Are you aged 16-35 and have (or are a sibling of someone who has) a rare #craniofacial condition? Then come and join us for our first-ever young persons' conference in London on Saturday 21st September. It's completely free. Email info@headlines.org.uk for further details.
Headlines Craniofacial Support
@HeadlinesCranio
Supporting all those affected by craniosynostosis and rare craniofacial conditions. Registered charity in England & Wales no. 1058461 and Scotland no.SCO50262
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Please consider taking part in this important new study
New study: Do you have a visible difference which can be inherited? Considering children in the future, or had children in the last 5 years? Please consider taking part in my study.View quoted post on X
Our Director Karen Wilkinson-Bell and trustee Charlotte Ashby are excited to be in Oxford today for the Annual Scientific Meeting of the British Association of Oral & Maxillofacial Surgeons @BAOMSOfficial - Karen & Charlotte are speaking at a session on ‘Humanising Healthcare’
Headlines trustee Charlotte Ashby joined @NicolaMarie and fellow ACCORD contributor and PhD student Sally Smith for the @CAR_UWE #AM10 conference in Bristol this week to talk about the Headlines/CAR ACCORD project for adults #craniosynostosis
As a dad, John found it hard to tell anyone how he really felt when his son was diagnosed with #Apertsyndrome. You can hear John’s story and how Headlines is helping other dads like John here:
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