30 Days of PF: My Mom Inspires Me to Be Positive

30 Days of PF: My Mom Inspires Me to Be Positive

Photo courtesy of Ann Reynoso Day 19 of 30 This is Ann Reynoso’s story: Never a day goes by that I don’t think of my mom. She was very important to me. She helped me to be brave when we found out about my having LIP/PF. She would…

30 Days of PF: My Faith Sustains Me

Photo courtesy of Diana Schmitz Day 18 of 30 This is Diana Schmitz’s story: In January 2019, I was diagnosed with idiopathic pulmonary fibrosis. Throughout my experience with IPF, people have used certain words to describe me: grace, bravery, strength, and inspiration. But for me, the key words…

30 Days of PF: Swimming Is My Happy Place

Photo courtesy of Terril McBride Day 17 of 30 This is Terril McBride’s story: My name is Terril McBride, and I have IPF, like my father before me, and my two brothers. I was diagnosed in 2015. However, I had many lung complications after having open heart surgery in…

Ofev Can Safely Treat Progressive Fibrosing ILDs in Japanese Patients

With reasonable safety, Ofev (nintedanib) slowed lung function decline in Japanese patients with progressive fibrosing interstitial lung diseases (ILDs), according to a subgroup analysis of the Phase 3 INBUILD trial. Overall, this analysis provides further assurance to clinicians in Japan on Ofev’s benefits to patients there, with “no new…

30 Days of PF: Staying Active While Living with IPF

Photo courtesy of Malcolm Mann Day 16 of 30 This is Malcolm Mann’s story: My first inkling that my lungs were under stress was around the year 2000, when I developed a cough while exercising. In those distant days, I was a 50-year-old, slow-ish triathlete, and I…

Why September Is Hard for Me as an IPF Patient

As a patient living with a chronic illness, I’ve become comfortable with people using clichés to try to comfort me. People naturally want to relate to others, but it’s often hard for someone who’s healthy to understand the experiences of a young adult who requires oxygen to breathe. One cliché…

30 Days of PF: I’ve Been Given a Second Chance at Life

Photo courtesy of Curt Strickland Day 15 of 30 This is Curt Strickland’s story: I had a double lung transplant 18 months ago, and I am doing very well. Given my good fortune, I wanted to share what I believed helped in both my recovery and the actual transplant…

New Institute Aims to Leave No Rare Disease Patient Behind

A newly launched non-profit institute is seeking to advance research, and the development of new therapies, for people with rare diseases — a patient community with some of the largest therapeutic needs, but one that is often left behind. Named the Institute for Life Changing Medicines, the project was…

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