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 » Kelly pushes for increased federal funding to fight Lyme disease

 - UBBFriend: Email this page to someone!    
Author Topic: Kelly pushes for increased federal funding to fight Lyme disease
zipzip
LymeNet Contributor
Member # 6226

Icon 1 posted      Profile for zipzip     Send New Private Message       Edit/Delete Post   Reply With Quote 
http://www.midhudsonnews.com/News/Lyme_funding-02Jun05.htm

Saying the Hudson Valley is the ``epicenter'' of Lyme disease in the nation and the State of New York has the highest instance of the disease that is transmitted to humans by deer ticks, Congresswoman Sue Kelly announced yesterday that she has re-introduced a bill that would appropriate $10 million for each of fiscal years 2006 through 2010 to provide research and educational activities concerning the disease.


Kelly's bill, which is also sponsored by fellow Hudson Valley House Member Maurice Hinchey, would require development of a diagnostic test to detect Lyme; authorize federal funding for increased educational activities and local community prevention information; and create an advisory committee of the Department of Health and Human Services on Lyme disease.


Orange County Health Commissioner Dr. Jean Hudson said those measures would be a great help in the fight against the disease. ``Early testing and a test that is responsive to treatment would help us enormously,'' she said. ``Now, when you are tested for Lyme disease and you are positive, you can get it again, still the test is no use the second time around. It becomes a clinical discussion.''


County Executive Edward Diana also endorsed the congressional efforts to pass the Lyme disease legislation.


Posts: 795 | From nyc | Registered: Sep 2004  |  IP: Logged | Report this post to a Moderator
Linda LD
Frequent Contributor (1K+ posts)
Member # 6663

Icon 1 posted      Profile for Linda LD     Send New Private Message       Edit/Delete Post   Reply With Quote 
zip,

Got any email addresses so we can email Kelly, Hinchey and Hudson for their efforts?

Linda


Posts: 1171 | From Knoxville, TN US | Registered: Dec 2004  |  IP: Logged | Report this post to a Moderator
cbb
Frequent Contributor (1K+ posts)
Member # 788

Icon 1 posted      Profile for cbb     Send New Private Message       Edit/Delete Post   Reply With Quote 
I hope it passes!!
This bill would be a giant step in the right direction!!

Want to express my opinion -
My concern is that in the past, too much money has gone to the wrong people & their "research" (?) has continued to fuel the debate about diagnosis & treatment of Lyme disease.

The result -
difficulty in getting a diagnosis & adequate treatment has caused so many people to suffer unnecessarily.
I have seen this in my family more than once.

I'm aware that there are exceptions to what I've just said.

"The powers that be" and those in charge of disbursing funds seem to favor the people at prestigious medical institutions, but that does not guarantee that they are the best.
I don't have any idea how this could be avoided.

Positive feedback would be great for the people sponsoring this bill.


Posts: 4638 | From South Carolina | Registered: Mar 2001  |  IP: Logged | Report this post to a Moderator
NP40
Frequent Contributor (1K+ posts)
Member # 6711

Icon 1 posted      Profile for NP40     Send New Private Message       Edit/Delete Post   Reply With Quote 
To e-mail your rep: http://www.house.gov/writerep/

Sue Kelly's office 202-225-5441 http://suekelly.house.gov/ContactInformation.asp

Maurice Hinchey's office 202-225-6335 http://www.house.gov/hinchey/ http://www.house.gov/hinchey/contact/#addresses


Posts: 1632 | From Northern Wisconsin | Registered: Jan 2005  |  IP: Logged | Report this post to a Moderator
Linda LD
Frequent Contributor (1K+ posts)
Member # 6663

Icon 1 posted      Profile for Linda LD     Send New Private Message       Edit/Delete Post   Reply With Quote 
NP40,

I already wrote my house rep over S5057 sponsored by Hannon--is this a different bill?

My representative actually knows my family--so I don't want to look too ignorant.

L


Posts: 1171 | From Knoxville, TN US | Registered: Dec 2004  |  IP: Logged | Report this post to a Moderator
brainless
LymeNet Contributor
Member # 6771

Icon 1 posted      Profile for brainless     Send New Private Message       Edit/Delete Post   Reply With Quote 
HR 2526 is a federal bill.

I believe Hannon is a state rep, not a federal rep. Hannon (et al) was the rep to write to for NY stuff only. This bill is for the entire country which means that you should NOT contact Hannon for this.

Use the URL above or ask the LDF at www.lyme.org for help in determining who your federal rep is.

b


Posts: 210 | From lalaland | Registered: Jan 2005  |  IP: Logged | Report this post to a Moderator
Ann-OH
Frequent Contributor (5K+ posts)
Member # 2020

Icon 1 posted      Profile for Ann-OH     Send New Private Message       Edit/Delete Post   Reply With Quote 
You can find your federal rep at this site http://thomas.loc.gov/

You can also put the bill number
HR 2526 in there and see what the status is and which representatives have signed on as co-sponsors. There are 15 so far, I believe.

The people at www.Lyme.org have lots of good info, including a nice script to use when e-mailing or calling your rep.

Please check it out and contact your Fed. representative.
Ann - OH


Posts: 5705 | From Ohio | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
Linda LD
Frequent Contributor (1K+ posts)
Member # 6663

Icon 1 posted      Profile for Linda LD     Send New Private Message       Edit/Delete Post   Reply With Quote 
HEY!

I'm on top of things! I checked my "sent" one emails and I asked my friends to email our house rep on H.R. 2526 AND asked them to write and thank Hannon for his efforts.

I had a good day yesterday too--I wrote one newspaper, two tv stations and the govenor.

Up for people to write letters!

Linda


Posts: 1171 | From Knoxville, TN US | Registered: Dec 2004  |  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.