News
News and updates from across every CLAPA region
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CLAPA40 | Your Stories |
40 years of CLAPA: An Interview with Michael Mars
One of our founding members, former Orthodontist Michael Mars has watched CLAPA grow from an idea into a national charity working to improve the lives of people affected by cleft all over the UK. In this interview, he looks back on how CLAPA was founded and how far it has come since 1979.
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CLAPA40 | Parent Stories | Volunteering Stories | Your Stories |
Amelia’s Story
Amelia is part of CLAPA's Board of Trustees. Our Trustees are a small group of volunteers who take responsibility for governing CLAPA as a charity and directing how it is managed and run. CLAPA's staff look after the charity's day-to-day work, but our Board of Trustees ensures everything we do is governed and directed by the cleft community.
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Adult Stories | CLAPA40 | Volunteering Stories | Your Stories |
Eleanor’s Story!
Eleanor, now in her early 20s, volunteers for CLAPA by helping to run Residential Weekends for young people born with a cleft. From adventure activities and team games to the opportunity to relax and have fun with others who have similar experiences, these weekends are aimed at tackling the isolation that can sometimes come with being born with a cleft.
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Grandparents | Research | Research Summaries |
The Psychosocial Impact of Cleft on Grandparents
The aim of this study was to explore the experiences and potential support needs of grandparents of children born with CL/P to inform future service provision.
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CLAPA40 | Updates from CLAPA |
CLAPA Turns 40
CLAPA has come a long way since that inaugural meeting, but we’ve remained committed to our founding principles of partnership, peer support and community. During June we’ll be publishing a series of interviews with people from CLAPA’s history who have had a major role in shaping the charity as we know it today. This week, we’ll be starting with some of our existing volunteers to get their view on how things have changed and what their hopes are for the future of CLAPA.
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Adult Stories | CLAPA40 | Volunteering Stories | Your Stories |
Oliver’s Story!
“I hadn’t thought about CLAPA in years,” Oliver admits. “I used to go to the Christmas parties when I was younger and I had really nice memories of them which came back when I saw the logo, they were fun parties.” CLAPA Trustee Oliver shares his story ahead of CLAPA's 40th birthday.
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Adult Issues |
Adult Services Project: An Update
Don’t let the name fool you, the Adults Services Programme is still down with the kids. Starting this month, we’re trying an innovative new way of delivering information - online panel discussions!
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Cleft Lip and Palate | Parent Stories | Your Stories |
#MyCleftStory a year on, through the eyes of Casper’s mummy
"What did that mean? Did that mean Casper would need more palate surgery? Did that mean Casper’s speech would still not develop? Again, I was overwhelmed and hit by a pang of too many emotions and my role of mummy being tested." In honour of Awareness Week, Jemma shared with CLAPA her experiences with her son, Casper over the past year.
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Adult Issues | Adult Stories | Cleft Lip and Palate | Your Stories |
Denise’s Story
All the treatment was being geared up towards the operation to close Kenny’s cleft lip at 3 months of age. Initially, that operation couldn’t come quick enough, but by the time he was 3 months old, I’d grown accustomed to how he looked and was a bit fearful of the change. Our son was a smiley, happy, very content baby. It seemed wrong that he had to go through this.
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NHS Cleft Services | PRS |
Pierre Robin Sequence Study for Trent Region Families
The Nottingham-based Trent Cleft Service are putting together a set of resources for families affected by Pierre Robin Sequence. Can you help them by completing a short online survey?