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 » Searching for LLMD in NY State

 - UBBFriend: Email this page to someone!    
Author Topic: Searching for LLMD in NY State
Kerry23
Member
Member # 28383

Icon 1 posted      Profile for Kerry23     Send New Private Message       Edit/Delete Post   Reply With Quote 
I need to find a LLMD in NY. Can someone email me or PM me but I don't know how to use this site yet. I am new: today, but would like to tell you all, my 22 year old son has lyme and was treated a year ago with 3 weeks of Doxy and he has gone downhill ever since. I am not even going to talk about me yet. Anyway, we went to an infectious disease specialist where we live around Middletown, NY and she claims there is no such thing as chronic lyme or post lyme. All his tests came back negative and sent us on our way. To nowhere, to no answers, to back to square one, to hear my son complain everyday of pain in joints, muscles, brain fog, memory loss, depression ect. You all know the deal. He has Medicaid which isn't helping either, most of these "specialists" won't except Medicaid. I might be able to convince PCP to put him on medication again, but somebody better tell me what kind, how much and for how long. We know he has the co infection which was never treated: The babiosis (spelling), why didn't they treat him with Mepron for that?
I am so lost....the movie "Under our Skin" was downright frightening!!
Thanks for listening

--------------------
30 Supplements
Awaiting new protocol
Diagnosed 2nd time 9/08/2011
with positive western blot
No co infection

Posts: 74 | From Pine Island, NY | Registered: Sep 2010  |  IP: Logged | Report this post to a Moderator
MidnightMoon
Member
Member # 26717

Icon 1 posted      Profile for MidnightMoon     Send New Private Message       Edit/Delete Post   Reply With Quote 
Pm sent. good luck

--------------------
The closer you get to G-D The closer He'll get to you.

Be who you are, and say what you feel...the people who matter don't mind...and the people who mind , don't matter.

Posts: 98 | From In the woods by a stream in beautiful Catskills NY | Registered: Jun 2010  |  IP: Logged | Report this post to a Moderator
littlebit27
Frequent Contributor (1K+ posts)
Member # 24477

Icon 1 posted      Profile for littlebit27   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sent you a Pm.

--------------------
*Brittany Lyme Aware on FB*
http://littlebithaslyme.wordpress.com/

Posts: 2310 | From Southeast | Registered: Feb 2010  |  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.