NHS SW Genomic Medicine Service Alliance
@SWGenomics
Improving Healthcare Through Genomics - working together to embed Genomics into standard care for patients and families across the South West.
We are incredibly proud to be working in partnership to support this cutting-edge #GenomicsResearch! Learn more about the Generation Study here: generationstudy.co.uk
Over 800 families have now joined the Generation Study at UHBW, which tests for rare genetic conditions in newborn babies. We’re proud that St Michael’s Hospital was the first site in England to recruit families and complete testing for the major research study. (1/2)
WE CAN NOT WAIT! See you then @jimconey - and thank you for all you do. Happy #RareChromoDay.
It’s Rare Chromo day! You can hear me and the comedy writer Shaun Pye chatting about raising children with a rare genetic condition today at 1pm for @Unique_charity Sign up rarechromo.org/get-ready-for-…
📕 Happy #RareChromoDay! All over the world, our members have been sharing their experiences of life with rare gene and chromosome disorders. Join us in celebrating them by visiting our website and reading our Little Red Book today! #MyUniqueStory rarechromo.org/little-red-boo…
🧬 IT'S RARE CHROMOSOME AND GENE DISORDER DAY 2025, #RareChromoDay We're so excited to share two publications. Have a read, share and let us know what you think in the replies💬 - The Little Red Book: rarechromo.org/little-red-boo… - 'Unique experiences' report: rarechromo.org/get-ready-for-…
Do you have or care for someone living with a rare chromosome and gene disorder? Unique is an open, supportive community for people who are looking for information, share experiences and connect. Join our free membership and access our services. 👉 rarechromo.org/join-us/
We are proud to support #RareChromoDay 2025, a day to raise awareness of rare chromosome and gene disorders, and celebrate all the brilliant families and carers involved. How are you celebrating next week?
Join @Unique_charity next week for an event not to be missed!
Yesterday we hosted a #PCUKStudyDay on genomic medicine in pancreatic cancer with Genetic Counselling Lead, Matilda Bradford and HPB CNS Hayley Turner. During the study day we were thrilled to highlight the positive difference genomic medicine can make to treatment and care now.
On 16 May, our Genetic Counselling Lead for Cancer, Matilda Bradford, spoke at @PancreaticCanUK’s #PCUKStudyDay on genomic medicine in pancreatic cancer! Catch up here: 🔗 pancreaticcancer.org.uk/health-profess…
