We Have Some Exciting Updates!

The TANGO2 Research Foundation is dedicated to providing transparent and accessible information about our mission, strategies, and impact. In line with this commitment, we are proud to announce the following updates:

Candid Gold Seal of Transparency

We’ve earned the Candid Gold Seal of Transparency! This milestone demonstrates our dedication to transparency.
Check out our Candid GuideStar profile to learn more about the foundation’s work and impact.

Global Genes RARE Advocacy Summit

We are thrilled to share that Kasha Morris, TANGO2 Research Foundation co-founder, and Deena Chisholm, Director of Research Engagement, have been invited to facilitate a panel discussion at the Global Genes RARE Advocacy Summit.
The panel will highlight the importance of natural history studies in rare disease and the potential they hold for unlocking the future.

Launch of the TANGO2 Research Learning Network

Introducing the TANGO2 Deficiency Disorder Research Learning Network—a new resource for researchers, clinicians, and families.
Visit the online forum today, sign up for a free account, and join in on conversations to connect with TDD stakeholders worldwide!

Amgen Global Advocate Grant

We are honored to receive Amgen’s Global Advocate Grant of $5,000! This grant will fund the creation of TDD Genetic Explainer videos designed for families, caregivers, and healthcare professionals.
Leading this project is the Early Detection & Diagnosis (ED&D) Committee, chaired by Farah Ladha, a genetic counselor at Baylor College of Medicine.

Stay tuned—these informative videos will be available on our website soon!