Kate and Harry’s story
Kate tells her story about Harry's cleft diagnosis and how CLAPA's support was so invaluable she became one of our volunteers.
Read news and stories from CLAPA and the UK's cleft community, and find opportunities to get involved.
Kate tells her story about Harry's cleft diagnosis and how CLAPA's support was so invaluable she became one of our volunteers.
Members of CLAPA’s management team recently sat in on a cleft clinic hosted by the South West Cleft Service - and tested out their new hi-tech speech investigation assessment suite.
We were pleased to have the opportunity to submit evidence to the Committee and hope our recommendations help ensure the reforms continue to support high-quality, equitable care for everyone affected by cleft.
In this research paper, Kingston University researchers explore the process of resilience for children with a cleft lip and/or palate (visible difference) starting secondary school in the United Kingdom.
“This response reinforces why the campaign remains necessary - and why we'll continue to work on this issue while our concerns remain unresolved."
Firefighter Rich recently shared his story of growing up with a cleft in CLAPA's latest Cleft Youth Magazine.
“The Appearance Matters conference was a great opportunity to share our findings with peers in the sector, from across the UK and internationally."
We’re looking for a new Involvement Coordinator.
We’re looking for a new Youth Engagement Coordinator.
Maddie tells her story of dealing with bullies and learning to love her authentic self.
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.
Charlotte tells us about overcoming anxiety, embracing your differences and her career in theatre.