🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

Thank you Steven for sharing your experience as a father of a child living with charge syndrome at the EpiGenRare - Rare Disease Research UK conference this afternoon. If anyone would like to learn about charge syndrome, check out their support group: chargesyndrome.org.uk

Check out my first podcast! Certainly a new experience & aside from nerves, I hope I did the #geneticcounsellor community proud & hope its interesting! Thank you Dr Stefan Tino Kulnik & #ACNAP! Listen here: esc365.escardio.org/event/1973 #cardiogen #genechat #podcast AGNC Royal Brompton and Harefield

Great to hear from Edel Robinson, Haemoglobinopathies Screening Practitioner from the West Midlands Haemoglobinopathies Team, gives us an overview of #sicklecelldisease and #betathalassemia and their antenatal screening pathway #AGNC2025 #genechat

Next we have an overview of amyloidosis from Dr William Moody, Consultant Cardiologist University Hospitals Birmingham and genetic counselling for amyloidosis from Emily Dixon, Principal GC from the National Amyloidosis Centre #AGNC2025 #genechat

We are very lucky to hear from Clinical Psychologist, Sally Austen, who makes the case for the integration of Clinical Psychologists into Clinical Genetics Services BWC NHS Trust #AGNC2025 #genechat

A strong focus on Lynch syndrome today! Andrew Beggs Consultant Colorectal Surgeon at University Hospitals Birmingham gives us an in-depth review of advances in Lynch syndrome management and research #AGNC2025 #genechat

Moving from paediatric to adult services can be daunting for young people with polyposis syndromes. Dr Ronald Bremner, Consultant Paediatric Gastroenterologist, tells us how they do things at the Polyposis Transition Clinic at Bham Children's Hosp 💙 #AGNC2025 #genechat

Research GC, Jonathan Robert’s asks what do people want from a genetic counselling research network? #AGNC2025 #genechat

The Gene People Partnership Network is an exciting collaboration between organisations working to improve the lives of those affected by genetic conditions. Check out our current members here buff.ly/Z8GTX3k

It's shaping up to be another busy month! Gene People will be attending or speaking at the following events in April to represent our wonderful community: PPP: The Important of Genomics Research in Advancing the Growth Agenda, the ABPI Annual Conference and the AGNC Conference

Gathering the views of 9,591 Europeans living with a rare disease and their family members, this survey report explores the barriers to full participation in all areas of society experienced across our diverse community. #RareBarometer 📊 Full report: tiny.cc/RB_DailyLife

DTC genetic tests raise ethical issues, which genetic counsellors Emma O'Donoghue and Cliona Carroll will expand on in later talks in this session Anneke Lucassen European Society of Human Genetics (ESHG) #precisionmedicine

Think #genomics isn’t relevant to your clinical role? Pls think again. Join us for 1st in a new series of lunch and learn webinars. Discover how genomics is being used across routine #healthcare. Let’s bring genomics into everyday #practice. Book here: bit.ly/4i2YNmH

Our award-winning #genomics course for patient-facing NHS professionals returns this year! Healthcare professionals from England are invited to apply for a funded place on 'Genomics and Counselling Skills', starting in September. Read more and apply today: genomicseducation.hee.nhs.uk/news/award-win…

The agenda for the Genomics England Research Summit is now live! This year’s programme brings together leaders across healthcare, research, and industry. View the full agenda and find out more about our speakers and their sessions here: ow.ly/gTyF50VRB4C #GERS2025

Who supports the mental health of those living with, and caring for, people impacted by rare diseases? matt johnson shares his insights with RARE Revolution Magazine, calling for holistic approaches to emotional wellbeing. 👉Read the full article on page 17: go.eurordis.org/AOiW9q

Recent reports in the media about the possible direction of SEND reform in England have caused concern and anxiety among families of children & YP with SEND. 📄 We urge you to write to your MP about this, and have produced a template email to help you: ipsea.org.uk/write-to-your-…

Dave McCormick (aka Twin Castor) and Bryan Matthews (aka The Rayne) have released a single called The A, the C, the G, the T which celebrates the extraordinary science behind the world of genomics medicine Spotify open.spotify.com/track/5Ebuq0ig… Apple Music music.apple.com/us/album/the-a…

Have you, or has someone you know, been newly diagnosed with a genetic condition? Visit our website to find out how you can best access support genepeople.org.uk/support-and-in…

With just one week to go, the final touches are coming together. We’re looking forward to welcoming you to the Genomics England Research Summit on Tuesday 17 June in London. Plan your day with the agenda: genomicsresearchsummit.co.uk/agenda2025 #GERS2025