About Us

The National Addison’s Disease Foundation was formed in 1985 by a young couple as a result of their experiences with Addison’s disease. At that time, there was no organization established to provide guidance and information about life with adrenal insufficiency. There was no way to contact others who shared this illness. Although Addison’s disease is considered a rare disease, it is estimated that at least 10,000, or 1 in 100,000 individuals in the United States have this condition (this is probably an underestimation). 

Incorporated in New York State in 1985, the name was later changed to National Adrenal Diseases Foundation to include individuals suffering from related diseases, such as Cushing’s Syndrome, Congenital Adrenal Hyperplasia, Pheochromocytomas. Support groups began forming in New Jersey, New York, Connecticut, Illinois and now include groups in 26 different regions of the United States, including a Spanish-speaking group, a Kids’ Pen Pal E-mail Network (NKPPEN), and a Young Adult (ages 18-29) group.
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As a result of the dedication of the Board of Directors, officers and members of NADF, patients with adrenal diseases now have a resource for their physical and mental health questions. The newly diagnosed can look to NADF for information from its page "Newly Diagnosed"  as well as “Facts You Need To Know” pamphlets. Anyone wishing to find support and share experiences with others can participate in one of our numerous support groups throughout the country, or can join an online discussion on the NADF Inspire website nadf.inspire.com. Even endocrinologists can stay informed through the efforts of the foundation with NADF’s Professional Membership.

​This page is dedicated by Mr. & Mrs. Thomas J. Foley in honor of the marriage of their daughter, Erin Ann Foley, to David Michael Moudry on November 16th, 2002.