Starting soon!

In-person attendance is fully booked, but please join discussions online…

How will we work together to scale #NewbornScreening so the rights of #EVERYchild to life & health are protected, promoted & respected?

mates4kids.org/wha77.html

#SDGs #Equity #NBS #INSD

20 años mejorando el pronóstico de la #anemiafalciforme con el #cribadoneonatal de los recién nacidos 🦶en #Madrid . 20 years of #sickle #newbornscreening

Breaking News 🚨 Ireland has initiated #NewbornScreening for #SCID ! This means that newborns in Ireland will undergo identification, diagnosis, and treatment, providing them with a crucial chance for survival. Find out if your country is on the list: bit.ly/41IDYpV

Proud of Goa Medical College's free newborn screening for genetic disorders, promoting early intervention and healthier futures. #TheGoaModel #HealthcareInitiatives #NewbornScreening #GeneticDisorders

Protecting Goa's youngest! Newborn screening initiative checks 53,767 infants for 5 diseases, 46 disorders within 72 hours, emphasizing early intervention for their well-being. #NewbornHealth #GoaHealth #TheGoaModel
#NewbornScreening #InfantHealth #ChildWellBeing

Goa Medical College leads the way with free newborn screening for genetic disorders. Empowering parents with genetic counselling, Goa’s Health Department is forging healthier future. #HealthcareForAll #GeneticScreening #TheGoaModel
#GoaMedicalCollege #NewbornScreening

We are thrilled to include a focus on #SickleCellDisease & #NewbornScreening at our upcoming side event at #WHA77

Please watch this terrific video to learn more about the importance of early diagnosis & treatment for #EVERYnewborn

youtu.be/Wn56LROFz2s?si…

“Newborn screening is a system, not an event”. Captivating talk about the future of #newbornscreening by Susan Berry at SIMD Presidential seminar. Also here STFU = short term follow up. 😂 🧠 🚼 🦶 🧬

EURORDIS-Rare Diseases Europe unveils new insights from a survey on newborn screening for rare diseases, conducted by the organisation’s Rare Barometer survey initiative and as part of the Screen4Care research project: eurordis.org/newborn-screen…
#newbornscreening #rarediseases

Leading up to #RareDiseaseDay , we’re talking about the importance of #newbornscreening for rare genetic diseases. We support the inclusion of Duchenne in existing #NBS programs so that that all patients have the chance to benefit from early diagnosis and treatment.

It was an honor to talk about the history and changing paradigms of #newbornscreening at the Child Neurology Society annual meeting. Shoutout to Jamie Fraser, MD, PhD, DABMGG🧬🧠🧫🔬, Laura Tochen, Jullie Rhee and Andrea Gropman who mentored me for the talk. Yasmin Khakoo, MD, FAAN, FAAP (she/hers) Monique Terrell Louis Dang

Breaking News 🚨 the Czech Republic has initiated #NewbornScreening for #SCID ! This wonderful news brings us closer to our goal of SCID screening worldwide. Early diagnosis saves lives! Find out if your country is on the list: bit.ly/41IDYpV

Please have a look at our latest paper on a Patient and Public Involvement and Engagement ( #PPIE ) activity focused on identifying parental information needs for families of infants with suspected #athymia after abnormal #SCID #newbornscreening results. tinyurl.com/PPIE-NBS-athym… 👇

CHF are proud to be part of The Newborn Screening Collaborative and share 'A Rare Find'.
This film is just one part of a broader campaign to push the subject of screening and to work towards positive progress within the current UK screening programme.🩷
#NewbornScreening

⚡Newborn Screening SAVES LIVES!⚡ In honor of #WorldPIWeek , physicians Antonio Condino of São Paulo, Brazil and Pere Soler-Palacín of Barcelona, Spain speak on the importance of #NewbornScreening for #SCID all around the world. Learn more here: bit.ly/41IDYpV #INFO4WPIW

1 in every 33 babies is born with a congenital disorder or anomaly. Congenital Heart Defects are the most common of all. Population health #NewbornScreening + followup care are the most impactful ways to save and improve lives + reduce inequities. #WBDD #CHD #BORNproject

#PedsHemeOnc Education Galore! What is Dr. Maa-Ohui Quarmyne from Phoenix Children's excited for? Learn about her presentation #Thalassemia in Transition, Saturday April 6 at #ASPHO2024 . #StandardsofCare #NewbornScreening #NovelTherapies #PHODocs
Register here: ow.ly/a6LN50QI39f

The Advisory Committee on Heritable Disorders in Newborns and Children voted Tuesday, January 30, 2024 to add #Krabbe to the RUSP. This recommendation will now go to the Secretary of HHS for approval. #newbornscreening #NBS #genetics