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| ·Remembering Leslie Wermers. One year ago today. | 2009-11-02 20:10:50 | | ·Lyme disease patients mourn passing of well known doctor | 2009-07-01 04:00:00 | | ·All she lost: My sister's battle with Lyme disease | 2009-05-19 04:00:00 | | ·Laura Treanor, 19, Lyme disease not ruled as cause of death | 2009-05-07 04:00:00 | | ·Lila Star Smith Harms, 25, dies from complications of Lyme disease | 2009-05-05 04:00:00 | | ·Lyme Disease Patients Loses a Hero and Friend | 2008-11-16 19:57:38 | | ·Nancy L. (Scully) Strayer: March 20, 1946 - March 12, 2008 | 2008-04-12 04:00:00 | | ·Bite from tick on holiday led to death leap | 2008-04-11 06:49:39 | | ·Rugby great, Mike Gregory, loses his battle with Lyme disease | 2007-11-24 23:51:00 | | ·Missouri teen, 15, dies from Ehrlichiosis | 2007-09-04 04:00:00 | | ·Steven F. Wells, 45, dies after battle with Lyme disease and ALS | 2007-08-14 07:03:39 | | ·Bruno C. Malvezzi | 2007-07-31 21:06:47 | | ·In loving memory of Dr. Edward McNeil | 2007-07-24 19:45:00 | | ·Lyme disease is a growing problem, Britteny Gallgher, Kansas City, MO | 2007-05-24 04:10:00 | | ·Lyme Disease Skyrockets In Maryland | 2007-05-23 04:00:00 | | ·C. Peter Thomas, 46; Sound Engineer | 2007-05-21 04:00:00 | | ·Jimmy Duarte, gifted musician, charismatic islander, dies at 70 | 2007-05-17 15:12:03 | | ·Obituary: Lyme Disease Advocate Karen Johnson ''Rose'' Rose, 1947 - 2007 | 2007-04-30 22:50:17 | | ·BETH'S QUEST: Family crusades against Lyme disease | 2007-04-29 04:00:00 | | ·Tick kit distribution aimed at heading off Lyme disease | 2007-04-28 12:40:00 | | ·Letter to the Editor: In Memory of Lyme Advocate ''Rose'' | 2007-04-26 11:00:03 | | ·Lyme Advocate ''Rose'' Succumbs to Lyme Disease | 2007-04-19 18:25:19 | | ·Body of Missing Woman with Lyme Disease Found | 2007-04-14 21:46:32 | | ·Michael Coers won Pulitzer Prize | 2007-03-21 10:00:43 | | ·E STREETER IN LYME 'SUICIDE' | 2007-03-19 12:33:30 | | ·Lost to Lyme Lyme disease facts | 2007-03-19 04:00:00 | | ·Musician remembered as battler against Lyme disease | 2007-03-19 04:05:00 | | ·Maine Musician Bill Chinnock Dies | 2007-03-08 13:45:18 | | ·Obituary - Eric von Schmidt - Singer and painter was in Dylan's circle | 2007-02-27 11:00:00 | | ·JAMES P. KOCH | 2007-02-22 00:53:49 | | ·Andrew Spielman, 76, Expert on Insect-Borne Diseases, Dies | 2006-12-26 04:00:00 | | ·Martin Frank Dumke | 2006-11-29 04:00:00 | | ·Bill Reynolds: For QB Coen, tragedy lies beneath the surface | 2006-10-29 04:05:00 | | ·Coen plays on without No. 1 fan | 2006-10-17 04:00:00 | | ·Librarian was dedicated to students, family | 2006-09-19 17:02:58 | | ·TORMENT OF BRAIN BUG PROF - Alasdair Crockett | 2006-09-19 13:43:35 | | ·Widow of Lyme disease victim appeals for help | 2006-09-18 22:44:57 | | ·Professor commits suicide after catching dementia from tick bite | 2006-09-17 22:17:12 | | ·Tick talk: Family blames member's death on tickborne illness | 2006-08-21 04:00:00 | | ·Death of York PA area doctor due to Lyme and ALS | 2006-04-29 20:40:02 | | ·Emmy-winner Scott Brazil dies of ALS and Lyme disease at 50 | 2006-04-22 11:37:59 | | ·Kym Cooper- Dead Woman's Own Letter Tells Her Lyme Disease Story | 2006-02-05 14:08:53 | | ·Kym Cooper - Worn down by Lyme | 2006-01-22 01:56:26 | | ·Kym Cooper, 1968-2006, After long battle with Lyme disease | 2006-01-19 13:51:02 | | ·Tribe leader Francis mourned | 2006-01-14 18:22:58 | | ·Easton mourns former selectman after fatal accident | 2005-12-17 13:04:17 | | ·Educator, union leader dies from complications of Lyme disease | 2005-12-08 09:25:32 | | ·'A TERRIBLE WAY TO GO' | 2005-10-22 14:39:56 | | ·Leo Bogart, R.I.P. (1921-2005) | 2005-10-21 15:55:28 | | ·Leo Bogart, 84, Sociologist Who Studied Role of Media in Culture, Is Dead | 2005-10-21 15:46:44 | | ·Passages: Pat Pepper | 2005-10-10 01:11:11 | | ·Man loses battle with Lyme disease | 2005-10-09 10:37:43 |
[ Read Obituaries ] | |
| U.S. Army, 1983-1996 Lyme Disease Risk Assessments |  |
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 | Obituaries: Remembering Leslie Wermers. Four years ago today |
LymeBlog News
Lexington, KY USA
By LymeBlog News Staff
~You've touched Countless Lives in so Many Beautiful Ways~She Was Always A Loving and Giving Sister; Daughter; Life- Partner; Jayde's Lessie; Ralphie & Dudley's Mommy; Cherished Lyme Patient Advocate; Aunt; Niece; Cousin; & Friend.
