About People Against Leigh Syndrome (PALS)
People Against Leigh’s Syndrome (PALS) was formed in 2013 by the friends of William Martin; a Houstonian diagnosed with a progressive and fatal form of a mitochondrial disease called Leigh syndrome. PALS seeks to build awareness of this unknown disease and support efforts that would lead to discover a treatment or a cure.
Currently, PALS is working in partnership with the Children’s Memorial Hermann, UT Mitochondrial Center of Excellence and the Memorial Hermann Foundation.
Medical and scientific information on mitochondrial disease and Leigh’s Syndrome is used with permission from the United Mitochondrial Disease Foundation.
Consult your physician before changing your care.
Mary Kay Koenig, MD