Hi, I’m Callie! I’m one of the only IC RDs in the world (in fact, I’m one of only 2 who focus only on IC- meaning I live and breathe it). But I’m also an IC Warrior, so I know first-hand how it feels to struggle day in and day out with excruciating pain. I’ve experienced symptoms since I was very young. When I was finally diagnosed at 18, I was glad to put a name to my pain, but I didn’t realize my struggle was only beginning.