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Recent press release from CDC who’s motto is “24/7  saving lives and protecting people” !!

http://www.cdc.gov/media/releases/2013/p0819-lyme-disease.html

…and it’s getting considerable attention…

http://lymedisease.org/news/touchedbylyme/cdc-lyme-number-coverage.html

TOUCHED BY LYME: “300,000? number catches media’s eye

21st August 2013
When the CDC bumped its estimate of annual Lyme cases from 30,000 to ten times that, it made the evening news.

I blogged last week about the unprecedented wave of recent media coverage about Lyme disease. Turns out, we hadn’t seen nothin’ yet.

On Monday, August 19, the CDC announced that it had raised its official estimate of how many cases of Lyme disease are diagnosed each year, from 30,000 to 300,000.  (No matter that way back in 2004, the CDC stated on the record that official numbers were likely underreported by a factor of 10. Suddenly, putting that big number—300,000—in an official government press release made the news media sit up and take notice.)

All the major news outlets carried the story, some of them going into deeper detail than others. Here are links to a sampling if you want to check them out yourself.

Boston Globe

Poughkeepsie Journal

PBS Newshour

NBC Virginia

CBS Chicago

San Francisco-area TV station KTVU

The New Yorker blog

In addition to a news story, the Poughkeepsie Journal (in New York state) ran an editorial entitled “Lyme fight must go beyond change in numbers.” In addition to having more accurate reporting of cases, the newspaper suggests a number of changes:

That would include providing doctors with more protections if they are treating long-term cases of Lyme. It also would include establishing a federal advisory committee to ensure that all medical points of view are being represented before public health policy decisions are reached in relation to Lyme.

Sound proposals have been offered for years, but little action has been taken. Armed with new numbers, advocates must continue the fight for a better and broader fight against Lyme.

Hear, hear.

TOUCHED BY LYME is written by Dorothy Kupcha Leland, LymeDisease.org’s VP for Education and Outreach. Contact her at dleland@lymedisease.org.

- See more at: http://lymedisease.org/news/touchedbylyme/cdc-lyme-number-coverage.html#sthash.VBV9I5Gl.dpuf

Well there you have it… from CDC themselves.  How are you going to deny that… Bartonella in Lice !!!

Volume 19, Number 2—February 2013

Dispatch

Transmission and Maintenance Cycle of Bartonella quintanaamong Rhesus Macaques, China

Abstract

We detected Bartonella quintana in 48.6% of captive rhesus macaques from an animal facility in Beijing, China. Prevalence of infection increased over the period of observation. Our findings suggest that macaques may serve as reservoir hosts for B. quintana and thatPedicinus obtusus lice might act as efficient vectors.

See link for full Article:

