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 » Are there any Funding or Patient Support Programs for Lyme Disease?

 - UBBFriend: Email this page to someone!    
Author Topic: Are there any Funding or Patient Support Programs for Lyme Disease?
springshowers
Frequent Contributor (1K+ posts)
Member # 19863

Icon 1 posted      Profile for springshowers     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am trying to research this and have not come up with anything really.

I am looking for any ideas that could help financially treat this disease.

Posts: 2747 | From Unites States Of America | Registered: Apr 2009  |  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 haven't heard of any, and I think there needs to be. It would be awesome if we could get a fund set up by someone, say, with a lot of money, I'm talking big league money, so they'd never miss it themself, who would like to help people get medical help.
Posts: 13116 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
riverpatrol
Member
Member # 12182

Icon 1 posted      Profile for riverpatrol     Send New Private Message       Edit/Delete Post   Reply With Quote 
I think Tina Garcia at www.leaparizona.com was attempting to establish help for some people. I don't know how successful she has been in fund raising though. I see the web site is off-line right now but it was up a couple of weeks ago.
Posts: 69 | From So Cal | Registered: Jun 2007  |  IP: Logged | Report this post to a Moderator
pmerv
Frequent Contributor (1K+ posts)
Member # 1504

Icon 1 posted      Profile for pmerv   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
In her testimony at the IDSA hearing, Tina said she had been too sick to do the fundraising necessary to help the many people who need help. I think that is what you will find across the board. No one has the kind of money needed to help sick patients, millions and millions of dollars. The LDA has their LymeAid4Kids fund but it only helps with expenses for testing. I don't know anyone else who can afford to give away that kind of money. Some of the drug companies have compassionate programs to supply meds to people. I've heard of a few people putting on benefits to help themselves or their families. Robin, if you have any connections to the "big league," see what you can do!

--------------------
Phyllis Mervine
LymeDisease.org

Posts: 1808 | From Ukiah, California, USA | Registered: Aug 2001  |  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 
Phyllis, I know they're around where I live - I see the money mentions in the paper all the time. Unfortunately, I do not clean house for any of them! Or clean mansion, I should say!

What I was wondering is I see items in the news from time to time, like Bill Gates has just given millions to xyz cause.

Has anyone approached the really big money people like Bill Gates and asked them to help? For them, I don't think they would ever feel a pinch from donating millions to a Lyme medical fund that could be managed by financially savvy people to earn interest and whatever else gets done for the money to keep generating money.

I notice that those who give big money for some cultural institution often like to be recognized with their name, or receive some really nice perks, like be able to attend rehearsals, that kind of thing.

Thinking outloud here - there are institutions where people are very, very wealthy. I know the names of some of them. I have actually been inside some of these institutions and heard the talk.

But it takes people who move in those circles and know people in those circles to do this work. I think it could happen through social relationships. That's usually how the big money is raised.

Posts: 13116 | From San Francisco | Registered: May 2006  |  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.