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Have many people here moved away from their parents, when going to college or just growing up? How did you find the experience, what did you find difficult about it?

Does anyone have any interesting ways of keeping organised and storing all of their equipment? Please post photos if you do. Also, do you think you would buy new table or shelf type product if it was specially designed for Cystic Fibrosis?? My cousin could really use one, he's always leaving...

I'm now looking at the possibility of making a product that will shift some day time treatments to night time, while we are sleeping. For example a new Vest that is designed for sleeping in. What are peoples thouhts on this? Do you do any treatments while asleep, would you prefer to be doing...

When you use your vest, do you like to do a high intensity for shorter period of time, or a low, less intense frequency worn for a bit longer? What are your preferences and habits?

Does anyone do anything creative or different with their therapy and medication aside from vest and nebuliser? Those seem to be the gold standard but I'd like to know if anyone uses their own techniques

I'm curious, are there any activities that you can't or won't take part in because of CF ? And what lengths do people go to to not pick up infections

Hello everyone, I'm a researcher in the University of Limerick in Ireland. My brother has cf so I've been around it for most of my life, but only recently realised its severity as his CF has gotten worse. For my final degree project I've decided to research the every day problems people face...