Interstitial Cystitis Association
Cafe ICA

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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

Shop iGive and Search iSearch.iGive -- And, Help Raise Money for the ICA
Here's a way to help raise money for the ICA, every time you shop online or search the web: www.iGive.com and www.iSearch.iGive.com.
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Posted -- November 2008 Issue of the Cafe ICA
Check out the latest medical highlights, self-help and copying strategies, and ICA news
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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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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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Question of the Week
What information does your healthcare provider routinely ask you to provide:








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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 November 27, 2008