Will you be one of the 250?

To continue our work in 2023, CLAPA needs 250 more regular donors by Christmas. Will you support the UK cleft community by investing in our future?

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Need to talk?

CLAPA's Parent & Peer Supporters are trained volunteers who can help you talk through any problems, worries or questions you have about cleft lip and palate. Get in touch today.

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In your area

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Annual Survey 2022

This annual survey is designed to give us a 'snapshot' of your needs, priorities and concerns. By taking part, you're helping us make sure our plans include you!

Take the Survey
  • Young Nora

    Nora’s Story

    My first memory was going to see the plastic surgeon Dr. Tanner. He was so gifted to be able to help me and my brother James,  who had a more severe cleft lip, and palate. He was born with no palate and no top lip and almost died at birth. His story deserves to be told.

  • Stacey's little boy

    Stacey’s Story

    I'm Stacey, and I was born with a unilateral cleft lip and palate. As a young girl, I was confident and happy, but when I got to secondary school, I was bullied about my appearance, and my self-esteem was low.

  • 26 Sep 2022 03:39 -26 Sep 2022 03:39

  • 26 Sep 2022 03:39 -26 Sep 2022 03:39