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 » TIME TO TAKE A STAND !!

 - UBBFriend: Email this page to someone!    
Author Topic: TIME TO TAKE A STAND !!
Mo
Frequent Contributor (5K+ posts)
Member # 2863

Icon 4 posted      Profile for Mo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Time to Take a Stand

LYME RIGHTS RALLY !!

[woohoo]

Friday, June 2nd

1 - 3 PM

State Capitol Building ~ Hartford, CT


� support Dr. Jones, Dr. Jemsek

and all our Lyme literate physicians


� Protect the rights of Lyme patients


� Gain recognition for this Public Health Crisis


Special Guest speakers

Dr Joseph Burrascano

Pat Smith, Pres., Lyme Disease Assoc. inc.


This is a NATIONAL call to action

For All Patients, Lyme families,

Medical proffessionals, Government officials

Children invited to tell their personal Lyme stories.


Time To Take a Stand Lyme Rights Rally!

Wear `lyme' green to show support!

Please RSVP TO [email protected]

Or call 203-270-3301 to register A child for a talk.

--------------------
life shrinks and expands in proportion to one's courage
-- anais nin

Posts: 8337 | From the other shore | Registered: Jul 2002  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Sure wish I lived within 100 miles of there; but I don't so you ALL rally for me and the rest of us LYMIES NATIONWIDE who can't attend.

Looked like an interesting program. Go get em lymies!

IP: Logged | Report this post to a Moderator
chainsaw joseph
LymeNet Contributor
Member # 6611

Icon 1 posted      Profile for chainsaw joseph     Send New Private Message       Edit/Delete Post   Reply With Quote 
If I may suggest an idea,it may be good it may stink.What if all the lymies held signs outside for an hour before the meeting,the signs would say OPRAH,PLEASE HEAR OUR PLEA FOR HELP WITH LYME DISEASE TREATMENT.Maybe Oprah will get the message through the media and even if she doesnt respond the enemy side will know we are trying to get someone who will tell the story lyme really is,maybe a little fear will get in them and do something to help us.I think it would be an offensive aggressive step weve needed to take for a long time.If the enemy thinks we have a chance to get on Oprah and the facts really told,well,it maybe a different ball game then.
Posts: 308 | From new bedford,Ma. | Registered: Dec 2004  |  IP: Logged | Report this post to a Moderator
Cucamonga
Member
Member # 2122

Icon 1 posted      Profile for Cucamonga     Send New Private Message       Edit/Delete Post   Reply With Quote 
WHAT A GREAT IDEA!!! Look at my post just above yours..I just e-mailed her AND I sent her a long letter with lots of extra info...I HOPE TO BE POSTING IT ON THIS WEBSITE IN THE NEXT FEW DAYS!!!

Great idea! AND I WILL BE GOING UP THERE!!!

--------------------
Cucamonga

Posts: 90 | From NYC, NY USA | Registered: Feb 2002  |  IP: Logged | Report this post to a Moderator
chainsaw joseph
LymeNet Contributor
Member # 6611

Icon 1 posted      Profile for chainsaw joseph     Send New Private Message       Edit/Delete Post   Reply With Quote 
She hasnt responded to e-mails but a big crowd with signs is a different story,not just to get Oprahs attention but IT will get the medias attention and questions.
Posts: 308 | From new bedford,Ma. | Registered: Dec 2004  |  IP: Logged | Report this post to a Moderator
Meg
Honored Contributor (10K+ posts)
Member # 22

Icon 1 posted      Profile for Meg     Send New Private Message       Edit/Delete Post   Reply With Quote 
Fantastic idea!! It's sure to be covered by some

media.....get the signs everyone. If we did that

for every rally it would make a huge difference.

--------------------
Success Stories---Treatment Guidelines

Posts: 10010 | From somewhERE OVER THE Rainbow | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
chainsaw joseph
LymeNet Contributor
Member # 6611

Icon 1 posted      Profile for chainsaw joseph     Send New Private Message       Edit/Delete Post   Reply With Quote 
If we did this right once with a huge crowd we could change things this year.If we could get 500 to 1000 people holding signs I think we would get someone like Pat Smith(if she would)on the Oprah show,I think it just might work,something would come of this.If we got all our family and friends to hold signs just once we could be the people that changed this.
Posts: 308 | From new bedford,Ma. | Registered: Dec 2004  |  IP: Logged | Report this post to a Moderator
WildCondor
Unregistered


Icon 6 posted            Edit/Delete Post   Reply With Quote 
Can we please keep this at the top as a hot topic? I tried emailing the moderators again to make it a sticky and they don't read their private messages. Just keep bringing it back to the top!
[Smile]

IP: Logged | Report this post to a Moderator
hatsnscarfs
LymeNet Contributor
Member # 6562

Icon 1 posted      Profile for hatsnscarfs     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm planning to head down from Boston. I can fit 4 additional people in my car. Who's coming with me?
hatsnscarfs

Posts: 956 | From MA | Registered: Nov 2004  |  IP: Logged | Report this post to a Moderator
trueblue
Frequent Contributor (1K+ posts)
Member # 7348

Icon 1 posted      Profile for trueblue     Send New Private Message       Edit/Delete Post   Reply With Quote 
^up^

--------------------
more light, more love
more truth and more innovation

Posts: 3783 | From somewhere other than here | Registered: May 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.