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Hi,

My name is and my daughter Meg, who is 18, is moderate-

severe mental retardation. No official diagnosis or syndrome, just

delayed since birth related to prematurity and anoxia. I'm just an

ordinary mother who belongs to no organizations related to my childs

disability, but trys to be active in school events and support

services. I'm now in the position of negotiating the transition process

into the adult services world. While Meg's school offers a wide variety

of support in this area, I'm finding that the process can be a

difficult and confusing one. I'm hoping to find ideas, suggestions,

thoughts, experiences... maybe in areas that I haven't even begun to

think of yet. This is yet another beginning of the road for us. From

what I have read so far, it seems as though most of the members here

are ahead of where I am in the arena of the adult world, but I'm always

willing to contribute whatever I can! Thanks. Steph

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