I am looking to start some sort of support group in the Minneapolis/St. Paul, Minnesota area. Are there any lymies out there with me?
Posted by bettyg (Member # 6147) on :
lyra,
may i suggest you add this to beginning of subject:
wanting to start ........;
just click on PENCIL, 3rd box to right and now they know you want to START one! many folks are in that area.
you can do a directory check.
click directory at top
go to left side and type in MINNEAPOLIS next line chose LOCATION hit send; and it will show members who showed minn. in profile
once you get it started, post info in SEEKING DR. AREA, so others know of it.
support groups on left side; did you check that out first??
Posted by pab (Member # 904) on :
quote:Originally posted by Lyra: I am looking to start some sort of support group in the Minneapolis/St. Paul, Minnesota area. Are there any lymies out there with me?
I'm interested in a support group. I live in Woodbury and my husband, 2 sons and I have Lyme and co-infections. There are quite a few posters from the Twin Cities area.
Posted by heiwalove (Member # 6467) on :
i grew up in the twin cities but don't live there anymore. when i go home to visit family (2 or 3 times a year) i'd love the chance to meet up with mpls/st paul area lymies. Posted by Lyme Wolf (Member # 5463) on :
Hi Guys,
I can't believe no one beat me to it, but here goes.
Now in it's 3rd year, a large, active, and awesome support group in the Twin Cities area is:
We invite anyone from the Twin Cities Metro area to attend. There is also an annual event that has grown quite large and raises funds dedicated to research in the great state of Minnesota.
Please contact the group at their website with any questions.
![[Smile]](smile.gif)