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The Champ Foundation supports research and clinical initiatives focused on Pearson Syndrome and related single large-scale mitochondrial DNA deletion syndromes. The organization funds scientific projects that develop therapies, including gene and mitochondrial-targeted treatments, small molecule approaches, and disease models. It provides
competitive research grants to academic and clinical investigators working on mitochondrial DNA deletion disorders. The Champ Foundation also convenes meetings and conferences to share research progress and develop care guidelines for affected patients. In addition, it runs fundraising campaigns and outreach activities to sustain its grantmaking and raise awareness of Pearson Syndrome. Through these programs, The Champ Foundation aims to advance new treatments and potential cures for mitochondrial DNA deletion syndromes.
