August 19, 2012
Having suffered for paruresis for over 30 years, finding that an organization like the IPA existed was a life-changer. For the first time, I realized I was not alone. The IPA is the only organization I'm aware of that exists to tackle this condition, which has a moderate to severe impact on a small but significant minority of the population. By providing resources such as books and workshops, spreading awareness and hosting an online discussion forum, IPA has greatly improved the lives of many who suffer from paruresis.
Will you volunteer or donate to this organization?
How much of an impact do you think this organization has?
When was your last experience with this nonprofit?
MY ROLE:General Member of the Public