Parents
CLAPA has many regional branches, who are all run by volunteers, and many other regional contacts in the United Kingdom, all committed to providing the support needed by families affected by cleft lip and/or palate.
Branches are run by people who have themselves benefited from the organisation, often working in partnership with local health professionals.
To access branch information click on this link http://www.clapa.com/members
Registration will take a few minutes.
Related Articles
- National Office News
- CLAPA Conference 2011 Videos
- Marianne Foot’s Story
- CRANE Database
- Branch Chairperson needed for CLAPA Essex
- Marianne Ryan’s story
- First meeting of East of England Young People’s Group
- Video: Easing The First Few Hours
- Volunteer Induction Day
- Katie Gore’s story
- Cleft Palate and Deafness
- Changing Faces Activity Days for Children
- South Thames Network Board
- Help prioritise cleft care on the NHS
- Regional Coordinator
- Parent Case Stories
- Having problems accessing an NHS dentist?
- The School Years - FACT SHEETS
- Mead Johnson feeding bottles to be discontinued
- Stickler Syndrome
- CLAPA National Survey 2010
- Launch of new CLAPA information leaflet
- Look at Me!
- Glossary of medical terms
- Grommets or Hearing Aids?
- Feeding Service
- Feeding Advice
- Express Feeding a baby with a cleft palate
- CLAPA websites for children & young people
- Branch Network
- Face Forward
- CLAPA’s Strategic & Operational Plan
Need to talk?
We have parent contacts available throughout the UK to support families affected by cleft lip and/or palate.
Parent Contacts >