Click here to watch Jo-Anne Mainwood interview on CTV News Ottawa --------- Jo-Anne Mainwood has been living with Pulmonary Arterial...

Click here to watch Ella's interview on Winnipeg City News --------- After getting a second lease on life following a successful lung...

I suffered from osteoarthritis for many years, or so I was told. I broke bones easily and had two knee replacements, one in 2013 and one...

My Husband Ron and I married in 1997. I didn’t know then, but the shortness of breath and fatigue I had been feeling for the previous...

In July 2015, I came down with what I thought was a chest cold that never seemed to get better. I spent the next three months going to my...

I first started noticing symptoms approximately seven months after the birth of my second child in 1996. In April 1997, I was diagnosed...

In 2016, I was an active 32-year-old. My boyfriend and I were trying to have a baby, and pulmonary hypertension, a disease I had never...

Each year, September 30 marks the National Day for Truth and Reconciliation. The day honours survivors of the residential school system,...

Having lived with PAH for over 12 years, I vowed never to let it control my life. Our family loves to travel, and I was not about to hold...

The first time I heard the words, "I think you have Scleroderma and Pulmonary Arterial Hypertension" was in January of 2012 was from my...

Bill C-22, the Canada Disability Benefit Act, has become law, marking a significant milestone for people with disabilities in Canada....

This is a big year, marking 15 years of inspiration with PHA Canada. This week we are honoured to get to celebrate this milestone in...

I applied to join the PHA Canada Board of Directors in 2018 because I wanted to give back to the PH community and contribute towards...

Twenty years ago, I first heard the words pulmonary hypertension. An emergency CT scan sent me to the hospital. I was in congestive heart...

15 years. Wow! Has it been that long since the small group of us got together with a vision of starting a national organization in...

Emily's story is featured by  Patient Voice   * “I was working as a litigator in Toronto when I was diagnosed with chronic thromboembolic...

The Pulmonary Hypertension Association of Canada Welcomes Federal Government Investment to Support Access to Rare Disease Drugs...

The Pulmonary Hypertension Association of Canada Welcomes Federal Government Investment to Support Access to Rare Disease Drugs...

There is a rapidly growing end-of-life or death doula movement across Canada. Over the last five years, there has been a significant...

Greetings. My name is Stephen Winter, and I’m from Oakville, Ontario. I want to share my story about chronic thromboembolic pulmonary...