http://wwwnc.cdc.gov/eid/article/19/2/12-0816_article.htm

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November 28th, 2012
Dear Nova Scotia MLA/MP:
RE: Lyme Disease in Nova Scotia
Lyme Disease (LD) is an emerging disease in Nova Scotia and Canada that is generating considerable attention from the media, advocacy groups and communities. Given this situation, I felt it important that you had accurate and up-to-date information on LD in Nova Scotia and the provincial response plan.
LD is a bacterial illness that can be transmitted to humans through the bite of a blacklegged tick (deer tick). There are a number of tick species in Nova Scotia, but only the blacklegged tick can carry the bacteria that can cause LD. Not all blacklegged ticks carry the bacteria and the risk of acquiring LD remains low in the province. LD is readily treatable with appropriate antibiotics.
The Department of Health and Wellness (DHW) has an active LD response plan which includes an interdisciplinary committee (public health, veterinary medicine, wildlife biology) that provides evidence-based advice and guidance to the provincial government on the control of LD. Nova Scotia has multiple infectious disease and medical microbiologist experts in the province who deal with treatment and diagnosis of LD. DHW has a close working relationship with these clinical experts through an Infectious Disease Expert Group, which meets regularly to advise DHW on public health and infection control issues. We also work closely with our partners at the Public Health Agency of Canada and the National Microbiology Laboratory who provide evidence based recommendations for the prevention and surveillance of LD and ticks.
Tick and Lyme Disease Surveillance
Lyme disease is a notifiable disease under the National Microbiology Laboratory. Health care professionals are required to report cases of Lyme disease to Public Health when they diagnose clients clinically or with laboratory confirmation. In 2011, there were 54 confirmed cases of LD reported to Public Health, corresponding to an incidence rate of 5.8 cases per 100,000 population. Surveillance of both human cases and blacklegged ticks in the province enables DHW to keep abreast of the current state of Lyme disease in Nova Scotia.
Over the past few years, DHW together with the Department of Natural Resources and the Public Health Agency of Canada have been identifying and testing ticks collected in Nova Scotia. Analysis of this data has identified six areas where blacklegged ticks carrying the bacteria that can cause LD are known to be endemic (i.e. have become established as part of the local ecology). These endemic locations are areas in Yarmouth County, Shelburne County, Lunenburg County, Halifax County, Pictou County and most recently Queens County. These known endemic areas can be found on the Department of Health and Wellness website at http://www.gov.ns.ca/hpp/cdpc/lyme.asp
DHW has had a tick surveillance program in place since 2002, which included both passive (ticks being submitted by the public) and active plans. In the fall of 2011, DHW restructured its tick surveillance program to place an emphasis on active surveillance. Active surveillance involves ‘in the field’ work including small mammal testing and dragging vegetation to collect
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ticks. We will continue with focused active surveillance to determine additional areas where ticks may be establishing.
It is expected the number of LD cases will increase over time as ticks become more densely populated and expand their geographical range when conditions permit. Climate change related to global warming is expected to contribute to the increase of LD in Nova Scotia and Canada.
Public Information
DHW regularly provides consistent, evidence based information about LD and its prevention to the public. Strategies are implemented each year to provide Nova Scotians with information about the prevention of tick bites and to ensure health care providers have the most up to date clinical information. The DHW website is regularly updated plus we work closely with partners to disseminate information regarding LD to the public and stakeholders via various methods (letters via schools, residential letters, media releases, websites, signs in parks/campgrounds). DHW has also provided an advertorial for newspapers as well as news release each year. DHW regularly responds to multiple media requests and letters to government regarding LD.
Nova Scotians and visitors to the province can help prevent exposure to blacklegged ticks and LD by taking some simple precautions. This is especially important when in areas where there may be increased risk. Prevention messages can be found on the DHW website at: http://www.gov.ns.ca/hpp/cdpc/lyme.asp
Information to Clinicians
Webinars have been provided to health care providers in the last few years, addressing prevention, surveillance, diagnosis and treatment of LD. In addition, the DHW provides updates to physicians in the province via Doctors Nova Scotia. The Infectious Disease Expert Group has developed a document entitled “Statement for Managing Lyme Disease in Nova Scotia” which has been widely circulated to physicians in the province. This document is based on current evidence and follows the guidelines endorsed by the Infectious Disease Society of America.
Testing
Laboratory testing for LD in Nova Scotia follows the guidelines established by the Public Health Agency of Canada and the Centre for Disease Control and Prevention in the United States. These guidelines have been endorsed by the Canadian Public Health Laboratories Network and the Infectious Diseases Society of America.
We are aware of the Canadian Lyme disease advocacy group, Can Lyme, who claim that the testing and treatment of LD is inadequate. However, the testing methods they promote, and the ones used by many private labs in the US, are not endorsed by infectious disease and laboratory experts.
Research
DHW supports and partners with many researchers in the field of LD and tick surveillance. Research that DHW is aware of and supports includes the Public Health Agency of Canada’s study on identification of emerging endemic areas for the blacklegged tick and prediction of the further spread of LD. Two other research initiatives that DHW supports include the human seroprevalence study on LD and the Deer Treatment Study. We are aware that other
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researchers initiate studies within the province with or without consultation or consideration of experts on the interdisciplinary committee.
If you have additional questions regarding LD, or if you would like to involve a regional Medical Officer of Health in any meetings with community or advocacy groups, please contact your local Public Health office which can be found through the following website: http://novascotia.ca/DHW/about/phs-offices.asp
We appreciate your ongoing support and cooperation to help ensure Nova Scotians receive evidence-based information on LD.
Sincerely,
Robert Strang MD, MHSc., FRCPC
Chief Medical Officer of Health
c. Dr. Frank Atherton – Deputy Chief Medical Officer of Health, Health and Wellness
Elaine Holmes, Director – Communicable Disease Prevention and Control, Health and Wellness
Regional Medical Officers of Health

Panel of experts bring new perspectives to Morgellons Research.

