Re: PMG anyone living in the uk? (angela in the USA)

[Guest guest]

Hi

 

Thanks so much for your reply. It does make such a huge difference to know that

there are other mums on the same journey as me. And yes it does not really

matter where we are in the world because we are all here in this group together.

Take care, hope your son is well at the moment.

From: louise loveridge <louloveridge@ yahoo.co. uk>

Subject: PMG anyone living in the uk?

To: polymicrogyria@ yahoogroups. com

Date: Tuesday, October 6, 2009, 4:54 PM

 

Hi

 

I have a 2 year old little girl who not long ago was diagnosed with PMG. Would

love to know if there are any other families in the UK in this group. There does

not seem to be many of us here. I am on the south coast not too far from

Brighton.

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