CLAPA was set up in 1979 as a partnership between parents and health professionals to support parents all around the UK. Since then, we have grown into a national charity with a network of staff, groups and volunteer-run Branches dedicated to supporting everyone in the UK affected by cleft lip and/or palate.
Whatever your situation, you’re not alone. In this section, you’ll find information on all our support services, from Parent Contacts to Facebook Groups. We hope you’ll find something that fits your needs, but if not please do get in touch with us directly.
Not sure where to start?
Check out CLAPA’s Services to see what we can offer parents and families as well as young people and adults with a cleft.