Re: I'd like to find an MCS group to meet up with

[Guest guest]

I think you can start meet up groups.... sue

>I don't have too many people I can talk to about this. People that

>really understand how it makes my life so stressful and fearful.

>I live in New York City but have a car and access to the boroughs

>(Queens, Brooklyn)Also Long Island.

>Does anyone have a website to find groups? The meet up thing has nothing

>for MCS.I'm not sure where else to look.

>I'm a little lonely I guess and I know that talking to likeminded people

>will definitely help me.

>Thanks for any suggestions

>

>

[Guest guest]

Here are the links to a couple of moderated

This is the first one I joined when my MCS became severe suddenly. It's based in

WA but people that didn't live there were also members.

WSMCSN/messages

This one I joined last summer. This group is international.

GreenCanary/messages

You may find people at these groups that have friends with MCS living in NY.

Some of them are too affected by EMF's to be on a computer. You can also search

for MCS. There are other groups listed there too.

Have you heard of The Chemical Injury Information Network ?

ciin.org

They put out a tiny publication called Our Toxic Times that you can run an ad

in.

>

> I don't have too many people I can talk to about this. People that really

understand how it makes my life so stressful and fearful.

> I live in New York City but have a car and access to the boroughs (Queens,

Brooklyn)Also Long Island.

> Does anyone have a website to find groups? The meet up thing has nothing for

MCS.I'm not sure where else to look.

> I'm a little lonely I guess and I know that talking to likeminded people will

definitely help me.

> Thanks for any suggestions

>