My niece Angelina has this devasting disease named Lafora disease and I want to help find a cure. Unfortunately, Angelina cannot take advantage of this new treatment but me and my family are dedicated to stop children from suffering and continue the fight.
On Wednesday March 19th, 2025, I will be hosting a morning tea at my workplace to raise much needed funds.
To learn more, view this fundraiser page or go to chelseashope.org.
*Please note that all donations are in US dollars as it is a US non profit organization.
Follow her story on social media @laforainitiative
Here is one of her latest videos that was shared on social media
Update from Angelina's mum with Chelsea's Hope Lafora Children Research Fund