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 » Activism » LymeMD in Maryland needs help

 - UBBFriend: Email this page to someone!    
Author Topic: LymeMD in Maryland needs help
radfaraf
LymeNet Contributor
Member # 11909

Icon 1 posted      Profile for radfaraf         Edit/Delete Post   Reply With Quote 
http://lymemd.blogspot.com/2009/02/please-read-this-it-may-be-my-last-post.html

Tuesday, February 3, 2009
PLEASE READ THIS- IT MAY BE MY LAST POST
This should be my last entry.

My lawyer has advised me to stop treating all Lyme patients.

He has advised me to send all my Lyme patients "somewhere else." Just where that is he doesn't say. The fact that there is virtually no one to send them to- underlines the point that I am the outlier- the target.

I have been under active investigation by the Maryland State Medical Board for over 18 months.

Five patient charts were subpoenaed based on a complaint filed by an infectious disease-IDSA doctor.

The cases have been sent to peer review. That means that 3 IDSA doctors will be passing judgment about my care of patients. In Maryland, Johns Hopkins is the final arbiter: They say there is no chronic Lyme disease. I will be evaluated to see if I am within the standard of care. The mainstream/IDSA sets the standard. Period.

I will loose. Bank on it.

My medical license may be suspended or I will be instructed not to treat Lyme
disease. Then I can take my case to court. I need political pressure to help in this fight.

I will end up in legal battle which will cost more than $100,000, which I do not have. This apparently will be the first case of its kind in Maryland. My colleagues who charge up to $3000 up front are in a financial position to fight this fight. I treat many patients for free or practically nothing.

If I am going to have a chance to win the inevitable court battle I need your help.

Please contact the Maryland General Assembly- you can get info on line.
Write/call your local congressman. Write call/fax the Senate President Thomas Miller, Jr 410-841-3700, 301 585 3700 and the speaker of the House Michael Bush 410 841 3800, 310 858 3800.

If I do not get support from my patients/readers- I will have to "go away."

The only issue is: Can I prescribe long term antibiotics for Lyme disease. That is all.

Thank you for your attention.
Posted by Lyme report: Montgomery County, MD at 9:18 AM

Posts: 526 | From NJ | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
lou
Frequent Contributor (5K+ posts)
Member # 81

Icon 1 posted      Profile for lou     Send New Private Message       Edit/Delete Post   Reply With Quote 
We need an organized response on this or he will end up like Dr. Jones, being dragged into hearings for trumped up cases.

I am trying to find out what the best procedure will be.

Hoping everyone will pitch in, before it gets to the stage of having to raise $100K for defense.

Posts: 8430 | From Not available | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
up; lou, contact wisc. mike, i;ll pm you his home email addy!

they had a successful campaign there on dr. h and NOTHING was done on him!!!

IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
please show ALL REPLIES and suggestions about this situation in medical on CD 57'S POST where all the replies are going so we don't repeat ourselves and miss important suggestions.


thanks all .... bettyg


http://flash.lymenet.org/ubb/ultimatebb.php/topic/1/77067

IP: Logged | Report this post to a Moderator
hcconn22
LymeNet Contributor
Member # 5263

Icon 1 posted      Profile for hcconn22   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Who is this Dr. At this point there should be no secrecy --- why does he not sign the letter-- and if he is treating he should NOT STOP because that by itself is almost an admission that he is doing something wrong.

Again the experts-- CAN NOT PROVE or DISPROVE Chronic Lyme. They only use words-- no research or science.

The ILADS guildlines have science behind them and describe a different standard of care. This Dr should contact ILADS and the LDA for help-- and not Lyme boards and patients. I am suspect of this letter, but maybe it's just me.

If he was being investigated there is a clear process in each state before you need to hire a lawyer etc. Also if he has and should have ANY malpractice insurance this normally covers defense of claims to a medical board.

--------------------
Positive 10 bands WB IGG & IGM
+ Babesia + Bartonolla and NOW RMSF 3/5/09 all at Quest

And still positive ELISA and WB two years after IV treatment
http://www.lymefriends.org/profile/blake

Posts: 607 | From Tick Town, Connecticut | Registered: Feb 2004  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
read this new blog for a little additional info.

yes, this is the GERMANTOWN, MARYLAND LLMD that i thought it was, and if you go to another area, he shows his city there.


http://lymemd.blogspot.com/2009/02/good-question.html

IP: Logged | Report this post to a Moderator
lymesly
Member
Member # 8528

Icon 1 posted      Profile for lymesly     Send New Private Message       Edit/Delete Post   Reply With Quote 
A fellow lymie just told me he is a good guy.
Posts: 92 | From Shepherdstown, WV | Registered: Jan 2006  |  IP: Logged | Report this post to a Moderator
Andromeda13
LymeNet Contributor
Member # 8314

Icon 1 posted      Profile for Andromeda13   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've been reading his blog for the last 6 months and it's obvious he's a principled and honest doctor, and also very knowledgable.

He hasn't slammed ILADS at all, but has openly discussed minor differences in the way he treats patients. You can tell this guy is a good man.

He has asked for help. Can people in the UK help at all?

Best wishes,
Andromeda

Posts: 180 | From UK | Registered: Nov 2005  |  IP: Logged | Report this post to a Moderator
lymesly
Member
Member # 8528

Icon 1 posted      Profile for lymesly     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm thinking anyone could write a letter. I'm not in Maryland, but I am going to send a letter to a MD politician.

This from the comments section of his blog:

Maryland Speaker of the House.
[email protected]

And Bryan Rosner added this...now this looks like a good thing!

"There is a bill that would allow long term antibiotic treatment."

http://www.cga.ct.gov/2009/TOB/H/2009HB-05625-R00-HB.htm

Posts: 92 | From Shepherdstown, WV | Registered: Jan 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  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.