LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Seeking a Doctor » Looking for doctor on west coast

 - UBBFriend: Email this page to someone!    
Author Topic: Looking for doctor on west coast
johnny_broadway
Member
Member # 14854

Icon 1 posted      Profile for johnny_broadway   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi everyone. I'm looking for a good LLMD on the west coast. I've been to Dr. H in CA and Dr. K... In fact I've been seeing Dr. K for about 2 years and have seen little to no improvement.

Does anyone know of any other good LLMD's? I'm actually willing to travel anywhere if it means I can see some kind of improvement.

I don't have a lot of physical symptoms, mostly just psychological, like confusion, bad memory, anxiety, depression, not coordinated, mood swings, hard time comprehending, inability to focus, general inability to think, yada yada.

Thanks everyone in advance! [Smile]

Troy

Posts: 30 | From Las Vegas | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
http://www.turnthecorner.org/content/selection-proper-physicians

Turn the Corner Foundation - Find Lyme Literate Medical Help

=======================

From what I've read of his work, Dr. K certainly seems thorough in the various aspects of his suggested treatments and I'm not sure anyone else has the range of things he considers - but each doctor does have their own eyes, ears, brain and set of experiences . . . so it does make sense to get another opinion. You might consider someone here:

Excellent reputation in the Seattle area:

http://www.thehealingartspartnership.net/index.htm

========================

http://bastyrcenter.org/

Near Seattle, Bastyr Naturopathic University Clinic also may have interns educated about lyme. Even if not for primary care, they may work well for adjunct treatment.

One of the NDs in the previous link is (or was) a professor there.

======================

There are no LLMDs in Oregon as the IDSA is harshly against doctors in Oregon learning the facts about lyme and other tick-borne infections.

However, there are couple good ILADS-educated LL NDs (naturopathic doctors) who can be located through:

http://oregonlyme.org

OLDN: Oregon Lyme Disease Network

=======================

See their support group listings for LLMD and LL ND recommendations:

http://www.lymedisease.org/

California Lyme Disease Association (CALDA)
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
Have you been assessed for Cpn? HHV-6? XMRV / HGRV ? More here about those:

In addition to the usual coinfections from ticks (such as babesia, bartonella, ehrlichia, RMSF, etc.), there are some other chronic stealth infections that an excellent LLMD should know about:
----------

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=069911#000000

TIMACA posted 03 August, 2008

I would encourage EVERY person who has received a lyme diagnosis to get the following tests.

- at link.
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
http://flash.lymenet.org/scripts/ultimatebb.cgi/topic/2/13964?

Topic: How to find an ILADS-educated lyme literate (LL) professionals in these areas:

Naturopathic doctor (ND); Acupuncturist (L. Ac.), a doctor of Oriental Medicine (O.M.D.), or a doctor of Ayurvedic Medicine (D.Ay.), certified herbalists or nutritionists, . . .

. . . Holistic MDs, and also Doctors of Osteopath (DO) and Doctors of Chiropractic (DC), etc.

** You can compare many LLMDs and LL ND's articles and books - Includes many professional links, articles and books on complementary / integrative methods - & RIFE links -- all by LL authors.

Also included are basic links explaining the principles of herbal medicine.

BODY WORK considerations (geared to lyme patients) are discussed; with links.
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Robin123
Moderator
Member # 9197

Icon 1 posted      Profile for Robin123     Send New Private Message       Edit/Delete Post   Reply With Quote 
Pm'ing you -
Posts: 13171 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
johnny_broadway
Member
Member # 14854

Icon 1 posted      Profile for johnny_broadway   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Wow, thank you guys! You are awesome! I posted this last night and didn't expect to get so many responses so soon [Smile]

Keebler
-----------
quote:
Have you been assessed for Cpn? HHV-6? XMRV / HGRV ? More here about those:
I was tested for HHV-6 which I had in addition to Bart and Babs, but the other ones are new to me - I've never heard about them before! I was diagnosed with KPU as well but I've taken care of that for the most part I believe.

And not to get down on Dr. K; he's an excellent doctor, but for whatever reason I haven't had much improvement (??). Not really sure why. He has me on Mepron and Azithro which I heard is a good 1-2 punch at the Lyme and I think Babesia?

Posts: 30 | From Las Vegas | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
Oh, I perfectly understand your need to find a new doctor if you aren't making the kind of progress expected from your doctor's input and your hard work, etc.

As for KPU, that might need on-going attention but I'm more familiar with other kinds of porphyria which needs constant mindfulness but that really just becomes a way of life with good health habits of a specific nature.

You might want to take a look at this:
------------------------

http://flash.lymenet.org/scripts/ultimatebb.cgi/topic/1/91842?

PORPHYRIA

Includes links from GiGi, Dr. K, and others about KPU / HPU (mauve factor) . . .

& links from TerryK regarding METHYLATION issues
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
You might want to find a doctor who is familiar with this issue. Just a bit from my notes - but the information is a few years' old, so you'd want an update, for sure.
-----------------------

(HLA DR 14-5-52B)

* HLA-DR

I don't have details about HLA-DR and HLA-DQ but you will want to search that out.

Do a cross search of these terms at Google: HLA-DR "chronic neurotoxins"

One set of links from that search:

http://www.prohealth.com/library/showarticle.cfm?libid=8849

New Theory Links Neurotoxins with Chronic Fatigue Syndrome, Lyme, MCS and Other Mystery Illnesses - PART ONE

-by Patti Schmidt - November 29, 2002

http://www.immunesupport.com/library/showarticle.cfm/id/4291/searchtext/neurotoxins/

New Theory Links Neurotoxins with Chronic Fatigue Syndrome, Lyme, MCS and Other Mystery Illnesses - PART TWO'

-------------

http://sunshine35446.yuku.com/topic/2073/t/Dr-Shoemaker-and-tests.html

A bulletin board post explains a lot about these:

* MSH: (MSH is a hypothalamic neuroregulatory/cytokine regulatory/mucus membrane regulatory hormone.)
In short: MSH stands for "MELANOCYTE-STIMULATING HORMONE".

* MMP-9 is activated by cytokine effect

* PORPHYRINS

* The HLA DR by PCR is a typing of immune response genes, that can show individual susceptibility to particular neurotoxins.

Dr. S's tests can be ordered by your physician from Esoterix Labs. He must set up an account with them, you cannot do it: 



Esoterix Labs, Inc. 
7540 Louis Pasteur, Suite 200 
San Antonio, TX 78229-4008 
1-800-661-4118 


www.esoterix.com
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.