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>

> I have 15 month old boy and he hath Lipomeningomyelocele. Is it here

> someone who have this same LipoMMC? Sorry my england is not so well,

> I`am from Finland. :)

>

I have the same. Was not diagnosed as a child. I think with an early

diagnosis you son may do better. Once permanent nerve damage has set

in, surgery won't help. How was he diagnosed?

Janine

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> >

> > I have 15 month old boy and he hath Lipomeningomyelocele. Is it

here

> > someone who have this same LipoMMC? Sorry my england is not so

well,

> > I`am from Finland. :)

> >

>

> I have the same. Was not diagnosed as a child. I think with an

early

> diagnosis you son may do better. Once permanent nerve damage has

set

> in, surgery won't help. How was he diagnosed?

>

> Janine

>

My son name is Santeri. He catch diagnosed when he born and he was a

surgery year ago, 3 month old. Surgery went very well. What proplems

you have to LMC? My son doesn`t have nothiong yet.

Meiju

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