Donate & Become a Member
The International Paruresis Association, Inc. (IPA) is a nonprofit organization formed in 1996 to help those afflicted with and affected by this social phobia. Won’t you support the cause with a gift today? Donors who contribute $100 or more are eligible for special “members only” benefits including savings on workshops, invites to special events, and access to classic IPA books and resources for free.
For nearly 30 years, the IPA has consistently worked to:
- educate the public and the medical establishment on the nature of Paruresis
- show that Paruresis has been the most neglected social phobia and yet afflicts a wide range of people
- sponsor workshops to help those suffering with Paruresis overcome this phobia
- help those afflicted with Paruresis overcome the stigma, embarrassment, and isolation associated with it
- disseminate the latest information about Paruresis
- facilitate the establishment of support or self-help groups across the world
- expand research to help identify the most clinically effective treatments
Operated by a small group of professionals and primarily staffed by volunteers, we have already helped thousands of men and women realize a difference in their lives though our educational workshops, newsletters, websites, research and outreach. Now we ask for your support to sustain the organization and help us continue to reach our long-range goals. Please….you can help others and yourself by giving to this worthy cause…
The IPA needs help in the form of money and volunteers. Can you contribute?
Maybe you’ve said to yourself in the past: “I’d pay any amount (maybe $10,000?!) if someone could help me with this condition”…. Well, now some people have come forward to help you, and they are not asking for what you may have previously been willing to pay.
Your donation goes directly to pay for online resource maintenance, information packets, administrative help and other costs. Select our official online donation portal, or print out and mail in the Donor Form. Our members are completely anonymous and we never sell our mailing list. While donations of any amount are sincerely appreciated, we encourage you to “join” IPA with a donation of $100.00 or more today!
If you are interested in considering a legacy or estate gift, click here for our wish list and contact us here. You can use the same form to let us know about your interest in volunteering, too!
THANK YOU,
Steven Soifer, Ph.D., MSW, Co-Founder, IPA
To make a donation online, click here for our official donation portal powered by CharityEngine.
To send a check by mail, click here to download, print and complete our Donation Form.
To join our e-mail mailing list, click here.
QUICK LINKS
INTERNATIONAL PARURESIS ASSOCIATION
P.O. Box 21237
Catonsville, MD 21228
You Are Not Alone.
There Is Help For You!
Shy Bladder, Bashful Bladder, Pee Shy
IPA OFFICE HOURS
Monday - Friday
10:00am - 6:00pm (ET)
844-I-CANT-PEE (422-6873)
US/Canada
443-315-5250 Office
Email: getinfo@paruresis.org
This website is NOT a substitute for medical or legal advice and does not constitute the practice of law, medicine, psychiatry, clinical psychology, clinical social work, or any other mental health profession. If you are having trouble urinating, you should always contact a physician since difficulty with voiding can be a symptom of a serious medical condition. We are a group of professional people and people who have suffered with paruresis. We have assembled a board and a board of advisors to help people cope with urinary dysfunction that has a psychological or social origin. On this website, we are NOT practicing medicine, psychiatry, clinical psychology, clinical social work or any other mental health profession. You should have your doctor evaluate your condition before diagnosing yourself, and seek the appropriate necessary mental health counseling if warranted. IPA, Inc. disclaims any and all legal liability whatsoever.