Here is an excerpt from the beautiful tribute that Andy Abrahams Wilson wrote in memory of Leslie. Andy is the Producer/Director of the Powerful Lyme Disease Documentary,"Under Our Skin". "The Lyme community has lost an important hero and friend–and so did I. Leslie Wermers, 41, died from heart failure in her sleep on November 2nd, 2008."
"It is hard to imagine Leslie’s heart giving out, because for anyone who knew her she was all heart."
"A dear friend to so many and a tireless worker on behalf of the Minnesota and national Lyme communities, Leslie gave everything she had to help others who were sick. And everything she had was an abundant reserve of love and support–even as her own health waned." Andy Abrahams Wilson, Producer/Director, UNDER OUR SKIN Click Here to read the entire tribute and to watch Leslie's interview excerpt from "Under Our Skin".
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Posted by Editor on Friday, November 02 @ 19:20:02 EDT (486 reads)
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 | Obituaries: Remembering Leslie Wermers. Two years ago today |
LymeBlog News
Lexington, KY USA
By LymeBlog News Staff
Source: Minnesota Lymefighters
Co-founded by Leslie Wermers
"If I die tomorrow and I save one life, I'll die happy."
Leslie Wermers 07/07/1967 - 11/02/2008
Leslie Gave Everything She Had, Cared & Loved So Deeply, Until the Very End.
~God Broke Our Hearts and Angels Rejoiced, the Day Leslie Entered Heaven~ November 2nd, 2008
~You've touched Countless Lives in so Many Beautiful Ways~She Was Always A Loving
and Giving Sister; Daughter; Life- Partner; Jayde's Lessie; Ralphie
& Dudley's Mommy; Cherished Lyme Patient Advocate; Aunt; Niece;
Cousin; & Friend.
Here is an excerpt from the beautiful tribute that Andy Abrahams Wilson wrote in memory of Leslie.
Andy is the Producer/Director of the Powerful Lyme Disease Documentary,"Under Our Skin".
"The
Lyme community has lost an important hero and friend–and so did I.
Leslie Wermers, 41, died from heart failure in her sleep on November
2nd, 2008."
"It is hard to imagine Leslie’s heart giving out, because for anyone
who knew her she was all heart."
"A dear friend to so many and a tireless
worker on behalf of the Minnesota and national Lyme communities, Leslie
gave everything she had to help others who were sick. And everything
she had was an abundant reserve of love and support–even as her own
health waned."
Andy Abrahams Wilson, Producer/Director, UNDER OUR SKIN
Click Here to read the entire tribute and to watch Leslie's interview excerpt from "Under Our Skin".
Other stories about Leslie:
North Iowa native, Story City woman advocate for Lyme disease victims
Lyme Disease Patients Loses a Hero and Friend
The Tick And The Time Bomb
Source: Minnesota Lymefighters
Co-founded by Leslie Wermers
Other stories about Leslie:
North Iowa native, Story City woman advocate for Lyme disease victims
Lyme Disease Patients Loses a Hero and Friend
The Tick And The Time Bomb
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Posted by Editor on Tuesday, November 02 @ 04:00:00 EDT (2244 reads)
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 | Chronic Illness Conference, 11/6/10, Plainview, NY |
 Doctors
and Patients Dealing with Chronic Illnesses: Great News About
The
Chronic Illness Center (CIC)
Chronic Illness Conference
Wave
of the Future ~
The Cutting Edge in Medicine Doctors may contact:
Josephine Cavallaro, Chronic Illness Center Consultant, 631-968-2723
November
6, 2010 Time:
1 PM to 9:30 PM Place:
Marriott
Residence Inn 9
Gerhard Road Plainview NY 11803 Phone:
516-433-6200
Registration
begins at 12:30 PM – see below
- Program
1 PM - 9:30 PM
- Opening
and Conference Speakers -1:00 PM to 3:30 PM
- Coffee
Break 3:30 PM to 4:00 PM
- Conference
Speakers and Closing 4:00 PM to 7:30 PM
- Dinner
& Social Hour - Marriott’s Solarium Room 7:30 - 9:30 PM
(Note:
To reserve a room - mention Empire State Lyme Disease Association)
Presenters- Dr.
