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  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Your experiences with New England LLMD's?

 - UBBFriend: Email this page to someone!    
Author Topic: Your experiences with New England LLMD's?
BostonLyme2005
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Hello,

Please tell me your experiences, (what has worked, what has not) with New England LLMD's.

MA, NH, CT, RI, VT, ME?

I would love to hear from you.

Thanks,

IP: Logged | Report this post to a Moderator
beachcomber
Frequent Contributor (1K+ posts)
Member # 5320

Icon 1 posted      Profile for beachcomber     Send New Private Message       Edit/Delete Post   Reply With Quote 
My MD in CT is great. I think he has used the cutting edge treatments for me and they seem to be working. Can't complain.
Posts: 1452 | Registered: Feb 2004  |  IP: Logged | Report this post to a Moderator
vitch
LymeNet Contributor
Member # 8094

Icon 1 posted      Profile for vitch     Send New Private Message       Edit/Delete Post   Reply With Quote 
CT LLMD and Boston LLMD were extremely kind and informative.

--------------------
[email protected]

www.lymediseaseassociation.org/Conflicts.doc

Worthless tests & labs, a dangerous vaccine, insurance companies refuse to pay, undertreatment the norm, all about money. MO.

Posts: 281 | From CT | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
humanbeing
LymeNet Contributor
Member # 8572

Icon 1 posted      Profile for humanbeing     Send New Private Message       Edit/Delete Post   Reply With Quote 
Haven't met an llmd I didn't adore. (BOth in CT...both different approaches and bedside manner both passionate about helping lyme pts.)

One does very aggrssive oral combos four weeks on two weeks off. He tests for all coinfections and watches symptoms for treatment changes. Extremely competent but not very warm and fuzzy.

The other has a one abx at a time strategy and thinks that length of therapy is more important than any other factor in getting rid of smptms. Watches for coinfections. Doesn't take breaks unless big herx.

Both don't recommend vitamins or other supps except acidophilus. Both are not big on IV.

Love them and wish there were hundreds more in our ignorant, lyme devastated state.

Best

--------------------
We are spiritual beings on a human journey...

www.ruggierogallery.com

Posts: 906 | From CT | Registered: Jan 2006  |  IP: Logged | Report this post to a Moderator
Christine202
LymeNet Contributor
Member # 6158

Icon 1 posted      Profile for Christine202     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've been to 5.... 1 in MA, 2 in CT, 2 in NY..

My current NY LLMD is my favorite... I feel this LLMD really looks at the individual and does not clump all Lymies into one catagory.... I didnt find that with the others.

Although he does not actually do alternative therapies he is agreeing and open to whatever else you want to do alternatively in conjunction with abx approach......

It works for me.

Posts: 437 | Registered: Sep 2004  |  IP: Logged | Report this post to a Moderator
sofy
LymeNet Contributor
Member # 5721

Icon 1 posted      Profile for sofy     Send New Private Message       Edit/Delete Post   Reply With Quote 
All posters:

I wish you would use initials and states so we might be able to guess who the doc is your talking about without pm,ing all of you.

Im not ready to change just yet but always keeping my eyes and ears open to the possibility. I dont know what will happen tomorrow.

Posts: 561 | From connecticut | Registered: May 2004  |  IP: Logged | Report this post to a Moderator
BostonLyme2005
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Good answers from good people. No one knows what tomorrow brings, hopefully a cure for Lyme Disease and its co-infects.
IP: Logged | Report this post to a Moderator
kelmo
Frequent Contributor (1K+ posts)
Member # 8797

Icon 1 posted      Profile for kelmo     Send New Private Message       Edit/Delete Post   Reply With Quote 
It was good to hear your answers. I know we are on the right track. There are very few options in AZ, but we have an LLMD who attends all the conferences with your docs on the east coast, and has his own lab.

Our doc pulled me aside while my daughter was getting dressed and said, "this is going to take a while, but don't lose hope, I have a lot of tricks up my sleeve". Hope. We were just running out of that!

His initials are Dr. F in AZ. Gentle, intelligent, but doesn't talk down. Spends as much time as his office manager will allow (she actually has an alarm go off when it's time to move to a new patient). I'm so impressed, and sounds like you are, too.

Kelly

Posts: 2903 | From AZ | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
BostonLyme2005
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Thanks,

Its nice to hear from Lymies who are in your area when you are considering options for your recovery....

I laugh at healthy people when they say they are tired!

IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  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.