Becky’s dream is that we can find a cure for Lafora disease. Can you help?
“Alone, we can do so little . . . together, we can do so much.”
— Helen Keller
Video
This page contains tributes, news stories, and other videos about Lafora and those it affects.
A Tribute to Becky
Becky’s Dream from Suzy Brooks on Vimeo.
Meet 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
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Help us find a cure!
Becky has a page on Chelsea’s Hope:
Click the image to visit her page.
Copyright © 2010, beckysdream.org, Bourne, MA 02532. All rights reserved.
This site, its design, graphics, and media are donations from family friends. Please help us find a cure for this disease.