The ICA was established in 1984 to put a face to all those affected by IC/BPS and remains today the only non-profit health association dedicated solely to improving the quality of healthcare and the lives of people affected by IC/BPS. To fulfill its mission, the ICA pursues three core functions

• Advocacy: By rallying a grassroots network, the ICA’s advocacy efforts empower people affected by IC/BPS around the country and the world, teaching them to become self-advocates for their healthcare needs. In addition, the ICA raises awareness among legislators and government leaders of the need for increased dedicated federal funding for IC/BPS research. The ICA specifically advocates for funding through the Centers for Disease Control and Prevention (CDC), the Department of Defense (DoD), and the National Institutes of Health (NIH) to explore and discover effective treatments and, ultimately, a cure for IC/BPS.
• Education: The ICA’s educational programs raise awareness of IC/BPS and empower those affected to change their lives. In all efforts, the organization serves as a curator and translator of the most current science-based information on the condition. Importantly, the ICA reach extends to healthcare providers; we work to improve professional education efforts to ensure optimal care with dignity for all people with IC/BPS.
• Community: The ICA provides support communities for those affected by IC/BPS. These communities are places for fostering connection, sharing experiences, and collective growth/learning. The ICA also serves as a powerful connection between IC/BPS healthcare providers, researchers, and those affected by IC/BPS.