That’s a wrap! Thank you to everyone that joined us for Rare Disease Day. Let’s continue to work together for a better tomorrow. #RareDiseaseDay #RDD https://t.co/3M047JIIQ5

COVID-19 Shared Prize 🥇 ‘Bastaa’ by Pulkit Tomar 🥇 ‘Buonanotte/Goodnight’ by Yohana Ambros

🥇 1st ‘This is not a Person’ by Miguel Rodríguez and Pablo Ostarek 🥇 2nd ‘Lumen’ by Sarah Seené 🥇 3rd ‘Fraser Syndrome & Me’ by Kyle Anne Grendys

Congratulations to our International Rare Disease Day Filmfestival winners! By sharing stories on the unique challenges rare disease patients face every day, we can continue to raise awareness together. #RareDiseaseDay #RDD https://t.co/OS1TwtrBPR

Showcasing work from 52 filmmakers, the International Rare Disease Filmfestival raises awareness of the challenges patients face every day. Join us in watching the finalists, and see who takes home the top prize! https://t.co/WsPUnpNVeC #RareDiseaseDay #RDD https://t.co/SvM9Yv2JLc

Our next Rare Disease Day discussion is about to start! Listen in as speakers from around the world discuss the importance of international cooperation for #RareDiseases. Join now to see how we can help: https://t.co/WsPUnpNVeC #RareDiseaseDay #RDD

Join the conversation with world leading medical experts and patient advocates, as we discuss the impact COVID-19 has had on rare disease patients. Tune in to our panel to learn how we can make a difference: https://t.co/WsPUnpNVeC #RareDiseaseDay #RDD

Our #RareDiseaseDay activities are beginning! CENTOGENE welcomes everyone joining us virtually for #RDD – bringing together patients, advocates, and physicians to raise awareness and support the community. Join now from the comfort of your own home: https://t.co/WsPUnpNVeC https://t.co/vukMHWe5Yu

The countdown is over! Rare Disease Day is finally here! Today we come together as one rare disease community – to share stories, insights, and hope. Join CENTOGENE at 2:00 pm CET today for our virtual event: https://t.co/WsPUnpNVeC #RareDiseaseDay #RDD https://t.co/iyEtoAzk1f

#RareFacts Did you know that more people die from #RareDiseases than from #cancer? Sign up for our #virtual two-part #RareDiseaseDay event tomorrow, and join the community. Together, we are rare. 👵👶 👨‍⚕‍🧕 👩‍⚕‍ https://t.co/WYMkbH10wR https://t.co/vlmH1uM07H

#RareFacts Did you know that 95% of #RareDiseases don’t have a treatment? 💊 By working together as a #scientific & #medical community, we can change that. Register for our virtual #RareDiseaseDay activities tomorrow, & join the conversation: https://t.co/WYMkbH10wR https://t.co/K5NIThQZsG

By working together with #patients, we can deliver #medical breakthroughs. Read the latest interview in @OutsourcPharma from Prof. Peter Bauer, our Chief Genomic Officer, to hear how patient-centricity is key to #RareDisease #research: https://t.co/Dg9RdY7dSw https://t.co/kgnSOOPOBI

#RareFacts Did you know that 80% of #RareDiseases are hereditary? 🧬 With the correct #genetic testing & planning, we can provide answers today for a better tomorrow. Sign up now for #RareDiseaseDay on Feb. 28th to learn more about rare diseases: https://t.co/WYMkbH10wR https://t.co/jOdkEujWZg

Únase con Pilar Guatibonza Moreno, MD, Enlace Científico en CENTOGENE, en el #DíaMundialdelaAudición, para aprender cómo la acción oportuna puede ayudar a prevenir y abordar la pérdida auditiva en todas las etapas de la vida. Reserve su lugar hoy: https://t.co/g8CUxQx11t https://t.co/mgyPlGZiRu

What can science do for you? 🧬 Join CENTOGENE’s Medical Sales Liaison Brittney Kraeer on #WorldHearingDay to learn how timely action can help prevent and address #HearingLoss at all stages of life. Reserve your spot today: https://t.co/xZmsnMR9RN https://t.co/dsjDlJ6LR2

Together, we are rare. Meet Mohinav Sharipov – Doctor, Medical Center Director, & Advocate for Medical Access for Rare Disease Patients 🏥 Join us for our #RareDiseaseDay Virtual Conference to hear how we can work together for a better tomorrow: https://t.co/XuaeTfSOZA https://t.co/TrQseJXP6w

#RareFacts Did you know that there are over 350 million #RareDisease #patients around the world? 🌏 Sign up for #RareDiseaseDay on Feb. 28th, & join the community of patients, physicians, partners, & advocates who are committed to creating change: https://t.co/WYMkbH10wR https://t.co/1L0fWAYnu7

#RareFacts Did you know that on average it takes over 8 years for #RareDisease patients to receive a diagnosis? Together, we can turn those years into days. Sign up for our #virtual #RareDiseaseDay event on Feb. 28th to help drive solutions: https://t.co/WYMkbH10wR https://t.co/1H79FyUKmP