Austin, TX (PRWEB) May 02, 2012 A multinational panel of medical and scientific professionals met on March 24 and 25, 2012 in Austin, Texas at the 5th annual Morgellons Medical Conference entitled, “Searching for the Uncommon Thread” to discuss the latest findings on Morgellons disease. Morgellons is a debilitating, systemic illness characterized by the formation of unusual fibers within the skin. In addition to slow-healing skin lesions, those afflicted by the illness also experience overwhelming fatigue, and an array of neurological deficits. Morgellons affects people of all ages and ethnic groups, worldwide. Sponsored by The Charles E. Holman Foundation (CEHF), the two-day event boasted attendees comprised of doctors, scientists, Morgellons patients and supporters. Much of this conference was dedicated to refuting the conclusions suggested by the 2011 study by Hylwa et al, of the Mayo Clinic, and the January 25th, 2012 Center for Disease Control (CDC)/Kaiser Permanente Morgellons study.

Highlights of the two-day event included many educational and thought provoking presentations. Canadian microbiologist, Marianne Middelveen, reported on ground-breaking research that she and prominent San Francisco-based physician, Raphael Stricker, published recently in Clinical Cosmetic and Investigational Dermatology, http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3257881. This research demonstrates similarities between Morgellons and a bovine spirochetal disease.

“The unusual filaments associated with Morgellons are likely composed of keratin and demonstrated photographic evidence that fibers stem from both pavement epithelial cells and hair follicles, tissues where keratinocytes are the predominant cell type,” stated Dr. Middelveen. According to Middleveen “these findings conclusively debunk the erroneous theory that this disease is caused by delusional beliefs and that patients self-implant fibers or are intentionally mutilating themselves”. A second publication related to this subject authored by Middelveen, Stricker and other collaborating researchers, is currently in-press and scheduled to be published soon.

Australian Dermatologist, Peter Mayne, showed clear slides of fibers taken from some of his many Morgellons patients, noting that fibers are subdermal in origin and some originate in the hair bulb. Dr. Mayne is the first practicing dermatologist to thoroughly examine the tissue of Morgellons patients and acknowledge the disease’s unique pathological characteristics. Mayne outlined differential diagnoses he considers in his Australian clinical practice. Dr. Mayne, along with Randy S. Wymore, PhD., Director of Research at the Center for the Investigation of Morgellons disease, reviewed the history of the CDC’s noninvolvement with Morgellons disease, and refuted the 2012 CDC/Kaiser study results. A presentation on Institutional Cognitive Dissonance by CEHF Director, Cindy Casey, RN, in collaboration with Elizabeth Rasmussen, PhD, further demonstrated the repudiation by the CDC in its lawful responsibilities towards Morgellons patients as well as to their confused and bewildered medical care providers.

CEHF Associate Director, Greg Smith, a pediatrician from Georgia, Dr. Amelia Withington, a Psychiatrist from Pennsylvania, Ginger Savely, DNP, a recognized authority in the medical management of Morgellons disease from Washington, D.C., and Carsten Nicolaus, MD, PhD from Augsburg, Germany, an esteemed medical provider for Morgellons patients in Europe, also gave informative presentations covering a broad range of Morgellons-related topics.

The Morgellons medical conference is an annual gathering in Austin, Texas of medical and scientific professionals and members of the Morgellons community. Sponsored by The Charles E. Holman Foundation in Austin, Texas, its purpose is to discuss the latest scientific discoveries in Morgellons research. The foundation was named for Charles E. Holman, a pioneer in the fight against Morgellons disease.

The official DVD of the conference is now available. To order a copy of the DVD, please visit http://www.thecehf.org.

###

Cindy Casey, Director The Charles E. Holman Foundation (415) 720-8752 Email Information

See link:

http://gma.yahoo.com/exciting-discoveries-morgellons-research-unveiled-annual-conference-070428812.html

Dr. Phil after the “Deadly Consequence’s” show stated he should have touched more on the “Key Elements” regarding the Conflicts of Interest pertaining to Lyme.
That comment was HUGE !!
Thankyou again !!

