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Just Because I Can’t Work Doesn’t Mean I Am Lazy

By Jenny Livingston August 08, 2019

In an ableist society, sometimes you just have to ignore comments that make you feel worthless for not working. If I had the chance, here is what I would tell people who judge those with an invisible illness.

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  1. Top 10 Blog Posts of 2018

    By Bethlehem Horn December 26, 2018

    With nearly 120 blog posts shared on the CF Community Blog this year, we're taking a moment to look back at some of your favorite posts. Check out the countdown to the most-read blog post below.

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  2. Reflecting on 500 Posts on the CF Community Blog

    By Margarete Cassalina November 20, 2018

    As the first contributor to the CF Community Blog, I was ecstatic when the Cystic Fibrosis Foundation reached out to me about authoring the 500th post. As I look back on all the stories the CF community has contributed over the past three years, I can’t help but feel grateful for the opportunity for connection.

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  3. Top 10 Blog Posts of 2017

    By Bethlehem Horn January 3, 2018

    In 2017, our most-read blog posts covered a variety of topics including parenthood, guilt, and loss. Check out the countdown below to see if your favorite post made the top 10 list!

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  4. A Holiday Message From Dr. Preston Campbell, III

    By Preston W. Campbell, III, M.D. December 26, 2017

    As we look forward to 2018, our President and CEO, Preston W. Campbell, III, M.D., shares a special holiday message to the cystic fibrosis community.

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  5. Committed to Community: Meet the 2017 Impact Grants Program Awardees

    By Piper Beatty Welsh, J.D., M.P.A. November 21, 2017

    As an adult with cystic fibrosis, I know just how powerful and creative the CF community can be. That’s why I’m excited to announce the four 2017 Impact Grant awardees who are making a positive impact on the CF community.

  6. Community Voice Brings Your Voice Into Everything That We Do

    By Christina Roman April 7, 2017

    The CF Adult and Family Advisors (AFA) just got a fresh new look and name: Community Voice. By joining this group, people with cystic fibrosis and their family members have an active say in the Cystic Fibrosis Foundation’s initiatives, driving improvements that benefit everyone impacted by CF.

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