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 » Lyme Letter To Editor

 - UBBFriend: Email this page to someone!    
Author Topic: Lyme Letter To Editor
cinderskenney
Junior Member
Member # 28044

Icon 1 posted      Profile for cinderskenney     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi All, just wanted to let you know I wrote a letter to the editor of my local paper about lyme and they printed it.
Here it is

I hope this has helped spread the word about this illness.

--------------------
looking at the world through lyme green glasses

Posts: 4 | From MD, USA | Registered: Sep 2010  |  IP: Logged | Report this post to a Moderator
chiquita incognita
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Bravo and well done! I think the more we write letters to the editor, the more we can raise awareness in the community.

And as awareness becomes the norm (if we all help it along with similar letters, again brava!) then there will be pressure on the health un-insurance companies to do what we pay them to do. Take care of us.

I think we also have outreach and influential power by posting to blogs. If we ask readers to seed our posts around the web, giving written reprint permission, then we can also spread word and raise awareness in this way. As readers are asked to spread word around the web, they will. They can also be asked to send our posts out in chain emails, to help spread word.

I also would like to see us raising awareness for the necessity of the removal of government over-controls in medical practice. No government entity, and no insurance company, has any business reaching into our bodies by remote control. Doctors should be free to prescribe for us as they see fit, based on individual patient needs and without strictures from the government. We may make the assumption that government controls protect us, but here is one prime example of how this illusion ends up becoming the reality of endangerment rather than protection.

This has to be stopped.

The first step is to raise public awareness about it. If we write letters and blogs in such a way as fosters critical thinking (asking questions is one way to go, rather than making statements, and appealing to common beliefs such as the assumption of "protections" which actually end up endangering us) then there will be increasing pressure on the powers that be to make changes.

[ 06-07-2011, 09:57 PM: Message edited by: chiquita incognita ]

IP: Logged | Report this post to a Moderator
sickofsick
LymeNet Contributor
Member # 29258

Icon 1 posted      Profile for sickofsick     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'd be interested in your letter, however, it isn't accessible from that link any more. could you send me a copy?
Posts: 312 | From Utah | Registered: Nov 2010  |  IP: Logged | Report this post to a Moderator
payne
Frequent Contributor (1K+ posts)
Member # 26248

Icon 1 posted      Profile for payne     Send New Private Message       Edit/Delete Post   Reply With Quote 
ditto... cinder, the link failed for me too

--------------------
TULAREMIA/rabbit fever ?

Posts: 1931 | From mid-michigan | Registered: Jun 2010  |  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.