Welcome to the ICN's Eosinophilic Cystitis Resource Center. There are very few resources currently available for EC on the web, but we hope to change that. This page was first created in 1999 and, in our journey, we've drawn dozens of patients for this "rare" bladder disease. We hope that we can unite you all to form a patient organization, put pressure on our government to provide seed money for EC grants and, most all, provide patient support.
      Our work began with one patient, Cricket, who has given so much care, love and support to other bladder patients in the past five years. We dedicate this web site to her and to each every EC patient out there struggling for information. (Read A Letter From Cricket About Her Experience With EC)
      Don't forget to sign up for our free e-newsletter! There is a special interest group on EC that we have just added.
      - Jill Osborne, Founder - ICN