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 » We can make this work! Band together ask others Share your story!! Calling ALL LYMIES

 - UBBFriend: Email this page to someone!    
Author Topic: We can make this work! Band together ask others Share your story!! Calling ALL LYMIES
victoria
Member
Member # 11267

Icon 1 posted      Profile for victoria     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am moving this post to Medical Questions because I believe it needs to be answered and responded to!

This is important for us to make the people who aren't suffering with Lyme understand why we're so passionate about our stories! This could really put an impact into our walk!! It's easy and FREE! Just 5 sentences.

Thanks guys! [Smile]

As the Lyme Walk- For those who can't of the Corning Finger Lakes area begins to get underway: we are asking for your help for contribution to the walk a free and easy way to give a voice to Lyme disease and those who suffer from it-

Our goal is to promote awareness and prevention of Lyme Disease with this we're asking you to contribute your story and face to the walk as a free way to get your story out there to make non-Lyme suffers understand a little more. The ideal goal is to have 100's of ''Lymie's'' to hand out for each walker so every walker has a person they are walking for.

What we need:

- Your name (First names only please!)

- Your state (no city or anything else)

- Your Photo (just a head shot is fine, we really just want to be able to put a face with the stories and having a photo- makes the story all more real to the person walking for you.)

- And of course a very brief description of what you have been through, symptoms, how long you've had it and how Lyme has affected you. We ask that you limit the story to 5 sentences or give us the liberty of editing your story for the walk due to lack of space on these cards we will be handing out

- *Upon sending in your story please have the photo and story either together as one document or clearly labeled with your name if it is two files*

Our Vision-

We hope to have each walker carrying with pride or pinning their lime green square to their shirt and throughout the upcoming year they are thinking of you and sending thoughts and prayers to you and your family. We want each person to have a personal touch and be able to take ownership in the walk itself so they are not only walking for a cause but also walking for an individual.

Please submit all stories by May 15th, 2008 to [email protected].

If you would like further information regarding the walk- we encourage you to visit our website at www.lymewalk.org or e-mail Victoria Wilcox at [email protected]

Posts: 82 | From New York | Registered: Feb 2007  |  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 hope to do this. Gotta find a pic!

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 14 posted            Edit/Delete Post   Reply With Quote 
hi V, you've got my mug and story.

for others, Victoria told me 2" of info is MAXIMUM LIMIT!

V, I suggest also you edit your post and show MAY 15 DEADLINE in it somwhere since we're working with all these other deadlines:

congress' lyme bills ... phone marathon;

may 7 lyme protest, etc.

thanks V

just click on paper/pencil icon to open up subject line, and perhaps add to your text 2" LIMIT OF STORY!

it's going to be GREAT!! thanks for all your work on this and SARAH! [group hug] [kiss]

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.