August 20, 2012
I've suffered with Paruresis since college and it rules my life. It conditions my leisure, my work - anything outside of my home. I stumbled upon the IPA webpage about 6 years ago and I literally cried. I wasn't alone. Not only that, those with this affliction shared their experiences. The IPA has many resources to deal with Paruresis as well as a support lifeline. I proudly support their work.
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When was your last experience with this nonprofit?
2012
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