In recognition of of National Rare Disease Day we would like to share The Faces of TANGO2 – a rare genetic disorder.
A disease may be rare, but hope should not be.
The Charles Dickens holiday classic, a Christmas Carol, was the backdrop for a TANGO2 Research Foundation fundraiser held on November 30, 2018 in Turin, Italy. The show was performed by Varallo’s Company, a local non-profitRead more
Davide, a friend of Rashmi and Giorgio, organized his farewell party in support of TANGO2 research. Thanks to his idea and the participation of many close friends, he raised nearly $2K dollars for the Foundation.Read more
Veronica, Thea’s Mom, has started a blog sharing her and her family’s TANGO2 journey – click here to go to Notes from a Rare Disease Mom From Veronica: “In 2017, my then 2 year oldRead more
The TANGO2 Research Foundation is excited to announce the funding of its first research award. The Foundation has committed $45,000 over a two-year period to help fund the cost of a Research Assistant dedicated toRead more