Take 5 Campaign – CSNK2A1 Foundation

2020 Awareness Day

April 5, 2020April 5, 2020Jennifer SillsLeave a comment

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Announcing our First OCNDS Awareness Day

March 17, 2020March 17, 2020Jennifer SillsLeave a comment

We are pleased to announce our first OCNDS Awareness Day Save the Date for April 5, 2020 for our Take 5 Campaign and learn more about OCNDS and why we chose this day. #ocnds #hopeintoaction #ocndsawareness #csnk2a1 #weareyou...

President, Jennifer Sills profiled by Global Genes

October 23, 2020October 23, 2020Jennifer SillsLeave a comment

We are a proud member of the Global Genes Foundation Alliance. Global Genes’ mission is to connect, empower and inspire the rare disease community. As an Alliance Foundation, we have the opportunity to collaborate and exchange best practices with other rare disease organizations to drive better outcomes for the rare disease community. Global Genes...

We are excited to launch our Parent Education Webinar Series

October 9, 2020October 9, 2020Jennifer SillsLeave a comment

We are excited to launch our Parent Education Webinar Series. As parents and patients try to navigate a new diagnosis, they can be overwhelmed with information. We want to provide informational videos to help parents and patients navigate their rare diagnosis and inform them about different types of interventions available. Our first webinar is...