This is topic St. Louis, MO has a suport group! in forum General Support at LymeNet Flash.


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Posted by she7 (Member # 11244) on :
 
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.
 
Posted by Lymetoo (Member # 743) on :
 
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....????
 
Posted by chroniccosmic (Member # 7789) on :
 
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.
 
Posted by Lymetoo (Member # 743) on :
 
cosmic....Can you swim?? [lol]
 
Posted by chroniccosmic (Member # 7789) on :
 
Better yet, I will just ride one of the many gambling boats across.

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


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