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CPFF’s new Board Chair is leading with lived experience and compassion
Mark Ashcroft is using his personal experiences from a career in community health and safety services, as a patient, a transplant recipient and as a Board member to help CPFF help you. Mark Ashcroft is a listener and he’s been where you are. He understands community organizations and board responsibilities – he is, and has…
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Every extra day I have with both of my parents is a gift
It’s been almost three years since Anne Hurding had her double lung transplant on April 19, 2023. She was in the hospital and it was not certain whether she would survive long enough for the right lungs to become available. As a small woman, she was especially fortunate to receive two lungs from a compatible…
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Travel Insurance 101: What to Know When You Have Pulmonary Fibrosis
Travel can still be part of life when you’re living with a chronic lung disease but it comes with extra questions, especially when it comes to insurance.
