About Us
The PK Deficiency Foundation is a self funded public charity which provides science-based education to patients, their caregivers, and the medical community. Founded by patients and caregivers, our Foundation advocates on behalf of our community for affordable and accessible treatment options. We support rigorous research that advances the understanding and treatment of Pyruvate Kinase Deficiency for patients of all ages, empowering healthy, long, fulfilling lives.
Meet the Team
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Alejandra Watson
Founder and Board President
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Laura Miller D'Angelo
Founder and Board Secretary/Treasurer
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Carla Kane
Founder
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Kylee Roney
Board Member