Megan Parker Artist

Megan Parker Artist Canadian landscape artist from Canmore, Alberta.

04/28/2026

Hey Fernie!! I can’t wait to see you this Thursday (April 30th!) for the opening reception of my solo art exhibition “Stories From the Trails: Unlikely Adventurers”. Come on by at 7pm to hear more about this project and what it’s meant to me.

Thank you to ❤️

(Part 2 of 2) “Stories From the Trails: Jill’s Story”From then on my life changed. I started taking digestive enzymes wi...
04/25/2026

(Part 2 of 2) “Stories From the Trails: Jill’s Story”
From then on my life changed. I started taking digestive enzymes with every meal, I needed chest physiotherapy twice a day, which had to be done by my parents. My teachers had to get pamphlets about CF. This disease taught me how to be responsible, but also determined and how to deal with hard things. As the years progress I had added more medications to keep me healthy, until the past year or two when I have actually been able to stop some medications, thanks again to Trikafta.

I have had my share of hospital stays and home IV antibiotics and as tough as that has been I am thankful that they happened when I was older and able to cope better with being that sick. I went through a stretch in 2016-17 where I needed 8 rounds of IV antibiotics that was unbelievably tough, especially when I had a 3 year old at home. I have come out the other side and cannot believe how much my quality of life has changed in just over 4 years.

I never let my CF hold me back, but now the future doesn’t seem like something that is in question. I think every person with a Cystic Fibrosis always has their mortality in the back of their mind. It is still there these days, but not as looming.
Hopefully, there is a pot of gold at the end of the rainbow.

(Part 1 of 2) “Stories From the Trails: Jill’s Story”This painting reflects a moment that was 41 years in the making. A ...
04/24/2026

(Part 1 of 2) “Stories From the Trails: Jill’s Story”
This painting reflects a moment that was 41 years in the making. A completed 5k Christmas Elf run in December of 2021, the first one I had ever done. When I signed up to do it with my then 8 year old, little did I know that less than a week before the race I would have the chance to start a medication that would change my life. For the first time in my life I was able to run without coughing at all, with only a few walking breaks. I had never experienced that before. In 7 days I went from coughing and coughing up sputum with any amount of exercise to not one cough the whole run. I had a wow moment after the race when I realized I didn’t cough the whole run, it was kind of surreal. In less than a week my lungs were acting like ‘normal’ lungs. It was and still is life changing. In the back of my mind I always wanted to be able to run for any length of time without hacking up a lung and thanks to Trikafta that has happened.

I have always been an active person. When I was growing up I played Ringette, golf, baseball, softball and skied. My cough never stopped me and being so active kept me healthy, even before I was diagnosed at 8 years old. I was a puzzle for our family doctor, my parents knew something was wrong with me, but they didn’t know what. I don’t think I had any of the obvious signs of Cystic Fibrosis. I was a “kielbasa baby” with rolls and a good appetite, and very active. I honestly don’t know or remember what other things the doctor thought was the issue before they ordered a sweat test to see if I had CF. Now, the sweat test... It was 1988, so before the fancy technology they use today for the tests. I literally had gauze taped to my inner elbow and had to sit in my Mum’s car with the heat cranking and bundled up in winter jackets. I had to stay like that until the gauze had enough sweat on it to test. When the doctor finally told my parents the diagnosis, I remember him apologizing for not figuring out what was wrong sooner. I can only image the stress of years of unanswered questions my parents dealt with.

(part 3 of 3) “Stories From the Trails: Brenda’s Story”I was officially placed on the waitlist on my 36th birthday. Then...
04/24/2026

(part 3 of 3) “Stories From the Trails: Brenda’s Story”

I was officially placed on the waitlist on my 36th birthday. Then, on July 27, 2003, my second miracle, a double-lung transplant after being on the waitlist for 3 years (by this time my lung function had dropped to 16% of normal). You can’t even describe your very first breath after they finally remove the oxygen. It is freedom! Post-transplant was like having a completely different life. However, the trade-off is the side effects of the anti-rejection medication, and general aging with CF has its own challenges not connected with transplant. But how amazing is it that I am even able to experience aging!

Transplant has given me an extra 23 precious years (so far!), and allowed me to continue on. In 2024, I turned 60 years old, along with it being my 20th year post transplant. Two huge milestones.

To celebrate, I fulfilled a dream of travelling to Scotland solo. This was a trip about self-reflection, ancestry, finding myself and proving that I still had the courage to be adventurous. It was beyond expectations and made me realize how amazing life is, and has been, even with all its hardships. Everything that has happened to me has shaped the person I have become. I am proud of her and all she has accomplished in life. I very much look forward to what’s ahead!

(part 2 of 3) “Stories From the Trails: Brenda’s Story”In my early twenties, my father passed away quite suddenly from c...
04/23/2026

(part 2 of 3) “Stories From the Trails: Brenda’s Story”

In my early twenties, my father passed away quite suddenly from cancer. Shortly after, I was hospitalized because of a massive bleed from my lungs. My health was already precarious, I was under 100lbs and the result was a 6 week hospital stay. Many years later my mother told me that they thought I would not make it. After discharge, returning to work was out of the question and I ended up having to go on disability. My fiancé and I were in the midst of separating. This was definitely one of the lowest points of my life.

