Remembering Mark

The following was posted in The Toronto Star, The Winnipeg Free Press and the Barrie Examiner.  Please note the change in venue for Mark’s memorial on January 22.

RUTHERFORD, Mark Campbell Comrie - September 13, 1950 to December 31, 2010 - Musician, husband, father, brother, son, grandfather and friend. Born in Winnipeg, Manitoba, Mark always referred to himself as a Winnipegger. Leaving Winnipeg to further his career as a musician in Toronto, Mark moved to Innisfil, Ontario where he raised his family for over 25 years. Six years ago, Mark and family relocated to Phelpston, Ontario where he skied the trails he established on his farm with his loyal canine companion Freddie. Mark’s love of the outdoors, skiing, cycling, running and general exuberance for life was curtailed by Myeloid Dysplastic Syndrome which progressed into Acute Myeloid Leukemia taking him from us New Year’s Eve. Mark leaves behind his wife Heather, daughters Willow Rutherford and Cassandra Rutherford-Epp (Bryn), grandchildren Peter and Dinah, brothers Ed, Gerry, Tom, Bruce, (predeceased by brother Peter), mother Willow Rutherford of Nanaimo, B.C., father Ed Rutherford of Pto. Escondido, Mexico . . . and half brother to David, Jose and Daniella of Mexico. A special thank you to all who have helped Mark on his journey, especially the staff on 15B Princess Margaret Hospital. A celebration of his life will take place at the Elmvale and District Lions Hall 1979 Flos 7 West, Elmvale, Ontario from noon until 4 pm on Saturday, January 22, 2011. The family requests that in lieu of flowers, a donation to the Princess Margaret Hospital would be appreciated.

The following are directions from Hwy 400 North & Horseshoe Valley Road  http://maps.google.ca/maps?f=d&source=s_d&saddr=Exit+117&daddr=44.538157,-79.898762&geocode=FcFKpwIdQ1g_-w%3BFS2ZpwIddtc8-w&hl=en&mra=dme&mrcr=0&mrsp=0&sz=14&sll=44.522091,-79.734478&sspn=0.032862,0.055361&ie=UTF8&ll=44.543995,-79.823914&spn=0.131398,0.221443&z=12

Additionally you will find a lovely article by Barrie Examiner writer Susan Doolan on Mark at this link:  http://thebarrieexaminer.com/ArticleDisplay.aspx?e=2926901&

The Journey Continues

On New Years Eve, 2010, Mark’s spirit left on its new journey.

After deciding that he had provided so many with the sense of adventure, love and joie de vivre he has said good bye to all of us that have loved him so.

Mark left surrounded by love and care, from family members, the staff at PMH and his wonderful friends who fueled his energy to the end.  May his life be an inspiration to all who have known him to go a little further, to listen a little harder and to care a little more as he would have.

Mark Campbell C. Rutherford   September 13, 1950 to December 31, 2010…husband, father, grandfather and friend.

There will be an open house on January 22, 2011 from 12 to 4 at the Elmvale Lions Hall 1979 Flos 7 West Elmvale Ontario @ L0LP10.

Below are directions from Hwy 400 North and Horseshoe valley Road:

http://maps.google.ca/maps?f=d&source=s_d&saddr=Exit+117&daddr=44.538157,-79.898762&geocode=FcFKpwIdQ1g_-w%3BFS2ZpwIddtc8-w&hl=en&mra=dme&mrcr=0&mrsp=0&sz=14&sll=44.522091,-79.734478&sspn=0.032862,0.055361&ie=UTF8&ll=44.543995,-79.823914&spn=0.131398,0.221443&z=12

 

Until we meet again

Heather, Willow, Cassandra and all who have loved you.

