Pulmonary Hypertension is a rare and life-threatening lung disease in which the high blood pressure in the arteries of your lungs. PH may cause symptoms such as shortness of breath with minimal exertion, fatigue, swollen feet, dizzy spells and fainting. As the disease worsens, its symptoms may limit all physical activity. There is no cure. However, new treatments today can help many patients live longer and healthier lives.
The PHA Canada - Toronto Chapter is a volunteer group of patients, families and caregivers. We are dedicated to improving the lives of people living with Pulmonary Hypertension through advocacy, awareness, education, and support. The PH support group meets on a regular basis in the GTA.
News
Vegas Fundraiser raised more than $10,873 for PH!
We were thrilled with the response to our first-ever PH Fundraiser "Let Me Breathe" on November 14, 2009.
Over 250 people attended a fun-filled evening which included casino games, live entertainment, door prizes and a live auction! Guests walked home with amazing prizes such as 40" LCD TV, netbook, a beautiful handmade quilt, yoga classes, skating lessons and many more!
Many thanks go out to the Brebeuf School, Club Brebeuf, the donors for providing us such amazing prize items, and all the volunteers who took their time, energy, talent and precious weekend to come help make our first fundraiser a successful one!
Lastly, thank you to everyone who came out to support our cause. We are grateful beyond words for your generous support on behalf of all patients living with pulmonary hypertension.
The Ombudsman needs your Help
The Ontario Ombudsman wants to hear from any and all Ontario PH patients who are concerned about the combination therapy issue and how they are or could potentially be effected. Bonnie Cameron didn't even reach out to the Ombudsman and their office needs to know if there are more people in her position. Please reach out to Loretta (loretta@phatoronto.ca) for more info or go to the Ombudsman to voice your concern - www.ombudsman.on.ca.
Newly diagnosed?
Some of us know what you're going though. It can be very overwhelming to hear you've been diagnosed with Pulmonary Hypertension. It's important that you can reach out to people who can support you. That is where we come in, we hope to answer questions you may have, and connect you with a network of people who know what you're going through. We are here for you.
If you wish to speak with a PH patient one on one in private, please contact us (info@phatoronto.ca) and we can arrange someone for you to talk too, or feel free to attend our monthly Support Group meetings.
PH Support Group
Most PH patients had never heard of pulmonary hypertension until they were diagnosed, and many go months or years before meeting another patient. Many newly diagnosed patients receive grim misinformation and receive limited services.
PH Support Groups change lives, and often they save the lives of their members. They provide spaces where patients, family members and caregivers can:
- Share their experiences
- Learn about PH, treatments and how others have adjusted their lifestyles around PH; and
- Learn from others about how to get involved in the fight against PH.
Upcoming Events
Support Group Meeting
February 6, 2010 1:30pm
North York, ON
Support Group Meeting
March 6, 2010 1:30pm
North York, ON
Support Group Meeting
April 3, 2010 1:30pm
North York, ON
Contact Us
Facebook: Toronto Chapter
E-mail: info@phatoronto.ca
PHA Canada
PHenomenal Hope
