News and Stories

A big thank you to the record nine walkers from our community north of the border, who’ve signed up for a Kiltwalk to raise funds for CLAPA this year.

An electronic music memorial for Will Helstrip, a much-loved member of our community who tragically died two years ago, raised more than £3k for CLAPA.

Connor founded Adore Dance London in 2021. He spoke to CLAPA about dancing, cleft, and Strictly Come Dancing.

Two-year-old Oakley has Apert Syndrome, a rare genetic condition that causes fusion of the skull, hands and feet bones. He was also born with a large cleft palate, which saved his life when his other airways became obstructed.

An Indian storytelling event for a festival called Navarathri/Dussehra has raised hundreds of pounds for CLAPA.

Peer supporter Andrew was born with a cleft lip and palate. He’s now trained to help others through our peer support service to talk through issues and experiences of living with cleft as an adult.

Many people affected by cleft say it has an impact on their mental health. For those struggling in the CLAPA community help is at hand with a free counselling service.

Next time you’re out shopping look up at the video boards and you might just see one of our CLAPA community babies advertising Pampers nappies.

In celebration of all our wonderful CLAPA grandparents we spoke to Audrey and Dave about their cleft journey with granddaughter Rebecca.

Three years since Harper-Lily was born, her parents reflect on their daughter's journey and why dad Callum has decided to take on a charity boxing match to raise funds for CLAPA.

Barry Jones, an adult born with a bilateral cleft lip and palate, has shared his story with the CLAPA community to inspire others to gain confidence in sharing theirs.

Sarah Mahone got in touch with CLAPA dring Cleft Lip and Palate Awareness Week to share her journey with her son Luca, who was born with a microform cleft lip.