Christmas carols

Yesterday Cassandra, mini-Dinah, Bryn, Mom and I met up at the PMH in Dad’s room. We’ve been here a long time! (Dad celebrated his 60th birthday here back in early Sept!) I have a cold and it is hard to control my over-protectiveness about him at this time. In fact it is hard to know if I myself should be even 10 feet away with my snotty nose dripping behind my sterilized hospital-issued facemask. Mom stayed with him again last night and I went to bed around 7 with a mug of Neo-Citron. This stuff reminds me of Flintstone vitamins melted in water. Hypochondria for my father aside, the nurse told me since Dad is on anti-biotics I can be around him if I wear one stylish pale peach facemask, so here I am, breathing in and out the odor of my garlicky kale salad I made for lunch, protecting my Dad not only from germs, Dracula, but also my temporary (I hope!) halitosis.
Seeing Dad in this condition breaks my heart, yet he so amazes me with his tenacious wit. He was telling us that there were leaches on his fingers, then he cocked one eyebrow and amusedly looked us square in the eye and said, “What do you think about that?” He is often answering questions in the most random ways and although there is a look of feeling lost, he seems kinda amused by the whole ordeal. Except of course he is often drifting off into sleep mid sentence. I was telling Dad about the car ride from the farm and how Sam (aka Cassandra) had a hard covered Christmas book and was sitting in the back seat beside Dinah, insisting on singing the entirety of ‘the Twelve Days of Christmas’ and how I managed to wrestle the book away, but realized that no, she had indeed memorized the lyrics at a young age and continued on with her amazing memory. Dad looked like he had fallen asleep and then he piped up “Sam’s a bugger.”
A little later on, Mom lead us in a round of Christmas carols. (If you know my Mom, you’ll know that historically she always sat back and watched, very rarely participated in the family’s music making, and we always find it such a gift when she chooses to sing with us.) We were ploughing on through with the usual kitchy melodies and harmonies when Sam and I noticed although Dad looked asleep he was mouthing the words to Jingle bells. What a guy. I’m choked up just writing this.
Christmas has never meant much to me, the tradition of gifts and cookies…, I mean it’s nice we get a day or two off from school/work/riding the public transit, but it always seemed like something was missing from the calculation of what is supposed to be the formula of ‘Christmas.’ I just watched this fantastic film about the Finnish chidren’s version of santa ‘Rare exports’ and basically Santa was a disciplinarian with horns and no red and white Coca-cola issued velvet parka-suit to be found. (Weird segue I know.) Cool film though! AND you get to learn some Finnish! (In fact this is not even a segue, it’s simply an interruption!) Talking about interruptions, Dad didn’t really want to talk on the phone today, so I’m sorry if any of you called and didn’t get an answer, or I turned you away, but he wasn’t in the mood to chit-chat, in fact the few times he spoke he fell asleep within the first or second sentence. I think it’s better to leave him be til he feels better, as stimulation (engaging him in conversation) often leads to his seizures. Back to X-mas…..
Perhaps it’s an opportunity to melt increasingly frosty hearts before the deep-freeze sets in. I dunno. All I know is I sure am glad that Dad’s still here, if only for a short while. He certainly has made his mark on the hearts of many, and with Mom, he gave Sam and I ours.
Merry Christmas everybody.
Love Willow, Mark and the rest of the sprawling clan here.

December 22 2010

Uncle Ger and I have decided to write a post for the blog today on
Dad’s behalf. Gerry’s packing right now so I guess I’ll start us off.
We have been by Dad’s bed side for approximately 2 weeks give or take.
Now allow me to refer to ourselves in the third person for rest of
this post! ;) Yesterday was a roller coaster of a day. The mixture of
joy and fear that we experienced was quite intense. The doc arrived in
the morning and uncle Ger and I witnessed him telling Dad that if all
went well he would be going home the next day as he was reacting
positively to the necessary change in medication that made a homebound
journey a  possibility. Throughout all of this Dad has insisted he
wanted to go home, so even though we had some misgivings we all agreed that going home was going to happen. So we lined up the necessities that would make the transformation from the ward to home possible such as oxygen, nursing care, and of course the standard issue hospital bed. Like so many things in life it’s so hard to figure out what is
the best thing to do.

