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CF Community Blog

The CF Community Blog is written by the community, for the community. It's about sharing our experiences, reflections, and perspectives — the good days, the bad days, and all the tough and wonderful things in between. With topics ranging from emotional health to treatments, the blog is a platform to share your unique story.

More community posts
Chris smiling outside with his wife, Kate.

BLOG

What To Do When “Most People Will Be Fine” And You Are Not “Most People”

Having CF has always involved doing things nobody else around us is doing because, well, we have to — and COVID-19 won’t be any different. As a post-transplant CF patient who happens to be a practicing pharmacist, I am writing about the tools we now have in a world of limited universal restrictions and precautions.

Chris Raybuck
| 8 min read
Meagan standing outside of an RV.

BLOG

A Look at the Pandemic Then and Now

I’ve had to make many changes in response to the COVID-19 pandemic to protect my health. Not all the changes were welcome, but now that I’ve adjusted, I’m enjoying my new normal.

Meagan-Tenyer-Headshot
| 5 min read
Lauren Molasky sitting down on the couch with her husband, two children, and dog.

BLOG

Year Two in the Pandemic

In my experience, the best way to support a loved one with cystic fibrosis is to listen closely and remember the details of his or her most common treatments and complaints.

Lauren Molasky headshot
| 5 min read

BLOG

Why Sharing My Positive COVID Results Mattered

What I thought was a cold turned out to be COVID. I shared my positive test result with my CF care team. Not only did they let me know of an important drug that was available to reduce the risk of getting severe symptoms, but they also helped me find it since the drug was in short supply.

Carmelina Hreinsson headshot
| 4 min read
Luisa sitting on the grass with a mask on outside with her dog.

BLOG

Giving You Permission to Accept My Chronic Illness

Although I don’t consider having a chronic illness like cystic fibrosis a good thing, I accept it and I think others should, too.

Luisa-Palazola-Headshot
| 3 min read
Katherine Finegan smiling with her husband at a baseball game.

BLOG

Prioritizing Myself This Holiday Season

Because I am immunocompromised after having a lung transplant, I still take extra precautions with COVID-19. I still feel awkward with turning down invitations and limiting my own guest list at gatherings, but I know my closest family and friends understand and do whatever they can to accommodate me.

Katherine Finegan headshot
| 4 min read