Alice's Journey
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Alice has a rare genetic condition called CDKL5 (Mutation in exon 18 - C deletion at position 2503), with a diagnosis of intellectual and physical disability, severe seizures, and digestive dysfunction. This is the story of our journey so far ***** To find out more about Cyclin-Dependent Kinase-Like 5 see: www.cdkl5.com ***** P.S This blog is getting very long! So please check 'Older Posts' at the bottom of the page for Doctors reports and more medical information.