Buoyed with the prospect of home Mark’s spirits soared and planning for tomorrow began. Gerry would stay with Mark overnight and pack up his stuff while Heather got things ready at home. It all seemed so fantastic. Willow and Sam were pitching in between feeding babies, gigging, work and everything else they have going on. And as sometimes happens in life just when things look like they’re going in the right direction, to use a baseball metaphor, the pitcher throws a sinking curve ball, over the plate, unhittable.

At about 9 PM Mark had the first of about 4 seizures last night. It appears that at some point in the very recent past there was a small
amount of blood that leaked from a capillary into the right side of
his brain where it is not supposed to be. Blood tissue irritates brain
tissue and causes a sort of short circuit. Fortunately care was
immediate and a CT scan revealed where the bleeding occurred.
Unfortunately in Mark’s case they cannot correct the situation with
surgery, they can only manage it with sedatives. Needless to say,
going home is going to be delayed for a while and we are all
disappointed. But true to form he soldiers on, cranky, sarcastic and
verbally sparring with the good natured nurses at every opportunity.
The respect is mutual and the compassion they show him knows no
bounds. The staff here have our eternal gratitude for the care Mark’s
received.

Mark is such a fighter………

 

Good wishes to all

 

love Willow and Gerry

Mark’s update continued December 17, 2010

Mark has asked the I (Heather) update you all since in his present state, he finds it difficult to concentrate on his blog or emails. After winning from another bout of fever, he has been experiencing pain in his back.  Now, this can be a number of issues, but the main thing that we have to concentrate on right now is to make him comfortable.  He is on numerous antibiotics which will treat whatever is causing the discomfort, but at this time the Doctor is of the opinion that we should not subject him to any more poking or probing, that the problem should resolve itself in time.  In the meanwhile, he is on Morphine and seems to be pain free.  So if you are calling him, and there are gaps in the conversation, it is the magic space that morphine provides, since the original term “spacey” certainly is the best description of his state of mind.  Mark tends to become distressed of the “stupid” state his mind is in and uses the term stupid to describe how he feels.  It is difficult for him since he normally has a quick brain reaction, but as we all agree, it is better to be stupid then to be in pain.  It may take him a bit longer to get his sentences out, and his attention span is similar to grandson Peter, but we all need to slow down and it’s a good opportunity to do so. Willow has been staying overnight at the hospital.  She is such a hero.  She looks after her dad with such care and attention, seeming to know what he needs and how to do it for him.  This hospital allows us to stay in his room with him and allows for visitors whenever they can come.  There appear to be very few restrictions, the only concern is the health of the patient, be it physical or mental.  I cannot explain about the heros in Mark’s life right now.  I see them everyday.  They are the doctors whose caring ways and positive attitudes lift their patients from the reality that is their fight that day to the steps that they must take to continue this journey.  They are the nurses, who despite working with heartache daily will come into a room, have a soft conversation with their patients, revealing the layers of their own lives while administering to the wants and the needs of patient.  They are the friends, who constantly give encouragement, through phone calls, emails, blogs and visits.  They are the families of the patients who carry the same look of someone who experiences the feelings of inadequacy that tugs at your heart strings.  They are the security guards who regularily check in to see how everyone is doing, especially Mark who they have danced and listened to over the last few months. They are the neighbours who come and help out with snow plowing, taking the dogs for a walk, bring a meal or a bottle of wine when they knew Mark’s family was here visiting.It has been difficult over the last while.  The snow has not stopped in weeks, the roads have been unplowed and driving to the train, to go to Toronto first thing in the morning and last thing at night has been a challenge.  But there is the conductor who waited for me to get to the train when he saw me coming rather then following his schedule to the minute, and the wonderful small acts that people do everyday that lift my spirits.  Cassandra and I will be going to Toronto tomorrow to see Mark with baby Dinah.  it has been difficult for her to go with a new baby, so she is quite excited.  Gerry, Mark’s brother arrives tonight and will stay with Mark tonight in his room.  Willow will go to work and allow them to be together, to talk and enjoy each other.
When Mark is off this medication, he will be returning to his blog.  Hope you all are well and enjoying the season.  This is time to be thankful, to reflect on what we have, to look to the future and to think of others.

