American Autonomic Society
This is an organization that brings together experts, from diverse disciplines, who share an interest in the treatment and prevention of autonomic nervous system disorders (such as dysautonomia).
Center for Hypotension-New York Medical College
This is the website of the clinic of Dr. Julian Stewart, a physician and advocate who treats children with dysautonomia. This outstanding facility and doctor need more research funding. Dr. Stewart first recognized the existence of NFD, in children, in 1999.
Dr. Thomas C. Chelimsky
Dr. Chelimsky is the chief of neurology at the Medical College of Wisconsin. His research concentrates on dysautonomia and interstitial cystitis.
Dysautonomia Clinical Trials, per the National Institutes of Health
Periodically check this website for updated research developments. This is also a good source for the expanding number of doctors who are performing dysautonomia research and treatment in various parts of the country. If you have trouble using this website see your local public librarian for assistance.
Dysautonomia, National Inst. of Neurological Disorders & Stroke
This is the leading federal government dysautonomia research facility.
Dysautonomias--Report of the National Institutes of Healths' 2002 Symposium
The recommendations of this symposium, as to increased non-familial dysautonomia disease awareness and educational efforts, had not generally been followed or implemented. However, the administration of the National Institutes of Health suggests that many of the recommendations are in the process of being effectuated. The recommendations are reproduced, below, while the summary of the entire conference is available by clicking on the link above:
The first workshop on dysautonomia successfully concluded with all attendees agreeing on several issues: (i) that it is imperative to expand clinical and basic research and put emphasis on translational research; (ii) to endorse patient advocacy and improve awareness and education; (iii) to develop resources that will aid research and treatment strategies, and possibly establish collaborative broad scale efforts in the form of multi-project applications and grants and multi-site efforts; (iv) to encourage collaborative efforts and enhance data sharing and management; (v) and to hold regular, follow-up scientific meetings.
Dr. Blair Grubb
This is a link to contact information for Dr. Grubb, a researcher/physician who treats non-familial dysautonomia at the University of Toledo Medical Center's Cardiovascular Medicine Clinic.
Mayo Clinic: Dr. Phillip Low, Dr. Philip Fischer
and Dr. Wolfgang Singer
These are Mayo Clinic physicians, with contact information for Dr. Low and Dr. Fischer. Both are physician/researchers who treat patients with non-familial dysautonomia. Dr. Low treats adults and Dr. Fischer provides care for children.
Another Mayo doctor, who provides adult care, is Dr. Wolfgang Singer. Dr. Singer has also received funding from the National Institutes of Health. We have provided research funding to both Dr. Fischer and Dr. Singer.
Mayo Clinic researchers were the first, in the world, to recognize the existence of non-familial dysautonomia (NFD). It was diagnosed in adults in 1993 and in children (by Dr. Julian Stewart, link below) in 1999. In 2006-2010 they affirmed that the number of people who have non-familial dysautonomia is far greater than previously suspected, even as recently as 2002. Additionally, many people "diagnosed" with migraine headaches (and chronic fatigue syndrome) may in fact have NFD.
National Library Service
Provides free digitized books (and a machine to play them) for many people with disabilities. Those with dysautonomia, who find it easier to listen to an audio book, as opposed to sitting up and reading, qualify for free services. This link helps you to locate the closest library to you. Don't be put off if the local facility is called the Library for the Blind.
Vanderbilt Medical Center-Autonomic Dysfunction Center
This is the website of what is in part a non-familial dysautonomia (NFD) research facility. Its staff includes many physicians who treat adults with NFD. The latest information suggests that Vanderbilt researchers support the view that more Americans have NFD than previously suspected.
Disclaimer: If you have any health problem you should seek the assistance of a qualified medical professional. Our efforts, to raise funding for research and to increase dysautonomia awareness, are not a substitute for capable medical care. At the same time information cited, about problems with accurate diagnosis, is correctly summarized.