PNA Exclusives

Surgical Management of Cushing's Disease

Webinar presented by Russell Lonser, MD, FAANS


Each Month PNA Shines a Light on one of Pituitary Medicine's
Best and Brightest

PNA Spotlight: Dr. Richard Murray


Dr. Richard MurrayThis month the PNA Spotlight shines on Dr. Richard Murray, a neurosurgeon practicing at Virginia Hospital Center in Arlington, VA. He was born in Tucson, Arizona and grew up in Stellenbosch, South Africa. He graduated from medical school at the University of Stellenbosch in 2001 and then worked as a physician in the fields of acute care and critical care in the United Kingdom, South Africa, and various other international locations. He then completed his neurosurgery internship, residency, and chief residency at the University of Vermont in Burlington, VT. He later did sub-specialty fellows...


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Pituitary Network Association

The PNA is an international non-profit organization for patients with pituitary tumors and disorders, their families, loved ones, and the physicians and health care providers who treat them.

The PNA was founded in 1992 by a group of acromegalic patients in order to communicate and share their experiences and concerns. The PNA has rapidly grown to become the world's largest and fastest growing patient advocacy organization devoted to the treatment and cure of pituitary disorders.

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Donate Today

The PNA is supported by an international network of the world's finest physicians and surgeons. Our goal is to reach every patient who may be forgotten, abandoned, or worse yet, undiagnosed after many years of suffering. We are doing this in three ways: (1) by providing public awareness programs and educational seminars, (2) by assisting the medical community in developing uniform standards for early diagnosis, surgery, radiation, pharmacological treatment and follow-up, and (3) by having interactive web sites and a referral program on these web sites.

Mission Statement

To support, pursue, encourage, promote and where possible, fund research on pituitary disorders in a sustained and full-time effort to find a cure for these illnesses. The PNA will disseminate information helpful to the medical community, the public and to pituitary patients and their families on matters regarding early detection, symptoms, treatments and resources available to patients with pituitary disease.

Note: The PNA does not receive federal or state funding for any of its work, projects or studies.