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.
Posted by Ann-OH (Member # 2020) on :
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.
Ann - OH
[ 01-05-2015, 11:02 AM: Message edited by: Ann-OH ]
Posted by eternal12 (Member # 45147) on :
Thanks, but that web-site doesn't exist.
Posted by TF (Member # 14183) on :
The correct website for the Michigan Lyme Disease Assn:
Thanks, got it.
Posted by TF (Member # 14183) on :
You can also get their email address by clicking on Support Groups on the left side of this page.
I couldn't get their email at their site.
Posted by eternal12 (Member # 45147) on :
Ok,thanks
Posted by hopingandpraying (Member # 9256) on :
Welcome to Lymenet! PM sent for MI.
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.
The top LLMD, Dr. H, has written a new book entitled, "Why Can't I Get Better?". It is an excellent source of information.
Read "Cure Unknown" by Pamela Weintraub. Get it at your local library or buy it used on Amazon.
View "Under Our Skin" for free on www.hulu.com Posted by Ann-OH (Member # 2020) on :
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