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.

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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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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.
PALS’ Annual Fundraiser Breaks Attendance, Fundraising Records

People Against Leigh Syndrome’s (PALS) fifth annual fundraiser – Viva la Vida! – broke both attendance and fundraising records recently during a sold-out fiesta at Saint Arnold Brewing Company.

Lindsey Klingensmith
May 30, 2019
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Leigh Syndrome Patient Registry Gets a New Name

To better reflect its international reach, the Leigh Syndrome Patient Registry has been renamed.

Lindsey Klingensmith
April 2, 2019
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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
March 26, 2019
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