In 2017 our son Ryan was diagnosed with a life-threatening genetic condition called TANGO2. There were no treatments and very little was known about this disease. In 2018 Mike and I started the TANGO2 Research Foundation to help fast forward research that would help Ryan and others like him live their best lives. In the short time since, research funded by the Foundation has uncovered a treatment for TANGO2 (B vitamins) that is improving the quality of life for Ryan and others around the world. The Foundation is primarily funded by grassroot efforts spearheaded by families like ours. Contributions from donors like you really make a difference.