Interstitial Cystitis Association
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The ICA is dedicated to helping all those living with interstitial cystitis, as well as the healthcare providers and researchers who strive to improve the lives of IC patients.

In the News

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We're Moving!  New ICA Address as of Jan 1, 2009   
Check out our new address on the Contact Us page. The good news is our phone and fax numbers are the same. Also, please continue to mail your donations and orders to the same PO Box.

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Sleep and IC Study -- Recruitment closed due to overwhelming response
A women's health nurse practitioner with 10 years of experience treating IC patients and a doctoral student in nursing are asking for your participation in an innovative study.
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Shop iGive and Search iSearch.iGive -- And, Help People with IC
Here's a way to help support programs and services for people wtih IC, every time you shop online or search the web: www.igive.com and www.isearch.igive.com.
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The Latest Pain Management Information for Healthcare Professionals
The Fall 2008 issue of ICA Professional Perspectives is now available online and is dedicated to information gleaned from PAINWeek2008, held in Las Vegas, Nevada, in late September.
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November is Bladder Health Month
November is Bladder Health Month and a good time to learn more about how to manage bladder conditions like interstitial cystitis (IC) that affect millions of people in the United States.
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En route -- Fall 2008 Issue of the ICA Update
Special research issue
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Interstitial Cystitis Association Announces Two New Board Members
The Interstitial Cystitis Association (ICA) welcomes two dedicated interstitial cystitis (IC) advocates to its Board of Directors, Barbara Zarkinow of Buffalo Grove, Illinois and Paula Whelan of Scottsdale, Arizona.
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Interstitial cystitis (IC) is pelvic pain, pressure, or discomfort related to the bladder, typically associated with persistent urge to void or urinary frequency. IC may also be referred to as chronic pelvic pain (CPP), painful bladder syndrome (PBS), or bladder pain syndrome (BPS).

More than one million Americans -- of all ages, genders, races, and ethnicities -- suffer from IC. Until recently, only 10 percent were thought to be men, but new estimates are as high as 30 percent. IC in men may often be mistaken for chronic prostatitis/chronic pelvic pain syndrome.

Many people with IC experience severe, chronic pain. Some feel like their insides are being cut apart with razor blades. Others compare the pain to red hot pokers stabbing at their pelvic area.

 

Revised December 12, 2008