I have always loved Halloween, but celebrating it with a chronic illness like cystic fibrosis has always meant having to be creative. Being chronically ill meant having to spend a few Halloweens in the hospital or at home, but my mom always made the most of it so that I’d…
Columns
Studies about healthy people with chronically ill siblings are rare. Almost every study examining the psychological impact of illness on the well siblings begins, “This is an underexplored demographic.” This doesn’t surprise me. I’ve been a well sibling since age 3,…
Through the sliding glass doors and down the stairs of the medical plaza, the midday news played — muted, but with captions running — on the TV mounted across from the reception desk. The water fountain hummed. Where I live, case numbers from the COVID-19 pandemic remain high, and medical…
This week’s thoughts are inspired by one of my childhood best friends. She lived down the street from me for most of my life. We’d drive to school together. We’d have lunch together. She’d visit me at the hospital and we’d talk about boys. Now, she’s a…
In 2016, my family spent weeks in the ICU with my brother, Bradley, who had cystic fibrosis and was dying from sepsis caused by an infection. I can’t fully describe what it’s like to have a family member in the ICU, but I need to try, because the…
Someone told me I had a “dancer’s body” the other day, and I pretended it was flattering. “Thank you,” I said, since I hate refuting compliments (and believe intent matters more than execution), but inside I felt conflicted. Gross. Sad. I felt conflicted-gross-sad because the term “dancer’s body” should mean…
Are you living or surviving? Most cystic fibrosis patients have dabbled with this question. To what extent does your health guide your life, rather than love or ambition? I knew the answer back in 2018, but after my bilateral lung transplant in June 2019, things grew complicated. Letting go…
I’m starting to doubt the reasons why I doubt myself. Let’s start this column in a weird place: constipation. If one of my best friends is constipated (I bet you didn’t think we’d drop BMs into your DMs that fast, did ya?), she might complain a little to me,…
I’ve witnessed the greatest acts of love at my sickest. Whenever I reflect on how love has shone through on my darkest days, my misty eyes reveal how much someone has touched my life forever. Sept. 30 is National Love People Day. It’s a timely reminder to love others;…
I was evaluated for my bilateral lung transplant in March 2019. I was transplanted on June 14, 2019, and graduated from physical therapy two months after that. Although transplant facts are more accessible today than in the past, many patients remain in the dark, so I’ll tell you about…
Your CF Community

Visit the Cystic Fibrosis News Today forums to connect with others in the CF community.
Recent Posts
- New gene-editing tool models and corrects cystic fibrosis mutations
- Long-term air pollution linked to faster lung decline in CF: London study
- How my life after lung transplant differs from my life with CF
- Finding a balance between supporting others and taking care of myself
- New UCLA research shows path for 1-time gene therapy for CF