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    What is cystic fibrosis?
    • Symptoms
    • Diagnosis
    • Causes and inheritance
    • Types of CFTR mutations
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    • Approved treatments
    • Experimental treatments
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  • Living with
    Living with CF
    Tips for preventing reflux
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    Heat and humidity tips
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    Upper and lower RTIs
    CF and GERD
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  • News
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    Columns
    • Air of Life — Ed Jordan
    • Living Beyond – Jennifer Cogliano
    • Valiant Voice — Lara Govendo
    • Victorious — Brad Dell
    • Mutations & Conversations — Tré LaRosa
    Archived columns
    • Advocacy and Abnormality — Kristin Entler
    • Understanding Nonsense — William Ryan
    Videos
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    • Shaping change in the CF community
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Due to the invisible nature of cystic fibrosis (CF), many people with the disease feel unseen in their challenges. To mark CF Awareness Month, we partnered with patient advocate Brad Dell to create a series of articles — released each Thursday in May — about how to make those struggles known and build supports that lighten the burden.

‘It’s not contagious’: How to address stigmas about the CF cough

This piece is part of a series about living with invisible illness for Cystic Fibrosis Awareness Month. Read more here. While cystic fibrosis (CF) is an invisible illness, it can be heard. That trademark gurgling, wet, productive CF cough sets many on edge because the cause remains invisible.

Breathing space: Advocating for CF needs without overexplaining

This is part of a series about living with invisible illness for Cystic Fibrosis Awareness Month. Go here to read more. People don’t need to explain themselves when they need to take a lunch break to eat or sleep after a long day. That would be exhausting. How much more exhausting…

CF fatigue isn’t laziness: How to build support when CF fatigue exhausts you

Living with cystic fibrosis means battling invisible fatigue and the weight of social assumptions others can’t see — or begin to understand. Raising awareness helps replace judgment with empathy, support, and connection.

Trusting your body: Guiding doctors to take CF symptoms seriously

Cystic fibrosis affects far more than just the lungs, but symptoms beyond breathing trouble often go overlooked or dismissed. Here’s how to advocate for the full picture of your health — and ensure you get the comprehensive care and attention you deserve.

‘You don’t look sick’: How to quickly explain CF in difficult situations

Explaining cystic fibrosis on the fly isn’t always easy — but having the right words can help others understand this invisible illness. Here are simple ways to advocate for yourself in any situation.

CF at work: Talking to employers about cystic fibrosis

Disclosing cystic fibrosis at work can feel daunting, but knowing your rights and preparing the right conversation can ease the process. Here’s how to advocate for the accommodations you need to succeed.

Training CF allies: Sharing the load in managing invisible illness

Living with cystic fibrosis can feel isolating, but learning to ask for help shouldn’t add to the burden. Here’s how to build a reliable support system that lightens your load and helps you thrive.

A leveled field: Ensuring equitable education with invisible illness

Balancing cystic fibrosis and school life isn’t easy, but having the right accommodations and support systems in place can make all the difference. Here’s how to advocate for the tools you need to succeed and safeguard your education at every stage.

Your CF Community


Visit the Cystic Fibrosis News Today forums to connect with others in the CF community.

Recent Posts

  • Small study finds GLP-1 drugs boost lung function in CF patients December 16, 2025
  • Inhaled therapy ETD001 well tolerated in healthy volunteers December 15, 2025
  • This winter solstice, I reflect on moving from darkness to light December 12, 2025
  • Safety concerns halt BX004 phage therapy trial for CF infection December 9, 2025
  • Trikafta cuts need long-term for other CF treatments in real world December 8, 2025


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