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» LymeNet Flash » Questions and Discussion » General Support » St. Louis, MO has a suport group!

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Author Topic: St. Louis, MO has a suport group!
she7
Member
Member # 11244

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Hi everyone!

I got together with another lymie in St. Louis and started The St. Louis Lyme Foundation, a state recognized support group and non-profit organization
in St. Louis!

We are still working out the details with everything, but we are going strong.

You can visit our new webpage for more info:

[email protected]

My partner runs the page most of the time- and we are always open to suggestions and support.

Finally finding others in St. Louis who can relate to my struggle for proper medical care and understanding has been so valuable to me-
I hope to make this available to others who struggle in St. Louis.

Posts: 35 | From st. Louis | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

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I'm so proud of you!!! Great going!!!

here is the link for all the lazy folks out there!:

[email protected]

The link still doesn't work....????

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
chroniccosmic
LymeNet Contributor
Member # 7789

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Get out of here! Finally something in my area.

I will check out your website and thank you. If I can drag myself across the river, i will be there.

Posts: 460 | From Illinois | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

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cosmic....Can you swim?? [lol]

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
chroniccosmic
LymeNet Contributor
Member # 7789

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Better yet, I will just ride one of the many gambling boats across.

That link didn't work for me. [Frown]

Posts: 460 | From Illinois | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
   

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