This is topic finding a doctor in Upper Peninsula of Michigan in forum Seeking a Doctor at LymeNet Flash.


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Posted by William Quackenbush (Member # 45850) on :
 
Trying to find a lyme doctor in or near the Western Upper Peninsula of Michigan. I live in Copper Harbor which is right on the tip of the finger that sticks out into Lake Superior. Have been suffering with symptoms that doctors say is mixed connective tissue disease. Had to quit my job driving a big rig because I became to ill and weak to do it anymore.

[ 05-19-2015, 11:53 AM: Message edited by: William Quackenbush ]
 
Posted by hopingandpraying (Member # 9256) on :
 
Welcome to Lymenet! PM sent with some names for MI & WI.

I don't know of any in the UP of MI. Contact the MI Lyme Support Groups I have listed below. They would know better.

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":

http://flash.lymenet.org/scripts/ultimatebb.cgi/topic/2/15615?#000005

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.

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

Maybe they can help.

Some more resources for you (including Support Groups info):
www.lyme-aware.org/michigan.html
www.mlda.org [Contact Linda at (888) 784-5963]

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

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

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. Thanks.
 


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