The Interstitial Cystitis Association (ICA) is a patient advocacy organization devoted to optimal care with support for people affected by interstitial cystitis/bladder pain syndrome (IC/BPS). IC/BPS is a chronic pain disease that is not well known by the public or even healthcare practitioners, yet millions of Americans suffer from it. The primary symptom of IC/BPS is excruciating bladder pain, and secondary symptoms include urinary urgency and frequency. Many patients suffer for years without a diagnosis and miss the opportunity to make important lifestyle changes that provide relief.
Join us for the ICA's Fall Fundraiser - Step Up for IC/BPS Awareness & Educational Event!
This virtual event can accomplish a lot of different goals, including:
- For those living with IC/BPS, we are providing great information on the condition from leading experts and the ability to have friends and family “Walk in Your Shoes” to better understand the condition.
- For our communities, we’re raising awareness of interstitial cystitis to help people get a better diagnosis and treatment.
- For the ICA, we’re raising funds (hopefully $25,000!!) to support the mission of improving the lives of those with interstitial cystitis across the country.
I was diagnosed with IC in 2021 and it is something that influences me every single day. I hope you'll join me in the fight against IC/BPS, either by joining my team and raising awareness...or by simply making a donation! Every dollar helps!
The Interstitial Cystitis Association is a 501(c)(3) charitable non-profit corporation with federal EIN# 13-3292137. Contributions are tax-deductible as described by law.
