Pulmonary Fibrosis Warrior
@PFWarrior
PF Warriors, a support network that provides education, inspiration, & hope to those living with pulmonary fibrosis.❤💙
Learn how sleep apnea and pulmonary fibrosis (PF) are connected in this PF Warriors educational session. Discover practical tips, treatment options, and early warning signs that can help improve sleep quality, oxygen levels & daily well-being. pfwarriors.com/videos-2025/
Exciting from Avalyn Therapeutics! Avalyn secured $100M to develop inhaled treatments for pulmonary fibrosis. PF Warriors welcomes this investment and encourages all research to center the voices of those living with interstitial lung disease. globenewswire.com/news-release/2…
Join us this Thursday, July 24th, at 10 am CT for our monthly Pulmonary Fibrosis Warriors Q&A. Patients + caregivers share, support, and answer your questions. 🔗 bit.ly/W2WJUL2025
Join us Thurs, July 24 at 10am CT for our monthly Pulmonary Fibrosis Warriors Q&A. Patients + caregivers share, support, and answer your questions. 🔗 bit.ly/W2WJUL2025
We’re thrilled to welcome Lisa Lancaster, MD, to our monthly PF Warriors educational meeting to lead a session on sleep apnea and pulmonary fibrosis, and answer your questions in a live Q&A. 🗓️ Friday, July 12 at 10am CT 🔗 Save your spot: bit.ly/PFWJUL2025
"These recommendations may catch pulmonary fibrosis or interstitial lung disease earlier, which is when treatment and monitoring can make the biggest difference." - Dolly Kervitsky, RCP, CCRC, CNP President, PF Warriors
The Blue Journal thanks Anna Podolanczuk, MD, MS, ATSF, for her contribution to the July issue Approach to the Evaluation and Management of Interstitial Lung Abnormalities: An Official American Thoracic Society Clinical Statement atsjournals.org/doi/full/10.11…
What’s the link between sleep apnea and pulmonary fibrosis? ❤️ It can worsen symptoms, lower oxygen, and drain your energy. 💙 Early diagnosis = better outcomes. 📅 Join us July 12 at 10am CT. 🔗 bit.ly/PFWJUL2025
PF Warriors supports the efforts of the @ERSpublications and the @EuropeanLung Foundation to make YOUR voice heard. Whether you are a patient, caregiver, or family member, you can drive understanding, compassion, and change. Share your voice today! europeanlung.org/en/projects-an…
🛌💨 Sleep Apnea & Pulmonary Fibrosis PF Warriors invites you to our next monthly meeting on Friday, July 12 at 10am CT! We’ll explore how sleep-disordered breathing affects those living with PF. 🔗 Register: bit.ly/PFWJUL2025
It’s 🔥 Great tips to stay safe and cool by @atscommunity
As the heat wave continues to affect much of the United States, be sure to stay hydrated, check the air quality, and take any necessary precautions when going outside, especially for those who have respiratory illnesses and conditions. For more tips, check out this graphic from…
Jim recently had the chance to be part of a very special school project. Alexa, a sixth grader he knows from church, reached out to see if she could interview him for a class assignment about respiratory conditions. Jim didn’t hesitate to say yes! facebook.com/pfwarrior
Living with pulmonary fibrosis? Caring for someone who is? Join our June Q&A Zoom Meeting on 6/26 at 10am CT. Ask questions or lend your voice. Register here: bit.ly/W2WJUN2025
We're excited to share that PF Warriors President, Dolly Kervitsky RCP, CCRC, CNP will present alongside Brittany Davis of Avalyn Pharma on "Collaborating with Advocacy Groups to Enhance Trial Access and Awareness."
Pulmonary Fibrosis Warriors monthly Q&A meeting is back on 6/26 at 10am CT! Patients + caregivers come together to ask, share, and support. Register: bit.ly/W2WJUN2025
Got questions about life with pulmonary fibrosis? Join our next PF Warriors Q&A, led by patients & caregivers on 6/26 at 10am CT. 💬 Register: bit.ly/W2WJUN2025
In the FIBRONEER-IPF phase 3 trial, nerandomilast slowed disease progression in patients with idiopathic pulmonary fibrosis as compared with placebo. Full trial results and Research Summary: nej.md/4mgWcIU
“I carry my donor with every breath.” This Father's Day, watch Craig’s powerful pulmonary fibrosis journey, and help him give back! 🎥 youtu.be/NBNBYbSfNF8 Make a tax deductible donation today! donate.stripe.com/cN23fHcyY2hH3J…
Craig got a second chance at life with his children and his Dad, and today on Father’s Day, we hope you'll watch his story. 🎥 youtu.be/NBNBYbSfNF8 Make a tax deductible donation today! donate.stripe.com/cN23fHcyY2hH3J…
This Father's Day, Craig is celebrating more time with his kids and his dad. Watch his story & support Pulmonary Fibrosis Warriors: 🎥 youtu.be/NBNBYbSfNF8 Make a tax deductible donation today! donate.stripe.com/cN23fHcyY2hH3J…
From diagnosis to transplant, Craig’s journey shows what family love and organ donation make possible. A Father’s Day story worth watching! @TODAYshow @USATODAY @nytimes Watch his story: youtu.be/NBNBYbSfNF8 #pulmonaryfibrosis #IPF #ILD #idiopathicpulmonaryfibrosis