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Asthma Canada, 124 Merton Street, Suite 401, Toronto, ON (2026)

03/30/2026

Asthme Canada est profondément attristé par le décès de Chloé Bélanger, 4 ans, de Gatineau (Québec), survenu le 17 mars 2026 à la suite d’une crise d’asthme.

Nous sommes de tout cœur avec la famille de Chloé, ainsi qu’avec toutes les personnes, partout au Canada, qui ont perdu une personne chère en raison de l’asthme.

L’asthme est une maladie grave. Pourtant, chaque année, trop de vies sont encore perdues. Asthme Canada poursuivra son travail pour sensibiliser, informer et prévenir ces pertes évitables.

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Asthma Canada is deeply saddened to learn of the passing of 4-year-old Chloé Bélanger from Gatineau, Quebec, following an asthma attack, on March 17, 2026.

Our hearts and thoughts are with Chloé’s family during this unimaginable time, and with all those across Canada who have lost loved ones to asthma.

Asthma Canada remains committed to raising awareness about the seriousness of asthma and asthma attacks, because too many lives are lost needlessly every year to this condition.

03/02/2026

Originally from France and now living in Toronto, Alissia Gesret’s family history has been shaped by asthma following the death of her uncle, Franck:

“My family name is known in the paramedical field for a breakthrough in non-invasive asthma treatment. What led to that discovery, however, is rooted in tragedy.

To understand it, you need to meet my uncle, Franck.

To tell his story, I need to take you back to July 15th, 1974.
This is not just any summer day. It is Franck’s tenth birthday.

For the occasion, my father – Franck’s older brother – has organized everything. Friends and neighbors gather to celebrate. Franck runs, laughs, and plays like any other child his age.

Later in the day, my father looks for his brother and finds him locked in the bathroom. Franck is using his inhaler, exhausted, trying to catch his breath after simply being a child. Between two puffs, he looks at my father and says, “You’re lucky you’re not sick.”

Those words carve themselves into my father’s memory forever.

Later that day, Franck’s parents are angry, he has used up all the inhalers. Franck is crying so hard that his breathing worsens. He is already gasping for air.

He runs toward his bedroom but never reaches it. Franck collapses in the hallway. An asthma attack, followed by cardiac arrest.

Because the family lives in the countryside, emergency responders arrive too late. Franck is pronounced dead at the hospital.

I am grateful that Franck at least spent that day laughing, playing, and being surrounded by other children he loved, one last time.

Franck’s story is one of countless stories shaped by asthma and trauma. But I choose to keep telling my uncle’s story. To advocate for him, and for the many children who are still fighting, every day, just to breathe.”

12/27/2025

A look back at 2025: during Asthma Awareness Month, we shared the story of Amber Marie McCollum.

Amber was just 14 years old when her life was tragically ended by an asthma attack.

We are deeply grateful to Amber’s mom, Kim, for bravely sharing her daughter’s story to raise awareness about how serious asthma can be and to help prevent asthma attacks in others.

See more of our work in 2025: link in bio.

12/12/2025

❤️ Safeguard your family’s health by staying protected against preventable illnesses!

Asthma Canada in collaboration with our Lung Vaccination Working Group partners, encourages everyone living with lung conditions to talk with your healthcare provider about the vaccines that are right for you and your family! 💙❤️💉

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❤️ Protégez la santé de votre famille en vous protégeant contre les maladies évitables par la vaccination!

Asthme Canada, en collaboration avec nos partenaires du Groupe de travail sur la vaccination contre les infections pulmonaires, encourage toutes les personnes vivant avec une maladie pulmonaire à discuter avec leur prestataire de soins de santé des vaccins qui leur conviennent et conviennent à leur famille! 💙❤️💉

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11/14/2025

“Imagine watching your child’s chest rise and fall so quickly, the wheezing loud and terrifying.

That’s what it’s like watching my daughter, Jordan, struggle through an asthma attack. In those moments, I’m reaching for her inhaler with one hand and my phone with the other—trying to stay calm while deciding if it’s time to head back to the ER.

My husband, Peter, and I live in New Brunswick, and both of our children have asthma. Jordan was diagnosed with severe asthma as a baby, and managing it quickly became a full-time job. Every day, three times a day, she sat through 15-minute nebulizer treatments—about 270 hours a year just trying to breathe.

While other kids were outside playing or heading to dance class, Jordan was inside, attached to her nebulizer. Every decision we make revolves around keeping her and her big brother, Henry, safe. We’ve driven eight hours to Nova Scotia for specialist care, missed work, and paid out of pocket for medications and treatments not covered by insurance.

One December, after a wonderful day at our local Christmas market, Jordan was hospitalized and put on oxygen. The twinkling lights were replaced with beeping monitors. Thankfully, after several days and a visit to the Asthma Clinic, she came home just in time for Christmas.

We know we’re fortunate—we can manage the costs and travel when needed—but I often wonder: what about families who can’t?

That’s why we share our story: to help others understand how serious and unpredictable asthma can be, and why families like ours need support.

