This is topic SEEKING Lyme Disease Literate Doctor (MD/DC/VA) who works with Workers Compensation in forum Seeking a Doctor at LymeNet Flash.


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Posted by huneekis (Member # 47468) on :
 
Hi all,

I am desperately seeking a lyme disease literate doctor in the md/dc/va. Particularly in southern maryland, annapolis, washington dc, and/or northern virginia. I cannot find a literate doctor (along with a co infection of bells palsy) who will take workers compensation. Most are saying self pay but I am hopeful someone out there can help us. Thanks!
 
Posted by me (Member # 45475) on :
 
Sending you PM
 
Posted by huneekis (Member # 47468) on :
 
thank you!
 
Posted by hopingandpraying (Member # 9256) on :
 
Welcome to Lymenet!

I don't know of any LLMDs who take Workers' Compensation.

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 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?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 to sooner by doing this.

Check the online state Lyme groups at:

https://groups.yahoo.com/neo/groups/MarylandLyme/info

Maybe they can help.

Some more resources (including Support Groups info):

www.lyme-aware.org/maryland.html

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

Here is a link found on Lymenet for "Financial Help and Other Information":

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=3;t=023463;p=0

The Lyme Disease United Coalition, (800) 311-7518, has good information for financial resources on their website:

http://www.lduc.org/lyme-disease-resources

Scroll down for financial help, etc., available from several sources.

Also call them to ask if they can recommend anyone to you.

The Lyme Test Access Program (Lyme-TAP) is a nationwide patient assistance program to provide assistance for initial Lyme-related lab tests to patients who demonstrate true financial need. I think coverage is up to 75%.
View on www.lymetap.com

"Help For You" link here...

https://sites.google.com/site/marylandlyme/help-for-you

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. Check the 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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