Dec 12

Recent days have crawled forward with periods of challenge and postponement. Fever has unpredictably crept in and out of the day to day, giving hope as it subsides. The two step forward one step back continues, although with maybe discernible differences in degree. As I am able I try to maintain some small routines, walking around the block a couple of times after meals, some gentle rhythmic breathing daily.

The beet juice was a great idea but it assumed control over my digestive system. Describing my ails to one of my nurses, her response was, ‘Mark are you still drinking that beet juice! Maybe your body is not really used to that!’ (you idiot!). Last night was rounding out to be of those joyful ‘can’t sleep cause of the fever’ experiences. So at 2AM I acquiesced and took 2 tylenol, whose job it is to crack the fever, give you 6 hrs of feverless sleep and dump you back into the fever again. Alright, whatever I’ll do it! But of course the fever needs to break and I wake up twice in short order lying in a puddle. But the girls are so on it, the bed is stripped, I’m freshly gowned before I know it.

I am comatose until 8 when breakfast arrives (and I’ve learned to eat that while it’s hot). Then I go for my morning training run (umm, ok shuffle), back to command central (bed, computer), look outside at the huge expansiveness of west Toronto and realize oh… the fever is waking up. I hunker down for another duller day.

The nurses do a 2nd Cup run in the morning and I’m becoming part of the club. Sasha is the ringleader and loves her double espresso short. I put in for a latte with weight-gain in mind, which is not doing too bad by the way. Then I phone my brother Bruce in BC. It’s 7:30AM there and he’s sleeping after his late-night company Christmas party. He calls me back a few minutes later after coffee’s on and Sasha arrives with my latte. Bruce and I must have have talked for at least an hour and a a half. About 10 minutes into that latte, my fever broke and was normal most of the the day.

Heather’s Update

As it turns out coming home this weekend was a tad optimistic. Fickle finger of fate I guess.

Heather elaborates.

Wish I had better news, but unfortunately, Mark will not be coming home tomorrow.  This crazy disease gives him some reprise and then stabs him in the back when we all tlhink everything is going well.  He would so love to be back with his piano, his dogs and his home, but until the infection and fevers stop, he is better at PMH.
Good news is that he will have nurse care when he is back at the farm.
We have had quite the visit from the Rutherfords.  First Bruce, Mark’s youngest (from the first brood), then Tom and finally Ed (next in line in seniority to Mark), his wonderful wife Marilyn and the special appearance of Sr. Ed, Mark’s dad who arrived from Mexico in sandals….So the first action was to find Ed shoes…Thank you Bryn and Grandad MacAskill who both have size 12′s.  So it snowed, and snowed and snowed….but everyone has had quality time with Mark and all the Rutherford clan out here.  Peter and baby Dinah got to meet all the uncles, aunt and great grand dad on a first hand basis and were totally entertained by everyone.
The fields are covered with snow now, and the turkeys were on the road this morning when I was heading to work.  They are so bold, they don’t want to move off the gravel, despite my honking.  I think they don’t understand that cars don’t know anything about hunting season and could end up with one in the freezer if they refuse to vacate the rite of way.
I am sorry if I have not been in touch, but I am bushed most of the time.  I may not be answering calls for the same reason, but will eventually get back to everyone.  Heading down to Toronto tomorrow morning to check up on Mark.  Willow Jr. is there now, as she draws while he sleeps.  He needs to sleep to fight this thing, so if he doesn’t answer the phone, it because he needs his shut eye.  It isn’t a bad idea to text or email him first.  Usually that’s what I do if he is not answering.  That way he can let me know when it is okay to call since he needs to rest right now to get strength.
Take care everyone and will update when I have more news.

Heather @ Coyote Crossing
705-322-5476

Mentor

It’s about day 42 since my re-admission on 15B. After a lot of ups and downs, the upswing is slow but coming along. I’m getting more mobile daily. My blood counts are stable if not increasing. A month of family visits has allowed for some moments of real joy and connectivity. It has been a family-wide affair with lots of shared time with me at PMH and Heather and the girls both in Barrie and at the farm. At 83 my dad just keeps keepin’ on and yesterday had lunch with his 89 yr old sister in Bowmanville. Living in southern Mexico, Dad just announced he was doubling the size of his morning coffee club walk to over 4 km.

