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 » LLMD near Pasadena or Los Angeles, CA

 - UBBFriend: Email this page to someone!    
Author Topic: LLMD near Pasadena or Los Angeles, CA
SkeptikSharon
Junior Member
Member # 17230

Icon 1 posted      Profile for SkeptikSharon     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have been diagnosed with Fibromyalgia, but a lot of the symptoms I experience seem to possibly be along the lines of Lyme Disease. I am looking for a good LLMD in the Pasadena or Los Angeles area (or anywhere else in Southern California, if the doc is good) that can evaluate me for this. Thank you!
Posts: 1 | From Monrovia, CA | Registered: Sep 2008  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 10 posted            Edit/Delete Post   Reply With Quote 
welcome sharon; glad you found us.


suggest you get a western blot igm and igg blood test drawn and have sent to IGENEX, CALIF. lab. read all about it in my detailed instructions below. start reading page 54 ok! takes 3 wks. for results.


sending you LA names; check your profile for them.

make appt. now...some take months to get in. you can always CANCEL!!


Welcome; i'm so glad you found us!! You've come to the right place for education and support!

Fyi: we have over 1000 viewers daily; 200 - 400 posting/replying; so specific titles get our time/replies. non-specific ones, i sob, scroll on by!

Also, please be very specific in the subject line what you will be discussing so more people will be able to assist you.


Dr. Burrascano's most recent "Diagnostic Hints and Treatment Guidelines for Lyme and Other Tick Borne Illnesses" @
http://www.ilads.org/burrascano_0905.html
suggests that you discuss with your doctor continuing treatment until you are symptom free for 2 months.


this link, making the most of your LLMD visit, may help you also.
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic&f=1&t=020605#000005


please see BettyG's newbie package info on the link below; click on link at bottom of my package. Check it out as time permits for you!
@ http://tinyurl.com/58eyou

IP: Logged | Report this post to a Moderator
Peedie
LymeNet Contributor
Member # 15355

Icon 6 posted      Profile for Peedie     Send New Private Message       Edit/Delete Post   Reply With Quote 
I PM'd you.
Good Luck

Posts: 641 | From So. CA | Registered: May 2008  |  IP: Logged | Report this post to a Moderator
ING2008
Junior Member
Member # 17244

Icon 1 posted      Profile for ING2008     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am looking for a good LLMD in the Pasadena or Los Angeles area too.Could you refer me to a good one.Thanks
Posts: 8 | From LA.CA | Registered: Sep 2008  |  IP: Logged | Report this post to a Moderator
Peedie
LymeNet Contributor
Member # 15355

Icon 6 posted      Profile for Peedie     Send New Private Message       Edit/Delete Post   Reply With Quote 
ING2008
I PM'd you.
Best wishes,
Peedie

Posts: 641 | From So. CA | Registered: May 2008  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Read my fibromyalgia story below!

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96239 | From Texas | Registered: Feb 2001  |  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.