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Welcome to the group. As you read, we are not all parents of kids with

PMG but a mixed bunch of auntes, uncles, brothers, sisters,

grandparents and parents of kids with PMG. I am suprised that the

doctors didn't mention any seizures becuase I think the majority of

these kids have some sort of seizures, ranging to once a month to once

every hour or so. My niece also doesn't look like she has PMG but she

does and is severely effected by it. The best advice I think any one

can give is to take this one day at a time and enjoy every minute with

your child. You will encounter many heartbreaking moments as well as

wonderful moments of watching your 5 year old just learning to walk

without support. (Congrats caleb, by the way. Thats just awesome!!!!)

That is what this group is here for, we support each other and give as

good advice as we can about situtaion we have already delt with or are

dealing with. It helps to talk to people who understand what your going

through and how you feel and understand why you feel that way. We

welcome you with open arms.

, Auntie to age:19 and 1/2 months

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