I must take a minute to again extend a heartfelt thanks to all who are engaged by my postings. There is no question that I can feel this power. Your responses through comments on the blog, emails and phone calls always give me a measure of solace – OK… maybe some self-importance. There has been a daily procession of visitors through my room and with my family being here on a daily basis it has been busy – but very stimulating. If we exceed the population standards of my room, we just move down to the lounge. There have been some notable spontaneous incidents. Two of my most unique and colourful longstanding friends – Gary Taylor, drummer, photographer, and morphing Italian – and Penner McKay, drummer, percussionist and proud father of 2 busy musicians (with whom he is doing a concert in Winnipeg this weekend) walked into my room not 5 min apart one morning. They had known about each other, subbed each others gigs for years but never met face to face – thoroughly enjoyable! Another drummer friend, Jim Hillman drove from Montreal specifically to see me. Jim and I first started playing together in Winnipeg. He lived with Heather and I for some months when Willow was born. Then he moved to Montreal and has made his living playing with the likes of Sonny Greenwich, Oliver Jones, Raneé Lee. We spent some very quality time together. Yesterday 2 spontaneous visitors arrived. Scott Hurst who is one of the most visionary proponents of the arts in Simcoe County (Greater Barrie Area) is an actor and director who works tirelessly to promote broader culture, plus is a regular performer at regional theatres (recent 6 mo Stratford) across Canada. Moments later, Chris McCulloch, who I have mentioned in this blog before as an orthodontist and researcher, formerly Junior Barnes, leader of  the hottest bar band in Winnipeg through the 70s and then in Toronto through the 80s, made his entrance. Chris is now an active supporter of performing arts and was most interested in what Scott had to say on the subject. Finally my brother Ed was coming up the overloaded elevator at PMH yesterday when he looked over with recognition and cuffed a fellow on the head. It was an icebreaker to say the least, kinda shocking the workaday Toronto folk. It was Bob Omar Tunnoch, Ed’s best friend and neighbour through his school years in Winnipeg. I’ve mentioned Omar as a frequent flyer visiting me here and bassist in Fathead, one of the most happening blues bands in Canada. Ed and Omar had a heartfelt reunion.

So my renewed energy has got me up and about and walking the halls again. I’m kind of the grand old man here. Last night I did some patient visiting and found myself in the role of mentor. There is definitely a fullfillingness in discussing people’s conditions and then relating to my own often more advanced experience. I have survived 2 fairly heavy rounds of chemo reasonably intact. I have managed to avoid some of the darker occurrances here on a daily basis and positively engage with the doctors and nursing staff. My friend Jan whose neighbour’s wedding we crashed (described in a older post) lost that neighbour plus the subsequent in demoralizing short order. We discussed the deleterious effects of her chemo and and the prospect of facing a second such treatment vs the quality of life at home on whatever supportive care could sustain her. One of the downsides of chemo is that it punches holes in you inviting infection while your immune system is disabled. Further chemo treatment has been ruled out at least for now in my treatment, which pleases me.

Plan C

OK. Time to change it up. Done the ‘dis and done the ‘dat and we are are treading some water. It’s all been good. Learned a lot. But definitely a ways to go here. I’ve gone the institutional route and made some great strides. I’m still here after 6 mo of transfusions, 4 months of remission with vidaza, 1 1/2 mo induction chemo and now 1 1/2 mo re-induction. My blood counts are apparently rising (touch wood), my blast counts unfortunately have not lowered to remission. This unfortunately rules out the stem cell transplant solution at least for the the time being. The doctors agree conclusively I could have 2 months or maybe 20 years. They are recommending I apply for some experimental trial treatment through hematology. This of course I totally plan to check out. However I really consider future treatment to include a wide rang of possibilities.

