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Hi all,

We are new to this support group. Our daughter Alana,

5, was first diagnosed with Schizencephaly when she

was just one. We recently sat down with her new neuro,

and she explained to us that Alana has the clefts seen

in Schizencephaly, but they were not deep enough to be

called a " true " Schiz. case. The radiologist gave

Alana the diagnoses of PMG with secondary Schiz. Makes

no sence to us, but we are eager to learn about this

" new " diagnoses. Alana is unable to sit alone, crawl,

talk, or do anything that requires any physical

strengths. Alana is able to, shake her head yes and

no, point to everything she wants, and has the most

contagious laugh you would ever want to hear. We

adopted Alana from India. She came home to us

believing she was a " normal " little girl. As soon as I

saw her come off the plane I knew something wasn't

quite right. As soon as Alana was put into my arms it

was instant LOVE. Alana has five siblings who dote on

her when daddy and mommy are busy. She is one of the

greatest gifts our family has been given. She is our

light in the darkness.

Lori Mom to Alana 5 1/2

__________________________________________________

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