A way to reach the world and tell our story.
The story of my precious daughter and her battle with a rare form of Epilepsy, Landau-Kleffner Syndrome.
And the story of me, a complete novice, learning how to blog. Hehehe.
Taylor has Landau-Kleffner Syndrome. A rare and severe form of Epilepsy that has left her neurologically deaf. Join us in our fight against this illness and support us in our efforts to ensure Taylor has access to deaf education, programs and facilities, so that she may continue to learn to communicate with the world.