Take on 11,000 steps a Day in Feb and raise money for over 11,000 people living with cystic fibrosis in the UK. Register and get your FREE t-shirt. | Cystic Fibrosis Trust
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Take on 11,000 steps a Day in Feb and raise money for over 11,000 people living with cystic fibrosis in the UK. Register and get your FREE t-shirt. | Cystic Fibrosis Trust
Cystic Fibrosis Trust. . Take on 11,000 steps a Day in Feb and raise money for over 11,000 people living with cystic fibrosis in the UK. Register and get your FREE t-shirt.
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Take on 11,000 steps a Day in Feb and raise money for over 11,000 people living with cystic fibrosis in the UK. Register and get your FREE t-shirt. | Cystic Fibrosis Trust
0:04
Take on 11,000 steps a Day in Feb and raise money for over 11,000 people living with cystic fibrosis in the UK. Register and get your FREE t-shirt. | Cystic Fibrosis Trust
FacebookCystic Fibrosis Trust
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Living with cystic fibrosis brings many unique challenges, and your voice matters in shaping the future of research, care, and support for everyone affected by CF. We want to hear from you, but we know that surveys can feel long and tiring, so we’re keeping this request short and sweet. There are just two questions: 🟡 What are the biggest challenges you face living with cystic fibrosis? 🟡 And where do you feel you, and your family, need the most help and support in the future? Sharing your vie
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Living with cystic fibrosis brings many unique challenges, and your voice matters in shaping the future of research, care, and support for everyone affected by CF. We want to hear from you, but we know that surveys can feel long and tiring, so we’re keeping this request short and sweet. There are just two questions: 🟡 What are the biggest challenges you face living with cystic fibrosis? 🟡 And where do you feel you, and your family, need the most help and support in the future? Sharing your vie
FacebookCystic Fibrosis Trust
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Ever wanted to ask you brother, sister or friend with cystic fibrosis a burning question about their life with CF? This video project may help with some answers! | Cystic Fibrosis Trust
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Ever wanted to ask you brother, sister or friend with cystic fibrosis a burning question about their life with CF? This video project may help with some answers! | Cystic Fibrosis Trust
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Take on 11,000 steps a Day in Feb and raise money for over 11,000 people living with cystic fibrosis in the UK. Register and get your FREE t-shirt. | Cystic Fibrosis Trust
0:04
Take on 11,000 steps a Day in Feb and raise money for over 11,000 p…
1.2K views4 months ago
FacebookCystic Fibrosis Trust
Living with cystic fibrosis brings many unique challenges, and your voice matters in shaping the future of research, care, and support for everyone affected by CF. We want to hear from you, but we know that surveys can feel long and tiring, so we’re keeping this request short and sweet. There are just two questions: 🟡 What are the biggest challenges you face living with cystic fibrosis? 🟡 And where do you feel you, and your family, need the most help and support in the future? Sharing your vie
0:28
Living with cystic fibrosis brings many unique challenges, and you…
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FacebookCystic Fibrosis Trust
Ever wanted to ask you brother, sister or friend with cystic fibrosis a burning question about their life with CF? This video project may help with some answers! | Cystic Fibrosis Trust
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Ever wanted to ask you brother, sister or friend with cystic fibrosi…
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FacebookCystic Fibrosis Trust
If it’s hard to explain CF to your family and friends why you look ok on the outside but not on the inside, watch and share this video to see how lungs normally work, and how CF can affect the lungs over time. Learn more about the basics of lung care: http://on.cff.org/2rZ5tK0 | Cystic Fibrosis Foundation
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If it’s hard to explain CF to your family and friends why you look o…
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FacebookCystic Fibrosis Foundation
Cystic fibrosis is not just the lungs 🎤 🫳 Our social media officer Eilidh explains how CF is a life-long, life-limiting condition that affects the whole body – and like Eilidh, over 30% of adults with cystic fibrosis are also living with CF diabetes, a number that hasn't changed over the last five years. It’s 24/7. 365 days a year. You never get a day off from CF. If you'd like to get involved and share your experience, join the conversation using #notjustlungs and don't forget to tag us! #cys
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Cystic fibrosis is not just the lungs 🎤 🫳 Our social media officer Eilidh exp…
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“You don’t get a day off from cystic fibrosis, it’s always there.” This is Charlotte, who features on the posters for our ‘No Day Off’ campaign. She shares the reality of living with #cysticfibrosis every day as well as what she would do if she had a day off from CF. Find out more about our awareness campaign and how you can get involved on our website now! ➡️ https://ow.ly/CI8T50RNuOX | Cystic Fibrosis Trust
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“You don’t get a day off from cystic fibrosis, it’s always there.” This is …
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Learning for the first time that your child has cystic fibrosis can be scary. Over the past few months, we've been working with families across the CF community to put together this video and a new information pack for those dealing with new diagnosis based on their real experiences. Download the pack and more information at http://cysticfibrosis.org.uk/about-cf/new-diagnosis | Cystic Fibrosis Trust
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