CF Community Blog

Morgan Barrett

Adult with CF

Learn more about Morgan Barrett

  1. Why My CF Clinic Visits Are a Family Affair

    By Morgan Barrett January 11, 2019

    The expression, “It takes a village,” sometimes seems to apply to my clinic visits. I like having my family accompany me. They support me emotionally and help me keep track of important health information.

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  2. 5 Things I Wish People Knew About My Life With CF

    By Morgan Barrett December 13, 2018

    Cystic fibrosis is a complex disease that affects each person living with it differently. I think it’s so important for us to learn to understand each other, so I’ve come up with things I wish others knew about me and my specific experiences with CF.

  3. Participating in a Clinical Trial Is Empowering

    By Morgan Barrett February 7, 2018

    Participating in clinical trials can be scary, but the sense of empowerment you get from knowing that you are contributing to a cure outweighs any second thoughts.

  4. Making the Hospital More Hospitable

    By Morgan Barrett August 9, 2017

    Calling an inpatient stay “ideal” may sound like an oxymoron, but having the things I need to be in better health by the time I head home from a hospital stay is important.

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  5. The (Birthday) Gift of Life: My Brother’s Liver Transplants

    By Morgan Barrett December 15, 2016

    My brother received a liver transplant the day before his 15th birthday but soon needed another.

  6. 5 Easy Ways to Make the Most Out of Hospital Stays

    By Morgan Barrett April 7, 2016

    Hospital stays are hardly a party. But since they’re a part of life with CF, let’s get the most out of them and help ourselves make them fewer and farther between.

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About Morgan Barrett

Morgan resides in her native Kansas City with her husband, Kory. She grew up with her two younger siblings, who also live with CF. Morgan graduated from Kansas State University in 2014, where she studied advertising, business, and Spanish, and also studied abroad in Costa Rica. She works full time, and enjoys volunteering for her local CFF chapter -- particularly for the KC Wine Opener fundraiser event. Some of her favorite things are reading, running, and traveling, and she fully believes in the importance of exercise to keep her lungs healthy.

This site contains general information about cystic fibrosis, as well as personal insight from the CF community. It is not intended as a substitute for treatment advice from a medical professional. Consult your doctor before making any changes to your treatment.