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 in Manhattan

 - UBBFriend: Email this page to someone!    
Author Topic: LLMD in Manhattan
marypart
LymeNet Contributor
Member # 27012

Icon 1 posted      Profile for marypart     Send New Private Message       Edit/Delete Post   Reply With Quote 
Please, can someone send me a list of LLMD in Manhattan or nearby? I have a friend with arthritic and neuro symptoms.

Thank you.
Mary

--------------------
Son, 26, Dx Lyme 4/10, Babs 8/10
Had serious arthritis, all gone.
Currently on Valtrex
Daughter, 26,bullseye 7/11
arthritis in knees, cured and off all meds. .
Self:Lyme, bart, sxs gone, no longer treating.

Posts: 496 | From Washington, DC | Registered: Jul 2010  |  IP: Logged | Report this post to a Moderator
Tincup
Honored Contributor (10K+ posts)
Member # 5829

Icon 1 posted      Profile for Tincup         Edit/Delete Post   Reply With Quote 
Mary part,

I am sharing below a large list of Lyme treating health care professionals names and contact info for you to consider.

Narrowing down your choices by contacting their offices and reading their websites in advance may help pick someone more in line with your friends needs.

Some take insurance and some charge MUCH less than others and it has nothing to do with their abilities.

If you go to www.MarylandLyme.org and look at the menu to your left you will see "DOCTOR REFERRALS".

Click there to find the site with the names and contact information for health care professionals treating Lyme & TBD's in your state (or any state). You may want to review options in states near-by also.

There is also a page with support group information, one for alternative medical professionals, educational conferences across the country, labs and their contact information, one for mental health providers, MTHFR and Morgellons providers.

There is also a list of TBD with how to diagnose (testing), a list of symptoms for each disease and treatment info with links to the treatment guidelines.

Here is a "Help For You" page that hopefully you can find some cost-saving tips to help them out.

https://sites.google.com/site/marylandlyme/help-for-you

Hope that helps in your search!

Good luck!

--------------------
www.TreatTheBite.com
www.DrJonesKids.org
www.MarylandLyme.org
www.LymeDoc.org

Posts: 20353 | From The Moon | Registered: Jun 2004  |  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 
PM sent with some names for CT. I don't know of any good ones in NYC.

When he/she calls for an appointment, have him/her ask if they have any cancellations or a waiting list. Patients have been able to get in sooner by doing this.

Also have him/her check the online state Lyme groups at:
https://groups.yahoo.com/neo/groups/NewYorkLyme/info

Maybe they can help. They would know better about NY.

Some more resources (including Support Groups info):
http://whatislyme.com/websites-and-support-groups-by-state/
www.empirestatelymediseaseassociation.org

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

Posts: 8981 | From Illinois | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
TF
Frequent Contributor (5K+ posts)
Member # 14183

Icon 1 posted      Profile for TF     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi, Mary. I remember you and your son's struggle with lyme.

I also don't know of any good lyme docs in NYC or nearby. So, be very careful about who you recommend to your friend.

I suggest you contact lots of lyme support groups in the area to find out who is getting people well. In general, the NYC lyme docs are VERY expensive. Don't want her to have a bad experience and spend a lot of money on it to boot.

Posts: 9931 | From Maryland | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
marypart
LymeNet Contributor
Member # 27012

Icon 1 posted      Profile for marypart     Send New Private Message       Edit/Delete Post   Reply With Quote 
Interesting.

I had already sent them a list sent to me for NY several years ago. I'm surprised that things have changed so much.

My son is in a complete 5 year remission and is a registered nurse working in cardiac critical care.

He's 26 now. Incredible. He was really sick as many know.

The person I am asking for will have no problems paying for expensive doctors, and having someone in Manhattan or nearby would be quite important. If someone knows anything please let me know.

What about Dr. H or Dr. R? Are they not treating Lyme anymore?

--------------------
Son, 26, Dx Lyme 4/10, Babs 8/10
Had serious arthritis, all gone.
Currently on Valtrex
Daughter, 26,bullseye 7/11
arthritis in knees, cured and off all meds. .
Self:Lyme, bart, sxs gone, no longer treating.

Posts: 496 | From Washington, DC | Registered: Jul 2010  |  IP: Logged | Report this post to a Moderator
TF
Frequent Contributor (5K+ posts)
Member # 14183

Icon 1 posted      Profile for TF     Send New Private Message       Edit/Delete Post   Reply With Quote 
Dr. H hasn't taken new patients in 3 years; he has a 2 year waiting list. And, he isn't in Manhattan anyway.

The news about your son is GREAT!!!! Maybe you would take the time to post it in the Success Stories thread. It would bless others to read it!

Here's the link to the thread:

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=3;t=015820;p=0

Posts: 9931 | From Maryland | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
marypart
LymeNet Contributor
Member # 27012

Icon 1 posted      Profile for marypart     Send New Private Message       Edit/Delete Post   Reply With Quote 
His story is on the third page. I wrote it 4 years ago.

--------------------
Son, 26, Dx Lyme 4/10, Babs 8/10
Had serious arthritis, all gone.
Currently on Valtrex
Daughter, 26,bullseye 7/11
arthritis in knees, cured and off all meds. .
Self:Lyme, bart, sxs gone, no longer treating.

Posts: 496 | From Washington, DC | Registered: Jul 2010  |  IP: Logged | Report this post to a Moderator
lymehope
Member
Member # 48581

Icon 1 posted      Profile for lymehope     Send New Private Message       Edit/Delete Post   Reply With Quote 
Your friend should NOT go to Dr. R in NYC.
He puts you on strong treatment but doesn't check your blood work during treatment. Which can be very dangerous.
They said you can communicate through emails, but it can take days if at all for him to respond. The office is also very bad.
As other members said, and from my experience there are no good doctors in NYC.

Posts: 68 | From new york | Registered: Aug 2016  |  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.