#RareDiseaseDay raises awareness for the 7,000+ #RareDiseases that affect over 25 million Americans! We will be joining National Organization for Rare Disorders (NORD) in celebrating the rare community. Learn how to #ShowYourStripes: bit.ly/US-RDD22

A focus on gender equity needs to be part of every society's DNA. #EmbraceEquity #IWD2023

To apply please visit: thinkgenetic.org/the-pro-gc-pro… #chiesiusa #horizontherapeutics #ovidtherapeutics #Takeda #vertexpharmaceutical #GeneticCounselors #geneticcounselingstudents #GeneChat

Today is World Sickle Cell Day! With new therapies on the horizon, awareness is more critical than ever. #SickleCell #Warrior #WSCD #June19 #KnowYourStatus #NewBornScreening #GeneTherapy #ClinicalTrials #treatment #Cureonthehorizon

Today is International Neonatal Screening Day and we are celebrating the life changing benefits of early detection of diseases. #InternationalNeonatalScreeningDay #NeonatalScreeningMatters #screen4rare #EveryLifeFoundation #RDLAteam #RUSP #rareadvocates

Looking for funding to attend meetings this Fall? Pro-GC scholarship applications are still open. Apply now at thinkgenetic.org! #GeneChat #GeneticCounselors #metabolicdietician #horizontherapeutics #chiesiusa #takedapharmaceutical #vertexpharmaceuticals #ovidtherapeutics

Accelerating Rare disease Cures (ARC) Program Emerges as a Conduit for Empowering Rare Disease Stakeholders fda.gov/news-events/fd…

There is still time to apply for funding in 2023! Apply now at thinkgenetic.org! #GeneChat #scholarships #GeneticCounselors #metabolicdietitians #geneticcounselingstudents #ProGC #TGF #horizontherapeutics #chiesiusa #takedapharmaceutical #vertexpharmaceuticals

We are committed to positively impacting the #raredisease community and invite other #nonprofits to join our Advocacy Organization Network - a free network where organizations can amplify their mission. Apply now at: loom.ly/6c37rAw #collaboration #advocacy #genetics

🌟We're grateful for our volunteers, contractors, and dedicated Board members who empower those living with genetic conditions and their care providers! 🙌 Discover their incredible work: loom.ly/sm-ydX4 💙 #ThinkGeneticFoundation #EmpoweringLives #GeneticConditions 🧬

There is still time to apply for scholarships for fall meetings! Visit thinkgenetic.org to apply. #NSGC2023 #ASHG2023 #GeneticCounselors #geneticcounselingstudents #geneticeducation #metabolicdietitians

September is National Sickle Cell Awareness Month. Approximately 100,000 Americans live with sickle cell disease. We are proud to stand with the SCDAA to push for better treatments, education and outcomes for sickle cell warriors. Learn more: sicklecelldisease.org

September is World Autoinflammatory Awareness Month and the theme for 2023 is patient access to genetic testing. #FMF&AID #rarediseases #genetictesting #patientadvocacy

National Hereditary Cancer Week (NHCW) and National Previvor Day serve as important reminders of the impact that hereditary cancer has patients on families. #HereditaryCancerWeek, #PrevivorDay #1FORCECommunity.

Our founder, Dave Jacob, was recently featured on the Grey Genetics Patient Stories Podcast. Dave recounts his diagnostic journey and shares how his experience as a rare disease patient inspired both ThinkGenetic Inc. and the ThinkGenetic Foundation. bit.ly/3HSnS3S

Rare Disease Day is only one week away! Let's join together to support the 300 million people worldwide affected by rare diseases. Together, we can raise awareness, advocate for better treatment, and offer hope to those facing these unique challenges. #RareDiseaseDay2024

Join us in raising awareness for Rare Disease Week on Capitol Hill 2024! This crucial event brings advocates, patients, and policymakers together to support those with rare diseases. Let's work together to make sure every voice is heard. #RareDC2024

Let's come together and raise awareness for Rare Disease Day! There are over 300 million people worldwide who are affected by rare diseases. For them, every day is Dare Disease Day. That's why supporting research and advocating for better resources and care is crucial.

🌟 Embrace Differences, End the Stereotypes! 🌟 Today, on World Down Syndrome Day, let's celebrate the unique abilities and talents of individuals with Down Syndrome. #WorldDownSyndromeDay #EndTheStereotypes 💙💛

We are grateful to continue supporting the professional development of many deserving genetic professionals! To stay informed about future rounds of the Pro-GC Scholarship Program, please visit bit.ly/4cs0toh.