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

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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Available Online -- October 2008 Issue of the Cafe ICA
Check out the latest medical highlights, self-help and copying strategies, and ICA news
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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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NIH Launches an Exciting New Chapter in Federally Funded Research on IC
An exciting new chapter in federally funded research on interstitial cystitis (IC) was just launched by the National Institutes of Health (NIH).
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National Study Recruiting Female Research Participants
Researchers at the University of Alabama at Birmingham still need a few more women to participate in a National Institutes of Health-sponsored study on pain and interstitial cystitis.
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Interstitial Cystitis Association Announces ICA Pilot Program Awards
Committed to finding the cause and ultimately, a cure for interstitial cystitis (IC), the Interstitial Cystitis Association (ICA) announced recipients of FY2007 ICA Pilot Research Program grants.
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Question of the Week
The ICA is setting its advocacy agenda and would like to hear from you. Please tell us which area you believe to be most pressing for the IC patient.





Submit Survey  View Results
 

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 November 1, 2008