Pulmonary Fibrosis Foundation

We imagine a world without pulmonary fibrosis.

[Pulmonary Fibrosis Foundation @PFFORG]

PFF Board of Directors member and lung transplant recipient, Laurie Chandler, wrote a letter for the New Hampshire Union Leader to urge lawmakers to pass the SOAR act.

Read it below:

📰 https://t.co/vgwYPyMOEW #SOARActO2

[Pulmonary Fibrosis Foundation @PFFORG]

PFF Summit 2023 sessions are now rolling out on YouTube! In our first Summit premier, join a panel of experts to learn how federal agencies play a crucial role in research for pulmonary fibrosis. Watch now! https://t.co/pCG8teXhnr

[Pulmonary Fibrosis Foundation @PFFORG]

Chronic cough has a significant impact on pulmonary fibrosis patients’ physically and mentally. Learn more about the causes, treatments and impact on quality of life by registering for EU-PFF’s webinar this Thursday, May 9th.

Sign up at https://t.co/9YdmE0e5Y0

[Pulmonary Fibrosis Foundation @PFFORG]

Have you ordered your Shop PFF merch yet? Raise awareness of PF everywhere you go at https://t.co/xV94820GU3

[Pulmonary Fibrosis Foundation @PFFORG]

Join the 18th annual FREE in-person patient/family education day event hosted by The American Thoracic Society’s Public Advisory Roundtable (PAR) in sunny San Diego!

Date: May 18, 2024
Location: San Diego, CA
RSVP: Email [email protected] by MAY 10, 2024

See flyer for details!

[Pulmonary Fibrosis Foundation @PFFORG]

In our newest post, Dr. Amy Hajari Case talks about how AI will improve healthcare for the PF community. Read it now at https://t.co/MM8chtBBdc

[Pulmonary Fibrosis Foundation @PFFORG]

April is National Volunteer Month. Today, we’re highlighting one of our PFF Hill Day volunteers, Marla Brady. Thank you Marla for your contributions to the PF community!

[Pulmonary Fibrosis Foundation @PFFORG]

THANK YOU to everyone who has joined the PFF Community Registry so far! 🎉🎉 As a token of our gratitude, you can show your support of pulmonary fibrosis research with this profile picture. Haven’t enrolled yet? Get started at https://t.co/o3IuMUAn07.

[Pulmonary Fibrosis Foundation @PFFORG]

April is National Volunteer Month. Today, we’re highlighting one of our class of 2022 PFF Ambassadors, Karen Smoot. Thank you Karen for your contributions to the PF community!

[Pulmonary Fibrosis Foundation @PFFORG]

Take it from our current enrollees. Your participation matters. Enroll now at https://t.co/o3IuMUAn07!

[Pulmonary Fibrosis Foundation @PFFORG]

April is National Volunteer Month. Today, we’re highlighting one of our PFF Ambassadors, Gretchen Cararie. Thank you Gretchen for your contributions to the PF community!

[Pulmonary Fibrosis Foundation @PFFORG]

PFF Ambassadors are available to speak at your next event! Find out more at https://t.co/vYrRfQKFdE

[Pulmonary Fibrosis Foundation @PFFORG]

April is National Volunteer Month. Today, we’re highlighting one of our PFF Hill Day volunteers, Julie Rossignol. Thank you Julie for your contributions to the PF community!

[Pulmonary Fibrosis Foundation @PFFORG]

With more than 50 full-length webinars available for FREE on our YouTube channel, we’re confident that you’ll find answers to your most pressing questions about pulmonary fibrosis. Check out the playlist and watch now!
https://t.co/oitj8etvyf

[Pulmonary Fibrosis Foundation @PFFORG]

@EU_IPFF invites you to the PF Patient Summit 2024! The third European PF Patient Summit will take place from April 26-28, 2024 in Castelldefels, Spain at the Gran Hotel Rey Don Jaime. A fully virtual option is available.

💻 Register at https://t.co/nPKqkAAcEE #PFSUMMIT24

[Pulmonary Fibrosis Foundation @PFFORG]

April is National Volunteer Month. Today, we’re highlighting one of our PFF Hill Day volunteers, Jamie Lederer. Thank you Jamie for your contributions to the PF community!

[Pulmonary Fibrosis Foundation @PFFORG]

@EU_IPFF invites you to the PF Patient Summit 2024! The third European PF Patient Summit will take place from April 26-28, 2024 in Castelldefels, Spain at the Gran Hotel Rey Don Jaime. A fully virtual option is available.

💻 Register at https://t.co/nPKqkAAcEE #PFSUMMIT24

[Pulmonary Fibrosis Foundation @PFFORG]

☀️🌷 With warm temperatures on the way, get ready for spring with merch from the Shop PFF store! Raise awareness of PF everywhere you go with tshirts, caps, bracelets and more at https://t.co/xV94820GU3

[Pulmonary Fibrosis Foundation @PFFORG]

This year’s 'Broadway Belts for PFF!,' held on March 18 at Sony Hall in New York City, shattered fundraising records with $516,00 in donations and continues to climb. Thank you Broadway Word for the press coverage of our annual gala!

https://t.co/1VRGPeGtvs

[Pulmonary Fibrosis Foundation @PFFORG]

Pulmonary rehabilitation (PR) can unlock the potential to live a better life with pulmonary fibrosis. Visit https://t.co/J0E05z0RMa to use an interactive map to find PR near you! Thank you to the American Thoracic Society for providing this valuable resource!