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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » Seeking LLMD in WI, Seeking Neurologist in WI

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Author Topic: Seeking LLMD in WI, Seeking Neurologist in WI
lookingforanswers11111
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Hello,

Looking for LLMD in WI please asap
Also looking for neurologist in WI please asap

Thank you.

--------------------
lookingforanswers11111

Posts: 1 | From US | Registered: Jun 2019  |  IP: Logged | Report this post to a Moderator
Bartenderbonnie
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Welcome to Lymenet lookingforanswers11111

We can help you.

You can request a LLMD through ILADS here;

https://www.ilads.org/patient-care/provider-search/

You can request a LLMD through Global Lyme Alliance here;

https://globallymealliance.org/education-awareness/find-medical-professional/

These are simple e-mail applications you fill out. There is a message box where you can write you are seeking a LLMD Neurologist.

Many LLMD"s don't participate with insurances, here's why;

http://flash.lymenet.org/scripts/ultimatebb.cgi/topic/2/25539?

Its important to get your finances in order, as your 1st initial visit can be costly. Start a folder and include in it all your medical records. Blood work, test results, procedures done with results, providers seen, diagnosises, daily symptom chart.

Also be sure to write down EVERYTHING your LLMD tells you, many of us have cognitive difficulties and have short term memory loss.

Any questions you may have along your wellness journey will be answered if you post questions in open forum. Be sure to utilize Lymenet's 'search' function. Such valuable information on all Tick Borne and Vector Borne infections in one website.

Healing wishes. You can do this!!!

I will send you a private message.

Posts: 1724 | From Florida | Registered: Nov 2016  |  IP: Logged | Report this post to a Moderator
hopingandpraying
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Welcome to Lymenet! PM sent for WI.

I don't know of any neurologists, but contact the WI Lyme Support Groups whose info I'm including below.

You need to be evaluated and treated by a 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 you call for an appointment, ask if they have any cancellations or a waiting list. Patients have been able to get in earlier by doing this.

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

Maybe they can help. They would know better about WI.

Some more resources for you:

http://wisconsinlymenetwork.org/patients/wisconsin-support-groups

https://www.facebook.com/Wisconsin-Lyme-Network_408459622540767/

http://whatislyme.com/lyme-in-wisconsin/

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

Read the books written by the top LLMD, Dr. H, titled, "Why Can't I Get Better?" and "How Can I Get Better?". They are an excellent source of information.

Also read "Cure Unknown" by Pamela Weintraub. View "Under Our Skin" and "Under Our Skin 2: Emergence" DVDs. Check your local library or buy them used online.

Posts: 8494 | From Illinois | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
   

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