You don't see CF |

#cysticfibrosis #cf #lifeunlimited
Cystic fibrosis is an invisible condition. You can’t see it or what it does to the body. But it’s not invisible to the 10,800 people in the UK whose lives are dominated by it every single day. The challenge of living with cystic fibrosis is invisible. Except to the ones who live it.
Speak out and share your #CFTruths.
Visit www.cysticfibr...

[@paulwarren8832]

Thanks for sharing your experience, Kieron. This video is very impactful.

[@Jojo-CyFi]

Your experience is articulated very well, thanks for that.

[@lesleyblaikie7031]

Thanks for sharing .

[@markcampion1029]

Ima cf in ireland 37 tabs per day. Fuk them its mental strength my friend. We'll break barriers.

[@AWayOfLiving84]

Does your family care for you? If they do that's a good thing. As long as they don't overcare. I've noticed families with no money problems care more. Is that because I have no money problems?

[@noahriding5780]

someone experiences coughing fits for a long time after eating... every time they eat is this not just asthma? And with constant lung infections, it seems like that wouldn't just be asthma?

[@gamingstore1589]

Don't be upset bro
I have cf i alls see problem 😅

[@AWayOfLiving84]

👣🌍☯️🤷🏻‍♂️ I am healthier than most. But I still get sick a bit. At the moment it's as bad as it's been in a while.🫣 I will have some money to get a nebuliser soon. Saving. Usually I'd go to hospital when I'm this bad but I can't. Believe what you want to believe. Cause that's what people do