jadescdkl5journey blogspot.com

Jades journey with CDKL5

Little is known about CDKL5. I am hoping by creating this blog, word will get out and parents will communicate more if their children have been diagnosed with this mutation. It is a devastating neurological condition causing a variety of problems, intractable epilepsy being one of the primary signs. Welcome to our blog.

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Sophie Jane Lewis

I hope you enjoy reading my story. Wednesday, 8 October 2008. My name is Sophie, I was born 26th June 1999 in The University Hospital of Wales. I live with my mummy Jane, daddy David and my two brothers, Thomas 5 years and Matthew 10 months. I have recently been given a diagnosis, I have an alteration in one of my genes called CDKL5. This gene helps brain development and is a rare genetic disorder. I hope you enjoy reading my story.

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Jades journey with CDKL5

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Little is known about CDKL5. I am hoping by creating this blog, word will get out and parents will communicate more if their children have been diagnosed with this mutation. It is a devastating neurological condition causing a variety of problems, intractable epilepsy being one of the primary signs. Welcome to our blog.

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This web page jadescdkl5journey.blogspot.com states the following, "Little is known about CDKL5." We saw that the webpage said " I am hoping by creating this blog, word will get out and parents will communicate more if their children have been diagnosed with this mutation." It also said " It is a devastating neurological condition causing a variety of problems, intractable epilepsy being one of the primary signs. Wednesday, March 21, 2012. So, we head back next week for another consult with the epileptologist and a follow-up with her new ."

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