Lesley Fein
Private
practice 1988-pres.
Medical Director, Lyme
Disease Society,
presented “Multivariable Analysis of 160 Patients with Lyme
Disease,” wrote foreword to Confronting Lyme Disease, 2007 IPPY
Award winner, featured on Discovery Health Mystery Diagnosis- Dr
Eva Sapi
Associate
Professor of Biology and Environmental Science at the University
of New Haven.
Research & investigates presence of different
formations of Borrelia burgdorferi, the Lyme disease bacteria &
has held three national Lyme disease conferences.
- Amy
Proal
Georgetown
University,
Author, “Autoimmune disease & the metagenome,”
in press at Springer Publications, will speak on Autoimmunity
Research & Metagenomics, http://vimeo.com/5106259
- Veny
Musum
Director
of the CIC Center, NJ
“To resolve these issues, my mission is to
provide educational information about tick & other vector
borne diseases & chronic infectious, systemic diseases.”
- Turn
The Corner Foundation
Nationwide
Advocacy Foundation on Physicians training, educational programs,
and on the facilitation and promotion of important research
- The
Lanford Foundation–Lifelyme,
Inc.
A
National Foundation that is one of the driving forces for cutting
edge medicine, on support, advocacy, & educational resources
for patients.
Admission
(Tax-Deductible Donation)
is $40.00 Dinner is Included Pre-register
& Save $5.00 by Reserving Your Tickets
Please
send check or money order for $35.00
to:
Empire
State Lyme Disease Association
PO
Box 874, Manorville, NY 11949
The
mission of LIFELYME, is to provide educational information for anyone
interested in tick-borne diseases, chronic infectious, systemic diseases
and related sutoimmune diseases. Information presented is intended only
for educational exchange. This information is not offered by LIFELYME
as medical advice for anyone.
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Posted by Editor on Tuesday, October 12 @ 10:42:48 EDT (5540 reads)
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 | Opinion / Editorial: NatCapLyme: Don't let IDSA be only voice at workshop! |
LymeBlog News
Lexington, KY
By LymeBlog News Staff
September 23, 2010
Dear Lyme Community:
As you know, some Lyme advocates have chosen to pull out of the IOM Lyme Disease workshop http://www.iom.edu/Activities/Disease/TickBorne.aspx.
They are legitimately concerned that the agenda is heavily biased
against the patients’ interest. We respect their concerns and their
decision to pull out of the workshop. However, upon careful
consideration, we have decided to participate in the IOM workshop to
represent the Lyme patient’s perspective and show support for our
presenters. While we have our own reservations, we are working hard to
improve the agenda.
Here are some facts and thoughts to consider in making your own decision:
-
The IOM Lyme workshop is not a forum to debate whose science is
right or wrong. It is, rather, an assessment of the state of the
science as presented from all points of view, for the purpose of
determining the science and research still needed. This workshop is not
designed to draw conclusions, but to determine where future research
needs to go.
- If Lyme patients and Lyme doctors fail to participate, the only
perspective presented will be that of the IDSA. If our Lyme doctors and
advocates don’t participate, the committee can’t include them in the
record and it will appear in the report as if we don’t exist or care.
- The IOM committee will accept comments for the record up to 3 or 4
days after the workshop. If you don’t know what was said at the
workshop, you cannot draw intelligent comments.
- Clinicians will have a microphone reserved solely for their use,
with extra time allocated to their questions or comments which will be
included in the final report. Lyme doctor participation is critical or
the IDSA clinicians will be the only ones at the microphone and on
record.
- A Congressman worked hard for the appropriation to fund this
project. Abandoning this workshop is abandoning him, and will compromise
his future ability to argue successfully for Lyme patients in Congress.
This Representative needs Lyme community support at this workshop. We
cannot “burn our Congressional bridges” with the very people who are
critical to our cause.
- When you withdraw from the Washington process, you won’t be asked
back again. Each time this happens, we lose our ability to be taken
seriously. History shows that progress is made when we work within the
system, not when we abandon it. Admittedly, it is by nature, a long and
arduous process.
Bottom line: the workshop will proceed with or without our community;
without representation we concede to the IDSA. We can’t let that
happen! If the situation warrants it, there will be time to write a
minority report.