Despite everything, Jordan has done something incredible—she’s run two 5K races, finishing first in her age group. Her strength gives us hope every single day.” ❤️

09/26/2025

“After surgery, everything changed!” 💪

For as long as he can remember, William Daniels has loved science and medicine. Born and raised in Vancouver, British Columbia, he studied biology and neuroscience, worked in cancer research, and is now a medical student.

Alongside his studies, William has lived with chronic rhinosinusitis with nasal polyposis (CRSwNP), a condition that began in his teens.

“It felt like plugging your nose completely shut and trying to live that way. I thought maybe everyone felt this awful all the time.”

For years, he was misdiagnosed with stubborn allergies until, at 19, an ENT finally confirmed CRSwNP. “For the first time, it made sense. It was validating to hear that all the medications hadn’t worked because I needed more than allergy pills. I needed surgery.”

At St. Paul’s Hospital, William underwent a three-hour endoscopic sinus surgery. “The surgery unleashed a potential I never knew I had.” His smell and taste returned, his sleep and mood improved, and his grades skyrocketed. “After surgery, everything changed! I went from the bottom of the class to the top almost overnight.”

To sustain his new quality of life, William relies on steroid rinses and a biologic medication. “Some medications are thousands of dollars per dose. If it weren’t covered, I simply couldn’t afford it. Access to these drugs is detrimental in terms of quality of life.”

“People don’t realize how devastating this can be. You lose smell memory… you can’t enjoy food, you can’t make new memories.”

Today, William is thriving in medical school and conducting research. “These treatments change lives, but they’re out of reach for too many people. We need better awareness, better access, and more research.” 💙

08/25/2025

Jasmine, a nurse and Certified Respiratory Educator (CRE) from Sault Ste. Marie, Ontario, knows the challenges parents face during back-to-school season.

Her six-year-old son Milo, born prematurely, began experiencing frequent croup episodes, nighttime coughing, and difficulty breathing after activity by age three.

“That was when I really started to notice patterns—he was red-faced and winded after running, and coughing at night even when he wasn’t sick.”

Trusting her instincts, Jasmine pushed for answers. A trial with a low-dose steroid inhaler immediately improved Milo’s symptoms.

“The results were immediate. He could play without stopping and sleep through the night. I finally had validation and a plan to support him.”

School brought new challenges.

Milo’s symptoms worsened with activity and exposure to viruses. In December 2023, a severe asthma attack triggered by RSV led to hospitalization.

“It was really scary. He was struggling to breathe, and as a parent, you feel helpless.”

Working closely with his pediatrician and Milo’s CRE, they adjusted medications, added allergy treatment, and created an asthma action plan for school.

“Ask questions. Make sure teachers know your child’s triggers and what to do if symptoms appear. Having the asthma action plan on hand really makes a difference.”

Today, Milo is doing well.

“Being a nurse gave me knowledge, but being a mom gave me determination. That’s what made the difference for Milo.”

Inspired by their experience, Jasmine became a CRE herself and now supports families like her own through Asthma Canada’s Asthma & Allergy HelpLine. She also helped develop Asthma Canada’s Mission Breathe, an interactive game that teaches kids how to understand and manage their asthma with confidence.

Jasmine’s advice for parents is simple: “Trust yourself as a parent. If something doesn’t feel right, keep asking questions until you get the support your child needs.”

07/17/2025

Charly Jarrett, from Vancouver, British Columbia, has lived with both the physical and emotional challenges of asthma for most of her life.

Her first symptoms appeared in high school, when she began frequently losing her voice. It wasn’t until after she developed pneumonia twice, however, that doctors finally suggested asthma as the cause.

Growing up in a community skeptical of medications and vaccines, her symptoms were often downplayed and misunderstood, even as she continuously battled yearly respiratory infections.

“I thought, ‘Is this just going to be the rest of my life? Having a piece of my life taken away every year was horrible.”

Charly was finally diagnosed with asthma while in university. After being advised to begin regular inhaler use, she was able to end the infection cycle and replace it with a sense of control and relief.

Despite these physical improvements, social struggles still remain. She has found her experience with the condition to be isolating and anxiety-inducing.

“The continuous outbreaks after COVID have been incredibly isolating. I get anxious about the wildfire smoke. There’s a constant worry about normal daily activities, like seeing friends in the summer, going outside, being able to breathe.”

No one should have to feel isolated or anxious because of their condition, yet for many, asthma makes that a daily reality. These struggles are exactly why Charly is so passionate about joining Asthma Canada and speaking out — to help others feel seen, supported, and empowered to live fully despite asthma.

06/23/2025

Dallas Lockhart, a 20-year-old student from Toronto, Ontario, has lived with asthma since childhood.

“At nine, I began experiencing shortness of breath and chest tightness, especially during physical activity.”

At first, her parents didn’t grasp the severity of her symptoms. But as they worsened, she was diagnosed with asthma.

In the early years, Dallas relied heavily on both controller and reliever medications—what her parents called her "dinner and dessert." She often faced name-calling and felt discouraged.

