This is topic Seeking LLMD in Michigan in forum Seeking a Doctor at LymeNet Flash.


To visit this topic, use this URL:
https://flash.lymenet.org/ubb/ultimatebb.php/topic/2/27836

Posted by Kamaji (Member # 50213) on :
 
Hello,

I am very new to Lyme. I have had what was diagnosed as NDPH, a specific type of constant headache, for over 6 years.

After looking for some treatment I have found NO relief. I found a Dr. who suggested Igenex testing for Lyme.

My B. burdorferi IFA - G/M/A was positive and by Igenex standards my Western Blot IgM was positive and IgG was indeterminate.

By CDC standards the Western Blots were negative. The Dr. says I have Lyme, but I don't feel as though I have many of the symptoms.

I'm looking for a second opinion, specifically an LLMD. If I have Lyme it would be late stage for sure and the local hospitals won't see my case based on the test results.

I would be willing to travel a bit if necessary. Anywhere in Michigan or northern Ohio or Indiana would be worth considering.

Any ideas appreciated!

[ 04-23-2017, 10:49 PM: Message edited by: Kamaji ]
 
Posted by hopingandpraying (Member # 9256) on :
 
Welcome to Lymenet! PM sent for MI, IN, & OH.

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/

Read the books written by the top LLMD, Dr. H, titled, "Why Can't I Get Better?" and his new one, "How Can I Get Better". They are 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 http://www.veoh.com/m/watch.php?v=v21055812yWtmpgB8

Btw - I know you are new to Lymenet, but 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.

To do this click the pencil/paper icon, make your changes, then click "Edit Post". Thanks.
 
Posted by Kamaji (Member # 50213) on :
 
Thank you so much!

I will look into those options.
 


Powered by UBB.classic™ 6.7.3