The UK's cleft lip and palate charity
Supporting, celebrating and championing the UK cleft community at every stage of life.
Jump for July!
Take the leap with a tandem skydive, face your fears on a bungee jump, or bounce your way through a family-friendly inflatable course — all while raising vital funds to support CLAPA’s work.
Sign up now for discounted rates and support from our friendly fundraising team throughout.
Our impact
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’.
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
Featured
Discussion Evening: School & Education
This event is for parents and carers of a child born with a cleft lip and/or palate in the United Kingdom.
Antenatal Support Group
This event is for new and expectant parents and grandparents of a baby born with a cleft lip and/or palate in the United Kingdom.
Carol and Anton’s story
CLAPA's celebrity patron Carol Vorderman, and her brother Anton, discuss the lack of support for families affected by cleft before CLAPA, and the importance of raising awareness.
CLAPA shows its strength in influencing Scottish Government policy
CLAPA has had its first big success in influencing government legislation – reinforcing our role as advocates for people born with cleft.