“When you’re the slowest person in the race, it gets a little bit defeating at times.”

But Dallas refused to let asthma hold her back. Determined to prove herself, she continued to play volleyball, basketball, and soccer—activities that not only helped improve her fitness but also strengthened her lung capacity.

She credits her confidence to a strong support system: “My parents were my number one supporters, my gym teacher always understood my condition, and my sister was my inspiration.”

In 2020, after years without symptoms, a cold and sinus infection triggered an unexpected asthma attack. Without updated prescriptions, Dallas had no medication on hand. She was rushed to a clinic to be treated.

“This made me open my eyes—just because I don’t have symptoms doesn’t mean my asthma is gone.”

Since then, Dallas has taken charge of her asthma, keeping her medication up to date and identifying her triggers: dust, pet fur, smoke, and unfamiliar environments.

Today, she not only manages her own asthma but also empowers the children in her care who live with it, reminding them:

“Just because you have asthma doesn’t mean you’re limited. You can do anything—and you have me as a support system.”

Dallas’s story reminds us on the importance of lung conditioning, never underestimating asthma, and always keeping your emergency medication close.

06/06/2025

Josée Michaud, from Quebec’s Laurentides region, has lived a life profoundly shaped by asthma—living with the condition herself and losing two brothers to it.

“My older brothers and I all had asthma—pretty severe cases. I was about seven when I began missing a lot of school. I had to repeat second grade because of it. I remember one time when all three of us—my brothers and I—were in the hospital together. My mother even slept there with us.”

Tragedy struck Josée’s family for the first time in 2002.

“Eric, my eldest brother, had very bad asthma. At home, we had a nebulizer, and he was on a lot of medications to manage his condition. He was the kind of person who would wait until the very end to ask for help. Even when he was very sick, he would say, ‘No, don’t call emergency. I’ll be fine. I’ll take my puffer.’ But one day, he just collapsed. He was in the ICU for a month, on a ventilator. He didn’t wake up. We had to stop treatment. He died at 26 from a severe asthma attack.”

Tragedy struck again when her younger brother, Luke, also lost his life to asthma.

“Luke had severe bronchopulmonary issues caused by asthma and collapsed suddenly. We weren’t able to save him. He was just 14.”

In recent years, although Josée's own asthma is mostly well managed, she finds spring especially difficult.

“My asthma was well controlled for many years. But for the last two springs, it’s been bad. I’ve had to use my puffers more often. Winter is usually great for me, but spring allergies have made the last two years difficult. When the trees start blooming, I have to take allergy pills, and my asthma flares up.”

Josée has worked as a nurse for many years and wants to help raise awareness of the dangers of asthma.

“In the ICU, I saw patients experiencing all levels of asthma attacks, and it was frightening. Asthma has always been part of my life, and I want to help others recognize the symptoms and get help early—before it becomes too severe.”

05/22/2025

“Asthma isn’t a simple disease. It’s incredibly complex, which makes it both challenging and fascinating for me. Even now, more than 20 years later, I’m still intrigued. I still want to understand what causes asthma and, more importantly, how we can do better for the people living with it.”

Dr. Teresa To is a trailblazer in asthma research, known for using big data to uncover the true burden of asthma in Canada. When she first began her work at SickKids Hospital, she was shocked to learn that asthma was the number one reason kids were hospitalized. “I thought it would be a simple task—just counting numbers and reporting them. But when I saw the numbers, I was shocked.”

That moment shaped her career. “I went to my boss and said, ‘I want to focus on asthma. This will be my research territory.’”

As the founder and Scientific Director of the Ontario Asthma Surveillance Information System (OASIS), Dr. To’s work has helped track asthma’s impact on thousands of lives and shape better care. In partnership with Asthma Canada, she also led a major study on the real-world use of biologics for asthma treatment.

But she’s clear: the work isn’t done.

“We’re still not done with asthma. Ten years ago, funding shifted toward COPD, and now lung cancer is receiving a lot of attention. But asthma is still here, we have not eradicated asthma, yet, and it’s still affecting a huge number of people.”

She urges more investment in asthma research:
“There’s still so much potential in asthma research. We need more support, and I want to give people hope that we can make a real difference.”

05/22/2025

As Asthma Awareness Month winds down, we invite you to join a powerful and personal event: “Asthma: Stories From the Community” on Thursday 29 May at 7:00 p.m. ET.

This free webinar isn't about stats or science, it’s about the human experience. Hear real stories from people living with asthma—stories of challenge, resilience, advocacy, and hope.

🔷 Moderated by Beyond the Wheeze Podcast Host, Josh Rheaume, the event will feature:
🔹 Vibhas Bapat: Asthma Canada Board Chair & living with asthma and eczema
🔹 Adrienne Lam: MPH student, passionate asthma advocate & living with asthma & allergies
🔹 Jaqueline Murdoch: Late-onset asthma patient & retired IT project manager

Register now: https://us02web.zoom.us/webinar/register/6617442385686/WN__eZkp7K7TGCdHN8dkCvonA

Asthma Canada

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