Archive for the ‘Transmission’ Category

NY Medical College & the 21st Century Plague

https://www.change.org/p/1120418/u/22746020?utm_medium=email&utm_source=petition_update&utm_campaign

New York Medical College and the 21st Century Plague

Carl Tuttle
Hudson, NH
MAY 14, 2018 — Please see the latest email thread below addressed to the president and chairs of New York Medical College who have refused to acknowledge the concerns identified in these letters. Please continue to read past the 19 references.

NOTE:

The primary focus of this petition has been to expose the deception and scientific misconduct while highlighting the fact that Lyme is life-threatening/life-altering ruining lives worldwide while public health officials follow what has been deceitfully established here in the United States.

All information provided is in the public domain available for use in future litigation

The evidence is overwhelming that Lyme disease is capable of death and disability as most data is easily accessed through Pubmed by an astute fifth grader.

If Lyme disease was classified as life-altering/life threatening as it truly is and elevated to Highest Alert in the same category as AIDS then we would get the funding needed to finance a Manhattan Project.

For nearly four decades Lyme is simply seen as a low-risk and non-urgent health issue.

What was the motivation for downplaying the severity of Lyme disease?

The rush to create a vaccine for Lyme led to the mishandling of the disease as laboratory testing was manipulated (Dearborn) to insure the vaccinated would test seronegative. All evidence points to those who were involved in the vaccine debacle. The vaccine by the way caused the same debilitating effects as the disease itself as identified in the class action lawsuit below. For the record, LYMErix was not withdrawn from the market due to slow sales.

REPORT ON LYMErix
Prepared by: SHELLER, LUDWIG & BADEY
Stephen A. Sheller, Esquire
Albert J. Brooks, Jr., Esquire
https://www.dropbox.com/s/sodqs3pdeeesktf/Sheller%20Lymerix.pdf?dl=0

JUDGEMENT, FINAL ORDER AND DECREE GRANTING FINAL APPROVAL OF THE CLASS ACTION SETTLEMENT:
https://www.lymediseaseassociation.org/images/NewDirectory/Government/Vaccines/2003_Vaccine_Judgement_Final_Sttle_Apprvl..pdf

Important background on Lyme vaccine controversy

The Vaccine Connection: Lyme Gets a Business Model
By Pamela Weintraub:
https://www.lymedisease.org/vaccine-chapter-of-cure-unknown/

Please read the following comment by Dr. Rosalie Greenberg in response to Dr. Bransfield’s recent article:

Aggressiveness, violence, homicidality, homicide, and Lyme disease
https://www.dovepress.com/articles.php?article_id=38295

Letters to the president of New York Medical College:

———- Original Message ———-
From: Carl Tuttle
To: Alan_Kadish@nymc.edu
Cc: Nicholas_Janiga@nymc.edu, Michael_Newman@nymc.edu, ddutko@hanszenlaporte.com
Date: May 6, 2018 at 11:01 AM
Subject: New York Medical College and the 21st Century Plague

May 6, 2018

New York Medical College
40 Sunshine Cottage Rd
Valhalla, NY 10595
Attn: Alan Kadish, M.D., President

Re: New York Medical College and the 21st Century Plague

Dr. Kadish,

It was once thought that the Black Plague (mid-1300s) was transmitted by the bite of a flea that acquired the pathogen from infected rats. This rat-flea theory may be in question but transmission regardless is believed to have been vector borne [1].

There is no question whatsoever that Lyme disease is transmitted to humans by the bite of an infected tick.

Lyme disease is capable of producing sudden death with no warning signs; [2,3,4] heart damage requiring transplant, [5] paralysis with seizures, [6] lymphoma [7] and persistent infection after antibiotic treatment [8,9,10,11,12] along with congenital transmission [13] and ability to create wheelchair bound patients [14] yet there are no Public Service Announcements informing the public that you could become horribly disabled or die from Lyme disease.

I ask you Dr. Kadish, “Why do you think there are no Public Service Announcements (PSA’s) describing the severity of Lyme disease?”

Please be advised that a racketeering lawsuit (RICO) has been filed in the United States by the law firm SHRADER & ASSOCIATES, LLP naming Dr. Gary Wormser of New York Medical College and six other academics.

The court document can be found at the following link:

Click to access LymeDisease.pdf

A worldwide community of physicians has been influenced by the ongoing disinformation campaign aimed at promoting the idea that Lyme is little more than a nuisance disease (Aches and pains of daily living) as health agencies across the globe are blindly following what has been deceitfully established here in the U.S. (New York Medical College)

We are dealing with a life-altering/life-threatening infection with faulty/misleading antibody tests, inadequate treatment, no medical training and absolutely no disease control.

