Celebrating ‘Company’: Visitors at the Hospital

“Phone rings./ Door chimes./ In comes company.” — from “Company,” from the musical of the same name There was a time I wasn’t a fan of hospital visitors. Living with cystic fibrosis (CF), I needed hours of maintenance to appear clean and put together. I’d spend an hour in…

Thanks to My Transplant, I Can Dream About the Future

I never really dreamed about my future until after my double-lung transplant in 2017. My friends who are also transplant recipients inspire me to dream bigger as we navigate this new world together. Although it’s been over four years, dreaming can still feel risky. But the more time that passes,…

The Pros and Cons of Sharing Medical News Online

Growing up, my older sister and I were tasked with calling relatives when our younger sister was hospitalized due to a cystic fibrosis exacerbation. We relayed the news while my mother hurried around, packing bags and getting ready for the inpatient stay. I assume it was helpful — one less…

I’ve Found Powerful Camaraderie in the CF Community

Two of the most powerful words in our vocabulary are “me, too.” Many of us tend to isolate ourselves when our circumstances are challenging. We turn inward rather than outward because we feel shame about what we’re going through. When we find that person or group of people that gets…

My CF Is My Burden Alone

It is natural that we grow attached to the people with whom we develop relationships. That’s just how it is. There’s not much more to it. The early days of friendship are full of tiptoeing around heavy topics or shying away from our truest selves. That’s what makes developing friendships…