Cystic fibrosis is nasty. Bacteria makes my breath stink. Malabsorption makes me fart a lot. I cough so much that my face turns red, and blobs of mucus often fly out of my mouth and onto the shirts and/or pants of those standing in my general area. If I could…
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7 Tips for Managing Your Pain
I’d been anticipating my bilateral cochlear implant surgery for more than a year. I knew it required some drilling into my skull, cuts behind the ear, and having devices shoved into my cochlea. I did not expect to be restricted to Tylenol…
Only 61.8 percent of cystic fibrosis patients comply with their daily respiratory medication and 41.2 percent comply with physiotherapy plans, according to a 2008 study. I’ve observed that most patients and their parents want to be perfectly compliant — they just haven’t formed good strategies for…
Cystic fibrosis (CF) is horrible. Say it again for the people in the back: It is horrible. To be transparent, I’m writing this article in a bad mood, so naturally, I look to my diagnosis as a means to understand my frustration. I don’t believe this is unfair…
I’ve always known that I wanted to be a writer. There were some rebel years, of course — short-lived times growing up when I claimed to have aspirations of teacher-hood or superstardom. There was even a year when I wanted to be a hydrologist, as I couldn’t seem…
You’ll meet legions of doctors throughout your life with cystic fibrosis. You’ll encounter doctors you adore and who will save your life countless times. And you’ll encounter some who make life a nightmare. Here are six “characters” you’re bound to meet, plus things they’re likely to say, at…
A Letter to CF Parents
Dear parent, I know you’re afraid. My parents were afraid, too. My mom left a college biology class crying; the lesson on genetics included the life expectancy of a child with cystic fibrosis. There’s an old home video of her talking to Baby Bradley before I was diagnosed. I was…
I fought cystic fibrosis for 15 years before the overwhelming burden collapsed. My family was driving to get dinner when my brain and heart suddenly exploded. I was sobbing and gasping for breath, able to hear every rapid pound of my heart against my ribs. I couldn’t think,…
Most of last summer was spent either in a hospital bed or lying on my couch — the couch I had watched my cat dying on just months before. I wasn’t in much better condition than my cat. I thought I was defeated, broken. The most activity I had in…
Chronic pulmonary infections are a hallmark of lung disease in patients with cystic fibrosis. Due to the variability in bacteria that can colonize the lung and the specific antibiotic treatments that may be effective, treatment strategies are often tailored to individual patients. But some bacterial infections are…
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Recent Posts
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