THE CPFF @THE_CPFF
The Canadian Pulmonary Fibrosis Foundation (CPFF) is a registered foundation established to provide hope and support for people affected by pulmonary fibrosis. cpff.ca Canada Joined September 2013-
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Our September Newsletter is here—packed with new treatment updates, impact stories, walk highlights, upcoming events, and ways you can make a difference! mailchi.mp/cpff/sep-2025
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🍓 Run the Farm for PF! 📅 Aug 16 | ⏰ 9:30 AM check-in 📍 Avonmore Berry Farm, ON 🏃♀️ 5km walk/run for Pulmonary Fibrosis. Join us to run, walk, or cheer—your support matters! 🔗 Register by Aug 15: p2p.onecause.com/cpffwalks/even… #CPFF #PulmonaryFibrosis #HopeBreathesHere
Join us as a volunteer at a CPFF Hope Breathes Here Walk! It’s a powerful way to give back, support families, and help fuel life-changing research. 📩 Sign up to volunteer: cpff.ca/volunteer-form/ 📧 Questions? Reach out to [email protected]
Our August newsletter is packed with inspiring stories, research updates, event highlights & more—take a peek! - mailchi.mp/cpff/aug-2025
🫁 Can blood vessel changes predict lung scarring? Dr. Albina Tyker studies abnormal vessels as early signs of pulmonary fibrosis. Next: CT scans to track progression & improve treatment. 🔗 cpff.ca/articles/inves… 💙 cpff.ca/donate
Meet the Phillips family — honoring David Andrew Phillips by hosting Run the Farm for PF at Avonmore Berry Farm. Join us Aug 17 to walk/run for PF awareness and research. Every step counts. Register: p2p.onecause.com/cpffwalks/even… #PulmonaryFibrosis #CPFF #LungHealth #HopeBreathesHere
This August, join CPFF walks across Canada to raise awareness, honour loved ones & fund research, support & hope. 🚶♂️ Register now: p2p.onecause.com/cpffwalks #WalkForPF #PulmonaryFibrosis #CPFF #LungHealth #HopeBreathesHere
🚶♂️Walk with us this August! Join communities across 🇨🇦 to raise awareness + hope for those with pulmonary fibrosis. Every step funds research + support. 💙 🌟 Register now: p2p.onecause.com/cpffwalks #WalkForPF #CPFF #LungHealth
🍁 Happy Canada Day from CPFF! 🍁 Whether you’re visiting family, enjoying a lakeside cabin, or heading to a new province, travelling with oxygen is possible with the right prep. Our travel guide can help you plan with confidence: 👉 cpff.ca/traveling-with…
Ray & Jo-Anne Palmer show how positivity & support make all the difference living with PF & Sjögren’s. From tough diagnoses to daily wins—they face it all, together. 💙 Read their story: cpff.ca/articles/a-pos… #PulmonaryFibrosis #CaregiverSupport #CPFFWalk
On August 3, 2025, Andres Moran-Macdonald takes on an Ironman — not just for the challenge, but to honour those facing pulmonary fibrosis every day. He's racing for breath. For awareness. For hope. 💙 p2p.onecause.com/cpffwalks/team… #IronmanForPF #HopeBreathesHere #PulmonaryFibrosis
On a plein de super ressources pour vous accompagner dans votre parcours avec la fibrose pulmonaire — vidéo éducative, groupe de soutien, groupe Facebook et même une marche à Montréal. Allez jeter un coup d’œil! cpff.ca
June 2025 Newsletter is here! Discover inspiring community stories, research updates, new t-shirts, and upcoming Hope Breathes Here walks —read it now! mailchi.mp/cpff/june-2025
Shine a light on PF by visiting the CPFF Shop to order your Tackle the Crackle t-shirt and cap. Pick up your gear at a CPFF Community Walk and wear it proudly to spark conversations and support those living with PF. cpff.ca/shop/
We’re excited to welcome you to Edmonton’s first-ever CPFF Walk for Pulmonary Fibrosis on June 28! Join us for an inspiring day of unity, support, and hope as we walk together for a cause that truly makes a difference. #Edmonton #PulmonaryFibrosis p2p.onecause.com/cpffwalks/even…
🫁 Connect, Share, and Support – Wherever You Are! Join PF patients and caregivers from across Canada for our virtual National Patient Support Group. 💬 All are welcome — patients and caregivers alike! cpff.ca/series/nationa… #PulmonaryFibrosis
From coast to coast people are gathering to walk, roll, and run to raise awareness, hope, and funds for people living with #pulmonaryfibrosis. Join us from June to October. Find a walk near you and register today! p2p.onecause.com/cpffwalks
Meet the 2025–2026 CPFF Robert Davidson Fellows! Dr. Na’ama Avitzur and Dr. Pourya Masoudian—two respirologists dedicated to advancing PF research and improving patient care across Canada. Learn more cpff.ca/research-and-h…
The Joly sisters share the heartwarming and heartbreaking story of supporting their dear Mother on her journey with #PulmonaryFibrosis. This is a must-watch for anyone affected by PF. Thanks to the Joly Family for sharing with us. cpff.ca/on-demand-vide…
May Newsletter is Here! From new Robert Davidson fellow announcements & powerful patient stories to practical videos and events happening this month, there’s something for everyone in our latest update. mailchi.mp/cpff/may-2025 #PulmonaryFibrosis #CPFF #PFSupport #TackleTheCrackle
Steve Jones @ActionPFsteve
2K Followers 373 Following Trustee of @ActionPFcharity, a patient organisation committed to supporting people living with pulmonary fibrosis. Board member of @EU_IPFF
Action for Pulmonary ... @ActionPFcharity
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