See link here:

http://www.drphil.com/uncut/page/uncensored/

Petition to Remove Outdated Lyme Treatment Guidelines from National Guidelines Clearinghouse

ProHealth.com

February 9, 2012

LymeDisease.org* has dedicated a page to an online petition requesting that the Infectious Diseases Society of America (IDSA) guidelines for medical treatment of Lyme disease be removed from the National Guidelines Clearinghouse list and be updated to reflect current research.

A key reason stated for the petition is that the current IDSA Lyme guidelines, established in 2006, do not recognize the possibility of persistent infection after initial 10 to 28 days of antibiotic treatment. Research since 2006 has found evidence that infection may persist after initial antibiotics where infection is established.

Find the petition here – http://www.lymedisease.org/petitionscript/index.php.

The list of more than 11,430 signatures appears to be growing moment by moment – and though signers are required to provide some information to ensure validity, they can elect to remain anonymous by clicking a box.

___

* LymeDisease.org, formerly the California Lyme Disease Association (CALDA), is now a national US nonprofit organization dedicated to providing a central voice for Lyme disease patient advocacy, education and research. Thanks to XMRV Global Action Facebook for this news.

See full story:

http://www.prohealth.com/library/showarticle.cfm?libid=16808

http://www.activistpost.com/2012/01/cdc-calls-morgellons-nanoworms-delusion.html

http://m.youtube.com/#/watch?desktop_uri=%2Fwatch%3Fv%3DFFeHIXGT0To%26feature%3Dshare&feature=share&v=FFeHIXGT0To&gl=CA

Joni Mitchell’s page:

http://www.jonimitchell.com/library/view.cfm?id=1996

The
Kaiser/CDC Morgellons Collaborationby Miguel Perez-Lizano
February 2008

Morgellons is a disease that has garnered widespread attention in the past few years. The cause of the disease is unknown.   The most  significant aspect of the disease is the growth of multicolored fibers erupting from lesions in the skin. Many patients with Morgellons also have documented Lyme disease, and Morgellons patients typically have symptom overlap with Lyme disease.

This disease is not a new disease. In the past doctors have dismissed Morgellons sufferers with a diagnosis of delusional parasitosis – a psychiatric condition in which a patient believes parasites are crawling in their bodies. I know one Morgellons sufferer who is an intelligent, normal professional and was given this diagnosis. Dismissive use of the term “delusional parasitosis” should be a red flag that signifies the uninformed, uncaring
doctors who parrot this diagnosis to hide their ignorance and laziness.

The Centers for Disease Control has awarded Kaiser Permanente a grant to study Morgellons in their patient population in Northern California.
The CDC uses Kaiser for studies because of their captive member base. All, or most, records for health care received reside at Kaiser and can be retrieved. In addition, patients included in clinical trials can be easily tracked.   This  also avoids the expense of enrolling people in clinical trials orstudies.

It is more than likely that this study will validate the theorem “garbage in, garbage out.” One potential flaw is the probability that
inadequate care has affected the reliability of
information contained in patient records. An example that would relate to this study is the fact that many (and perhaps all) Morgellons sufferers also have Lyme disease. 

See Article here:

http://lyme.kaiserpapers.org/kaiser-cdc-morgellons-collaboration.html

DALLAS (CBS 11 NEWS) – Five years ago, CBS 11 News began investigating a bizarre medical condition known as Morgellons Disease. Those who claim to have it describe unusual symptoms like strange fibers poking through their skin. But, the question all along has been is it real, or is it just in the patient’s mind?
In 2008, CBS 11 was the first to report that the Centers For Disease Control would be launching its own investigation to determine if Morgellons was in fact a new and real disease. Now, the agency is making its findings public in this report. But, it may not be what patients hoped to hear.
I feel the itchy and the creepy crawly,” said Cindy Casey when we first met her in 2007. “It’s been extremely disfiguring… every part of my body, hands, legs, arms, and back.”
Casey has been dealing with effects of a mysterious illness for more than a decade.
“I don’t escape it for one moment of the day,” she said. “I’m constantly aware of it.”

See full story

http://dfw.cbslocal.com/2012/01/26/cdc-releases-results-of-morgellons-disease-investigation/

* There is also two links that contain CDC’s full report of investigation and a response from Cindy Casey

*There are about 4 Article’s in circulation at the moment. This is about the only I would post. The others seem to be “what the media would like you to believe”…beware of them !!