A plague denied; essentially classifying this disease as a low-risk and non-urgent health risk.

Lyme disease is spreading across the globe through migratory birds with no continental boundaries destroying lives, ending careers, causing death and disability while leaving victims in financial ruin.

Through an elaborate racketeering scheme the disease has been downplayed because it became “too expensive to treat” as outlined in the SHRADER & ASSOCIATES, LLP court document.

Wormser of NYMC has been identified as a kingpin for disseminating the disinformation globally.

Here is just one example of the negative influence Dr. Wormser has had on the global scientific/medical community while promoting his bias against persistent infection:

Summary:

In 2001 Prof. Gerold Stanek, MD (Medical University of Vienna) clearly reported persistent Borrelia infection in a 64 year-old patient despite treatment with four courses of ceftriaxone. [15]

When publishing a paper in 2012 [16] with co-author Dr. Gary Wormser of New York Medical College, Stanek claimed:

“Most manifestations of Lyme borreliosis will resolve spontaneously without treatment.”

In 2014 Stanek published the following paper promoting antibiotic treatment in a patient requiring a pacemaker after Lyme caused complete heart block. And this is a nuisance disease?

Lyme Borreliosis (Book Chapter)
https://www.scopus.com/record/display.uri?eid=2-s2.0-84942739356&origin=inward&txGid=D355DFF083BF00E79EB6ABEAFE4BBD9F.wsnAw8kcdt7IPYLO0V48gA%3a13
Stupica, D.a, Stanek, G.b, Strle, F.a
a Department of Infectious Diseases, University Medical Centre Ljubljana, Ljubljana, Slovenia
b Institute for Hygiene and Applied Immunology, Medical University of Vienna, Austria

Abstract

A 49-year-old male, living in a Lyme borreliosis (LB) endemic region, noticed an erythematous skin rash about 10 days after a bite that in the next 2 weeks evolved to a ring-like skin lesion with diameters of 18×9. Cm, i.e., presenting as typical erythema migrans (EM). The lesion disappeared spontaneously in 5 weeks; however, in the following 2 months the patient developed radicular pains, complete heart block that required insertion of transient heart pacemaker, and knee arthritis. Cerebrospinal fluid (CSF) analysis revealed lymphocytic pleocytosis. High levels of serum and CSF borrelial IgG antibodies and intrathecal production of the specific antibodies were ascertained, and treatment with ceftriaxone 2. G OD intravenously for 14 days was initiated. The patient regained his physical capacity, radicular chest pain and knee swelling declined, and heart conduction abnormalities resolved. The pacemaker was removed during antibiotic treatment, and the patient’s further course was uneventful. The patient had all major manifestations of LB, which could have been prevented if EM had been recognized and properly treated. However, instead of antibiotic treatment, the physician who saw the patient at the time of EM ordered tests for the presence of borrelial antibodies, and misinterpreted negative serology as an indication against antibiotic treatment.LB is the most frequent tick-transmitted illness on the Northern Hemisphere. It is caused by certain species of Lyme borreliae. In the present report, epidemiology, etiology, mode of transmission, pathogenesis, clinical features, diagnosis and differential diagnosis, treatment and prevention of this emerging disease with increasing incidence are discussed. © 2014 Elsevier Inc. All rights reserved.
_______________________

A recent pilot study of twelve patients from Canada were culture positive for Borrelia infection (genital secretions, skin and blood) even after multiple years on antibiotics so there was no relief from current antimicrobials. Some of these patients had taken as many as eleven different types of antibiotics.

Persistent Borrelia Infection in Patients with Ongoing Symptoms of Lyme Disease (2018)
http://www.mdpi.com/2227-9032/6/2/33

We have lost nearly four decades to Wormser’s racketeering scheme where the focus was to discredit the sick and disabled (while suppressing evidence of chronic disease) as opposed to finding a new approach for treating persistent infection from a pathogen known to cause immune suppression.

“Spirochetes disseminate to the lymph nodes, bone marrow, spleen and brain within a week of infection [17] . Lymph node germinal centers, where B cells are supposed to mature and be assigned an immune system function, are rendered incompetent” [18]

Now the rest of the world is suffering.

Might I remind you Dr. Kadish, as president of New York Medical College, you are 100% responsible for Wormser’s scientific misconduct which continues to this day.

As spokesperson for the 55,000 individuals calling for a congressional investigation into the mishandling of Lyme disease [19] , I ask that you stop Dr. Wormser from publishing his junk science and remove him from his position of influence over the student population of New York Medical College.

