Working to support, connect and empower everyone affected by cleft in the United Kingdom

Community

Over 20,000 parents, patients and health professionals

Support

A network of trained volunteers around the UK

Information

Unique information in the right place at the right time

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?

Be a Champion

Events for everyone: find yours today!

CLAPA runs a variety of online events, from topic-focused coffee clubs to live Q&As to children's parties.

Find an online event

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

Find cleft services, events and support near you

Join the CLAPA community

Join the UK's only charity dedicated to supporting people with and affected by cleft from infancy through to adulthood.

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Latest news & events

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.
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26 Jun 2022 07:40 -26 Jun 2022 07:40

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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.
Eva’s Story

In February 2021, we headed off for our 20-week scan. We were so happy to be told we were expecting another girl, but a lot of silence soon followed, and the sonographer said, “I suspect little one may have a cleft lip.”
26 Jun 2022 07:40 -26 Jun 2022 07:40

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26 Jun 2022 07:40 -26 Jun 2022 07:40

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