Baby's First Test
@BabysFirstTest_
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Baby's First Test is the nation's newborn screening education resource center for families and health professionals.
Joined July 2022
Embracing #RareDiseaseDay today and every day because awareness is just the beginning. Our fight for #raredisease equity is a daily commitment, and together, we can make sure that no one feels alone on their journey. Visit @rarediseaseday to learn more! #showyourstripes
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The rarest day of the year is finally here: it's #RareDiseaseDay! 🦓 Tag us in your posts today as you #ShowYourStripes and check out our website to add to our "Faces of Rare" dedication wall, download social media graphics, and more: https://t.co/YDwja7Arjg🦓
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In celebration of #InternationalWomensDay, we are hosting a webinar during which our presenters will share insights on the importance of women being included in #healthresearch while exploring the impact of diversity in #advocacy efforts. Register here: https://t.co/6ShJHYMq4Y
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Looking for even more #CHD resources? Visit our website ( https://t.co/VY0sZ75nqA) to find information, resources, organizations, and more all dedicated to CHD. #newbornscreening
What are Congenital Heart Defects (#CHD)❓ CHDs are present at birth and can affect the structure of a baby’s heart and the way it works. To learn more about CHD and access our support resources swipe to learn more➡️ Information provided by @CDC 🔗 https://t.co/M833ojxTQG
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Happening tomorrow - join us as we dive into the unique experience of being Black with a rare disease. We will provide insights, share stories, and offer practical tips we can all use to raise awareness and further our collective pursuit of #healthequity. https://t.co/lo4yM4mxvs
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It’s #WorldCancerDay! 🌍 Each patient and caregiver, irrespective of age and type of rare cancer, share the same challenges linked to the rarity of the disease. Let's unite to call to improve rare cancer patients' timely access to adequate care and a better quality of life.
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Join us on February 14th at 1:00 PM EST for a meaningful discussion about the unique challenges Black individuals face when navigating the #raredisease space. Discover ways we can collaborate to improve these experiences. Register here: https://t.co/lo4yM4mxvs
#healthequity
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This is a HUGE day for #krabbe and #leukodystrophy families! We’re going to make sure they add #MLD next! Huge work by @JimKelly1212 @HuntersHopeFDN and other Krabbe organizations and families.
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
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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
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This Friday, join us and our founder, @Nat_Bonhomme, to kick off the @NASEM_Health study, which will examine the current landscape of NBS systems, processes, and research in the US and considerations of sustainable adoption of screening for new conditions using new technologies.
Join us on Jan. 26 for a public information-gathering session from the Committee on #NewbornScreening: Current Landscape and Future Directions. Register to attend here: https://t.co/yGYWagpVkM
#HealthEquity #Bioethics
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The @AmerAcadPeds EHDI program is hosting a 4-part series of virtual office hours featuring real-time technical assistance on key #EHDI topics. Click here to learn more and register to attend: https://t.co/ubLwWQzu82.
#hearinglossawareness #hearinghealth #accessibilityforall
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How has medical gaslighting influenced your #RareDisease journey? How do you feel we can address medical gaslighting - and transform the care landscape for the better?
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It's #TakeoverTuesday with @rarediseasesint! With #RareDiseaseDay just 44 days away, join us in a quiz to test your knowledge. How did you fare? Did you score 5/5? Share your results in the comments! 👇 Visit our website & learn more: https://t.co/Fa6iNxlrwr
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Many #rarediseases can be detected through #newbornscreening. Visit https://t.co/DwrKOnFovy to learn more about the screening process, different rare diseases and conditions, and which diseases your state screens for.
Did you know that the majority of rare genetic diseases begin in childhood? These conditions can have a profound impact on a child’s life.🧬 This Rare Disease Day, let's raise collectively raise awareness and advocate! #RareDiseaseDay #ShareYourColours
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Join us this #RareDiseaseDay 🙌. You're part of a 300-million-strong community. Share your story, raise awareness, and remember: we are many, strong, and proud! 💪 https://t.co/E6jbKDOOUX !
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Julian Polaris (@manatt) is discussing ways that state programs can minimize barriers to quality healthcare, including working with managed care programs to waive prior authorizations required for prenatal vaccines. #RSV #maternalhealth #newbornhealth #MCH @WomenInGovt
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Sue Kendig (@NPWH) is sharing how waving out-of-pocket costs helps to remove access barriers to preventive services, like vaccines and prenatal appointments. @WomenInGovt #RSV #maternalhealth #newbornhealth
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Currently engaged in this webinar, learning about the new #RSV vaccine, which offers immediate protection to newborns against RSV right from birth. #prevention #publichealth
Join Women In Government TOMORROW at 2:00 pm ET for an #AccessToHealthCare webinar featuring Connecticut Representative Kathy Kennedy as moderator! https://t.co/kaa6d9aIEm
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