ICA board members, staff, and volunteers went to Capitol Hill to advocate for IC!
ICA staff, board members, and IC patients spoke at an FDA Advisory Meeting.
For many people with IC, an effective treatment plan requires a team approach.
Check out ICA's Diet Section! Focusing on what you CAN eat!
Struggling with bladder pain, urinary urgency/frequency? You may have IC.
The Interstitial Cystitis Association (ICA) is the only nonprofit charitable organization dedicated solely to improving the quality of healthcare and lives of people living with interstitial cystitis (IC).
IC is recurring pelvic pain, pressure, or discomfort in the bladder and pelvic region, often associated with urinary frequency (needing to go often) and urgency (feeling a strong need to go).
IC can affect anyone. More than 12 million people in the US have IC:
Revised Wednesday, February 24th, 2016
20 June 2019
ICA is excited to share this great resource for interstitial cystitis/bladder pain syndrome (IC/BPS) patients! We are working with Hannah Matluck, Founder, Producer & Host of The Women’s Pelvic Health Podcast to promote her podcast series that is a source … Continued
20 June 2019
Summer is officially here. Will you be attending picnics and cookouts? This can be an issue for interstitial cystitis/bladder pain syndrome (IC/BPS) patients who follow the IC diet. What are some tips you can share with other IC patients to … Continued
May God Bless your organization for all the wonderful work they are doing.
- Michelle
