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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » LLMD needed! Location is not important!

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Author Topic: LLMD needed! Location is not important!
stefi42
LymeNet Contributor
Member # 48591

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Hello,

I was recently diagnosed with lyme disease after having it for over a year. My health has been quite a struggle. I had brain surgery in September of 2016. During my recovery period I began to feel worse. No one was sure what it could be.

Ive been laughed at, told I was an idiot, completely dismissed, and passed of from neurologist to endocrinologist, and then back again. Finally I have a diagnosis.

The only problem is finding an LLMD. I love in florida but traveling isn't a problem for me, as I fly for free. The only thing would be doctors who accept insurance.

If anyone can please send me a list of doctors, I would be more than grateful. Location isn't important. If the doctor doesn't accept insurance, thats okay. I'll figure something out. I just want to feel better again.

Thank you so much!

...........................................

(breaking up a paragraph for easier reading for many here)

[ 08-20-2016, 05:25 PM: Message edited by: Robin123 ]

Posts: 113 | From Hollywood, Florida | Registered: Aug 2016  |  IP: Logged | Report this post to a Moderator
TF
Frequent Contributor (5K+ posts)
Member # 14183

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Welcome to LymeNet! We will help you here all we can.

I sent you the name of a good lyme doctor and lots of information on him.

I don't send a list of names. I send the name of the best doc in the east that I know of who is currently taking new patients without much of a wait.

So glad you found us!

Posts: 9931 | From Maryland | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
hopingandpraying
Frequent Contributor (5K+ posts)
Member # 9256

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Welcome to Lymenet! PM sent for FL & MD.

I am so sorry you have experienced such terrible treatment. Unfortunately, you are not alone, because many have gone through the same!

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

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

Maybe they can help.

Some more resources (including Support Groups):
http://whatislyme.com/websites-and-support-groups-by-state/

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

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 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. Thanks.

Posts: 8981 | From Illinois | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
   

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