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 » Dr V says hypochondria instead of lyme-vexed

 - UBBFriend: Email this page to someone!    
Author Topic: Dr V says hypochondria instead of lyme-vexed
adamm
Unregistered


Icon 5 posted            Edit/Delete Post   Reply With Quote 
I just had a phone conversation with Dr V. in which she said

that, given my past history of hypochondria and the facts that the

tick that bit me was a wood tick and was never actually

embedded,

she does not beleive that my symptoms are from a TBI. These

symptoms include the constant presence of floaters, petechia on

arms, an almost unremitting headache with concomitant

cognitive

impairment, periods

during which I become very dizzy upon shifting my gaze, and an

increase in crepidation (sp?). She told me that if I was worried

about Babs, I could definitively ascertain whether or not I have it

by taking some test for hemoglobin in the urine.


So...what do you guys think?

She WILL still see me, but my first appointment with her won't until December. I have an

appointment scheduled with Dr. M much sooner, but I have

heard better things about her. What would you advise doing (and

what is the name of and how reliable is this test) ? Please PM your responses.

Oh, and one more thing: I find the tick that bit me immediately

after showering, and when I removed it, there was a small bump

where it had been. Is it possible that, while being sprayed with the

water, it could have gone into some sort of distress and

vomitted pathogenic microbes into me?


sigh...
I simply do not see how, without physically examining me, she

could acquire a valid basis from which to draw her conclusion.


Thanks all,

Adam

[ 30. August 2007, 07:58 PM: Message edited by: adamm ]

IP: Logged | Report this post to a Moderator
sixgoofykids
Moderator
Member # 11141

Icon 1 posted      Profile for sixgoofykids   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Is she an LLMD? I would get to an LLMD!! I was diagnosed as having Somatization Disorder ... my LLMD was the first doctor who believed me.

A true LLMD knows that many people never see the tick ... you didn't necessarily contract Lyme from that particular tick.

--------------------
sixgoofykids.blogspot.com

Posts: 13449 | From Ohio | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
adamm
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Yep, she's an LLMD (one of the most highly regarded, from what

I've gathered on the boards.)

IP: Logged | Report this post to a Moderator
sixgoofykids
Moderator
Member # 11141

Icon 1 posted      Profile for sixgoofykids   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Wow, that seems very odd. I'm glad my LLMD did not base his diagnosis on a phone call and my previous diagnosis of Somatization Disorder!!

I'd see someone else.

--------------------
sixgoofykids.blogspot.com

Posts: 13449 | From Ohio | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
RoadRunner
Frequent Contributor (1K+ posts)
Member # 380

Icon 6 posted      Profile for RoadRunner     Send New Private Message       Edit/Delete Post   Reply With Quote 
run from this doc and find a better one....

crazy over the phone.

RR

--------------------
"Beep Beep"

Posts: 2630 | From ct | Registered: Nov 2000  |  IP: Logged | Report this post to a Moderator
lymeladyinNY
Frequent Contributor (1K+ posts)
Member # 10235

Icon 1 posted      Profile for lymeladyinNY     Send New Private Message       Edit/Delete Post   Reply With Quote 
She can't come up with a valid conclusion about you over the phone.

She already has a preconceived notion about you.

I'd see someone else, no matter how "good" a Lyme doctor she is.

And the babs test would not accurately tell you if you have babs. I had a negative babs test right at the time my babs was raging.

I'm sorry this has happened to you. [Frown]

--------------------
I want to be free

Posts: 1170 | From Endicott, NY | Registered: Sep 2006  |  IP: Logged | Report this post to a Moderator
TerryK
Frequent Contributor (5K+ posts)
Member # 8552

Icon 1 posted      Profile for TerryK     Send New Private Message       Edit/Delete Post   Reply With Quote 
Is she a member of ILADS? The whole "it's all in your head" with just a phone conversation is not the quality of care that I would expect from an LLMD.

Her remarks about babs concerns me. I do not believe that one must have blood in their urine in order to have babs. If that were true, that's all any of us would have needed for testing and many on this board have had clinical diagnosis for babs, been treated and had great improvement.

