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Hi, I've been posting a lot about this lately on other forums. I'm a student of Industrial Design in Ireland and for my degree project I'm looking to solve this problem for you guys by making a marketable stand alone product for CF storage and organisation :) .. Threads like this really help my...

Hi, I've been posting a lot about this lately in other forums. I'm a student of Industrial Design in Ireland and for my degree project I'm looking to solve this problem for you guys by making a marketable stand alone product for CF storage and organisation :) .. Threads like this really help my...

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...

Hey, Im researching life with CF and need all the quality info I cant get mrdavidrandles@gmail.com Thanks a mil.

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

Thanks for your quick response. Would you mind telling me more? Like what are some of these things that you know will send you in into a coughing fit?

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

That is an idea that I have been considering. Perhaps using ultrasound waves to loosen the mucus? I also really like the other ideas because they address care givers as well. Ideally we can come up with a contemporary solution to a problem all CF sufferers experience as well as those around...

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...