The Future of leigh syndrome starts here

Do you or someone you know have Leigh syndrome? Help change the future of this disease by joining TRiaLS: The International Registry for Leigh Syndrome. Register today.

Upcoming Events

Every contribution gets us one more step closer. Thanks for your heart ♥.

The Fourth Annual PALS Fundraiser – Viva la Vida! – will be held on Wednesday, May 15, 2019 at Saint Arnold Brewing Company.  

Thousands Needs

tRiaLS: The International registry for leigh syndrome

Contribute today to help us cure Leigh Syndrome once and for all.
Thanks for your heart ♥.
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Latest Causes

PALS Leadership

Working towards a brighter future.
Lori Martin

President

Tahra E. Peterson

VP and Founding Member

Peyton Jones

Treasurer and Founding Member

Melissa Knight

Secretary

Lindsey Klingensmith

Executive Director

Latest News

We're always working on new leads.
NIH seeks Leigh syndrome patients for study

NIH is seeking patients for a natural history study of Leigh syndrome and its relationship to infection.

Lindsey Klingensmith
November 7, 2017
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In The News: A New finding

Mitochondrial DNA from Fathers Could Lead to New Therapies, Study Suggests

Lindsey Klingensmith
November 7, 2017
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