This is topic Michigan but will travel in forum Seeking a Doctor at LymeNet Flash.


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Posted by lucecaboose (Member # 13058) on :
 
I had my tick bite in 1999, symptoms since 2003. My LLMD retired in 2021.

I’m in Michigan but will travel.

I have contacted Global Lyme Alliance and other sources but all I get is a list of functional medicine/naturopaths.

Ive already tried 3 of these…I need someone who understands and actually treats chronic Lyme.

Michigan says they have support groups but they don’t seem to exist anymore.

Thanks.
 
Posted by Bartenderbonnie (Member # 49177) on :
 
Welcome back to LymeNet lucecaboose.

You can request LLMD’s through Global Lyme Alliance
https://www.globallymealliance.org/lymedoc

You can request LLMD’s through LivLyme Foundation
https://livlymefoundation.org/resources/doctors/

You can request LLMD’s through ILADS
(International Lyme and Associated Disease Society)
https://www.ilads.org/patient-care/provider-search/

You can request LLMD’s through Lyme Disease.org
https://www.lymedisease.org/find-lyme-literate-doctors/

Project Lyme
https://projectlyme.org/providers-landing/

Lyme Basics
https://lymebasics.org/patient-support/lyme-doctor-referral/

Lyme Advice
https://www.lymeadvise.com/lyme-literate-physicians

LymeDoc.org
https://sites.google.com/site/lymedoctors/home?authuser=0&pli=1

Some of these are simple e-mail formats that you fill out and they respond with LLMD’s in your area. You MUST research each LLMD referred. To do this, google for patient reviews and call each LLMD provider and ask what their treatment protocols entails.

These lists are not exhaustive and may be outdated. Call the doctor to see if they are taking new patients!

Lyme Facebook Groups

Lyme disease support groups are abound on Facebook.
There are probably a couple hundred to choose from, including city- and state-specific forums, treatment-focused groups, and an assortment of national groups. Because people discuss the challenges they face and the symptoms they endure while living with Lyme, most groups and forums are kept on a "private" setting so others outside the group won't see what you post.

To locate a group, type a description of the kind of group you're hoping to join, such as,
"Lyme disease lowa," and review the selections that pop up. When you find one that interests you, request to join it. Each group may have certain posting and privacy guidelines, but once you're a member, you can crowdsource information regarding Lyme-literate medical doctors and Lyme disease specialists who may be able to help you. Plus, you can get feedback from others about the kinds of treatments they've found beneficial.

There’s lots of support groups in Michigan.
http://mlda.org/resources/support-groups/

Sending pm for Michigan.
Healing wishes 🙏💚
 


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