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 » General Support » Some doctors doubt whether Lyme disease exists

 - UBBFriend: Email this page to someone!    
Author Topic: Some doctors doubt whether Lyme disease exists
RDaywillcome
Frequent Contributor (1K+ posts)
Member # 21454

Icon 1 posted      Profile for RDaywillcome     Send New Private Message       Edit/Delete Post   Reply With Quote 
http://www.wwlp.com/dpp/news/massachusetts/some-doctors-doubt-whether-lyme-disease-exists
Posts: 1738 | From over the rainbow | Registered: Jul 2009  |  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 
Unbelievable, isn't it!?

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

Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
RDaywillcome
Frequent Contributor (1K+ posts)
Member # 21454

Icon 1 posted      Profile for RDaywillcome     Send New Private Message       Edit/Delete Post   Reply With Quote 
It is but with all that we've all been through, I doubt any of us are surprised.

I don't know what it's going to take for ego trippers to start thinking outside the box and listen to their patients some of our top authorities on lyme disease have to offer.

Posts: 1738 | From over the rainbow | Registered: Jul 2009  |  IP: Logged | Report this post to a Moderator
poppy
Frequent Contributor (1K+ posts)
Member # 5355

Icon 1 posted      Profile for poppy     Send New Private Message       Edit/Delete Post   Reply With Quote 
Some patients wonder why these doctors were ever allowed to practice medicine.

Maybe they also don't "believe" in TB, or AIDS, or any other infectious disease.

Posts: 2888 | From USA | Registered: Mar 2004  |  IP: Logged | Report this post to a Moderator
signs9
Member
Member # 37116

Icon 1 posted      Profile for signs9     Send New Private Message       Edit/Delete Post   Reply With Quote 
My husband was seen last month by a neurologist at the Hospital of the University of Pennsylvania. We had the experience of this Harvard educated MD actually laugh at us sarcastically and say that she didn't believe in chronic Lyme disease. She claimed that the Lyme bacteria were, "weak and could easily be removed with 2-3 weeks of oral antibiotics". ....OK

She never did diagnose my husband who has a lot of neuro symptoms but did insisted that he probably had something that could be helped with steroids. My husband refused to consider them and this brilliant MD couldn't understand why.

We didn't go back.

Posts: 34 | From Bucks County, Pa | Registered: Apr 2012  |  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 
Some patients wonder whether real doctors exist.

At least I felt that way until I found my LLMD.

I was at a meeting this past weekend with several doctors, who remarked about their humility in the face of medical diversity and the unknown. It was very refreshing to hear, like some honesty for a change...

Posts: 13171 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
tickled1
Frequent Contributor (1K+ posts)
Member # 14257

Icon 1 posted      Profile for tickled1     Send New Private Message       Edit/Delete Post   Reply With Quote 
That is refreshing to hear Robin. My child's pediatrician once said to me after I told her of my struggles that it's possible I could have something that hasn't yet been identified. I'd prefer to hear something like that than "nothing is wrong with you".
Posts: 2541 | From Northeast | Registered: Jan 2008  |  IP: Logged | Report this post to a Moderator
Catgirl
Frequent Contributor (5K+ posts)
Member # 31149

Icon 1 posted      Profile for Catgirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have to say, I lost all faith in the medical community until I found a great LLMD. The man is brilliant, kind, and compassionate. Even his staff is awesome.

I've had a lot of doctors in my life time (middle aged) and moved all over the country. The worst docs I've ever had are here in MA. It blows my mind. They are so closed minded!

I have never had docs (pre lyme) treat me as if I was making up my symptoms before. Maybe they are just getting so many patients with lots of little complaints (lyme) that they think we're all a bunch of hypochondriacs.

One tick lays 2000 eggs. Once they get out of the office, they'll get it (or a family member). It's just going to take some time. What goes around comes around...

--------------------
--Keep an open mind about everything. Also, remember to visit ACTIVISM (we can change things together).

Posts: 5418 | From earth | Registered: Mar 2011  |  IP: Logged | Report this post to a Moderator
poppy
Frequent Contributor (1K+ posts)
Member # 5355

Icon 1 posted      Profile for poppy     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sorry to say, catgirl, that has already happened. When the bad guys or their families get lyme, they get treated right and they keep quiet about it. So, you see, they don't even use their own guidelines when they care about the patients. And that is not very many people. Did you think that having lied about us, they would get honest when faced with it closer to home? Nope. They are all around liars.
Posts: 2888 | From USA | Registered: Mar 2004  |  IP: Logged | Report this post to a Moderator
Catgirl
Frequent Contributor (5K+ posts)
Member # 31149

Icon 1 posted      Profile for Catgirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
Not everyone finds the bite though. Sometimes it's on the head. I'm hoping they get it in the winter time and think it's just the flu. Whoops, my evil twin is coming out (ha ha)!

--------------------
--Keep an open mind about everything. Also, remember to visit ACTIVISM (we can change things together).

Posts: 5418 | From earth | Registered: Mar 2011  |  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.