posted
Looking for LLMD in SE MI. I've had Lyme disease since 2011, been on antibiotics and herbs and supplements. Did Cowden Protocol. Thanks for any help.
Posts: 4 | From Michigan | Registered: Jan 2015
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Ann-OH
Frequent Contributor (5K+ posts)
Member # 2020
posted
Go to MLDA.org to e-mail the head of the Assoc., Linda. On MLDA you will find a whole list of support groups and contacts who will know all about the Michigan docs.
You need to be evaluated and treated by a Lyme-literate doctor (LLMD). Non LLMDs have no clue about this horrible disease or its complex treatment!
They are far and few between, unfortunately. You need to go where they are.
Also, most LLMDs do not accept insurance due to the politics surrounding this horrible disease. Read poster TF's explanation, "Why Lyme Doctors Don't Take Insurance":
When calling for an appointment, ask if they have any cancellations or a waiting list. Patients have been able to get in sooner to see a LLMD by doing this.
Ann-OH
Frequent Contributor (5K+ posts)
Member # 2020
posted
Whoops! I did mean MLDA.org!
If you go to their website, and look down the right side, you will find you can click on an email link - and there is a "contact" box on the menu across the top of the website.
Hope you have found what you need by now. Ann - OH
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