Australia trip with cystic fibrosis?
A trip to Australia with a camper van entails risks for a cystic fibrosis patient. Even so, the PARI blog author, Alex, risked the trip and describes the challenges, the tour and her unforgettable experiences.
A trip to Australia with a camper van entails risks for a cystic fibrosis patient. Even so, the PARI blog author, Alex, risked the trip and describes the challenges, the tour and her unforgettable experiences.
From spa bath to recognised therapy. The history of the PARI BOY leads through from room nebulisers to what we know today as the PARI BOY, which has become the epitome of inhalation therapy.
Christine Braune has primary ciliary dyskinesia (PCD). In an interview she talks about why running is so important to her despite having this lung disease.
When a child is diagnosed with cystic fibrosis, parents usually have a hard time. Three families share their experiences with getting the diagnosis on the PARI blog.
Carola Landerer has cystic fibrosis. In this interview, the 24-year-old describes how she started working out and what respiratory therapy means for her.
The articles found on the PARI Blog are written by the PARI Blog editorial team. The editorial team consists of PARI employees as well as external guest authors and freelance editors, some of them suffering from severe respiratory diseases themselves.