Funded Research Studies
Standing Up to POTS is making a difference in the POTS community through research. To date, we have funded $41,250 USD of POTS research for teams around the globe. Our primary research interest is to improve the quality of life for people living with POTS right now through better diagnosis and treatment options.
Dr. Heather Edgell - York University, School of Kinesiology and Health Sciences, Canada - February 2018
The overall aim of this study is to examine how hormonal changes related to a woman's menstrual cycle affect symptoms of POTS, and whether the time of the month matters in diagnosis POTS for women of childbearing age. Further, a novel therapy for alleviating symptoms will be tested. Results are expected in 2020.
Dr. Andrea Maier, Dr. J.B. Schulz, Dr. Roman Rolke, and Dr. Joacim Weis - University Hospital RWTH Aachen, Germany - February 2018
Many patients with POTS report attention deficits and “brain fog” with problems in their everyday life and work, predominantly in upright posture. Specific symptomatic or medical therapies do not exist. This study will investigate problems of concentration, attention and/or cognitive dysfunction in people with POTS, autoimmune autonomic neuropathy, small fiber neuropathy and Ehlers-Danlos Syndrome compared to healthy controls. Results are expected in 2020.
Dr. Svetlana Blitshteyn - Dysautonomic Clinic, New York, USA - June, 2017
This study examines the connection between Lyme Disease and POTS, a particularly important issue for our friends in the Northeastern United States and other places where Lyme disease is prevalent. Results are expected in 2018.