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 » Best Lyme Doctors US?

 - UBBFriend: Email this page to someone!    
Author Topic: Best Lyme Doctors US?
stiffyoungman
Member
Member # 40067

Icon 1 posted      Profile for stiffyoungman     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hello all. I'll post the question first so that its the TLDR version and anybody wanting backstory can read further.

Essentially I'm wondering some names and locations of what could be considered a top10 list of LLMDs in the US. And Drs that can actually be seen by patients that is. I know Dr. H is basically impossible to see, and Burascanno and others don't see patients anymore.

I know some people on here have been involved in this community for years beyond years and can help with this.

Non-TLDR version

I am in Florida. The only legit LLMD I could find info about was Dr. C in Tampa. I was mid treatment with him and he retired out of the blue due to health concerns.

I couldnt find another LLMD in Florida and at the time felt I was on the right path and thought I could continue fighting with only herbs. (Mostly Zhang protocol but not ordered via Zhang)

I believe I am relapsing rather quickly lately and heading in the wrong direction and going to be in CA. I posted on this forum about Socal doctors and bumped the thread multiple times and only one user seems to respond to requests about Socal. They are insanely helpful the issue is when I look into these doctors, as expected, the comments found on the net are INSANELY back and forth. SO its hard for me to accept just what one person has heard on here-say cause clearly this one forum-user has not been to all of these Drs. Therefor I wanted more people who had been in-the-know of Doctors in Socal or near, so that I could see which doctors are consistently being mentioned as good around here. That didn't seem to be possible.

I want to be confident when I go to this next doctor that he/she is very good and among the best. I feel that is important for my mental state/health during this whole thing.

Depending on what I can find about these "best lyme doctors" im asking about, and if I keep hearing the same names from multiple knowledgeable people on here, and depending on where it is, I luckily have a job that allows me to travel and I have friends in many cities that I could potentially find something out of state.

Posts: 52 | From USA | Registered: Feb 2013  |  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 - you could contact support groups in the areas you're considering for some feedback about the doctors, since S CA folks would be going to them!

Support groups are listed at the left - click on United States, California

We have several "bests" in the state, if you want to discuss with me again.

Posts: 13116 | From San Francisco | Registered: May 2006  |  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 
Sadly, most LN members do not come to Seeking a Doctor very often. Even a similar thread in Medical a few weeks ago elicited few responses on who the best LLMD's are.

Florida is in a bind with few LLMD's . . always has been that way.

If you need more names for FL, I do have some.

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

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
stiffyoungman
Member
Member # 40067

Icon 1 posted      Profile for stiffyoungman     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm going to be in CA most likely. But like I said, considering traveling if I feel more comfortable with another DR
Posts: 52 | From USA | Registered: Feb 2013  |  IP: Logged | Report this post to a Moderator
hopingandpraying
Frequent Contributor (5K+ posts)
Member # 9256

Icon 1 posted      Profile for hopingandpraying     Send New Private Message       Edit/Delete Post   Reply With Quote 
I think you need to get to a LLMD sooner than later, because you wrote you are rapidly relapsing. You have received a lot of good information. Poster "Robin123" is the one who is very knowledgeable about CA.

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

Some more resources for you (including Support Group info):
www.lyme-aware.org/california.html

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

When you get the name of a LLMD, write a new post in "Seeking a Doctor" and title it "Need Feedback on Dr. _ (last name initial only) in CA (no cities allowed, per Lymenet rules). You can do the same for any LLMD in any state.

Posts: 8981 | From Illinois | 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.