Welcome to The Dysautonomia Project.
We’re a nonprofit with a mission of educating healthcare professionals, patients and communities about dysautonomia.
Overcoming dysautonomia is a group project, and ours comes with instructions.
We have organized our up-to-date dysautonomia information based upon the stage of your journey to help you quickly find the answers, advice and inspiration you can use. We invite you to read on, watch the videos, find a physician and connect with others through our social channels and find a support group perfect to you through our external resources. With all of us working together, dysautonomia doesn’t stand a chance.
Our definitive guide.
“The Dysautonomia Project” is a much-needed tool for physicians, patients, or caregivers looking to arm themselves with the power of knowledge. It combines current publications from leaders in the field of autonomic disorders with explanations for doctors and patients about the signs and symptoms, which will aid in reducing the six-year lead time to diagnosis.
Frequently asked and finally answered questions.
Do I have dysautonomia?
Disorders of the Autonomic Nervous System
Two most common dysautonomias
How is dysautonomia diagnosed and treated?
and help finding a healthcare professional
Just diagnosed with dysautonomia?
tips for the newly diagnosed patient
Support Groups, Patient Research Opportunities, and Events
How can I manage my symptoms?
Everyday advice for living with dysautonomia
School, Job, Financial Assistance
What is the connection between dysautonomia and COVID-19?
Long-covid Autonomic Dysfunction
How can I spread the word?
The #1 treatment is education
Read all about it.
Our annual newsletter is a great way to catch up on the past year! You’ll also be informed about our tireless efforts to advance our mission to educate healthcare professionals, patients, and communities about dysautonomia.