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 » Lyme Disease Worldwide Protest - Gains Top Spot in Google - CNN iReport

- UBBFriend: Email this page to someone!    
Author Topic: Lyme Disease Worldwide Protest - Gains Top Spot in Google - CNN iReport
Paul Mall
LymeNet Contributor
Member # 27581

Icon 1 posted      Profile for Paul Mall   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hello Lyme Friends

an Ireport by Lisa H has gained a top spot in the google search feed.

"Lyme Disease" NEWS (top spot)

"Lyme Disease" general google search (1st page)

Please submit your Lyme Stories in the comment section and share the page.

Also click the CNN should report on this button.

Sorry for posting in the wrong area but this is just Awesome!

http://ireport.cnn.com/docs/DOC-973150?hpt=us_bn3

Paul Mall
Posts: 925 | From Connecticut | Registered: Aug 2010  |  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 
I just tweeted it. Maybe that will help too!

--------------------
--Lymetutu--
Opinions, not medical advice!
Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
jlf2012
LymeNet Contributor
Member # 36002

Icon 1 posted      Profile for jlf2012     Send New Private Message       Edit/Delete Post   Reply With Quote 
I posted it on my FB page. Shouldn't we all consider sharing/posting in order to help spread awareness?
Posts: 463 | From Sandusky, Ohio | Registered: Jan 2012  |  IP: Logged | Report this post to a Moderator
droid1226
Frequent Contributor (1K+ posts)
Member # 34930

Icon 1 posted      Profile for droid1226     Send New Private Message       Edit/Delete Post   Reply With Quote 
I added story on the page, tweeted it. We can't complain about the IDSA, CDC, insurance, or Dr.s if we aren't vocal when opportunities like this arise.

--------------------
http://www.youtube.com/user/droid1226/videos?view=0&flow=grid
Posts: 1181 | From ohio | Registered: Nov 2011  |  IP: Logged | Report this post to a Moderator
feelfit
Frequent Contributor (1K+ posts)
Member # 12770

Icon 1 posted      Profile for feelfit     Send New Private Message       Edit/Delete Post   Reply With Quote 
Infirm? Home-Bound? You can still have a voice. Pls. take the time to make yours count.
Posts: 3975 | From usa | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
jlf2012
LymeNet Contributor
Member # 36002

Icon 1 posted      Profile for jlf2012     Send New Private Message       Edit/Delete Post   Reply With Quote 
Why are so many people afraid to be vocal about lyme disease? Is it because we think we'll be looked upon as contagious? Or is it just because many of us are too sick to care? Maybe it's because the disease is so confusing. I wish everyone on this site would share this information no matter how controversial lyme disease is. The word needs to get out there to the public. If we all share this it will help so much.
Posts: 463 | From Sandusky, Ohio | Registered: Jan 2012  |  IP: Logged | Report this post to a Moderator
map1131
Frequent Contributor (5K+ posts)
Member # 2022

Icon 1 posted      Profile for map1131     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thurs night at our support meeting a new member told us she had been to see ID doctor on Wed.

She had documentation and positive tests results from filria (sp) and mongellons.

This ID ripped her up oneside and down the other. He actually said "I bet you are part of that cult of lime green t-shirt wearing group."

I guess the ID society of Louisville has become very aware of our large growing group of Lyme supporters.

I'm thrilled they know of our existence and our threat to lies.

Pam

--------------------
"Never, never, never, never, never give up" Winston Churchill
Posts: 6478 | From Louisville, Ky | Registered: Jan 2002  |  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 
I'd say, excuse me, the word is not cult - it's culture. We are part of a culture that wears Lyme green T-shirts...

Whatever they say, listen, then respond with the truth.

More T-shirts! Design more lime green T-shirts and wear them visibly.

So how do we keep this top google spot search going? Just by posting the link on our social networks?
Posts: 13116 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
jlf2012
LymeNet Contributor
Member # 36002

Icon 1 posted      Profile for jlf2012     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, click on the link and then you can share it on Twitter or FB.
Posts: 463 | From Sandusky, Ohio | Registered: Jan 2012  |  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.