This is topic Need Feedback on Dr. M in WI in forum Seeking a Doctor at LymeNet Flash.


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Posted by 6Hypnone (Member # 47629) on :
 
Much appreciated
 
Posted by hopingandpraying (Member # 9256) on :
 
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/
 
Posted by 6Hypnone (Member # 47629) on :
 
Thanks so much.
I tried those last 2 links and they didnt' work/vacant domain.
 
Posted by hopingandpraying (Member # 9256) on :
 
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/
 
Posted by hopingandpraying (Member # 9256) on :
 
Here is another link for WI Support Groups to try:

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


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