Imagine having a condition so rare that the top specialists are unable to diagnose you. In fact, after further research, they explain they need to name your condition after you. This is the story of Kate Kobbermann and her remarkable life with Kobbermann Syndrome.

This episode is Part 1 of a 2 episode podcast. In this episode, Kate and her mother discuss the timeline of her life beginning with her birth and ending with the diagnosis of Kobbermann Syndrome

About Kobbermann Syndrome:
Based on Kate's experiences, her syndrome has been classified as one that causes skeletal fragility, which is potentially caused by a unique strand of DNA.