This page contains tributes, news stories, and other videos about Lafora and those it affects.
A Tribute to Becky
She’s an amazing 20-year-old young woman, with the ability to light up a room with her bright eyes and beautiful smile. We all adore her and love her to pieces.
Becky was recently diagnosed with Lafora disease, an extremely rare form of Epilepsy. To help Becky, her family and Lafora research, we have started beckysdream.org.
Be sure to stop by the website to offer your support, as it will mean so much, to so many.
There is no hand so small, that it cannot make a difference in the world....Please make a difference in our world.
A News Story about Chelsea Gerber
A news story about Chelsea Gerber, whose parents started Chelsea’s Hope.
The news station’s site: http://abclocal.go.com/kgo/video?id=6843181
Help us find a cure!