You see, I’m not really an institutional guy. I’ve more or less avoided being a part of society’s institutional makeup, doing just what I have to do to get by, and relating to large organizations through individuals with whom I can establish some kind of personal bond. But I am mightily apprehensive about sliding into that hole where my name is relegated to that 7 digit # on my wristband. Whew! Sorry.
So the the short of this diatribe is that I am casting my hook out to that big open sea that includes alternatives. Best case scenario is that through a combination of nutrition, excercise, meditation, good vibes and perhaps a dollop of an appropriate experimental trial program I can keep myself alive long enough to figure out how to stay here. Friends and acquaintances have offered me tips and programs that have worked for them. Zibi is one of my fellow patients and former roommate here on 15B came in here with the ‘car accident’ variety of AML I described in a recent post. That’s the one where you check into emergence with a sore leg, and they tell you it’s leukemia and you’re on 15B at PMH the next day. His family are very devout Polish Catholics and very quietly pray together, with as many of the the 5 kids that can be in attendance. The first time I heard it I was amazed at how inspired and strong it was. The intonation was so quiet and in sync as one voice that you could hardly hear it, but you sure could feel it. Beata, Zibi’s lovely wife and a math teacher, brings me fresh beet juice every day.
My current crop of guests includes my brother Ed and his wife visiting this week from Sydney BC. They also flew my Dad up from Mexico for the week. My daughter Willow drops by every afternoon. Yesterday I announced to everyone that it was time to go play the piano in the atrium. I had been pretty restricted in my mobility because of low blood pressure, but was feeling a bit better. So downstairs we went. Willow had seen one of Zibi’s kids who told his family. They all showed up a few minutes into the concert. Marc (a wonderful musician from Barrie) and his wife Maryse walked in the door just as I got started and I played for about an hour with a wonderful audience. Of course I pestered Willow to get up and sing and the magic reached new heights.
It is truly amazing how wonderful life can be!

A Truly Special Friend

I met him on a school excursion that Flor, my Dad’s wife had organized. It was maybe 1991.  We were the chaperones. Pierre was going in support of some of the the kids in his neighborhood that were in Flor’s class. Flor had asked me if I was interested in coming along with my own kids and meeting some Mexican teenage girls. It was a trip to the Manialtepec Hot Springs. We showed up at Dad and Flor’s at dawn. I hadn’t the least inkling what a life changing experience that day would prove to be. At first impression, there was something slightly odd about Pierre. He was willowy tall and white as a ghost. Though he spoke perfect English in an almost upper – crust vernacular, culturally he was overwhelmingly French. At first I thought he might be gay, but as he warmed up, his back-slapping British soccer fan mannerism was a first reveal of a very deep and multi-dimensional character.

Flor drove us in her truck, throwing my little 7 and 5 yr old half-brothers David and Jose into the mix. Pierre had a cute little Suzuki Jeep (still can be seen bouncing over the pot-holes of Puerto Escondido today) which he filled with his neighbor’s kids. The rest of the journeyers were waiting for us at their Dad’s ranch at the trailhead in Manialtepec. Well it was a test just to get to the village, driving an hour up the mountain on a dirt road. We were greeted by a few more teen girls and a row of saddled horses. It was obvious we wouldn’t be driving any further… except Pierre as it turned out, was offering seating to Flor and myself. But I had my sneakers, prepared to run the distance after my butt gave out on the Mexican saddle. The trek was another 10 interminable miles up the mountain from the ranch. The trail itself was nothing more that a goat path etched into the side of the river gorge, constantly impeded by rockfall from above. Below, Pierre with incredible conviction bumped that little Jeep along up the river bed winding around huge stones, getting stuck regularly and figuring it out to keep going. For the first while I rode a horse that turned out to be one-eyed blind on the downside. But after trying to ‘ride’ him initially, I realize he had way more business being on that trail than I did. So I  just sat on him until I could not longer handle the threat of immediate peril. Then I ran the rest of the way. Well, the Jeep finally mired itself, as the increased water flow and steepened pitch of the river signified our approach to the hotsprings. The Mexican and Canadian girls had bonded so well that whether anyone else was there or not mattered less. They were having a ball. We found the hot springs and hung out there for a few hours. Flor lay right out in the springs, ignoring the protestations of her little boys who were understandably bored of this long trip. Pierre and I talked, finding all kinds of things to like about each other.

