Mental health in PAH
A webinar hosted by the Pulmonary Hypertension Knowledge Sharing Platform this week talked about a couple of studies on mental health in...
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NEWS & MEDIA
PH Blog
Putting the PH in PHamily.
Welcome to PHA Canada’s community blog. Here, you can hear from patients, medical providers, caregivers, and much more.
If you are interested in submitting an article, contact us at info@phacanada.ca.
PHA Canada
Oct 28
Interview with Liss Cairns from Plan Institute - RDSP Awareness Month
💜 RDSP Awareness Month is almost over , but it’s not too late to learn about the benefits of a Registered Disability Savings Plan (RDSP)...
Traveling with PH: Angele's Family Adventures Across Canada - Blog 4/6
Blog 4/6 - Getting there Guillaume and I love road-tripping! Ever since we met in 2001, we have frequently hit the road in search of...
Traveling with PH: Angele's Family Adventures Across Canada - Blog 3/6
Blog 3/6 - Easter Seals When a family welcomes a child, many will say that "it takes a village"; I would say the same when someone...
Traveling with PH: Angele's Family Adventures Across Canada - Blog 2/6
Blog 2/6 - PLANNING Planning is key, as long ahead as possible. I started in December 2023 for a trip in June 2024, and worked on this...
Traveling with PH: Angele's Family Adventures Across Canada - Blog 1/6
Introduction: Blog 1/6 We are the Belliveau-Thibeault Family from Dieppe, New Brunswick. This year we received an opportunity to fulfill...
How Timely Diagnosis Changed My Life
I was a healthy and fit 59-year-old woman living in Winnipeg, MB, at the start of 2020. Then I started feeling like something was wrong....
PHA Canada
May 24
PHaware Podcasts
Phaware was founded by a group of pulmonary hypertension awareness activists. Comprised of patients, caregivers, and medical...
Life's Twists and Turns: My Story of Living with PH for Over 40 Years
Hi, my name is Suzanne Martin Wagnell, and I’ve just turned 60 years old in January. My husband and I are both retired and living our...
Rare Disease Day Summit Recap: Advocacy, Unity, and the Fight for Equitable Access
Board member Joan Paulin and PHA Canada Ambassador Jennifer Bryson attended the Rare Disease Summit hosted by the Canadian Organization...
PHA Canada
Mar 20
Tax Season is here!
Tax season is here! Before filing your taxes, determine which benefits you may be eligible for. Check out the article below to learn...
Selena McAlpine
Mar 7
Make-A-Wish trip to Disney World
Our daughter, Georgiana McAlpine, 10, was fortunate to receive a wish from Make-A-Wish Canada this past July! She was diagnosed with PAH...
Managing life with multiple rare diseases
Lupus is an autoimmune disease that causes inflammation of the body. The most common form of lupus is systemic lupus erythematous (SLE)....
Living with Scleroderma and Pulmonary Arterial Hypertension: A Journey of Rare Resilience
Scleroderma and Pulmonary Hypertension Comorbidities, the simultaneous presence of two or more medical conditions in a patient, present...
Recognizing Black History Month
As we celebrate Black History Month, I think of how far we’ve come and still have to go regarding race. Being a mixed-race child raised...
Jennifer Bryson, Patient
Jan 29
Third Time's a Charm: Finding My Footing at Canada’s Rare Disease Conference
I have had the privilege of attending multiple Canadian Organization for Rare Disorders (CORD) Conferences over the last few years. It is...
The value of volunteers
On this International Volunteer Day, I am reminded of the incredible support we receive from our community. From our Board of Directors...
CTV News / Jo-Anne Mainwood, Patient, Ottawa
Nov 24, 2023
CTV News - Ottawa school teacher living with rare Pulmonary Arterial Hypertension
Click here to watch Jo-Anne Mainwood interview on CTV News Ottawa --------- Jo-Anne Mainwood has been living with Pulmonary Arterial...
Jane Macleod, Patient
Oct 29, 2023
Jane's Journey: Overcoming PAH and Scleroderma
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...
Terri Hamm, Patient
Oct 26, 2023
Living with Hope: My PAH Journey and the Power of Perseverance
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...
Ella MacLeod, Patient
Oct 26, 2023
Surviving the Storm: My Journey with Pulmonary Hypertension and Transplantation
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...
Carolyn Mathur, Patient
Oct 25, 2023
Getting the Most of Each Day
I first started noticing symptoms approximately seven months after the birth of my second child in 1996. In April 1997, I was diagnosed...
Lea George, Patient
Oct 24, 2023
A testament to the strength and resilience of the human spirit
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...
Marion Roth, Patient
Aug 17, 2023
Ready, Set, Let’s Go!
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...
