Taking a holiday can require a lot of extra planning when you or your child have cystic fibrosis (CF). From travel insurance to taking medication on flights, there can be plenty consider. In today’s episode, we explore what you need to know about travel and CF.Our host Lucy shares some top tips from the CF community, Matthew from our Helpline answers some of your questions on travel, plus we hear from travel enthusiast Ryan about his experiences – and top do's and don'ts – when it comes to holidays with CF. For more information and support on any of the issues we've talked about in this podcast, you can call our Helpline on 0300 373 1000, or email [email protected], or message us on WhatsApp.Visit our website to find out more about going on holiday with CF.Find out more about travel insurance.Sign up to our monthly e-newsletter for all the latest CF news, personal stories and different ways you can get involved in our work.Be sure to speak to your CF team if you have any questions about travelling with CF.

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“What did the council decide on item 42?” — answered with the speaker and the moment.

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