On returning to Puerto Escondido, Pierre invited us up to his house for dinner and drinks. He had begun moving from Paris to Puerto Escondido and was doing so in steps over a couple of years while he built his house. His wife Martine was still in Europe, liquidating his home and business. He had found an incredible high point on the hill overlooking Marinero Beach. During the wet season the gorge above which his house presided filled with the flood that burst the main PE laguna, flushing it and all the dead and decaying matter collected in the gorge and laguna over the previous year into Marinero Beach, then quickly sucked out to sea. In the winter season it dried up and became the main thoroughfare for all human and animal traffic from up the hill for miles accessing the beach. In later years when the house was finished, the light on the corner of Pierre’s garden wall was the highest landmark visible looking up the hillside at night while standing on the bridge by the laguna. Looking down night or day the view was a unique vantage point of Marinero Beach that one would never know existed without being there to see it from Pierre’s garden.
On our first visit that day, Pierre’s house was in the early stages of construction. There were six or seven teenagers including my two, and the rest the Mexican girls. Pierre had strung up some Xmas/party lights on his construction-zone terrazza, broke out the soft drinks and pumped up the music, The girls were having a wonderful time. One thing I’d like to point out. When it comes right down to it, there aren’t many impediments to a teenage girl party. Language is definitely not an issue. The less verbally understood, the more fun everyone has. And the girls spent the rest of that week together mostly giggling out of control over at the pool at my condo. But that first night on Pierre’s unfinished rooftop under beautiful starry Puerto skies, Pierre and I were establishing a friendship that would bond us together as few ever had for me. I told him about my life as a musician in Canada and he recounted tales of being a French kid attending a British boarding school, hence his crazy accent. Then he spun stories of his years of knowing and hanging out with rock stars like David Bowie and Freddie Mercury.
How the heck did he end up in Puerto Escondido? Well he’d spent time there often, beginning as a young traveller and when the doctors had given him the leukemia 6-months to live death sentence, he and Martine packed everything up, sold what they could and cast their fate to the wind. He said ‘leukemia’ so quickly I nearly missed it – my first personal contact with the word. He explained in a very offhand and inconsequential manner that he had nothing to lose moving to Mexico. He had no faith in the tubes and drugs of the medical system. That was the last we spoke of his illness. He just seemed so invincible. I did not really think about it until shortly before he passed away. Each yearly visit to Puerto, reconnecting with Pierre was the top of my to do list. Before long he became friends with Heather, my Dad and all my brothers.
As time passed his illness became increasingly apparent, but his spirit remained undaunted. His leukemia never clouded my image of him. Even as the end neared and his body was breaking down, he continued working supplying plumbing and electrical services to the growing population of snowbirds landing in Puerto for the winter. I remember vividly the last time I saw him. He was fixing Nolan’s (a friend of my Dad’s) water system. I drove past him and stopped to chat our my way to the airport. His mouth was still bleeding from teeth being freshly pulled by the dentist because of the deteriorating effects of the illness. But he was smiling and insisted he was looking forward to see us on our next visit, reminding Heather that they still hadn’t spent a day in bed together, twinkling his crazy frenchman’s eye. You just had to love that guy.
When my Dad told me he was invited to Pierre’s funeral a few months later I was so devastated and really couldn’t believe it, tearingly phoning all my brothers with the news. At that point in my life I had only felt two deaths so personally – my brother Peter’s passing in 1987 and now friend Pierre’s about 10 years later. How ironic that they should have the same name.
How many times in the past year have I wished that I had had the foresight to learn from Pierre about the nature of the illness from his experience. There’s no more valued opinion could I have had. I have dreamt so often we could have had this conversation. Probably it’s one of the biggest regrets I have today.
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