PFF Insights Blog

  • “It’s important to connect with people who understand.”

    Why I’m Looking Forward to the PFF Education Symposium

    From IPF diagnosis to lung transplant, one caregiver’s questions keep changing. Join her at the virtual PFF Education Symposium, November 12-13.
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  • “I wanted to live but didn’t fear dying.”

    Six Insights from a Lung Transplant Journey

    Ten years after his lung transplant, a pastor diagnosed with pulmonary fibrosis in 2014 shares the challenges he faced and his advice for families.
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  • “I still had more living to do.”

    I Was on the Fence About Lung Transplant. Here’s Why I Said Yes.

    Unsure about a lung transplant? At 70, one person with IPF explains why going through the evaluation and keeping the option open mattered.
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  • “Choosing not to pursue a lung transplant was not about giving up.”

    I Decided Not to Pursue a Lung Transplant. Here’s Why.

    Weighing a lung transplant? A person with IPF shares the factors behind choosing not to pursue one: caregiving, travel, and quality of life.
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  • Thumbnail image cover of 5 questions answered with Dr. Kim

    Personalized ILD Medicine Webinar Q&A: 5 Questions Answered

    Read answers to top questions from our webinar on personalized medicine and precision treatments for interstitial lung disease.
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  • Why I Walk: Honoring My Mom and Fighting for a Future Without Pulmonary Fibrosis

    Read a heartfelt story about walking in the PFF Walk to honor a mother's legacy and support a future without pulmonary fibrosis.
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  • precision-medicine-doctor-lungs

    Personalizing ILD Care: Understanding Precision Medicine

    Learn how precision medicine and genetic insights are transforming targeted therapies for interstitial lung disease care.
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