CF Community Blog

Ashling Knight

Former Digital Content Manager, Cystic Fibrosis Foundation

Learn more about Ashling Knight

  1. Meet Our CFF.org Homepage Heroes: The Weyandt Family

    By Ashling Knight February 1, 2018

    Hear about our homepage hero, Jeremy Weyandt, and his journey to a lung transplant.

  2. Meet Our CFF.org Homepage Heroes: The Egan Family

    By Ashling Knight July 6, 2017

    The Egan family, currently featured on the homepage of CFF.org, share more about their sassy little girl, how much their support system means to them, and what inspires them in the search for a cure for cystic fibrosis.

  3. Meet Our CFF.org Homepage Heroes: The Woods Family

    By Ashling Knight May 4, 2017

    The Woods family, currently featured on the homepage of CFF.org, share their favorite part of Great Strides walk day, their proudest moments as parents of a child with CF, and more.

  4. Our Top 10 Posts of 2015

    By Ashling Knight December 30, 2015

    Our top blog posts of 2015 focus on big decisions, difficult struggles and small battles against CF.

    Topics:

  5. Real Talk: Expectations vs. Reality – Part 3

    By Ashling Knight November 13, 2015

    In their final “Real Talk” video, Emily, Piper and Somer talk about defying expectations, how every person with cystic fibrosis is different and the reality that there is no set reality for this disease.

  6. Real Talk: Expectations vs. Reality – Part 2

    By Ashling Knight October 20, 2015

    Emily, Piper and Somer continue their “real talk” about living for each day, reinventing their future and being up for a good challenge.
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About Ashling Knight

Ashling previously worked at the Foundation as a digital content manager. She helped keep the Foundation's website and blog up to date with news and information that's important to the CF community. Ashling first got involved with the Foundation through Delta Phi Epsilon sorority at York College of Pennsylvania, where she earned her B.A. in public relations. Originally from New Jersey, she now lives in Pennsylvania with her husband, son, and two dogs.

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.