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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » Need Feedback on Dr. M in WI

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Author Topic: Need Feedback on Dr. M in WI
6Hypnone
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Much appreciated
Posts: 606 | From sw suburbs of chicago, Illinois | Registered: Mar 2016  |  IP: Logged | Report this post to a Moderator
hopingandpraying
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I already sent you info, but this will also bring your post back up to the top so others may "re-visit" it and respond.

Check the online state Lyme groups at:
https://groups.yahoo.com/neo/groups/WisconsinLyme/info

Maybe they can help.

Some more resources for you:
www.lyme-aware.org/wisconsin.html
www.wisconsinlyme.net

http://www.lymenet.org/SupportGroups/UnitedStates/Wisconsin/

Posts: 8991 | From Illinois | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
6Hypnone
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Thanks so much.
I tried those last 2 links and they didnt' work/vacant domain.

Posts: 606 | From sw suburbs of chicago, Illinois | Registered: Mar 2016  |  IP: Logged | Report this post to a Moderator
hopingandpraying
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You're very welcome - glad to help.

I didn't know there was a problem with the two links. Have no idea what is going on!

Try the online WI state Lyme groups instead and if you get any more info about the groups, please let me know.

Here are some other links I found on google:

http://wisconsinlymenetwork.org/patients/wisconsin-support-groups/

https://www.facebook.com/Wisconsin-Lyme-Network-408459622540767/

Posts: 8991 | From Illinois | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
hopingandpraying
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Here is another link for WI Support Groups to try:

http://whatislyme.com/lyme-in-wisconsin/

Posts: 8991 | From Illinois | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
   

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