The Dysautonomia Project
The Dysautonomia Project is a not-for-profit collaborative effort of hundreds of volunteer physicians, patients, and community leaders. Our aim is to bridge the wide knowledge gap between community-based physicians and decades of validated clinical research about Dysautonomia.
June 15 serves as a reminder of our mission to change the 6 year average time to diagnose Dysautonomia, to just 15 minutes.
Because we are a not-for-profit organization, we solely operate on your donations. Help us continue our mission to educate community-based doctors, patients, and our community!
We are so appreciative of all of your efforts in supporting us and our mission!
Kelly Freeman, the Founding Director of The Dysautonomia Project and co-author of The Dysautonomia Project Book, holds an objective in line with TDP’s. Kelly, a dysautonomia patient herself, aims to transform the care of patients with dysautonomia through the education of physicians, patients, and community leaders with the mission of speeding time to diagnosis, proper assessment, and treatment of patients in community based clinics and hospital settings around the world.
Nate Freeman is the co-founder of both The Dysautonomia Project and his company Network People. Nate holds a strong desire for educating the medical community about Dysautonomia because his wife, Kelly Freeman, is a Dysautonomia patient. After watching his wife, and his family struggle for so long to find an answer, Nate knew he had to create something to raise awareness and education in his own community. With the help of his wife, The Dysautonomia Project was born.