Sincerely,

Carl Tuttle
Lyme Endemic Hudson, NH

Cc: Nicholas S. Janiga, Esq., Chief Counsel NYMC
Daniel R. Dutko, HANSZEN LAPORTE

New York Medical College Guiding Values:

https://www.nymc.edu/about-nymc/guiding-values/

Aptitude for Patient Care – The best reasons for providing patient care shouldn’t be a big paycheck. A strong desire to help people and the ability to provide exceptional care comprise the key traits every medical and health service professional should possess. Some of these things can be taught, but we find that NYMC students self-select our school because they truly wish to make a difference in people’s lives.

References: (Please read them)

1. Maybe Rats Aren’t to Blame for the Black Death
https://news.nationalgeographic.com/2018/01/rats-plague-black-death-humans-lice-health-science/

2. Cardiac Tropism of Borrelia burgdorferi: An Autopsy Study of Sudden Cardiac Death Associated with Lyme Carditis. (March 2016)
http://ajp.amjpathol.org/article/S0002-9440(16)00099-7/abstract

Excerpt:

“Fatal Lyme carditis caused by the spirochete Borrelia burgdorferi rarely is identified. Here, we describe the pathologic, immunohistochemical, and molecular findings of five case patients.”

3 CDC Case Study #1: Three Sudden Cardiac Deaths Associated with Lyme Carditis: http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6249a1.htm?s_cid=mm6249a1_w

4. CDC Case Study #2: A case report of a 17-year old male with fatal Lyme carditis
http://www.cardiovascularpathology.com/article/S1054-8807(15)00025-3/abstract?rss=yes

5. Professor Neil Spector: Duke physician uses near-death experience to encourage patient self-advocacy
http://www.dukechronicle.com/articles/2015/05/28/duke-physician-uses-near-death-experience-encourage-patient-self-advocacy#.VYlYnxtViko  Dr Neil Spector from Duke University required a heart transplant after his Lyme disease went undiagnosed for four years.

6. Nashua Mom in the ‘Lyme Light’ on Katie Couric Show
http://patch.com/new-hampshire/nashua/nashua-mom-talks-chronic-lyme-on-katie-couric-show  Fifth-grade teacher Kelly Downing was paralyzed from the neck down and interviewed by Katie Couric.

7. Infection by Borrelia burgdorferi and cutaneous B-cell lymphoma (Cancer)
https://www.ncbi.nlm.nih.gov/pubmed/9331890  Specific DNA sequences of Borrelia burgdorferi were identified in cutaneous lesions from 9 patients (follicle center lymphoma: 3/20; immunocytoma: 3/4; marginal zone B-cell lymphoma: 2/20; diffuse large B-cell lymphoma: 1/6).

8. Application of Nanotrap technology for high sensitivity measurement of urinary outer surface protein A carboxyl-terminus domain in early stage Lyme borreliosis.
http://translational-medicine.biomedcentral.com/articles/10.1186/s12967-015-0701-z  41 of 100 patients under surveillance for persistent LB in an endemic area were positive for urinary OspA protein after antibiotic treatment.

9. Culture evidence of Lyme disease in antibiotic treated patients living in the Southeast.
http://danielcameronmd.com/culture-evidence-of-lyme-disease-in-antibiotic-treated-patients-living-in-the-southeast/  Rudenko and colleagues reported culture confirmation of chronic Lyme disease in 24 patients in North Carolina, Florida, and Georgia. All had undergone previous antibiotic treatment.

10. DNA sequencing diagnosis of off-season spirochetemia with low bacterial density in Borrelia burgdorferi and Borrelia miyamotoi infections.
https://www.ncbi.nlm.nih.gov/pubmed/24968274  Faulty/misleading antibody tests landed a sixteen year old male in a psychiatric ward when his lab results did not meet the CDC’s strict criteria for positive results. His Western blot had only four of the required five IgG bands. Subsequent DNA sequencing identified a spirochetemia in this patient’s blood so his psychiatric issues were a result of neurologic Lyme disease misdiagnosed by antiquated/misleading serology. This patient was previously treated with antibiotics.

11. Granulomatous hepatitis associated with chronic Borrelia burgdorferi infection: a case report
http://www.labome.org/research/Granulomatous-hepatitis-associated-with-chronic-Borrelia-burgdorferi-infection-a-case-report.html  The patient had active, systemic Borrelia burgdorferi infection and consequent Lyme hepatitis, despite antibiotic therapy.

12. Scotty Shelton and Persistent Infection in Saginaw MN
https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/u/11685820  “Scotty’s brain (cerebral cortex) was positive for Borrelia burgdorferi and Borrelia myamotoi, his testicle is positive for Bb. We are now testing other tissues. Seven years of antibiotics and 3.5 years of natural treatments (along with antibiotics) and he was highly highly positive.”

