CLAPA
(The Cleft Lip and Palate Association)
CLAPA is the representative organisation
for all people with and affected by a cleft lip and/or palate in
the UK.
CLAPA was set up in 1979 by a group of
parents of children born with clefts and health professionals
involved in their treatment.
CLAPA work closely with the specialist cleft teams and generic
health professionals to ensure that people receive the best
possible care.
CLAPA offers free membership for anyone affected by or
interested in cleft lip and palate. For more information
visit CLAPA’s website: http://www.clapa.com/
Local branch
Your local branch is CLAPA Bristol and South West. Our main aim
is to encourage children and adults with clefts and their families
to come together to share experiences and give each other support.
This is usually through social events.
We aim every year to host a Christmas party (usually the first
Saturday In December) and a summer picnic in June.
Funds and donations permitting, we provide all new parents with
2 free bottles and teats. We also support the Cleft Unit, where
possible, by buying specialist equipment not otherwise funded by
the NHS.
For details of local events, see the branch section on CLAPA’s
website: http://www.clapa.com/services/entry/branch_network/
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One in every 600-700 children in the UK is born with a cleft lip and or palate
CLAPA Bristol and West
Branch Committee Members
Samantha Jones
0117 302 6718
Natalie Rigg
0117 924 5445
Michelle Bower
0117 962 3987
Cora Jones
0117 9086157
Parent Contact Bristol
Natalie Rigg
0117 924 5445
Parent Contact Devon
Esther Rookes
01822 853862