Kathy Geertsma

Kathy Geertsma

As the parent of a young adult with Salt Wasting Congenital Adrenal Hyperplasia, Kathy Geertsma became Chair of the Congenital Adrenal Hyperplasia Parent and Support Group. She has extensive contact with parents and patients from all over the world who struggle with confirming a CAH diagnosis and getting proper treatment. As a result, she offers a unique perspective about how practitioners can better serve the needs of their patient population.

Affiliations and Expertise

Chair, Congenital Adrenal Hyperplasia Parent and Patient Support, London, UK


Authors: Peter C Hindmarsh & Kathy Geertsma Release Date: 01 Apr 2017
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