Kevin Whitaker, peintre / painter, Galerie Gillygooly Gallery

Kevin Whitaker, peintre / painter

Vernissage 11:30 à 14:00 / 11:30 a.m. to 2 p.m., samedi le 25 aout  / Saturday August 25

96 chemin Hatley Centre, Canton de Hatley

Le Dernier Souper (devinez qui vient souper) / The Last Supper (guess who’s coming to supper)

Kevin Whitaker: Judge and Painter with LBD Parkinson’s 

By Marie Moliner

Not so many years ago, a movie came out entitled: “We Need to Talk About Kevin.” Since my spouse’s name is Kevin, it was a bit of a family joke until things started to go terribly wrong. At first it was nothing obvious. His excellent driving record was slightly marred while at the cottage in Hatley Acres, when he reversed the car into a tree and dented the bumper. Later, he drove into an underground parking lot in Kingston, where we were visiting our daughter, and cracked the Thule. He was forever forgetting his keys or misplacing things and blaming the dog, the housekeeper, and sometimes me. When he asked his family doctor whether there might be something wrong, the doctor laughed and said, “No, you’re just aging. You have CRAFT disease (Can’t Remember a Frickin Thing.)” That was 6 years ago when he was 55. He had just been appointed to the Superior Court of Ontario. General speculation, given his wide renown as fair-minded and brilliant, was that the appointment was a stepping stone to higher courts. So, when he asked to take a leave of absence from work because he was finding it hard to concentrate in court and to hear the litigants, we both knew there was something else going on.

The next four years were a jumble of doctors’ appointments, where each medical specialist would pass him on to the next one. His heart and lungs were in great shape. His fitness was excellent. His hearing was normal especially given that he had spent time as a Fort Henry guard firing cannons, an environment where hearing loss would not be unforeseeable. He spent a few summers at the cottage with symptoms that could best be described as premature aging. Our daughter would gently call him “the Codge.” Our son knew his father was fragile. He walked stiffly. His facial expressions were increasingly difficult to discern. He was generally listless and unhappy. This was behaviour that was completely out of character for a man who had excelled as a partner, parent, lawyer, public servant, and, ultimately, judge. 

As luck would have it, my brother, a physician, was the first to suggest it might be Parkinson’s Disease. This was later confirmed by a Toronto neurologist. When this first diagnosis came in, we were relieved. At least we knew that there was a name for this disease and could get on with treatment. 

When the second diagnosis came in, of Parkinson’s with Lewy Body Dementia (LBD), we were dumbstruck. While the disease is not hereditary, we were well aware that his grandfather had early onset dementia and his aunt had died with a diagnosis of LBD.

LBD Parkinson’s is an insidious disease. It eats your brain. It destroys your mobility and generally kills you within 8 years of diagnosis. Needless to say, our two children grew up very quickly as we all realized that time with their father was precious. There is no cure, and the only medication is dopamine for the motor symptoms, and a cocktail of antidepressants, memory medication, and antipsychotics (for the hallucinations). Every now and then Kevin pops an aspirin when he feels the need for a little ‘something extra.’

The most remarkable part of the story is what has transpired since the diagnosis. Kevin is a beautiful man. By beauty I am talking inside and out. Let’s just say that no one would ever kick him out of bed for eating crackers. Needless to say, when I met him in law school in 1981, I was attracted to him. And then I fell in love with his brain. That brain was able to process faster than the average computer and certainly faster than most human beings. And even now that the disease is manifesting itself much more cognitively, he sees things and understands things more quickly than most. Given his strength of character, it is not surprising that he would explore a second career as an artist, even in the face of such adversity. Kevin has dabbled in drawing and painting since his father was on his deathbed twenty years ago. At that time, painting became an outlet to express complex emotions toward his father who survived, only dying last October on our wedding anniversary. 

This past February, we were visiting friends in Santa Barbara, California to get the requisite dose of vitamin D and to enjoy some warmth before returning to the glories of Canadian winter. We were walking by a large canvas in a Santa Barbara art store. Kevin turned to me and said, “Someday, I would love to be able to paint a canvas that size.” My inside voice noted that we were in California — a long way from home — and for a nanosecond a 6’ x 8’ canvas seemed to be too big a dream. However, the next day was Valentine’s Day. With the help of Sam, a lovely painter who worked at the art store (and who also paints large canvases), a 6 foot canvas for Kevin was delivered. He began to paint in the backyard. He went on to paint three large scale canvases in one week. They were bright, bold and filled with energy. Later he called them: Dictator, Beach Boy, and Pink Lady. 

