Introducing NASCARR: A new partnership connecting researchers, families, TSF, and the NIH to advance research for X&Y Chromosome Variations

Introducing NASCARR: A new partnership connecting researchers, families, TSF, and the NIH to advance research for X&Y Chromosome Variations

 

Join us for an informative webinar introducing NASCARR and its potential to advance research and clinical trial readiness for Turner syndrome.

With a combined 40+ years of experience in medicine and clinical research, including the care of individuals with Turner syndrome and other sex chromosome aneuploidy (SCA) conditions, this session will explore how NASCARR can help strengthen the research landscape and create new opportunities for progress.

Attendees will gain a clearer understanding of this new funding mechanism, emerging research initiatives, and what greater clinical trial readiness could mean for the Turner syndrome community. We’ll also discuss how healthcare professionals, researchers, individuals with Turner syndrome, and families can become involved and help shape the future of research.

Whether you are a clinician, researcher, patient, family member, or advocate, this webinar offers an opportunity to learn how NASCARR is working to accelerate meaningful research and build the foundation for future clinical trials.

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Cost:
Free. Donations are appreciated.

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