I'm no expert on the wood tick but I think it is possible that the wood tick DOES carry lyme and we know that it does carry other disease so it's not impossible to think that it may have carried some sort of infection.

http://www.canlyme.com/ticks.html
Rocky Mountain Wood Tick (click on photo) Dermacentor Andersoni.
This and Dermacentor Variabilis as shown below have been shown to carry lyme but it is still under study as to their ability to pass it on through a bite3. It is 'theorized' that by scratching at an attached wood tick or dog tick (seen below), or by removing it with fingers you may force bacteria into your skin that otherwise would not be transmitted. Click here for proper removal methods

http://findarticles.com/p/articles/mi_m3225/is_12_71/ai_n14730369/pg_7

Sorry you are having a tough time. Don't accept the diagnosis of hypochondria. Personally, I don't believe in hypochondria. It is a convenient label that is used when the doctor can't or won't go to the trouble of finding an answer.

Terry

Posts: 6286 | From Oregon | Registered: Jan 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 
Forget it! Find another dr!

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

Posts: 96223 | From Texas | Registered: Feb 2001  |  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 
quote:
Originally posted by TerryK:
Don't accept the diagnosis of hypochondria. Personally, I don't believe in hypochondria. It is a convenient label that is used when the doctor can't or won't go to the trouble of finding an answer.

ditto to that!!

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

Posts: 96223 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
Michelle M
Frequent Contributor (1K+ posts)
Member # 7200

Icon 1 posted      Profile for Michelle M   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by adamm:
[QB] She told me that if I was worried

about Babs, I could definitively ascertain whether or not I have it

by taking some test for hemoglobin in the urine.


So...what do you guys think?

That is complete hooey.

You'd need to do an antibody titer test, and/or a detailed analysis of a peripheral blood smear -- rarely done anymore. Even then, it's difficult to find -- many strains exist and only two are tested for.

This really does NOT sound like an ILADS doctor.

If you threw out everyone on this forum with a previous diagnosis of "hypochondria," "conversion disorder," "malingering," or "affective disorder," it would be pretty lonely.

True LLMD's hear this all the time and read this frequently in their new patients' medical records, and it rarely raises an eyebrow.

Find someone else. Please!

Michelle

Posts: 3193 | From Northern California | Registered: Apr 2005  |  IP: Logged | Report this post to a Moderator
adamm
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Thanks you guys! I'll keep my appt. with Dr. M in wisc.

(BTW, any further comments on him would be greatly appreciated!_

IP: Logged | Report this post to a Moderator
robi
Frequent Contributor (1K+ posts)
Member # 5547

Icon 1 posted      Profile for robi     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have been around Lymenet for 4 years or so. Never heard of a Dr. V... anyone else? Not that I know all the LLMD's but who told you about her?????


You said: "Yep, she's an LLMD (one of the most highly regarded, from what I've gathered on the boards.) " What boards exactly?


robi

--------------------
Now, since I put reality on the back burner, my days are jam-packed and fun-filled. ..........lily tomlin as 'trudy'

Posts: 2503 | From here | Registered: Apr 2004  |  IP: Logged | Report this post to a Moderator
minimonkey
LymeNet Contributor
Member # 8693

Icon 1 posted      Profile for minimonkey     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've never heard of a Dr.V, either -- but I definitely wouldn't see anyone who was swayed by a previous diagnosis of hypochondria, or even hinted that she thought I was not truly ill --- in the 18 years I spent searching for a diagnosis, I've had every form of psychiatric label thrown at me, and then some... turns out, I'm CDC positive for Lyme, and also positive for mycoplasma fermentens. In my head? Not quite...

Babesia is hard to detect, even with sophisticated testing techniques. Hemoglobin in the urine??? That's one I haven't heard before...

--------------------
"Looks like freedom but it feels like death..
It's something in between, I guess"

Leonard Cohen, from the song "Closing Time"

Posts: 822 | From California | Registered: Jan 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 
robi....clear out your PM box!! [Smile]

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

Posts: 96223 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
Boomerang
Frequent Contributor (1K+ posts)
Member # 7979

Icon 1 posted      Profile for Boomerang     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'd get a second opinion!
Posts: 1366 | From Southeast | Registered: Sep 2005  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 10 posted            Edit/Delete Post   Reply With Quote 
Dr. V is who I went to last year. you can read below for more info.

never heard anything about adam is discussing above!!


