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 » ? for Activists

 - UBBFriend: Email this page to someone!    
Author Topic: ? for Activists
seibertneurolyme
Frequent Contributor (5K+ posts)
Member # 6416

Icon 1 posted      Profile for seibertneurolyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
See this link.

http://flash.lymenet.org/ubb/ultimatebb.php?ubb=get_topic;f=2;t=003621

My question is, "Is this legal?"

Can a state and federally funded institution such as Virginia Commonwealth University/Medical College of Virginia categorically deny treatment for all diagnosed Lyme patients?

This is not a question about the 2 standards of care -- I just don't understand how this situation can exist. This is discrimination in my book.

Maybe this is where the next Rally should be held.

Bea Seibert

Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
up for Tincup, Ellen Lube, and other knowledgeable activists!

I can't believe that is true! They need to be turned in.

IP: Logged | Report this post to a Moderator
riversinger
Frequent Contributor (1K+ posts)
Member # 4851

Icon 1 posted      Profile for riversinger   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Bea, I don't see this as the institution saying they deny treatment. It looks more like no one knows enough about Lyme, or chooses to take on the controversy over treatment.

Individual doctors have a right to limit the scope of their practice. What seems like is needed here is education about Lyme, and the NEED for someone to treat in Virginia. Perhaps these doctors don't consider it an important illness in the state.

--------------------
Sonoma County Lyme Support
[email protected]

Posts: 2142 | From California | Registered: Nov 2003  |  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 
I once stayed in a Virginia state park campground where a tick ed folder was given to me by camp host. It included lyme disease warning. Put out by state health dept. So, they ought to know it is disease that can be acquired in the state. However, I think this is their way of avoiding the whole controversy.

Too bad Virginia lymies. You will have to be ignored until it becomes safe to think about and treat this disease. Hope you last long enough to see this happy day arrive.

BTW, Johns Hopkins does this too. Mention that you have chronic lyme and you will be ejected immediately.

But, for sure they are on the watch for the dreaded bird flu. Diseases we don't have yet are preferable to the ones we do have. Much easier to cope with. More lucrative.

Posts: 8430 | From Not available | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
seibertneurolyme
Frequent Contributor (5K+ posts)
Member # 6416

Icon 1 posted      Profile for seibertneurolyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
I don't necessarily have a problem with an individual doc deciding what illness he wants to treat -- but I do have a big problem with state and federal tax dollars supporting research universities and medical schools which exclude specific illnesses. I know they can't specialize in everything, but to exclude you solely on the basis of your diagnosis is discrimination in my book.

They are the ones who have the money to hire specialists if they see fit to do so.

Bea Seibert

Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
riversinger
Frequent Contributor (1K+ posts)
Member # 4851

Icon 1 posted      Profile for riversinger   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I agree with you. They SHOULD be putting time and money into this. I just don't think what they are doing is illegal, only immoral.

--------------------
Sonoma County Lyme Support
[email protected]

Posts: 2142 | From California | Registered: Nov 2003  |  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 
This is very interesting because one of the "expert witnesses" on the virginia Medical Board Panel at Dr. Z's hearing last year was from MCV!!!

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
   

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.