13. Congenital Transmission of Lyme/TBD
https://www.dropbox.com/s/z10em0szgpm8bll/Congenital%20Transmission%20of%20Lyme%202015.doc?dl=0

14. Wheelchair-Bound Girl Calls Blessing By Pope Francis ‘Most Precious Moment Of My Life’ http://newyork.cbslocal.com/2015/09/24/pope-francis-blesses-girl-in-wheelchair/
NEW YORK (CBSNewYork) — A 12-year-old girl who has been confined to a wheelchair since being diagnosed with Lyme disease said meeting Pope Francis as he arrived in New York Thursday was “the most precious moment of my life.”

15. Isolation and polymerase chain reaction typing of Borrelia afzelii from a skin lesion in a seronegative patient with generalized ulcerating bullous lichen sclerosus et atrophicus. (2001) Breier F1, Khanakah G, Stanek G, Kunz G, Aberer E, Schmidt B, Tappeiner G.  http://www.ncbi.nlm.nih.gov/pubmed/11251580

16. Lyme borreliosis. (2012)
Stanek G1, Wormser GP, Gray J, Strle F.
http://www.ncbi.nlm.nih.gov/pubmed/21903253

Gerold Stanek published in the British Journal of Dermatology in 2001 reporting that:  “Borrelia [the Lyme disease bacteria] may possibly be able to remain dormant in certain tissue compartments”

17. Lymphoadenopathy during Lyme Borreliosis Is Caused by Spirochete Migration-Induced Specific B Cell Activation (2011)
Stefan S. Tunev, Christine J. Hastey, Emir Hodzic, Sunlian Feng, Stephen W. Barthold, Nicole Baumgarth
http://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1002066

18. Suppression of Long-Lived Humoral Immunity Following Borrelia burgdorferi Infection (2015)
Rebecca A. Elsner, Christine J. Hastey, Kimberly J. Olsen, Nicole Baumgarth http://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1004976

19. Calling for a Congressional investigation of the CDC, IDSA and ALDF
https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf
__________________________

Letter to the Academic Chairs of New York Medical College:

——— Original Message ———-
From: Carl Tuttle
To: john_fallon@nymc.edu, lnewman21@aol.com, mkittleson@nymc.edu, william_frishman@nymc.edu, Gregory.almond@nychhc.org, joseph_etlinger@nymc.edu, ernest_lee@nymc.edu, robert_amler@nymc.edu, vilma_bordonaro@nymc.edu
Cc: Alan_Kadish@nymc.edu, Michael_Newman@nymc.edu, ddutko@hanszenlaporte.com
Date: May 8, 2018 at 7:52 AM
Subject: Fwd: New York Medical College and the 21st Century Plague

To the Academic Chairs of New York Medical College;
Please see the letter below and supporting references addressed to Alan Kadish MD, President of NYMC.

Dr. Gary Wormser of New York Medical College has played a pivotal role in the mishandling of a disease destroying lives all across America as he continues to spread the disinformation which has misguided an entire medical community.

“Last September, France became the first country to release a national plan to address tick-borne diseases like Lyme. It ranges from ramped-up surveillance of ticks and infections to better treatment protocols and diagnostic tests.”

Marisol Touraine Launches National Plan to Combat Lyme Disease and Tick-borne Diseases
http://solidarites-sante.gouv.fr/archives/archives-presse/archives-communiques-de-presse/article/marisol-touraine-lance-le-plan-national-de-lutte-contre-la-maladie-de-lyme-et

Excerpt:

Marisol Touraine said: “This plan aims to avoid the feeling of abandonment and the therapeutic wandering faced by Lyme patients. It helps to better understand the disease, to treat patients more effectively and to mobilize all available tools to prevent the disease. ”

_____________

It is time for New York Medical College to recognize that Wormser is toxic to the advancement of the knowledge and treatment of Lyme disease which has been misclassified and downplayed as a low-risk and non-urgent health issue.

Might I remind everyone reading this email; you or a loved one is a single tick bite away from experiencing this travesty.

