Newly diagnosed?

We are here to help you.

Linda and Chelsea Gerber

We are a worldwide team of Lafora Disease family and friends dedicated to finding a cure. We have been where you are now, and we understand the emotions you are experiencing.

We want to connect with you and answer any questions you have. You have a Lafora disease family to support you.

As founder Linda Gerber said, “Together, we can maintain hope.”

Stay connected with Chelsea’s Hope