Those three paintings were the beginning of what has now become his raison d’etre. Eight weeks later he opened his first show on Friday, the 13th of April, at a local Toronto gallery. He titled it “Chasing monsters” to capture the reality of his daily hallucinations. Hundreds of people came out over three weekends to see his work. He received coverage in several newspapers, had an amazing interview on CBC’s Metro Morning and emerged into his next career as a painter. All proceeds were donated to LBD Parkinson’s Research.

That show crystallized a pent-up creative energy that continues to fuel his need to paint large canvases, despite an increasing number of Parkinson’s freezes and erratic memory. His next show will take place in the Eastern Townships in Quebec on the last weekend in August. Perhaps what is most remarkable is the creative process behind this show’s theme. The show’s theme is entitled “The Last Supper.” The paintings depict figures of note, whom Kevin has selected as having earned the right — based on their achievements — to be invited to the “Last Supper.” As of this writing, all of the characters, other than Jesus, are women. They include Frida Kahlo; Mary, Mother of God; Nadezhda Krupskaya; Emma Goldman and Rosa Parks. While the painter’s style has changed over time (and you will be able to see some of his earlier works) there is no doubt that the man who was once a judge is now an artist 

We hope you will be able to join us August 25 and 26th or by appointment the following week ([email protected]), at the Gillygooly Gallery, 96 Hatley Centre Rd. North Hatley, Eastern Townships, Quebec.

Protégeons les plans d’eau, ensemble / Together, let’s protect our lakes

Mylène Paquette, qui a traversé l’océan atlantique, seule à la rame, a donné son appui à la cause de la protection de nos lacs. Elle a traversé le lac de North Hatley à Ayer’s Cliff et elle nous encourage tous à ramer ensemble pour la protection du lac Massawippi.  – Michel Clairoux, Bleu Massawippi

***

Yesterday (August 11), Blue Massawippi celebrated its 50 years of existence. We had with us Mrs Mylène Paquette, a very determined lady, who crossed the Atlantic ocean alone in a row boat from Halifax to France. With her team, she canoed lake Massawippi from North Hatley to Ayer’s Cliff.

You will find below very good articles on this event and on the importance of working together (all rowing in the same direction) to keep lake Massawippi healthy. – Michel Clairoux, Bleu Massawippi

« Pour ses 50 ans, Bleu Massawippi a organisé, samedi, une traversée de son lac. C’est une activité que Mylène Paquette n’allait pas manquer : après avoir connu la pollution des eaux sur l’Atlantique Sud, la navigatrice ne manque pas une occasion d’encourager la préservation des eaux partout au Québec. »

Judith  Desmeules, La Tribune

https://www.latribune.ca/actualites/protegeons-les-plans-deau-ensemble-337201d80e40690fa417fce21506a48a

Blue Massawippi celebrates 50th ­anniversary with flotilla across the lake

On Saturday, well-known rower Mylène Paquette led a group of boaters across Lake Massawippi in celebration of 50 years of conservation efforts by Blue Massawippi on the lake. Under the theme ‘Paddling for Beauty’, the symbolic 14.5 km trip was organized to represent the millions of paddle stroked made during Blue Massawippi’s half-century of protecting the lake.

Matthew McCully, Sherbrooke Record

https://www.sherbrookerecord.com/blue-massawippi-celebrates-50th-%C2%ADanniversary-with-flotilla-across-the-lake/

fanhca.org soutient les organisations bénévoles qui travaillent pour les citoyens de North Hatley. S’il vous plaît soutenir ces organisations. Merci!

fanhca.org supports volunteer-based organizations working for the citizens of North Hatley. Please support these organizations. Thank you!

Une comédie d’erreurs

(English follows)

Les quelque trente-cinq participants à la dernière réunion du conseil municipal à North Hatley, tenue le 6 août, ont assisté au spectacle des membres du conseil, du maire et du directeur municipal qui tentaient de défendre une résolution sur l’accès à la plage publique (ou ‘parc’, comme on semble la nommer maintenant – toute référence, même implicite, à la présence d’un lac semble avoir été bannie), une résolution qu’ils ne semblaient avoir ni tout à fait comprise ni rigoureusement définie. Ce qui n’a pas empêché les membres du conseil municipal de l’adopter à l’unanimité.

