A blonde lady with glasses and her 5 year old blonde son. She is holding him and looking down laughing. The young son, Dylan, is holding her face and doing a cheeky look to camera. They both have repaired clefts.
Stacey and her son, Dylan, were both born with a cleft

The UK's cleft lip and palate charity

Supporting, celebrating and championing the UK cleft community at every stage of life.

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Our new look...

Introducing our new look and feel as Cleft Lip and Palate Action. The CLAPA you know and love - but with a bold new energy.

Our impact

Discovering CLAPA's community and services has changed lives.

Kazzi's Story

Kazzi talks about growing up with a cleft – after being adopted from Mother Teresa’s orphanage in Calcutta – and finding CLAPA.

CLAPA’s like a lifeline – to know you’re not alone and there’s someone else who’s feeling exactly how you’re feeling. Finding the CLAPA website was the best thing I ever did. I’ve loved being part of the CLAPA community ever since.
Kazzi

Billy's Story

Finding CLAPA, it was such a relief to know I'm not the only person to have gone through all of this. It's more common than you think.

Kevin and Sanjana's Story

When we found CLAPA there were 100 things going on in my mind, but this made me think, ‘okay, there’s a plan of action, we're not alone’.

Find a CLAPA Support Service

CLAPA has a range of support services for every stage of the cleft journey, from diagnosis through to adulthood.

Donate

CLAPA relies on your generosity to continue our work supporting, celebrating and championing the UK cleft community.

Fundraise

Whether you’re baking cakes, running marathons, or raising awareness at work or school, every effort makes a difference.

Latest news and events

Browse the latest news, stories and events from CLAPA.

Grandparents’ Coffee Club

This event is for grandparents of a child born with a cleft lip and/or palate in the United Kingdom. If you are a parent (including those who are expecting) or carer, you are also welcome to join.

Information Evening: Weaning

This event is for parents/carers of a child born with a cleft lip and/or palate in the United Kingdom.