Carl Tuttle
Lyme Endemic Hudson, NH
_____________________________________________

2nd letter to the president of New York Medical College:

——— Original Message ———-
From: Carl Tuttle
To: Alan_Kadish@nymc.edu
Cc: ddutko@hanszenlaporte.com, Nicholas_Janiga@nymc.edu, john_fallon@nymc.edu, vilma_bordonaro@nymc.edu, Michael_Newman@nymc.edu, ernest_lee@nymc.edu, robert_amler@nymc.edu, mkittleson@nymc.edu, Gregory.almond@nychhc.org, lnewman21@aol.com, william_frishman@nymc.edu, joseph_etlinger@nymc.edu
Date: May 9, 2018 at 8:21 AM
Subject: Re: Fwd: New York Medical College and the 21st Century Plague

Dr. Kadish,

Please see the attached list of “Deaths From Lyme Disease” compiled from scientific literature by John D. Scott, Research Scientist dated 17 April 2018.
https://www.dropbox.com/s/eo794dx7zspc1ln/Ld%20deaths.doc?dl=0

Lyme disease patients have fatal outcomes and deaths are documented in alphabetic order.

If you search through this document you won’t find anything published by Dr. Gary Wormser of New York Medical College. In fact, none of his publications refer to these outcomes as Wormser has had a career long history of downplaying the severity of Lyme disease as identified in the racketeering lawsuit.

You have to ask the question Dr. Kadish:

“What is Wormser’s motivation for downplaying the severity of Lyme disease?”

Furthermore, congenital transmission of Lyme disease has been documented as well but you won’t find any references to this mode of transmission in Wormser’s publications. (See attached list of references) https://www.dropbox.com/s/xlju8w25phkypy0/Congenital%20Transmission%20of%20Lyme.pdf?dl=0

There is a refusal to recognize that untreated/undertreated Lyme evolves into an entirely different disease similar to untreated strep throat which, as you know progresses to rheumatic fever causing irreversible heart damage.

What happens to the Lyme patient who went months, years or decades before obtaining a diagnosis? Patient experience is describing a disease that is destroying lives, ending careers, causing death and disability while leaving victims in financial ruin.

It is this stage of disease that Wormser refuses to recognize as he has spent a career discrediting the sick and disabled as we have seen in the Lancet article where he is a coauthor; Antiscience and ethical concerns associated with advocacy of Lyme disease. Six of the seven defendants named in the racketeering lawsuit are coauthors of this disgraceful article.
https://www.thelancet.com/journals/laninf/article/PIIS1473-3099(11)70034-2/abstract

Once again I want to remind you Dr. Kadish that as president of NYMC you are 100% responsible for Wormser’s scientific misconduct.

Respectfully submitted,

Carl Tuttle
Lyme Endemic Hudson, NH

Cc: Nicholas S. Janiga, Esq., Chief Counsel NYMC
Daniel R. Dutko, HANSZEN LAPORTE
Academic Chairs of New York Medical College

 

 

 

 

 

 

 

Lyme Disease Has Arrived. Why Hasn’t a Reliable Treatment?

https://www.theglobeandmail.com/opinion/article-lyme-disease-has-arrived-why-hasnt-a-reliable-treatment/

Until we know better how to diagnose and cure, we must do battle with ticks.  GETTY IMAGES/GETTY IMAGES

Mary Beth Pfeiffer, an investigative journalist from New York State, is author of Lyme: The First Epidemic of Climate Change.

Like soldiers in an advancing front, blacklegged ticks are today marching across Canada armed chiefly, but not solely, with a pathogen that indiscriminately sickens and disables: Lyme disease.

In 1990, ticks that carried the infection were found only in Long Point in far southern Ontario. But hitched to birds and enabled by a warmer climate, these blood-sucking arachnids have found a new and rich frontier across vast tracts of the country. They are in Ontario’s provincial parks, in Quebec’s Montérégie region, where temperatures have risen 0.8 degrees Celsius since 1970, along Manitoba’s Lake of the Woods, and in many parts of Nova Scotia, New Brunswick and British Columbia.

Climate change did not cause this scourge but it is surely abetting it. In Canada, white-footed mice that infect baby ticks when they take their first blood meal are also moving north, further setting the stage for the disease to grow.

 

The upshot: Canada is well into an epidemic that has exploded in the United States since the disease emerged in a small coastal town in Connecticut in the late 1970s. Today, these ticks reside in half of the continental United States’ 3,000 counties, twice the number of two decades ago. Evidence suggests that “case numbers will increase rapidly in the coming years in Canada as I. scapularis” – the blacklegged tick – “invades the most heavily populated southern parts of Canada,” according to a 2015 article in the journal Applied and Environmental Microbiology.

Of paramount concern amid this invasion is that the standard treatment for Lyme disease used in Canada and other countries – a short course of antibiotics – leaves a significant share of patients ill for weeks, months and sometimes years. This treatment is based on care guidelines developed in the United States that new research suggests are flawed. Until the medical establishment stops denying a problem exists, more people will suffer.

