Niki's Update on Angelina | Living with Lafora Disease | February 2025

Board member and Director of Family Support Niki Markou shares an update on her daughter's battle against Lafora disease. As of February 2025, Angelina's childhood dementia and other symptoms have significantly progressed. Her family is speaking out to help raise awareness and save other children. Give here: www.chelseashope.org/donate - Chelsea’s Hope Lafora Children Research Fund is an IRS 501(c)3 non-profit organization. Our mission is to improve the lives of those affected by Lafora Disease and help accelerate the development of treatments. Learn more: https://chelseashope.org/