Health Professionals
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 on take a few minutes.
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1 comment
Hello there, my son was born in February 2006 with a cleft palate. He is now almost 4 and still has no speech. We have been told he has a severe global development delay. I just wondered if anyone else with a cleft child has experienced anything similar.I would love to hear from anybody.
Many thanks and Merry Christmas!x