Saturday, January 21, 2012 by: Ethan A. Huff, staff writer

(NaturalNews) Remember when it was considered crazy talk to suggest that mainstream medicine viewed humanity as being born lacking in pharmaceutical drugs and vaccines, as if these synthetic inputs are necessary miracle nutrients for proper human development? Well, researchers from the US Centers for Disease Control and Prevention (CDC) recently showed that they adhere to this lunatic philosophy, having released a study that recommends women withhold breastfeeding their children in order to boost the “effectiveness” of the rotavirus vaccine.

Ten researchers from the CDC’s National Centers for Immunization and Respiratory Disease (NCIRD) released the ridiculous paper, entitled Inhibitory effect of breast milk on infectivity of live oral rotavirus vaccines, which claims the immune-boosting effects of breastmilk are a detriment to the efficacy of vaccines. The paper goes on to say that, rather than remove vaccines so that breastmilk can do its job, women should instead remove the breastmilk to allow vaccines to do their job.

See full story here:

http://www.naturalnews.com/034722_breastfeeding_vaccines_CDC.html

http://www.voltairenet.org/Morgellons-Victims-Across-the-US

Three weeks ago, we wrote about a “disease” known as Morgellons that very few people in the world know anything about. We placed the word disease above in quotation marks only because a large number of physicians refuse to recognize Morgellons as a medical affliction, with some even refusing to treat patients who suffer from it.
We have listened to a long litany of accounts about doctors who have literally laughed in the faces of Morgellons sufferers, male and female, young and old, with many attempting to make referrals to psychologists. Remarkably, other physicians have mounted web sites mocking and attacking people who report they have Morgellons and those who write about it. Some physicians have dubbed the disease Delusions of Parasitosis, meaning it’s all in the patient’s head. Additionally, there is a website entitled morgellonswatch.com “dedicated to examining the claims made regarding what is termed ‘Morgellons Disease’” and to preventing “sick people into thinking they may have a terrible disease.” Oddly, there are no formal individual or institutional sponsoring names identified on this site.
Despite this seemingly general stance from the “medical community” there are clear exceptions. Nearly every state across the US, and country in Europe, has at least several medical professionals who regard Morgellons as “a serious emerging infectious disease deserving study and research.” Dr. Ahmed Kilani, Laboratory Director of Clongen Laboratories, Germantown, Maryland, says, “I have personally listened to detailed descriptions of the symptoms of this disease and something has got to be done.”
At present, the Center for Disease Control (CDC) in Atlanta, Georgia is conducting a study of Morgellons in partnership with Kaiser Permanente’s Northern California Division of Research. The study was formally announced and launched in January 2008. The stated objective of the study was “to learn about an unexplained skin condition known as Morgellons.” The study, said a CDC spokesperson, was expected to “Take up to 12 months or longer to complete.” Said the CDC’s Dr. Michele Pearson, the principle investigator on the study, “We earnestly want to learn more about this unexplained illness which impacts the lives of those who suffer from it. Those who suffer have questions, and we want to help them.”
Over two years past the CDC’s announcement it appears unknown as to when the study will be completed or be released. About a month ago there were unconfirmed reports that the study had been handed off entirely to the Armed Forces Institute of Pathology in Washington, D.C., an identified partner in the study as explained by the CDC in 2008.
Morgellons Symptoms
The initial symptoms of Morgellons involve patients experiencing the discomforting sensation of insects crawling on and biting or stinging their skin. This sensation results in skin lesions that can appear much like mild to severe cases of acne. The lesions can appear anywhere on a patient’s body and quite often contain fiber-like strands or fibrous material. The fibers are the most perplexing visible feature of Morgellons. Often when an attempt is made to remove or extract the fibers the material will resist and act to withdraw or move away from whatever instrument is being employed.
Skeptics have put forth various explanations for the presence of the fibers that plague sufferers of Morgellons disease. Some have suggested that the fibers are merely clothing fibers, and other common everyday material, that become attached to scabbed lesions accidentally; the sufferers, skeptics claim, are falsely convinced that the fibers are being produced by their bodies.

Implement Recommendations Outlined in Schmidt Report 2010 Petition | GoPetition

 

Chelsey Livingstone and her mom, Angela Rector, organize the many pills Chelsey needs each day as she battles Lyme disease. It’s a costly process that could take from one to three years. Jennifer Vardy Little – The News
Published on May 26, 2011

 

Mom blames poor tests that failed to diagnose Lyme disease

Topics :
Department of Health , Sutherlands River , Ontario , Port Hawkesbury

SUTHERLANDS RIVER – For 8 1/2 years, Angela Rector brought her daughter to doctor after doctor, looking for answers.

