CLAPA

CLAPA

At a glance

Causes

  • Health and well being / research and care

Other details

Organisation type: 
Charity
Geographical remit: 
National - Britain

Objectives

The Cleft Lip and Palate Association (CLAPA) is the national charity supporting people born with a cleft and their families in the UK.

We bring together people affected by cleft to help them connect with others who share their experiences, welcoming them into a supportive community for life.

Our vision is to ensure one affected by cleft lip and palate in the United Kingdom will go through their journey alone.

Activities

Services include:

  • Vibrant social Facebook, Twitter and Instagram profiles which promote positivity, bust myths and celebrate differences with regular content created by and for the cleft community.
  • Online support groups moderated by trained volunteers provide an instant connection for those looking for an informal support network.
  • Regular events give people the chance to talk about their experiences and worries and hear from others at all stages of the cleft journey.
  • Confidential one-to-one support provided by trained volunteer patients and parents who reassure those most in need that they can cope with whatever lies ahead.
  • Accredited information on cleft led by our community, reflecting their experiences and emotional needs as well as medical facts.
  • An Advocacy Service that provides tailored information and signposting to those with complex enquiries.
  • A Children and Young People’s Council made up of 9-17-year-olds who meet to share their thoughts and experiences, helping to improve our support services as well as cleft research and NHS care.
  • A consultancy service for researchers which connects their work with our community.
  • A feeding service that supplies 15,000 subsidised items of specialist equipment for babies born with a cleft each year, including free of charge items for new and vulnerable families.

No current opportunities

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