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For #cranioawareness month @HeadlinesCranio is sharing stories of its shining #craniosynostosis stars. Here is Ben Edwards’ story. @AlderHey @GOSHCharity @BCH @OxfordCranio. Please share so we can support other children like Ben to have #positivelives
PLS RT** 1 child is born with #craniosynostosis almost every single day in the UK, but hardly anyone has ever heard of it. Learn about the challenges children like Ben face growing up with craniosynostosis and help Headlines help them achieve their dreams #CranioAwarenessMonth
Great opportunity for a upcoming young researcher with an interest in Craniofacial research
Funded PhD Studentship now available at the world-leading @CAR_UWE investigating Medical Traumatic Stress in #Craniofacial conditions. Supervised by a highly experienced international team & embedded within CAR's thriving #PhD community. Apply by 12 Feb bit.ly/3XnNT1m 🥳
Wendy Edwards retweeted
Please share our press release #evusheldfortheuk getevusheld.uk/ Please join our group and make our voices louder.
Thank you. It’s been an amazing 7 years with a few ups and downs but I feel I am leaving the charity in very safe hands and am delighted to accept the role of Chair of the new Research Committee.
Wendy Edwards retweeted
Fantastic new edition of @HeadlinesCranio newsletter featuring @oxfordcranio Unit’s own Professor Andrew Wilkie @Wilkie_Lab
Glad to see this is now ready. Great resource and a great day for #PSPAresearch
Recordings of the recent Research Information Day and Research Strategy Launch are now available to view.
The day, which took place via Zoom on 23 January, has been split into two sessions for the morning and afternoon, for ease of viewing.
pspassociation.org.uk/resear… #PSPAResearch
Wendy Edwards retweeted
F1’s Virtual Grand Prix Returns:
George Edwards reviews the opening two rounds of the increasingly popular Formula 1 Virtual Grand Prix series. ⬇️
exepose.com/2021/02/11/f1s-v…
So excited to be running this today
We're looking forward to welcoming Chairs, Speakers and attendees to our Research Information Day and research Strategy Launch this Saturday. If you're attending, what session are you looking forward to most? #PSPAResearch
Wendy Edwards retweeted
Looking for an environmentally-friendly alternative to Christmas cards? You can support Headlines by sending e-cards with DontSendMeACard instead. Just log in, create an account & send! dontsendmeacard.com/ecard/aV… #dontsendmeacard
So proud to be Chair of Headlines
Wendy Edwards retweeted
Interested in learning about the latest advances in the genetics of #craniosynostosis? You can now watch the session led by world-leading geneticist Prof Andrew Wilkie @Wilkie_Lab at our 2020 Virtual Conference & Information Day on our website headlines.org.uk 🙌
Thank you to all our amazing speakers today. An awesome first virtual conference
Wow! Almost 100 delegates and 7 outstanding speakers - a huge thanks to all those who joined us for our first-ever Virtual Conference & Information Day today. We’ll be making the content available shortly, so watch this space for details #cranioaware #craniosynostosis
Thank you to my son Ben for sharing his story. He’s a star both on stage and off. Please share his story so everyone knows what #craniosynostosis is.
PLS RT** 1 child is born with #craniosynostosis almost every single day in the UK, but hardly anyone has ever heard of it. Learn about the challenges children like Ben face growing up with craniosynostosis and help Headlines help them achieve their dreams #CranioAwarenessMonth
Wendy Edwards retweeted
In honour of #CraniosynostosisAwarenessMonth we are highlighting when the @OxfordCranio Unit Prof Andrew Wilkie and colleagues identified: ‘Reduced dosage of ERF causes complex craniosynostosis in humans and mice and links ERK1/2 signaling to regulation of osteogenesis’
Wendy Edwards retweeted
#Craniosynostosis is classified as a rare disease. As one of the busiest centres in the world, the @OxfordCranio Unit are committed to world-class research to better understand the multidisciplinary care of this condition #CraniosynostosisAwarenessMonth ow.ly/6UhI50ASrV3
Wendy Edwards retweeted
Did you know - In 1995, @OxfordCranio Unit clinical geneticist, Professor Andrew Wilkie and his team discovered the cause of Apert syndrome - two specific mutations within the gene encoding fibroblast growth factor receptor type 2 (FGFR2). #CraniosynostosisAwareness
Great news for Headlines. We can now operate in Scotland
We've finally gained registration with the Scottish Charity Regulator (OSCR),which means that we can now move forward with plans to develop services in Scotland. If you live in Scotland and want to know more, email our Charity Director via [email protected]
