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Re: Gavins great

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Amy,

The people have spoken, and we want you to stay. That is of course

if you want to. But I really think that you could be a wonderful

resource to other parents. I remember when you first started with

this group that you were looking for someone whose child had

scaphocephaly like Gavin. As far as I can remember, we've had one

member whose son did have scapho but I don't know if the two of you

ever connected. What I'm trying to say is, as unfortunate as it is,

there will be more parents out there whose kids will have

scaphocephaly and they will be searching for other parents to talk

to, like you did. You could really help many parents out there if

you hang around. Plus, you are a great example of following your gut

instinct!

Take care Amy, and I hope to see you around!

Niki

Kaylie & Danny (STAR grads)

Phila., PA

> Hi Niki,

> Gavin dosent need to wear anything on his head at all. We were

totally amazed

> that he did'nt need any protective wear. It's funny how he's so

careful with

> his head on his own. Do you really think I could still be of help

to people

> here? I kinda thought I was out of the loop because it turned out

he was not

> a plagio baby after all. I would be more than happy to help anyone

at all!

> Amy, WI

> mom to Gavin

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