has been one of the hardest and most rewarding weeks of my life, and Wendy, Steve, JAZ, and all of you have made it so.

But the rest of that enormous thank you will wait for another day.

Later: Thanks to everyone.  I’ve ended the campaign; it made a terrific difference in our lives.

Posted in Life, Wall-E—The Neuroendocrine Tumor | 5 Comments

Show Time

Richie

Keep a good thought for me as I head to surgery today.

Kristina and a few friends might provide updates on social media when there’s something to say.

I’ll be fine. I’ll see you on the other side.

Slainte!

Posted in Life, Wall-E—The Neuroendocrine Tumor | 4 Comments

The Nick Pick Solution

One of my young work colleagues, Nick Pick, has discovered the beauty of martial arts. In between calls, he’s full of questions and brimming with enthusiasm, so I occasionally teach him a few moves from Shotokan karate to help focus his mind, and drain some excess energy.

Since I’m not likely to see him — or any of my friends there — for about two months, I created a little video. I hope a little goes a long way.

I expect him to train hard. Osu!

Posted in Life, Wall-E—The Neuroendocrine Tumor | Leave a comment

End Game

Rl1

I am a patient man, but I wish I had a heavy bag to punch.

I’ve grown tired of waiting. Wall-E, the little neuroendocrine tumor, has overstayed his welcome. Cheeky little devil.

So, here’s how the Battle Royal of my life will play out. I’ve been lead to believe that my surgery will occur any day now, and that I will only have a few days’ notice. I have been through the pre-op drills, and marked and sent for another MRI and CT scan — and those results only have a shelf-life of 30 days. I have ten remaining.

I like my neurosurgeon, Dr. Clarke, and he comes highly-recommended. He’ll be working with Dr. Massoud, who is an ENT man; I know him very well because he was Mom’s doctor, too. He’s a wonderful, gracious man from Egypt, and I will always be grateful for the kindness he showed to Connie.

Mostly, I find the news encouraging.

The procedure is expected to take about five hours, but sometimes it takes the better part of a day. I will only spend three to four days in the hospital, and I should be out of bed on the second day. I should not be scarred because they’ll be going in through my sinuses. So my hair will not be affected!

Whew!

My recovery will last six weeks or more, and I’ll need to act like a dandy. I won’t be painting our office and I won’t be returning to karate any time soon. Perhaps I’ll be able to work on my second book, he wrote optimistically (which seems important to me now since the first book seems to be going nowhere).

I’m hoping the odds will be ever in my favor. I have a 50 percent chance of losing all pituitary function, and a minute chance of regaining some that I’ve already lost.

As a former wine taster and food writer, my heart does turn icy when I think about losing my senses of taste and smell. The chances are only ten percent, but know that I’ll be crossing my fingers on the table.

It gets better from here. I have less than a one percent chance of losing my vision, suffering a stroke, or dying on the table.

I’m not a betting man, but I like those odds.

What I don’t like is that Wall-E is expected to return. Dr. Clarke says it’s unlikely he’ll get it all, and that the sneaky little bugger will once again take up residence.

But that’s a story for another day. And hopefully a day that’s far, far away.

Right now, I’m thinking that I’d like to live happily ever after. At least for a little while.

Posted in Life, Wall-E—The Neuroendocrine Tumor | 9 Comments

Fire It Up

Sometimes I feel sorry for Americans who never get to listen to the Canadian music I hear every day.

Johnny Reid

The music video is here.

Posted in Canada, Entertainment | 2 Comments

Light a Candle

Amnesty

You’ve seen the Hollywood propaganda a dozen times. The intrepid hero is caught by the bad guys, tied and stripped, revealing a knotted chest and bulging biceps. He remains defiant, but then the sadistic torturer arrives, eyes gleaming with cruel delight. The camera cuts, but we hear sickening thuds, blood-curdling screams, and the brutal grind of metal against metal.

Yet the hero remains true, and he dies nobly without betraying his comrades.

I call bullshit. Amnesty International has been telling us it is so for a generation, and now I know it firsthand.

The Opening Salvo

This blog has been quiet seven weeks, but not because I was kidnapped or tortured. I’ve been silent because I fell ill.

That sentence feels so impotent. It’s like suggesting that Everest is just a big hill.

It began harmlessly enough on a Wednesday night with a difficult migraine that robbed me of sleep. I’ve had hundreds that bad in the last decade. I popped an Imitrex and waited for the sweet trickle of relief. It didn’t come, and I grew a little panicky. I called in sick to work, something I never do, popped a second Imitrex and crawled into bed. It still didn’t work, and now the pain crested my threshold, a full ten out of ten.

I’ve endured more than 6,000 migraines over the last 19 years, but now I found myself in an undiscovered country. Not to find a even a modicum of relief after swallowing two Imitrex was, in my experience, unprecedented. I thought the obvious, that my pituitary adenoma had ruptured, and my life might be in danger. But some part of me didn’t want to wallow in drama. Instead of calling an ambulance, I drove Kristina to work, and headed for emergency.

