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NHS Choices Condition

Content supplied by NHS Choices

Lauren, 14, talks about living with cystic fibrosis and how she doesn’t let it stop her from doing the things she loves

"Cystic fibrosis stops me from going out with friends sometimes and from doing sports because it makes me cough a lot.

"I also have to go to doctors’ appointments and to hospital when I’d rather be with my friends and doing social things. It can get a bit annoying at times.

"My personal symptoms are things such as coughing, wheezing and being unable to do things that I normally could do if I wasn’t ill. For example, if I was coughing a lot, then I couldn’t do any sports or dancing because it would make me more productive, which means bringing up lots of phlegm and isn't very nice. Sometimes it makes me sick in front of my friends, which can be embarrassing.

"My treatments are things like medication, or I have IV antibiotics through a needle in my hand or portacaf, which is a piece of metal under the skin. I also have inhalers and physio twice day. The physio is basically percussion, tapping on the chest to make me bring up phlegm. It helps because it can stop me from getting bugs and brings up all the nasty stuff that can do my body harm.

"I was 12 years old when I learned how to do my physio by myself properly. I also learned how to use my inhalers, the PEP (Positive Expiratory Pressure) mask and the flutter. My mum taught me how to do it and I think it was easier for her to teach me than a doctor because she has been with me the whole way through. I wouldn’t say there was a proper age for people with cystic fibrosis to start learning their own treatments, just when they feel confident. It’s quite important that people learn to manage their own treatment because it makes you feel more independent and happy that you’re not relying on somebody else.

"Having CF doesn’t stop me from doing everything I want to do, but when I’m unwell, it can stop me from swimming and dancing. When I’m well, I can do anything that someone who doesn’t have CF can do. I love to dance and sing, and I want to be an actress on Broadway or dance in musicals.

"When I’m unwell I always plan something and try to have something to aim for. When I’m in hospital and can’t go out for a few days, I always plan something nice so that I have something to look forward to. So you can fight anything bad that comes along because there’s something positive at the end." 

view information about Cystic Fibrosis on www.nhs.co.uk »

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