This is topic MI LLMDs in forum Seeking a Doctor at LymeNet Flash.


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Posted by alemicham171 (Member # 47737) on :
 
Hi all,

I'm new to the site and forum and this is my first post, so please excuse me if I'm in the wrong place!

I'm a 35-year-old male and I've been experiencing several distressing symptoms for close to two years (too many to list here, I will pass them on if requested). The variety, frequency, and seemingly random nature of the symptoms are very concerning. While I haven't been diagnosed with Lyme, my symptom list grows on almost on a daily basis and it sometimes feels like I'm losing my mind! My search has lead me to believe that Lyme may be the answer, so I'm hoping someone can help.

I have been passed around to different physicians in my area and most everyone scoffs when I bring up my symptoms and the possibility of Lyme. One nurse practitioner agreed to order a Lyme test (which came back negative -- to be honest I'm not sure exactly which test was ordered), but I'm learning that a false negative test can be common. I'm looking for an LLMD in Michigan, if possible, but I'm willing to travel regionally and look elsewhere in the state/Midwest if necessary.

Thank you for your time, it is greatly appreciated.

Regards,
alemicham171
 
Posted by paulieinct (Member # 17514) on :
 
Hopefully someone here will help you with names of LLMDs near you.

I tested negative on standard two-tier testing for decades. When I finally was tested by IGENEX it was positive, altho still "CDC-neg."

Get thee to a LLMD and get tested by IGENEX.
 
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!

A LLMD is one who has treated Lyme disease and the co-infections which come with it for many years and has gotten patients well. A good one will follow Dr. B's Guidelines, the "gold standard" for Lyme treatment.

Here is a link for them:

http://www.lymenet.org/BurrGuide200810.pdf

Unfortunately, LLMDs are far and few between. You need to go where they are.

Also, most LLMDs do not take insurance due to the politics surrounding this disease. Read poster TF's explanation about this:

"Why Lyme Doctors Don't Take Insurance"
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=2;t=025539;p=0

When calling for an appointment, ask if they have any cancellations or a waiting list. Patients have been able to get in sooner 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):
http://whatislyme.com/websites-and-support-groups-by-state/

www.mlda.org

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

The top LLMD, Dr. H, has written a 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 https://www.viewster.com/movie/1193-15367-000/under-our-skin/

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.

[ 04-19-2016, 11:33 AM: Message edited by: hopingandpraying ]
 
Posted by kathiekg (Member # 47750) on :
 
could I get a MI referral also?
 
Posted by hopingandpraying (Member # 9256) on :
 
kathiekg - Welcome to Lymenet!

I know you are new to Lymenet, but you should write a new post instead of adding on to an existing one, so more people will see it and respond. Most don't re-read old posts.

PM sent for MI.
 
Posted by alemicham171 (Member # 47737) on :
 
Thank you very much for all of the information, I appreciate it!!
 
Posted by michlyme (Member # 17845) on :
 
http://www.lymenet.org/SupportGroups/UnitedStates/Michigan/MLDA.shtml
 


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