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Resources for PMG kids

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Hi everyone,

We are new to this whole PMG experience. My granddaughter, Brie, is 12 weeks old

today and was diagnosed with PMG at 3 weeks old. We still do not have a doctor

who has a clue about PMG. So, we heard about Dr. Dobyns in Seattle but trying to

find a way to finance the trip from ville, FL to Seattle (could it be any

further away?) is extremely daunting, to say the least.

Does anyone know of any organizations or resources for families of PMG kids that

might help with expenses to travel for care?

Thank you so much for any input!

Catrina, Brie's Gram

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