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 » Need LLMD in California

 - UBBFriend: Email this page to someone!    
Author Topic: Need LLMD in California
Isadora
Junior Member
Member # 51415

Icon 1 posted      Profile for Isadora     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have had various symptoms over last three years creep up but since August they are more consistent with flares.
I have had 5 falls that start with dizziness felt in my eyes with drunk like gait,.

My symptoms include: muscle twitching, double , blurry and loss of vision; headaches, stiff neck with pain and back of head pain; numbness, tingling and prickly sensations in hands, feet and legs accompanied by limb heaviness; nystagmus and hyperflexia with achy, painful joints causing disruptive sleep.

I’ve been diagnosed with mild neuro cognitive impairment, I forget how to do basic math and have short term memory problems. White hyperintensities have been found in brain.I had a tick embedded when I was 10, 30 Year’s ago.

MS and lupus seemed to be ruled out. I tested positive on Western Blot IgM 41 and 23 and IGenex IgM 18,
23-25, 34, 39 I, 41 and Western Blot IgG 30 and 41.

Not diagnosed by Kaiser or UHC. Outside MD prescribed Minocycline for one month. Symptoms decreased greatly.

Now off antibiotics. Symptoms back and worsening.

Thank you for any feedback.

Isadora

--------------------
I

Posts: 1 | From S. Califonia | Registered: May 2018  |  IP: Logged | Report this post to a Moderator
Bartenderbonnie
Frequent Contributor (1K+ posts)
Member # 49177

Icon 1 posted      Profile for Bartenderbonnie     Send New Private Message       Edit/Delete Post   Reply With Quote 
Welcome to Lyment Isadora

Yes, we can help you.

You can go to Global Lyme Alliance and request a LLMD here;

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

Watch the Lyme documentary " Under Our Skin" here ;

http://www.veoh.com/m/watch.php?v=v21055812yWtmpgB8

Read about why LLMD's don't accept insurance and other important information you NEED to learn about the medical maze you now find yourself in. Here ;

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

Get your finances in order, Lyme is expensive to treat.
Start a folder that contains everything medical, blood tests, all doctors visit, speciality tests, all medicines.
Start a journal to moniter all symptoms. This helps to track all reactions to different treatment protocols.
Expect a long chunk of time to get well. Atleast 1 year, probably longer. Patience is needed.

I will send you a private message. Good luck to you.

Posts: 2977 | From Florida | Registered: Nov 2016  |  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 
Hi - sending a private message -
Posts: 13116 | From San Francisco | Registered: May 2006  |  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.