In the United States, authorities estimate that reported Lyme disease cases – 36,000 in 2016 – are one-10th of the actual number. Canada’s official disease count, which grew nearly sevenfold from 144 in 2009 to 992 in 2016, is also likely far below the real number. In a recent visit to Nova Scotia, the hardest-hit province, I frequently encountered people in restaurants and shops who shared stories of Lyme disease, suggesting the disease is more common than the 326 cases reported in 2016.

At this crucial juncture, Canadians would do well to learn from the mistakes of the U.S. model of Lyme disease care, which has cost patients dearly in delayed diagnoses and inadequate treatments. Since 2000, when the first treatment guidelines were issued in the United States, Lyme disease has been framed as an infection that is straightforward to both diagnose and treat. It is not.

Science has repeatedly found that the standard Lyme test fails to diagnose many infections – especially early in the disease, but later as well – leading to illness that is more difficult to treat. Moreover, some 10 per cent to 20 per cent of treated patients go on to suffer what American medicine calls “posttreatment Lyme disease syndrome,” a condition called “severe” in a recent Johns Hopkins University study. Symptoms may include muscle, bone and joint pain, memory and sleep disorders, fatigue, depression and neurological problems including numbness and tingling in hands and feet.

Beyond its early rash and flu-like symptoms, Lyme disease has also been linked to problems of balance, sight and cognition, facial palsy, meningitis, arthritic symptoms and, when the pathogen invades heart tissue, Lyme carditis.

In Canada, Britain, the Netherlands, Sweden, Germany and many other countries with Lyme disease, the U.S. guidelines have set the standard for – have essentially dictated – management of this epidemic. Yet, at least 20 scientific publications since 2012 have reported that the way Lyme disease is treated, with 10 to 28 days of antibiotics, may not be working. The pathogen survived in infected monkeys and mice and in test tubes when exposed to an array of antibiotics used in people.

Mainstream medicine has been slow to acknowledge and accept these new findings, clinging to dogma that a bottle of antibiotics cures. Extended antibiotic courses don’t always resolve advanced cases of Lyme disease. The problem is that medicine rejects the notion that Lyme lingers, so has done little to find treatments that work.

In research for a book on the global spread of ticks, I met patients who travelled across oceans and borders in search of care for intractable Lyme disease. I spoke to a woman from Thunder Bay, Ont., who drove 14 hours to bring her son to a doctor in New York State. Others included a British man who flew to California, a young Swedish woman who went to England and a Dutch woman who went to Belgium.

These are the patients whose tests failed to diagnose them; who did not get or see the variable reddish rash that signals infection; or who were inadequately treated. To be sure, a significant share of early treated patients recover. These are the patients around whom the dogma of Lyme treatment has been fashioned.

But thousands of other patients in hundreds of Lyme disease support groups around the world are testament to the failure of a faulty model of care. Canada should listen to them.

Medicine does not have a handle on this epidemic. What is controlling it now, to a far greater extent, are the environmental forces wrought by human influence over the planet.

As temperatures rise, ticks have moved poleward – into Scandinavia, Russia, China, even Siberia and Australia. There and here, they lurk where children play and outdoor laborers work and hikers brush against the edges of trails.

 

Until we know better how to diagnose and cure, we must do battle with ticks. Be vigilant to check our children after spending time outdoors; avoid tall grasses and leaf litter, and even consider chemical repellents and clothing treatments. We must recognize our role in enabling an eight-legged menace and a single-celled pathogen that for eons existed quietly in nature but that today wreak havoc for many.

_______________

**Comment**

A few things to ponder:

  • Ticks have been all over the place for decades but authorities have refused to believe & recognize it.  Sick patients & the doctors who dare to treat them are the proof in the pudding, but these sick people have repeatedly been denied diagnosis and treatment by mainstream medicine based on ancient, faulty testing and faulty maps supposedly showing where ticks are.

Ticks are all over the place:  https://madisonarealymesupportgroup.com/2017/10/06/remembering-dr-masters-the-rebel-for-lyme-patients-who-took-on-the-cdc-single-handedly/  This expose’ by Pam Weintraub shows Dr. Masters has been screaming bloody murder about a Lyme-like illness in the South for decades.  Crickets…..

https://madisonarealymesupportgroup.com/2016/09/24/arkansas-kids-denied-lyme-treatment/  It’s in Arkansas….crickets.

https://madisonarealymesupportgroup.com/2016/11/03/ld-not-in-australia-here-we-go-again/  A Lyme-like illness is in Australia……crickets.

https://madisonarealymesupportgroup.com/2018/02/06/lyme-in-the-southern-hemisphere-sexual-transmission/  It’s clearly in the Southern Hemisphere…..crickets.