Jeannette MacKeen, Patient
Jun 28, 2023
One Day, One Breath at a Time: Surviving Adversity
The first time I heard the words, "I think you have Scleroderma and Pulmonary Arterial Hypertension" was in January of 2012 was from my...
PHA Canada
Jun 28, 2023
Canada Disability Benefit Act: Advancing Financial Independence for Individuals with Disabilities
Bill C-22, the Canada Disability Benefit Act, has become law, marking a significant milestone for people with disabilities in Canada....
Nicole Dempsey, Patient
Jun 4, 2023
Patients at the Boardroom Table: Dr. Sanjay Mehta Interviews Retiring Board Chair Nicole Dempsey
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...
Ed Rathonyi, Caregiver
May 30, 2023
Adding My Voice as a Parent Caregiver to PHA Canada’s Board of Directors
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...
Sonya Collins, Patient
May 18, 2023
Sonya: Twenty Years and Counting…
Twenty years ago, I first heard the words pulmonary hypertension. An emergency CT scan sent me to the hospital. I was in congestive heart...
Sharon Proudfoot, Patient
May 15, 2023
Born from a Vision: Why I Joined the Other Founders to Start PHA Canada.
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, Patient
May 2, 2023
Patient Voice: Emily's story
Emily's story is featured by Patient Voice * “I was working as a litigator in Toronto when I was diagnosed with chronic thromboembolic...
Members of the Death Doula Ontario Network
Feb 26, 2023
End-Of-Life Doulas
There is a rapidly growing end-of-life or death doula movement across Canada. Over the last five years, there has been a significant...
Stephen Winter, Patient
Feb 20, 2023
My CTEPH Diagnosis
Greetings. My name is Stephen Winter, and I’m from Oakville, Ontario. I want to share my story about chronic thromboembolic pulmonary...
Nancy Lewis, Patient
Nov 23, 2022
My Journey to Chronic Illness
My journey to chronic illness has been a long one. My official diagnosis came in 2007, but I’d had signs and symptoms for quite a long...
Jas James, Patient, Cobble Hill, BC
Nov 20, 2022
Jas' Life In Purple: 21 years since being diagnosed with PH
The 21st anniversary of my PH diagnosis came, and I had to pinch myself. I started thinking about all the things that happened on the...
Vanda McLean, Patient
Oct 26, 2022
Vanda's Travel Blog: Part two
We have now returned from our trip west, unloaded the truck and now trying to relax. That isn’t about to happen with my aging parents and...
Vanda McLean, Patient
Oct 23, 2022
Vanda's Travel Blog: Part One
Summer 2022, and things are opening up after being shut down by the COVID pandemic. Although COVID is certainly not over, more people...
Deb McCoy, Patient
Aug 2, 2022
The Canada Disability Benefit and PH
The Canada Disability Benefit (CDB) was first introduced as Bill C-35, and was originally tabled in June, 2021. Due to the 2021 federal...
Esther, Patient
Jul 12, 2022
Patient Voice: Esther's story
Esther's story is featured by Patient Voice * “Since I moved to Canada from Trinidad and Tobago, I’ve always been on the go — working,...
Jessica Marks-Cullum, Caregiver
Jun 27, 2022
My PHighter is Graduating!
Being the mom of an ambitious, artistic dreamer has been a fun journey. From a very young age, Brinley always said, “mom, I want to...
Saeid Maghsoudi, Research
Jun 8, 2022
What Is Persistent Pulmonary Hypertension of the Newborn?
That any of us survive nine months in the womb is amazing. The level of oxygen available to a developing baby in the uterus is equivalent...
Kaitlyn Salonga, Patient
Apr 21, 2022
PH is a full-time job
No matter where you are on your journey, pulmonary hypertension (PH) takes up a lot of time. Between doctors’ visits, the tests they...
Miriam Bergeret, MSc, Research
Feb 8, 2022
Want to improve your heart health? Get more sleep.
You have probably always been told to sleep at least eight hours a night, but people with pulmonary hypertension (PH) know that their...
Dr. Sanjay Mehta
Jan 26, 2022
Life In Purple During A Pandemic: A COVID-19 update
By Dr. Sanjay Mehta, MDCM, FRCPC Founding Board Member, Eternal PHriend, Director & Past-Chair, PHA Canada Director, Southwest Ontario PH...
Ashok Pandey, Research
Nov 29, 2021
Advancement In PH Research
There has been immense progress in the diagnosis and treatment of PH! Research and clinical trials held around the world, much of it here...
Michael Mayville, Caregiver
Nov 18, 2021
Being a PH parent: Michael Mayville's story
My name is Michael Mayville, and I live in Toronto with my wife, Nicole. We are the proud parents of two children: Vance, our 8-year-old...
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