PFF In The Media

  • Jan 04, 2021

    Resolve to talk to your doctor in the New Year

    The New Year is the perfect time to advocate for your health and commit to listening to your body for any new symptoms or warning signs.

    Link to Article
    Source: Newswire
  • Feb 01, 2021

    PFF Patients Advocate and Inspire for National Patient Recognition Week

    Sharing patient stories can help spread awareness for little-known diseases like pulmonary fibrosis, empowering patients to build support systems, pinpoint symptoms and take action early.

    Link to Article
    Source: Medium
  • Feb 01, 2021

    The pulmonary fibrosis treatment landscape: An interview with an expert

    In 2014, FDA approved two medications for idiopathic pulmonary fibrosis (IPF) — nintedanib from Boehringer Ingelheim and pirfenidone from Roche (OTCMKTS:RHHBY).

    Link to Article
    Source: Drug Discovery & Development
  • Feb 15, 2021

    My Breath, Made Possible by Another: Lung Transplants and Pulmonary Fibrosis

    According to the Organ Procurement and Transplantation Network, a patient in need of a life-saving organ transplant is added to the national waiting list every 9 minutes*.

    Link to Article
    Source: Medium.com
  • Apr 01, 2021

    Early Diagnosis for Pulmonary Fibrosis is Key

    Pulmonary fibrosis (PF) continues to be relatively unknown among the public, making awareness and education critically important.

    Link to Article
    Source: VFW Magazine
  • Mar 23, 2021

    Local pulmonary fibrosis ambassador goes to Washington

    On March 10, Debbie Herndon, Boise resident and ambassador for the Pulmonary Fibrosis Foundation, traveled (virtually) to Washington, D.C., with a group of fellow advocates from around the country to drive awareness and research funding for the disease.

    Link to Article
    Source: Idaho Press
  • Apr 03, 2021

    The Deadly Lung Disease You've Probably Never Heard Of

    Pulmonary fibrosis (PF) is an uncommon and frequently fatal lung disease, and the road to diagnosis can be long and difficult.

    Link to Article
    Source: Scientific America
  • Sep 05, 2019

    September Marks Pulmonary Fibrosis Awareness Month

    September has been designated Pulmonary Fibrosis Awareness Month — a time during which researchers and clinicians aim to improve the public’s knowledge about the disease.

    Link to Article
    Source: Healio
  • Sep 03, 2019

    Charlotte pastor turns near-death experience into chance to help community

    A Charlotte pastor is turning his near-death experience into an effort to help his community.

    Link to Article
    Source: WSOC-TV Charlotte
  • Jul 27, 2019

    He Was a First Responder on 9/11—Why He’s Telling His Story Now

    Tom Frey spent years recovering victims of the 9/11 attacks. His time working to bring families answers resulted in his own poor health.

    Link to Article
    Source: The Healthy.com
  • Mar 18, 2019

    Pulmonary Fibrosis Foundation Warns Against Stem Cell Infusions

    In response to an uptick in direct-to-consumer advertising for stem cell therapies by for-profit centers, the Pulmonary Fibrosis Foundation (PFF) has issued an updated warning against any type of stem cell treatment of pulmonary fibrosis (PF) outside of an approved clinical trial.

    Link to Article
    Source: Medscape Medical News
  • Oct 18, 2018

    Pulmonary fibrosis organization creates registry for research

    The Pulmonary Fibrosis Foundation has launched its first phase of a patient registry with 2,000 patients on board.

    Link to Article
    Source: Health Data Management
  • Oct 08, 2018

    West Hartford Spreads Awareness of Pulmonary Fibrosis, Delamar Turns Fountain Blue

    For several days during the last week of September, the water bubbling out of the fountain in front of the Delamar West Hartford Hotel glowed blue, as the hotel joined other buildings and structures throughout the country in raising awareness for pulmonary fibrosis.

    Link to Article
    Source: We-ha.com
  • Sep 03, 2018

    After Hours with Rick Kogan: The Pulmonary Fibrosis Foundation

    Tonight on the show, Rick is joined by Dorothy Coyle, Amy Kozyra with Dr. Daniel Dilling to talk about the Pulmonary Fibrosis Foundation.

    Link to Article
    Source: WGN Radio
  • Jul 25, 2018

    How Can I Find the Best Pulmonologist?

    Our lungs work hard every day to make sure we're able to do all the things we need to do, extracting oxygen from the air we breathe and sending it onward to cells in every corner of the body.

    Link to Article
    Source: U.S. & World Report News
  • Jun 22, 2018

    Putting the Spotlight on Pulmonary Fibrosis with Julie Halston

    It’s a moment Broadway actress Julie Halston will never forget.

    Link to Article
    Source: Media Planet
  • Jun 16, 2018

    Why investors injected $62 million into a Peninsula biotech targeting a deadly lung disease

    Pliant Therapeutics expects to have 50 employees by the end of the year and is recruiting for its first clinical trial.

    Link to Article
    Source: San Francisco Business Times
  • Mar 30, 2018

    Spurred by personal tragedy, Jordan Howard seeking to change lives

    The Bears’ star running back is more than a bruising football player. He’s a man motivated by previous trials using his platform for a cause close to his heart.

    Link to Article
    Source: Windy City Gridiron