This is topic WI LLMD in forum Seeking a Doctor at LymeNet Flash.


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Posted by jsnyde2 (Member # 7888) on :
 
Hi, 2nd time around for me. Last time was 10 years ago.

I used an LLMD in MN, and wondering if anyone knows any right in WI.

I have the rash and I don't want it to turn into full blown Lyme. I love my GP but 200mg doxy she prescribed might not be sufficient.

The rash is going away, but still not gone. Thanks!

[ 10-06-2016, 02:23 PM: Message edited by: faithful777 ]
 
Posted by hopingandpraying (Member # 9256) on :
 
PM sent for WI. I don't know of any right in LaCrosse.

Unfortunately, LLMDs are far and few between. You need to go where they are.

When you call for an appointment, ask if they have any cancellations or a waiting list. Patients have been able to get in earlier by doing this.

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

Maybe they can help.

Some more resources for you:

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

https://www.facebook.com/Wisconsin-Lyme-Network_408459622540767/

http://whatislyme.com/websites-and-support-groups-by-state/

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

Btw - please break up your posts into 2-3 sentence paragraphs, as there are people on Lymenet who cannot read large blocks of text due to neurological problems from Lyme.

To do that, click the pencil/paper icon, make your changes, then click "Edit Post". Thanks.
 


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