The Record is Hazy

The recounting that follows may be inaccurate. If so, Kristina can correct the record in the comments, if she chooses. I don’t really know how it all played out.

At emerg, I was admitted within minutes, hooked to an IV line, and injected with yet another migraine drug and an antihistamine. I was placed in a cubical with an old woman who had had a stroke. I had a CT scan and returned to my cell.

Time stopped. I was there for barely a few hours, but it felt like a week. I learned quickly that half a day of intolerable pain had stripped my humanity from me. That poor old lady was facing a life-altering illness, but all I wanted for was her and her husband to shut the fuck up.

I am so ashamed.

The CT scan was negative. My doctor — I couldn’t pick him out of a line-up today — wanted to dope me up, but since that generally doesn’t help, and we’re amongst the working poor, I refused. I couldn’t pay for a $40 cab ride. In one of my life’s stupidest decisions, I drove home.

I know Kristina called, but I couldn’t find the phone, even though it was on the bed beside me. The hospital had told her that I left against my doctor’s wishes, and she was scared shitless. She called my sister, and I finally answered and let them know I was alive.

Barely.

Kristina tried to make me drink that night, but I was nauseated. I threw up the few morsels of food I forced down. I apparently refused to cooperate with her in any way; she said that I was my difficult mother reborn. I do remember her words, but I simply couldn’t act. As with the old woman at the ER, I wished she would just be silent.

And then muscle spasms, perhaps from dehydration. Neck, back, shoulders, arms, feet. Wrenching me. Pulling me from myself. Every movement brought excruciating pain, and I screamed throughout the night.

The 1960s

I don’t remember sleeping. I believe that I lived a month in that one day.

On Friday, the hallucinations started. I would close my eyes, and colors and images would fly through my mind at warp speed. Most were geometric and pleasant enough, but a few frightened. All were exhausting. When I snapped awake, I’d ask Kristina how long I’d been out, only to learn that my hour had been 30 seconds.

We don’t have sick leave, so she had to work. We need her pay cheque. My sister Lorraine arrived from Hubbards, arranged to get a prescription of (marijuana-based) Sativex from my doctor, and my brother-in-law Don went to fetch it. I wiped away tears waiting for him. He was gone for weeks.

When he arrived, he explained that the pharmacist said I should take single dose and, if it didn’t help, I could take another in a few hours. But I had used it before. I unwrapped the bottle and pumped three burning sprays under my tongue. After they left the room, I took two more. Maybe, just maybe, the pain was dialed back a fraction. I tried to rally my courage.

The Slow Return

The following week was a blur. I’ll hit a few lowlights. I know that I was moved to my sister’s house while Kristina and my family members worked on an important fundraiser, and I hated both of them for the pain they caused me. Yet some tiny part realized I had to ease my girl’s anxiety. While there, I imagined social-media friends would worried about my silence, but I couldn’t log on because I couldn’t see the letters on the screen. I went back to see my endocrinologist in the hospital, but I did so in a fucking wheelchair.

Eventually, maybe Tuesday or Wednesday, the pain softened to a nine. Weary beyond belief, the joints in my spine now seemingly fused, I kept my 90-year-old self company. I apologized to Kristina, read status updates on FB with great difficulty, and thought that maybe I would live.

I missed the benefit to raise money for my sister’s cancer treatment on Thursday. It was a huge success.

The migraines slowly became less painful, back to my usual 7s and 8s, and the spasms occurred less frequently. I discovered that the world had gotten along fine without me.

But my recovery was not smooth. I’ve been exhausted since, not to mention shaky and off-balance. On two separate occasions, I lost touch with reality, believing myself to be trapped in a different world where the laws of physics no longer applied. Panic rose like bile, and only years of martial arts discipline brought me to a stark meditative state which allowed me to sleep. When I woke, the psychosis had gone, but the fear of its return lingered.

The Point

But now I know the truth. I can take a punch better than anyone, but now I can imagine myself tortured by some brutal regime, and I know that I would cave within a week. I would sell out my comrades and betray my country. Anything to make it stop. If I were innocent, then I would proffer the most convincing lie my mind could conjure.

So imagine what humanity does to prisoners of conscience. Imagine the thousands tortured under the One Percent Doctrine. Imagine what Omar Khadr and Maher Arar endured despite their innocence. Explain to me why business always trumps human rights, or why Dick Fucking Cheney hasn’t been tried at the Hague for war crimes.

Torture is inhumane, and evil, and barbaric.

I have always supported the work of Amnesty International and Human Rights Watch, and have sent Amnesty money as often I can afford. This experience has convinced me I need to do more, and that you need to join me.

Together, we are mighty. It will always be better to light a candle than curse the darkness.

Posted in High Horse, Life, Politics | 4 Comments