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Hello All,

I'm Kim Raub (39) and I live in Connecticut with my husband Bob (40) and our

four children. They are BJ (11), Duncan (9), and twins Hunter & Teddy (27

months). Teddy was diagnosed at 5 weeks with Lissencephaly when an MRI was

done to look for reasons for his difficulty in eating, but I didn't discover

the loop until he was 18 months old. It has been wonderful to have so many

people to talk to when you have questions or even when you don't. His

diagnosis was changed to Polymicrogyria (PMG) by Dr. Dobyns at the Dallas

Lissencephaly Convention.

Teddy and Hunter are identical twins. Their cords became tangled when their

sacks were perforated during an amniocentesis. Hunter has developed

normally and Teddy is doing pretty well himself. We don't have his latest

developmental results but I figure it's around 18 months. He rides a big

wheel, plays tag and is learning sign language. We have problems with him

eating but are still fighting the idea of getting a tube, although listening

to how much Merritt's gained is making me a bit jealous. We've also

been having problems with his oxygen level and are trying various strategies

to keep it above 90%.

Teddy's not having seizures so his list of current medications aren't too

long. He's taking Albuterol and Prednisolone in the hopes that his current

respiratory problems are from asthma. Thanks to all who responded to my cry

for help, the information was helpful when I went back to the doctors

office.

Welcome all to the loop.

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