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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » Michigan

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Author Topic: Michigan
lucecaboose
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Member # 13058

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Michigan. Need LLMD in Michigan.

Mine retired four years ago.

There are only naturopaths or holistic docs in the state who claim they are LLMDS.

They are not. And have not helped.

I had the bullseye in 1999 and have fought symptoms since 2003.

I also know a woman who has "fibromyalgia" but I have no one to recommend anymore.

Thank you.
Posts: 45 | From Grand Rapids, MI | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
Bartenderbonnie
Frequent Contributor (1K+ posts)
Member # 49177

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Welcome back lucecaboose.

Yea, I have quite a few LLMD’s in Michigan that are ILADS trained, for you and your friend.

Start by gathering referrals.

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/

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.

I’m sending pm for Michigan.
Good Luck to you.
Posts: 3217 | From Florida | Registered: Nov 2016  |  IP: Logged | Report this post to a Moderator
   

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