Chelsey Livingstone, 11, lives in pain. She describes joints that ache so badly it keeps her up at night and a sharp pain in her stomach.

“It feels like someone’s stabbing me in my belly,” she says softly.

From the time she was a small child, she’d call out to her mother as she lay in bed at night, and in the time it took Rector to get across the hallway, she’d find Chelsey lying there, staring unresponsively at the ceiling with blue lips. Doctors thought she had epilepsy at first, but ruled that out, instead calling the nightly events “episodes.”

Doctors didn’t believe Chelsey when she said how bad the pain was, either.

“You know how they always ask how bad the pain is on a scale of one to 10? She’d say a 15, and they said that was impossible,” said Rector.

She was tested for rheumatoid arthritis, bladder infections, Crohn’s and irritable bowel, but all the possibilities were rejected. Eventually, says Rector, physicians at the IWK suggested it was all in Chelsey’s head and gave her a book on ways to cut back her stress levels.

Rector wasn’t willing to give up, however. All along, she begged the doctors to consider Lyme disease. When Chelsey was just 2 1/2, the family was living in Borden, Ont., and Rector believed her daughter had been bitten by a tick.

See Story here:

http://www.ngnews.ca/News/Local/2011-05-26/article-2538390/Child’s-illness-mystifies-doctors/1

SafeMinds demands long-overdue independent review of vaccine/autism research for data manipulation and conflicts of interest. Vaccine safety remains questionable.

ATLANTA, April 14, 2011 /PRNewswire-USNewswire/ — Poul Thorsen, the principal coordinator of multiple studies funded by the Centers for Disease Control and Prevention (CDC) used to deny a vaccine/autism link was indicted on April 13th on 13 counts of fraud and 9 counts of money-laundering.  The charges relate to funding for work he conducted for the CDC, which claimed to disprove associations between the mercury-based vaccine preservative, thimerosal, and increased rates of autism.

SafeMinds first voiced concerns in 2003 regarding a series of epidemiology studies out of Denmark and under the jurisdiction of Thorsen that provided the basis for the Institute of Medicine’s claim that there was no association between thimerosal and autism.  That claim has been responsible for the continued unsafe use of mercury in influenza vaccines in the United States and infant vaccines around the world.

“The quality of this epidemiological research has always been questionable,” states Sallie Bernard, SafeMinds president.  ”Many biological studies support a link between mercury and autism, but these Danish studies have been used to suppress further research into thimerosal.  With clear evidence of Dr. Thorsen’s lack of ethics, it is imperative to reopen this investigation.”

ATLANTA, April 14, 2011 /PRNewswire-USNewswire/ — Poul Thorsen, the principal coordinator of multiple studies funded by the Centers for Disease Control and Prevention (CDC) used to deny a vaccine/autism link was indicted on April 13th on 13 counts of fraud and 9 counts of money-laundering.  The charges relate to funding for work he conducted for the CDC, which claimed to disprove associations between the mercury-based vaccine preservative, thimerosal, and increased rates of autism.

SafeMinds first voiced concerns in 2003 regarding a series of epidemiology studies out of Denmark and under the jurisdiction of Thorsen that provided the basis for the Institute of Medicine’s claim that there was no association between thimerosal and autism.  That claim has been responsible for the continued unsafe use of mercury in influenza vaccines in the United States and infant vaccines around the world.

“The quality of this epidemiological research has always been questionable,” states Sallie Bernard, SafeMinds president.  ”Many biological studies support a link between mercury and autism, but these Danish studies have been used to suppress further research into thimerosal.  With clear evidence of Dr. Thorsen’s lack of ethics, it is imperative to reopen this investigation.”

http://pharmalive.com/News/index.cfm?articleid=774819&categoryid=32

Randy Sykes message to Lyme Patients asking patients to put aside their personal differences and act together for positive change. Mr. Sykes was a DOT working in Connecticut before being stricken down with Lyme.

He isn’t lazy, rides Harleys and is not someone to bellyache.

More information:
http://starkravingviking.blogspot.com…

http://www.youtube.com/watch?v=0tO-TVfeSTU&feature=related