Please attend this workshop and explain your views on the gaps in
science and the research you think is needed. For example, the gaps in
diagnosis that caused your disease to go unrecognized; the lack of
uniformity in approaches of the states; the problem of underreporting;
the unreliability of testing and the other issues you believe should be
addressed by the science.
Thank you,
Monte L. Skall
Executive Director, the National Capital Lyme & Tick-Borne Disease Association
Linda Lobes
President, Michigan Lyme Disease Association
Lisa Torrey
President, National Tick-Borne Disease Advocates
Judith Weeg
President, Lyme Disease United Coalition
Affiliates:
Lyme Disease Association of Iowa
Minnesota Lymefighter’s Advocacy
Nebraska LDUC
Ohio LDUC
South Dakota LDUC
Nevada LDUC
Indiana LDUC
Kansas Lymefighters, Inc.
Oklahoma LDUC
Washington (State) LDUC
North Dakota LDUC
In the Lyme Light, MN LDUC
Wright County Minnesota LDUC
Georgia LDUC
Annondale MN LDUC
Tracie Schissel
Chairman, Minnesota Lyme Fighter’s Advocacy
Vice President, Lyme Disease United Coalition
Tina J. Garcia
Founder, Lyme Education Awareness Program
Mac McDonald
Editor, LymeBlog News
Note: By the Editor
-
This letter is regarding the: Lyme Disease and Other Tick-Borne Diseases: The State of Science
-
Activity Description
- At the request of the NIH, National Institute of Allergy and
Infectious Diseases, the IOM will convene a committee to plan and
conduct a scientific workshop to assess the state of the science of Lyme
and other tick-borne diseases. The workshop will represent the broad
spectrum of scientific views on Lyme disease and should provide a forum
for public participation and input from individuals with Lyme disease as
requested in congressional appropriations report language in House
Committee Report 111-120 and Senate Committee Report 111-66. The product
to be delivered will be a committee authored meeting summary that
highlights workshop presentations and discussions.
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Posted by Editor on Friday, September 24 @ 13:05:48 EDT (1727 reads)
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 | Proof That Chronic Lyme Disease Exists |
LymeBlog News
Lexington, KY USA
By LymeBlog News Staff
Dr. Cameron's latest article presents several findings and pieces of data from research and studies related to Chronic Lyme Disease,
including but not limited to the following issues; diagnosis, current
limitations of and costs for treatment, the severity of symptoms, and
mixed long-term outcome for children with the disease. Dr. Cameron
includes research from his own practice, 32% of a consecutive case
series of Lyme disease cases (confirmed by an ELISA and 5 or more
positive bands on a IgG Western blot) had an average treatment delay of
1.8 years. Of these, 60% conformed to Centers for Disease Control (CDC)
and Prevention epidemiological criteria, presenting with a rash, Bell’s
palsy, or arthritis, yet there was still a diagnostic delay. Patients
in this case series were significantly more likely to fail their
initial antibiotic treatment since they had delayed treatment. Dr.
Cameron also addresses the risk to society of emerging
antibiotic-resistant organisms – the fact this should be weighed
against the societal risks associated with failing to treat an emerging
population saddled with Chronic Lyme Disease. He believes once we
acknowledge and accept the evidence that Chronic Lyme Disease exists,
the medical community will be able to focus on developing solutions for
this debilitating disease.
This research article is the first of its kind,
in that no one has ever summarized the proof that Chronic Lyme Disease
exists before in this type of format. In addition, no one has focused
on the consequences of denying that Chronic Lyme Disease exists, or on
the opportunities if one accepts that Chronic Lyme Disease exists.
Please find embedded in this release, the full version of Dr. Daniel
Cameron’s Research Article – Proof That Chronic Lyme Disease Exists.
About Dr. Daniel Cameron:
Dr. Cameron remains active in the practice of medicine, personally
attends to all the patients who visit his practice, and is affiliated
with Northern Westchester Hospital in Mt. Kisco, NY. He served as the
president of the International Lyme and Associated Diseases Society
(ILADS) from October 2007- October 2009, and he has published and
presented more than 30 scientific papers.
Photo: lymeproject.com
Dr. Daniel Cameron, a board certified primary care physician in Mt. Kisco, NY, considered one of the pioneers in successfully treating recurrent or Chronic Lyme Disease, has recently published a research article detailing clinical studies that support the conclusion that Chronic Lyme Disease exists – Proof That Chronic Lyme Disease Exists. Dr. Cameron diligently researched and sourced information, leveraging credible research studies and evidence to outline and prove that Chronic Lyme Disease does exist in his research article. The goal of this article is to inform the public and medical community on the implications of Lyme disease when left undiagnosed and untreated.
Photo: lymeproject.com
Dr. Cameron latest publication
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Posted by Editor on Saturday, June 19 @ 10:40:50 EDT (2377 reads)
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