Bettyg's 4-20-06 new LLMD in Minn. Office visit summary, complete BODY lab results of 15-18 labs nationwide, all info the lab sent back about specific high/low testing, $$ costs involved, and what each test specifically involved what ... VERY DETAILED!

I did this for other newbies who had NEVER had complete body testing like I did! Hoped it would give them guidance what they entail, how costly if OUT OF POCKET PAID like my $ 4300, and which specific labs nationwide are the best for these SPECIFIC lab work.


http://flash.lymenet.org/ubb/ultimatebb.php?ubb=get_topic;f=1;t=043234;p=1

IP: Logged | Report this post to a Moderator
AliG
Frequent Contributor (1K+ posts)
Member # 9734

Icon 1 posted      Profile for AliG     Send New Private Message       Edit/Delete Post   Reply With Quote 
Has anyone here ever actually had a telephone conversation with an LLMD prior to first visit?

I just can't imagine a truly LL-MD actually getting into a detailed assessment of a possible new patient over the phone.

Not to mention, not charging a fee for a specialist opinion? Maybe it's not the same Dr.V?

Seems really strange.
[confused]

--------------------
Note: I'm NOT a medical professional. The information I share is from my own personal research and experience. Please do not construe anything I share as medical advice, which should only be obtained from a licensed medical practitioner.

Posts: 4881 | From Middlesex County, NJ | Registered: Jul 2006  |  IP: Logged | Report this post to a Moderator
cactus
Frequent Contributor (1K+ posts)
Member # 7347

Icon 1 posted      Profile for cactus     Send New Private Message       Edit/Delete Post   Reply With Quote 
Adamm, glad you're keeping that appt with another LLMD.

The bite of a wood tick can carry a lot of infections, and a wood tick bite made me extremely ill although I can't pinpoint exactly which infection came from which tick (I've had hundredsd over the years).

I can't imagine an LLMD getting into a detailed assessment with a patient over the phone (prior to an appt) either.

I did, however, speak to my LLMD by phone prior to my first appt - but I had pos test results and a non-LL NP who was willing to work with LLMD while I waited for the appt.

Different circumstances, because LLMD had received calls from both of NP and me asking her to work in conjunction with NP while I was on the wait list.

Adamm, hang in there till your next appt!

--------------------
�Did you ever stop to think, and forget to start again?� - A.A. Milne

Posts: 1987 | From No. VA | Registered: May 2005  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 5 posted            Edit/Delete Post   Reply With Quote 
adam,

this really puzzles me as i never talked to her prior.

how much did she charge you for consult call?
--------------------------------------------

what city is she located in?

IP: Logged | Report this post to a Moderator
Hiawatha922
Member
Member # 10796

Icon 1 posted      Profile for Hiawatha922     Send New Private Message       Edit/Delete Post   Reply With Quote 
I also see a Dr. V in Minnesota (LLMD). I have found her to be very thorough. Telephone assessment? This sounds very strange.
Posts: 83 | From Minnesota | Registered: Dec 2006  |  IP: Logged | Report this post to a Moderator
Anneke
LymeNet Contributor
Member # 7939

Icon 1 posted      Profile for Anneke     Send New Private Message       Edit/Delete Post   Reply With Quote 
Adam,

There is always a possibility that our self-diagnose is based on fear and not fact.

Only you know your history - past and present. If you know that self-diagnose and huge fear issues around illness have been a pattern for you, it may help to talk to a professional about it.

Knowing all that I do know now - if I were not disabled, if my symptoms were very, very minimal and not growing - I would not go into Lyme treatment. It is not something to take lightly.

Another thing to keep in mind for all of us is that sometimes the primary issue really is depression. Depression is a horrible illness in and of itself. Depression alone can cause obsessive thoughts and fears re: illness issues, and it can actually cause various physical symptoms, including chronic pain and headaches, appetite changes, weight loss or gain, and severe fatigue.

It may be wise to see a psychiatrist to rule out depression as an illness. Thank God if that alone ends up being your issue - though depression alone is horrible.

Best wishes.

Posts: 364 | From California | Registered: Sep 2005  |  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.