International Paruresis Association

The International Paruresis Association (IPA) was founded in 1996 to raise public awareness about Paruresis, provide support, and give out the latest information.  Most of IPA’s members and leadership are treatment professionals, people suffering from Paruresis or recovering from it, and their loved ones.  Membership is open to anyone touched by Paruresis as well as those with an interest in supporting others with Paruresis, advocating for their rights, and advancing scientific knowledge about the disorder.

The International Paruresis Association is a non-profit organization under the terms of the US Internal Revenue Code section 501(c)(3).  As such an organization, contributions to IPA are tax-deductible. EIN#06-1509744.

Vision: To champion Paruresis awareness.

Mission: The IPA is dedicated to supporting people with Paruresis; providing information, recovery strategies and advocating in the mental health, medical and legal communities.