La résolution oblige à obtenir une carte électronique pour accéder à Pleasant View Park – à la pelouse, à la plage, aux quais, mais PAS à l’eau, car la baignade continuera à être interdite. On peut se demander quel problème ce nouveau système compliqué est censé régler, puisque l’accès à l’eau reste interdit.

Bien entendu, le Conseil sait bien que les gens vont se baigner, mais il espère pouvoir prétendre qu’il ne s’attend pas à cela – et ainsi se protéger de poursuites, si quelque chose de fâcheux se produit. Voilà, en bref, le but de toute cette charade – une charade qu’un juge trouvera certainement peu convaincante, à moins que la municipalité décide de faire respecter l’interdiction de se baigner. Mais il est peu probable que cela arrive, car des reportages décrivant l’arrestation de personnes âgées et de jeunes enfants, parce qu’ils se sont baignés dans le lac, ne constitueraient probablement pas le genre de publicité pour North Hatley que souhaiterait le conseil municipal.

Pour obtenir une carte, la résolution adoptée stipule que les ‘citoyens’ (c’est ainsi qu’elle nomme les ‘usagers’) devront signer une lettre de renonciation – bien que le contenu exact de cette lettre soit toujours inconnu. Et qui pourra obtenir une carte en versant une caution? Cela aussi reste à déterminer, et sur ce sujet il y avait lors de la réunion des affirmations contradictoires de la part du maire et du directeur-général. Ces incohérences sont des indications que la municipalité a agi sans bien comprendre ce que sa propre résolution impliquait.

Afin de justifier cette ‘politique’, la conseillère Farrugia a longuement cité la règlementation pour défendre la position que la baignade à partir d’une plage accessible au Québec ne peut être permise que pendant la période de surveillance. Peu importe que les législateurs du Québec n’exigent pas de clôtures autour des plages publiques, que celles-ci sont accessibles vingt-quatre heures sur vingt-quatre, et que les législateurs du Québec acceptent – implicitement du moins – que les gens se baignent en dehors des heures de baignade surveillée.

Une autre conseillère – Elizabeth Fee – a noté que cette résolution n’était qu’une première étape et que des améliorations y seraient apportées ultérieurement. Cela constitue, peut-être, quelque chose de positif, si cela se produit réellement; on peut espérer qu’une solution intelligente et raisonnable puisse encore se trouver. Des membres du public ont fait des propositions pour qu’il y ait un arbitrage exécutoire impliquant un organisme (l’Académie de sauvetage du Québec, par exemple) ou une personne (un avocat reconnu dans le domaine de la responsabilité civile, par exemple) sur lequel les deux parties s’entendraient. Le coût d’un tel arbitrage, tout comme le système de carte électronique lui-même, pourrait être couvert par des donations. Quant à la source des donations, dans le cas du système de carte électronique, le maire n’a voulu rien préciser à la réunion du 6 août. Il a simplement affirmé que l’argent avait été promis, et, en partie, déjà obtenu. Il serait certainement intéressant pour les contribuables de North Hatley de savoir qui subventionne cette mesure que nous impose le Conseil municipal.

Mais ces propositions d’arbitrage exécutoire semblent être tombées dans l’oreille de sourds. Il en va de même pour la demande de renseignements sur le coût de la gestion de la plage publique cet été, même avec des services très réduits, ainsi que pour la demande répétée que les membres du conseil municipal consultent ceux qui les ont élus. La réaction du maire a été  de nous comparer encore une fois – nous les résidents et non-résidents – à des enfants, cette fois-ci à des enfants qui, ayant perdu la clé de la boîte aux lettres, ne devraient plus y avoir accès. 

Si « tout est bien qui finit bien », tout n’est pas bien à North Hatley.

Paul St-Pierre

Les opinions exprimées sur ce site Web reflètent celles de leurs auteurs. L’espace est offert à titre de service à la communauté et FANHCA et ses administrateurs ne peuvent en aucun cas être tenus responsables des opinions qui y sont émises.

la voix du village the voice of the village