As you can clearly see, this is about WAY MORE than testing and treatment.  It’s a collective disgrace that makes Pandora’s Box look like a cookie jar.

Time to roll up the sleeves and get to work because there’s a lot to do.

Image

Lyme & Other TBI’s – 3rd Rocky Mountain Forum – May 19, 2018

SaveTheDate2018

Rheumatological Presentation of Bartonella Koehlerae & Henselae: A Case Report – Chiropractors Please Read!

https://journals.lww.com/mdjournal/Fulltext/2018/04270/Rheumatological_presentation_of_Bartonella.32.aspx

Rheumatological presentation of Bartonella koehlerae and Bartonella henselae bacteremias: A case report

Mozayeni, Bobak, Robert, MDa; Maggi, Ricardo, Guillermo, PhDb; Bradley, Julie, Meredith, BSb; Breitschwerdt, Edward, Bealmear, DVMb,*

Medicine: April 2018 – Volume 97 – Issue 17 – p e0465
doi: 10.1097/MD.0000000000010465
Research Article: Clinical Case Report

Abstract

Introduction: Systemic Bartonella spp. infections are being increasingly reported in association with complex medical presentations. Individuals with frequent arthropod exposures or animal contact appear to be at risk for acquiring long standing infections with Bartonella spp.

Case report: This case report describes infections with Bartonella koehlerae and Bartonella henselae in a female veterinarian whose symptoms were predominantly rheumatologic in nature. Infection was confirmed by serology, polymerase chain reaction (PCR), enrichment blood culture, and DNA sequencing of amplified B koehlerae and B henselae DNA. Long-term medical management with antibiotics was required to achieve elimination of these infections and was accompanied by resolution of the patient’s symptoms. Interestingly, the patient experienced substantial improvement in the acquired joint hypermobility mimicking Ehlers–Danlos Syndrome (EDS) type III.

Conclusion: To facilitate early and directed medical interventions, systemic bartonellosis should potentially be considered as a differential diagnosis in patients with incalcitrant rheumatological symptoms and frequent arthropod exposures or extensive animal contact.

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**Comment**

Bartonella isn’t even on most GP’s radars regarding tick borne illness, and in fact many deny ticks can even transmit it, yet here we see that those with arthropod exposure and/or animal contact need to consider it.  Isn’t that just about everyone under the sun?

You need to know this for yourself, friends and family.  Educate the doctors!

This poor female veterinarian was put on clindamycin & rifampin but had to discontinue after becoming pregnant.  She had a thousand symptoms:  axillary lymphadenopathy from cat scratch disease (CSD) at 12 years of age, a tibial sesamoid bone fracture, plantar fasciitis, generalized muscle/joint pain, muscle weakness, headaches, tingling, and fatigue, cervical lymph node enlargement, extremity edema, ligamentous laxity, tenosynovitis, shoulder and elbow subluxations, elbow joint crepitus, progressively worsening joint hypermobility (Beighton score 7/9), multiple joint subluxations daily, and breast cysts, meeting criteria for benign classification.

Please note the joint popping with each articulation and continual joint subluxation issue.  

Chiropractors need to be told about this.  Please educate!  Send them this article.

I too had this bizarre popping of the joints with a lot of instability in the knees.  Treatment completely ameliorated this issue so treatment is primo important.

For more on Bartonella:  https://madisonarealymesupportgroup.com/2016/01/03/bartonella-treatment/

https://madisonarealymesupportgroup.com/2018/05/07/fox-news-bartonella-is-the-new-lyme-disease/  (Tons more links on Bart after this article)

 

 

 

 

 

Tens of Thousands Likely to Get TBD in Massachusetts This Year

https://www.bostonglobe.com/metro/2018/05/07/state-expert-tens-thousands-likely-will-get-tick-borne-disease-mass-this-year

Tens of thousands likely to get tick-borne disease in Mass. this year

06252007_25tick-5985597An adult deer tick.  MARK WILSON/GLOBE STAFF/FILE

By Felice J. Freyer and Martin Finucane GLOBE STAFF MAY 07, 2018

Few experiences are creepier than finding a tick attached to your body — except, perhaps, pondering the harmful germs the eight-legged critter may be injecting.

But ponder no more: If you send a tick to the University of Massachusetts Amherst, you can find out exactly what manner of microbe may have infected it — and possibly, you. Lyme disease is the most prevalent, but ticks carry several other viruses, parasites, and bacteria.

People who find a tick on their body can put it in a plastic bag — dead or alive — and mail it to the UMass lab. For a fee, confidential results come by e-mail within three days.

The germs ticks carry are a matter of growing concern: Last week, the Centers for Disease Control and Prevention said that reported illnesses from mosquito, tick, and flea bites more than tripled from 2004 to 2016.

