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Westminster

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Here's how you can make sure your voice is heard in Parliament.

Unite with us to make sure cystic fibrosis is high on the agenda for your local parliamentarian.

  • What are Cystic Fibrosis Trust’s key campaigns?

    Cost of living with CF

    CF creates additional costs for those who live with it. That's why we're calling on the Government to tackle the financial burden of CF through fairer benefits and free prescriptions.

    Find out more

    Access to treatment and care

    We’re taking action to make sure everyone with CF can get appropriate treatment and care when they need it.

    Find out more

    Learn more about all our campaigns

  • How can you engage your local parliamentarian?

    There are lots of ways you can help us to spread the word about CF and get your voice heard in Parliament. This might include: 

    • emailing your local parliamentarian. Download our email template here. If you feel comfortable, please do copy us into your email at [email protected]. 

    • meeting with your local parliamentarians

    • raising awareness on social media

    • sharing your story with the media

    Your MP can be found here.

  • Why does it matter for people with cystic fibrosis (CF)?

    Your local parliamentarian is there to represent your voice in Parliament, so it’s important they know the issues that matter to you most. They can put pressure on the Government by speaking out in debates and asking questions in Parliament. 

    We encourage you to contact your MP to tell them about some of the things we’ve been campaigning for and how CF impacts your life. If you live in Scotland, Wales or Northern Ireland, you can also contact your MSP, MS or MLA.

Latest news

The latest news and research from the world of cystic fibrosis, keeping you up-to-date and in the know.

Our Helpline

Our Helpline is available to anyone looking for information or support with any aspect of cystic fibrosis, a listening ear, or just to talk things through.

Financial support

We provide a range of grants for people with cystic fibrosis and their families, support for those applying for benefits and information about prescription charges.