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The Interstitial Cystitis Association of America: lessons learned over the past 30 years

  
@article{TAU8043,
	author = {Vicki Ratner},
	title = {The Interstitial Cystitis Association of America: lessons learned over the past 30 years},
	journal = {Translational Andrology and Urology},
	volume = {4},
	number = {5},
	year = {2015},
	keywords = {},
	abstract = {In 1984, interstitial cystitis (IC) was considered a rare psychosomatic disorder in post-menopausal women. In 2014, the Interstitial Cystitis Association of America (ICA) celebrated its 30th anniversary. We’ve come a long way since 1984 and great progress has been made. IC is now recognized as a condition that afflicts both men and women of all ages, including children and teenagers. It is not a psychiatric disorder. Though it was once thought to be an orphan disease (defined as affecting less than 200,000 people), we now know that there are millions of women and men who suffer from IC/BPS (bladder pain syndrome). In looking back over this period, there were seven key reasons why the ICA became so successful: an extremely dedicated ICA staff, Board of Directors and volunteers; a very strong Medical Advisory Board and participation of many other urologists from across the country and around the world; cooperation of the media; epidemiological studies; the ICA’s Pilot Research Program; our representation in Congress; and a strong working partnership with the National Institutes of Health (NIH). Our history may prove useful to other advocacy groups.},
	issn = {2223-4691},	url = {https://tau.amegroups.org/article/view/8043}
}