This blog is our voice.
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.
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Hi Peta
ReplyDeleteI just stumbled on your blog. I'm a speech pathologist and I always have LKS in the back of my mind when working with children whose language skills have declined significantly. You're doing a wonderful job of educating people about LKS and supporting your beautiful daughter.
Regards,
Erin