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Breathing Easier on the Canadian West Coast

For as long as I can remember, I have always been passionate about traveling. While this has become more difficult since my idiopathic pulmonary fibrosis (IPF) diagnosis, I am grateful that it is not impossible. Having to pull an oxygen concentrator behind me wherever I go was not…

PF Brain Fog Struggles and Solutions

Lately, I’ve noticed I’m not thinking through things as well as I used to. It is very hard for me to accept since clear thinking was a strength for me. I was diagnosed with pulmonary fibrosis four years ago. Here’s what my brain fog looks like. Forgetting information…

Quiet Hobbies Bring New Opportunities

A recent discussion in our new Pulmonary Fibrosis News forums was about quiet hobbies that are beneficial for patients living with idiopathic pulmonary fibrosis (IPF). As the forum’s moderator, I shared a post about my own quiet hobbies and asked patients to share some of the relaxing…

A Gratitude Miniseries: April 2018

Editor’s note: A continuation of Charlene Marshall’s monthly “Gratitude Miniseries.” Unfortunately, April was not my best month. While many good things happened, which I am excited to share below, last month was full of unexpected hardships for both my friends and me. I have a concussion…

What I Wish I’d Known When I Was Diagnosed

I’m coming up on the fourth anniversary of being diagnosed with pulmonary fibrosis. It’s caused me to ponder what I wish I’d known before my diagnosis. Three things are at the top of my list. Ignore information online about life expectancy My disease progressed rapidly because it…

The Benefit of Having Friends with Chronic Illness

No one wants to be plagued with the symptoms, medications, management, or label of living with a chronic illness. For most, a diagnosis of a life-threatening illness such as idiopathic pulmonary fibrosis (IPF) can be an extremely emotional, confusing, and scary time. I remember this vividly when I…

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