Articles

Navigating the pandemic with two kids under five is no joke. I feel like I’m in a game of dodgeball and am just ducking and pivoting to narrowly escape the...

Planning a weekend break, a long haul trip or just a family holiday has always been difficult with CF. After Covid, many patients are struggling with traveling again due to...

When you are diagnosed with a rare disease like cystic fibrosis, you might feel overwhelmed about what to expect. Because few people have your disease, there may be a lack...

As more women with CF reach childbearing age and start families of their own, the question of how to feed their baby is becoming much more commonplace. Many new CF...

I was talking to someone about relationships recently. More specifically, we were talking about how hard boundaries can be, but how they can help relationships so much. At one point...

There are so many ways to get involved with cystic fibrosis advocacy and research – from talking to loved ones about life with CF to donating to CF foundations, and...

Numerous healthcare professionals are involved in CF care. Most often, people don’t think of their pharmacist as part of their CF team. There are many reasons for this; one reason...

At the NACFC (North American CF Conference) in October 2021, some very exciting news was announced for people and families living with CF. During the first plenary session, it was...

When the COVID-19 pandemic broke out in March 2020, nearly everyone had increased anxiety and stress. Fears of getting sick, dying, or feeling helpless were common. COVID-19 is a respiratory...

If you haven’t had a chance to read my previous articles, just know that I’ve always been inspired by the colors of Joseph’s Technicolor Dreamcoat. While I viewed them in...

Distal intestinal obstruction syndrome (DIOS) is a condition where the small intestines get blocked by thickened stool. About 15 percent of people with cystic fibrosis (CF) experience DIOS. It happens...

Cystic fibrosis (CF) brings its own sets of challenges that are unique to us as patients. I know everybody deals with depression and anxiety in their own ways, and have...

Living with a long-term health condition requires us to stay on top of everything: doctor’s appointments, new symptoms, insurance, and, of course, managing treatment – all while taking care of...

The excitement, or dread, that surrounds the holiday season is hard to ignore. People are busy. Shops are open late. Lines are long. And sometimes people can get overwhelmed. During...

The CF community has seen the advent of disease altering treatments in the last few years and a spurred interest from researchers and companies for bringing even better therapies that...

We asked our advocates on Cystic-Fibrosis.com to share their perspectives on the COVID-19 pandemic, and how their lives have been impacted so far. Life has changed in some ways and...

When I stepped out of my comfort zone and started raising awareness, I never thought I would actually teach someone about cystic fibrosis. And it was very naive of me...

A published study finds that certain people of color with cystic fibrosis (CF) have poorer lung function than white people with the condition. In our 2020 Cystic Fibrosis In America...

Entering into parenthood with CF can be an exciting and anxious time for many couples. However, first you need to give birth to welcome your precious baby. Labor and delivery...

For decades, many people living with cystic fibrosis struggled to gain and maintain their weight. Once enzymes were introduced in the 1950s, weight gain and the absorption of nutrients from...