Top Tweets for #fnait
Leidse onderzoekers achterhalen mechanisme achter zeldzame bloedingsziekte bij baby’s - Nationale Zorggids https://t.co/FRIHBNvFuz #FNAIT #bloedplaatjesziekte
#FNAIT #AwarenessDay please watch and share!!! If you have been diagnosed with or suspect you may have fnait contact @naitbabies
https://t.co/5jod4zVHSY
Lisa Shea Shares Key Takeaways from 2025 National Organization for Rare Disorders (@RareDiseases) Summit
@allofound
https://t.co/Ob7zzJVMo9
#BleedingDisorders #FNAIT #HDFN #Health #Hematology #Hemostasis #HemostasisToday #Medicine #NORDSummit #RareDiseases #Thrombosis #WAIHA #WAIHAWarriors #MedEd #MedX
Proud to announce the safe delivery of the first UK baby whose mother took part in the FREESIA-3 study. This is an open label randomised phase 3 trial investigating Nipocalimab vs ivig in women previously affected by #FNAIT @Ox_wrh @TeamOUHMat @DrChristinaAye

Autoimmune neonatal thrombocytopenia, which can mimic fetal and neonatal alloimmune thrombocytopenia (#FNAIT), may be the initial indicator of an undiagnosed maternal autoimmune condition. @CureusMedical
Read More: https://t.co/DQEYcxRciu
#RareDisease
Delighted to have been featured in the latest FREESIA-3 Newsletter after recruiting the 2nd and 3rd worldwide recruit for this groundbreaking FNAIT study! @DrChristinaAye @TeamOUHMat @Ox_wrh #FNAIT #Fetalmedresearch

#FNAIT Awareness Week may be over but we must continue raising awareness throughout the year - with all #RareConditions.
@naitbabies
Wishing all who celebrate a joyous and peaceful Christmas and a Happy New Year.
If you suspect your #baby may have #FNAIT we can be contacted 24/7 [email protected]

These findings make a compelling case for universal screening of pregnant women for FNAIT risk, regardless of race or ethnicity, and we’re proud to play a part in advocating for a future where this is the norm.
#HealthEquity #FNAIT #MaternalHealth #NORD #NORD24

Congrats to @VersitiResearch Senior Investigator Debra Newman, PhD, who was awarded more than $2.2M from @nih_nhlbi to study fetal/neonatal alloimmune thrombocytopenia. Learn more: https://t.co/gyEZoABb0j #FNAIT

The time to prioritize the health of women and babies is now, and preventative testing for rare diseases like #FNAIT is just the beginning of the work to be done. Read more from CNN here: https://t.co/OY8vGhSOVE
Jennifer Harrison is fundraising for NAIT babies after her daughter suffered severe #ICH due to #FNAIT. Check out their @JustGiving page - please donate & share if you can. Thank you! #JustGiving https://t.co/OrwYrVjQdZ
#RDD This little girl has complex #disabilities due to #FNAIT she is blind has epilepsy, a shunt in her head, cerebral palsy, fed via a gastronomy tube and other disabilities which have required major surgery. https://t.co/5uBqwRGb1B
Our #NAIT Babies are fighters ❤️

There are 300 million people worldwide living w/ a #raredisease. DYK: #FNAIT is a rare disease that occurs when there is a mismatch between the mother’s platelets & those of the baby, resulting in the destruction of platelets in the fetus or infant.
#RareDiseaseDay

Check out @PatientWorthy's latest profile on our co-founder and CEO Steve Uden for a deep dive into his career path, why we chose to focus on #rarediseases, and how RLYB212 has the potential to transform the #FNAIT treatment landscape: https://t.co/ec0dYfVPbC
Rare Community Profiles: A Conversation with Rallybio CEO Stephen Uden on the Need for Rare Disease Drug Development https://t.co/9dnHDqqViM #RareCommunityProfiles #FNAIT #FetalAndNeonetalAlloimmuneThrombocytopenia #RareDisease
#MaternalHealthAwarenessDay is intended to increase awareness of the urgent need for maternal access to care. We’re focused on progressing research and improving outcomes for mothers and infants including in #FNAIT - one of many #maternalhealth areas that need more research.

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