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Cystic Fibrosis Research Institute > About CF > CF Community Blog
November 2, 2026
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From the Front Lines of Caregiving to the RN Calling

Life rarely hands you a predictable roadmap. For me, the journey changed forever the day my oldest son was born. He was constantly sick as an infant and toddler, but for years, doctors brushed off my concerns, telling me it w [...]

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October 5, 2026
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A Therapist’s Journey Navigating One Diagnosis After Another

I have had cystic fibrosis (CF) my whole life and began in a role as an advocate when I was 15. Around that same time, I was diagnosed with a bacterial lung infection called Mycobacterium avium complex (MAC). The two bec [...]

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September 16, 2026
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Beyond Pushing Through: The Power of Accommodations

When people hear that I graduated from UC San Diego, they often see the degree as proof that I pushed through. I did work hard, but “pushing through” is not the whole story. I graduated because, at crucial moments, I was not [...]

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August 31, 2026
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82 Years Living With & Researching Cystic Fibrosis

I am almost as old as cystic fibrosis (CF). That is, Dorothy Anderson initially described CF as mucoviscidosis in 1939, and I came along in 1944. In this way, we are both over 80.  Since early childhood, I have had a pro [...]

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August 3, 2026
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Living with Invisible Symptoms of Cystic Fibrosis

In the media worldwide, we know cystic fibrosis (CF) as a fatal lung disease where patients are bound to hospital beds and oxygen masks. While this is true, it doesn’t represent the CF community as a whole. Due to the complex [...]

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June 30, 2026
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Seeking Answers and Establishing Care in the US

My journey with cystic fibrosis (CF) has been long and, at times, uncertain. When I was five, I started having recurrent lung problems. My childhood in Chile was shaped by hospitalizations, procedures, and treatment [...]

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June 1, 2026
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Coming to Terms with My CF Diagnosis

It’s often said that every person experiences grief differently. For many years, I struggled to come to terms with my CF identity. Writing this blog is an effort for me to achieve the final stage of grief, which is accep [...]

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May 5, 2026
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Building My CF Support System

Navigating young adulthood is already a complex journey. Not to mention adding another layer such as growing up with cystic fibrosis, which can make the path feel even more isolating. Growing up with CF, I [...]

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April 6, 2026
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A Cup of Courage a Day Keeps Fear Away

As a cystic fibrosis (CF) warrior, I am someone who over the years has been riddled with fear and anxietystemming from medical trauma. I couldn’t realize it sooner because I was in survival mode. I had learnedfrom an early ag [...]

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March 2, 2026
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Skipping A Colonoscopy Almost Cost Me Everything

It started like any other routine clinic visit, with the familiar checklist of questions and reminders. One of them was that I was overdue for my next colonoscopy. I already knew that. I just didn’t want to deal wit [...]

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About Us

  • Overview
  • Mission & History
  • Financial Information
  • Board of Directors
  • Infection Control Policy
  • Privacy Policy
  • Contact Us

Advocacy

  • Overview
  • CF Awareness Month
  • Cancer & Cystic Fibrosis
  • Become An Advocate
  • Resources & Reports
  • Diversity and Inclusion

About CF

  • Overview
  • Causes
  • Symptoms
  • Diagnosis
  • Treatment
  • CFRI Resources
  • CFRI Resources: Spanish

Events

  • Overview

Ways to Give

  • Donate Now
  • Fun And Easy Giving
  • A Breath of Fresh Air Gala
  • Research Challenge
  • Fundraising Events
  • Planned Giving
  • Non Monetary Donations

Research

  • Overview
  • Funding Opportunities
  • Patrick Nash Fellows Training Program
  • Research Awardees
  • Research Publications

Education & Support

  • Overview
  • Psychosocial Support Programs & Classes
  • Wellness Classes
  • National CF Conference
  • CFRI Community Retreats
  • CF Adult Retreat
  • CFRI Community Newsletters
  • Patient Assistance Resources
  • CF Community Voices Podcast Series

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