Support group for Selective Mutism

[sunflowervalley]

Hi,have just set up a basic web page in order to start a support group in my area for selective mutism.

Having searched for support in my area and found none thought I would try and get one together myself,although not sure where to start.

So have set up this freeweb site to see if their is any other parents in my area with a child with selective mutism.

Would it be ok to put the website address on here?

Definiteyl Sunflower.

Thanks moondog.

It's
link

It's very basic as have just set it up but really just want to gage any interest and hopefully will get some people posting in order to offer advice and share experiences.
Maybe get togethers with the parents and their children also.
Would be great to set up coffee mornings ,fund raising etc,whoops getting ahead of myself I think?

I am astounded at the lack of knowledge of SM within school and childrens services. Most of the information I have recieved has been from googling SM or mumsnet.
In fact I think you yourself moondog may have replied and offered good advice on one of my previous posts.
My son also has speech problems with compound with his SM.

Here's hoping I get some replies as I myself 2 years ago had never heard of SM and it makes me wonder how many othr chlden are in the system with this problem and it is not being recognised.

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