A letter from Dr. Judy Mikovits to all ME/CFS patients, families and advocates
Many of you have asked, "where is Dr. Judy Mikovits and what is she doing? Is she still doing research? Where can we go for testing?"
Dr Judy Mikovits remains passionately committed to the patients and to a search for treatment and a better life for all of them.
She refuses to compromise her integrity or the truth in a search for causes and treatment of disease. It is unfortunate, yet a sign of the society we live in, that politics and personal gain have interfered with science and the attempts of committed researchers to pursue the goal of scientific research.
Dr Mikovits is pursuing opportunities with a variety of new research institutions and collaborations which show promise to continue in her research and to provide patients with new resources for diagnosis and treatment.
She will make this information available on public sites for all patients to access and participate as they choose.
Dr. Mikovits is no longer with the Whittemore Peterson Institute and has no role or responsibility for any of the activities of the Institute and never had any role in the clinical laboratory (VIPdx or Unevx)
All patients or other individuals who wish to contact Dr. Mikovits may email via:
Lilly Meehan at:
See also: A big thank you to Dr. Judy Mikovits