The Headway Cork Choir have entered the Novartis Ireland Patient Choir Contest, and NEED YOUR VOTE!
Please vote at this link:
https://t.co/TM4KWzLomN...
You can listen to their entry and use the "VOTE NOW" button. Share with your friends!
The National Healthcare Outcomes Conference takes place on 16 April in RCSI. This year’s theme is ‘Improving health outcomes through AI’.
Topics include AI potentials and pitfalls, AI and patient care and more! Register at https://t.co/OFlds6AVF8
Supported by @NovartisIreland
Prof Jan Sorensen, @RCSI_Irl and Caitriona Walsh, @NovartisIreland delivering the opening remarks at the National Healthcare Outcomes Conference exploring Improving Health Outcomes through AI.
#NHOC24#AI#healthcareoutcomes
"Neonatal screening is a crucial public health provision for the future of the European Union”🇪🇺
Thank you @Konecna_K, Screen4Rare & the S4R MEP Alliance are delighted to count on your consistent support!
Questions about #INSD? Check out our website
👉 https://t.co/G6velY0ju9
For treatable rare disorders, the early detection offered by #neonatalscreening can be life-changing and can prevent long-term disability and death.
Join us on #INSD to find out why #NeonatalScreeningMatters
More info 👉 https://t.co/fvFrmeLOKW
Do you know why we celebrate #INSD on 28 June?
To mark the birthday of Dr Robert Guthrie, who launched the field of neonatal screening & dedicated his life to underlining that #NeonatalScreeningMatters
Follow us for more INSD content.
👉https://t.co/0OuKVjSaft
In 2021, only 27% of babies born around the world were screened at birth
Despite its potential to diagnose many treatable diseases, there are still too many disparities when it comes to accessing neonatal screening
More info 👉https://t.co/fvFrmeLOKW
#NeonatalScreeningMatters
Congratulations to Croí Chief Executive, Neil Johnson on receiving this prestigious award for his outstanding performance and advocacy work #patientengagement#CVD#MakingADifference 👏🎉
Newborn screening for rare diseases can help affected persons avoid costly and difficult diagnosis journeys.
The #EU should promote cross-border collaboration in the field of newborn screening for rare diseases as a way to reduce healthcare system expenditure.
At 12 noon today Lyndsey @raisingrareness will share story of journey to get a diagnosis for her daughter. Please join us to learn about challenges facing people living with a rare disease to get a diagnosis and importance of genetic services.
Register at https://t.co/SezUKNDVjs
Thanks to National Rare Diseases Office @HSELive for joining us in Stormont for our #RareDiseaseDay celebration with @NI_RDP . We are all looking forward to getting a new National Rare Disease Plan in place.
@CcoHse @DonnellyStephen @CMOIreland