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.
On June 26th, our Foundation had a successful virtual event celebrating on TANGO2 community. We celebrated our amazing team captains, participants and donors for surpassing our fundraising goal. We also heard from one of ourRead more
We are pleased to announce the transition of leadership for our Fundraising Committee. Our outgoing chair, Kara Dort, has accepted the role of Board Treasurer after successfully leading the fundraising committee and campaign to exceedRead more
This Rare Disease Day, the TANGO2 Research Foundation highlights “Living with a Unicorn” – a blog by Gloria McDonald, Olivia’s mom. Gloria talks about Olivia, her diagnosis of TANGO2 disease, how their life changed, whatRead more
In Spring of 2020, the TANGO2 Research Foundation granted Dr. Michael Sacher and Dr. Felix Distelmaier an award for their research proposal entitled Characterization Of Human TANGO2: From Biological Function To Therapeutic Strategies. Less than a year later, weRead more