Sheer determination kept me going. I knew things would get better… they had to! In my mid-twenties my health improved, I met a wonderful guy who eventually became my husband, and life was pretty darn good. After 10 years of stable health, things deteriorated. First came the incessant coughing, increased hospitalizations, home IV meds, increased physiotherapy and decreased lung function. Everyday life became harder. Next came oxygen only at night, then 24/7. By this stage the doctors suggested to me that it may be time to consider being listed for a lung transplant. I knew in my heart that this was coming but it was still a shock.

(part 1 of 3) “Stories From the Trails: Brenda’s Story”In 1964, the year I was born, a diagnosis of cystic fibrosis was ...
04/22/2026

(part 1 of 3) “Stories From the Trails: Brenda’s Story”

In 1964, the year I was born, a diagnosis of cystic fibrosis was considered a death sentence – most children would not survive to school age. Yet… here I am at the ripe old age of 62. How can that be?

I believe a series of miracles over my lifetime has brought me to where I am today. The first was being removed from my birth family as an infant by Child and Family Services, resulting in me spending most of my first year of life at Sick Children’s Hospital in Toronto, where a new CF clinic had just opened under the guidance of Dr. Douglas Crozier. Coincidentally, another young CF patient was also on the same ward where her grandparents had come to visit her. It was during this time that the grandparents learned of my story and that I was to eventually go to a home for incurables. Well, they were having none of that! So at 50+ years old, having raised 4 boys, the youngest of whom was 21, they started the process of becoming my legal guardians.

My guardians rose to the challenge of keeping me as healthy as possible. Daily medications, special diet, inhaled treatments, manual “clapping” to clear think mucus from my lungs and endless doctors’ appointments which required travel to Toronto from our home in Northwest Ontario. It was a huge cost and commitment on their part. Even with the extensive health regime that I required, they raised me to be strong and to believe that I could accomplish anything I set my mind to.

(part 2 of 2) “Stories From the Trails: Deb’s Story”“I tried to process the miracle of it all:  strong lung function, a ...
04/18/2026

(part 2 of 2) “Stories From the Trails: Deb’s Story”

“I tried to process the miracle of it all: strong lung function, a life filled with joy and purpose, beloved friends and family. And a promising, healthy future. I told myself to hang on to this feeling—contain it, keep it tight inside—chase away the worry with this memory.

To stay ‘in the moment’ is a hard skill to conquer for most people. Add CF to the recipe and it’s nearly impossible. Even after many decades of practice, I still struggle with this.

However, I try.

When joy and happiness come, I sit with them. I welcome them for tea.

“Have a seat,” I tell them. “Stay awhile.”

I remember the birds so vividly, with their fluttering wings, their tiny beaks nipping at the banana. Their delicate feet tap, tapping on the branches.

I thank them for their visit and for the reminder of the miracles.”

(part 1 of 2) “Stories From the Trails: Deb’s Story”“A few years ago, in my early fifties, I found myself in a Costa Ric...
04/17/2026

(part 1 of 2) “Stories From the Trails: Deb’s Story”

“A few years ago, in my early fifties, I found myself in a Costa Rican rainforest, surrounded by all its awe-inspiring beauty—the colourful flowers and leaves, the sounds of frogs and howler monkeys, the smell of fresh rainfall.

I sat on the back deck of my bungalow in the rainforest and watched the birds, brought close to my hammock by slices of banana skewered on a stick. There were at least six different species that morning, all of them glistening with metallic blues and greens, lemon yellows and blood reds. Deep, dense colours, perfectly patterned and symmetrical. Science, sure, but that day the colours seemed more like magic.

I wept, and felt my heart expand with gratitude. I was a small-town girl with a chronic illness, told she would not live past twelve, sitting in a rain forest in Costa Rica, listening to the singsong of birds. I sat still and thought of how lucky I had been year after year, thanks to my relatively good health.”

Getting ready for my upcoming solo exhibition at The Fernie Arts Station - opening April 30th!! Last night that meant ca...
04/12/2026

Getting ready for my upcoming solo exhibition at The Fernie Arts Station - opening April 30th!! Last night that meant capturing my paintings in high res RAW image format , for my own records and in case I want to create prints or products.

Before I dove all-in to painting, I’d been taking classes at MRU in photography and learning all that I could, mastering manual mode and how to nail the creative perspectives I always envisioned. About two-ish years ago, after trying many different companies and options for making high quality, archival prints, I came across a Calgary photographer with an artist wife that had a small fine art print operation from his basement. We scheduled a “5-minute” introduction call and ended up talking for over an hour, needing out about photography and physics and the intersection of how to leverage them both to make high quality fine art prints that accurately captured the essence of original paintings. He ended up recommended some equipment, but I was far too cheap to blow over a grand and went down a giant rabbit hole and rigged up my own setup for less than $100. But WOW does it work!! 🙌🏻

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Calgary, AB

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