In Massachusetts in 2017, some 8,692 people tested positive for Lyme disease, up from 5,829 four years earlier. But most cases are not reported, so Dr. Catherine M. Brown, deputy state epidemiologist, estimates that about 87,000 people a year are getting Lyme disease in the state.

Anaplasmosis/ehrlichiosis, the second most common tick-borne disease, was reported 341 times in 2013, and rose to 1,226 in 2017. That’s a 260 percent increase.

“So many people in Massachusetts are being impacted by at least one of these diseases,” Brown said. “It’s increasing dramatically.”

Stephen Rich, a microbiology professor and director of the Laboratory of Medical Zoology at UMass Amherst, said the increases probably reflect both more illness and more awareness. The biggest changes are in areas, such as upstate New York, where ticks are just starting to move in, he said.

In Massachusetts, ticks are always abundant statewide, so fluctuations in the tick population have little meaning, he said. People need to think of protecting themselves from bites in the same way they put on sunscreen at the beach — a necessary precaution, every year. To avoid tick bites, wear clothing treated with permethrin, apply DEET to the skin, check for ticks after being outside, and treat your yard and pets.

The TickReport program at UMass, which Rich runs, tested 14,000 ticks last year and expects to see many more in 2018. The program, which has received ticks from all 50 states, demonstrates the power of crowdsourcing, by gathering a wealth of information on the location of different tick species and the disease-causing microbes they carry, he said.

The only other way to track ticks is to drag a cloth over bushes and test the ticks that stick to it, he said. But that just gives a snapshot of a limited area on a given day. “That doesn’t reflect the ticks that are biting people,” Rich said.

TickReport goes directly to the source — the ticks’ human targets.

People who send a tick pay $50, $100, or $200, depending on how many microbes are being tested for.

A $100,000 federal grant announced Monday will subsidize those tests for Massachusetts residents. The goal is to get a better idea of the prevalence of the 23 potentially disease-causing microorganisms that ticks can carry.

Along with a discount added by the laboratory, the federal grant will lower the cost of the $100 test to $15 for the first 1,000 ticks the lab receives; then it will lower the $50 test to $15 for the next 1,500 ticks.

TickReport has been testing ticks since 2006. About 43 percent come from Massachusetts but not evenly across the state. Rich hopes to get more ticks from underrepresented areas, particularly the North Shore, the Berkshires, and Worcester County.

The tests don’t diagnose a person but they provide information that can guide medical decisions, Rich said.

TickReport has a partnership with another crowdsourcing project — TickSpotters at the University of Rhode Island, which is free:  http://www.tickencounter.org/tickspotters

With TickSpotters, people e-mail photos of bugs they think are ticks and provide basic information such as how long each was attached. The URI group identifies the species of tick and describes the risk of illness. Often the bugs pictured aren’t even ticks — the program has received photos of weevils and lice, said Thomas N. Mather, director of URI’s TickEncounter Resource Center:  http://www.tickencounter.org

Once participants get the basics from TickSpotters, those who want to know more are urged to send the tick to TickReport to find out if it was infected.

For example, a Rhode Island woman recently sent TickSpotters a photo of a tick that had been attached to her for less than a day, Mather said. The program identified it as an adult, female, black-legged tick, and advised that the risk of infection was low because the tick hadn’t been attached long enough to transmit illness. Still concerned, the woman sent the tick to UMass, where it was found to be infected with Lyme disease.

That doesn’t mean the woman has Lyme disease. A tick must feed for 36 to 48 hours before it transmits Lyme disease. (Please see my comment below)

“If I were her, I would just be alert for symptoms. But we try to stay out of it at this point,” Mather said. The rest is up to the woman and her physician.

After years of trying to educate the public about ticks and the risk of illness, and finding that misinformation remains rampant, Mather has found TickSpotters to be a useful educational tool.

“I don’t think there’s anyone more engaged in learning about ticks than someone who has had a tick on them,” he said. “We’re personalizing education, approaching people at their most needy and receptive.”

TickSpotters, which started in 2014, has received nearly 46,000 submissions, collecting a wealth of data about locations of different species of ticks nationwide — data no one has had time to analyze, Mather said.

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**Comment**

While I love the work going on here a huge faux pax has been made regarding transmission times – and it’s a big deal:  https://madisonarealymesupportgroup.com/2017/04/14/transmission-time-for-lymemsids-infection/  

Transmission Time: Only one study done on Mice. At 24 hours every tick had transmitted borrelia to the mice; however, animal studies have proven that transmission can occur in under 16 hours and it occurs frequently in under 24 hours. No human studies have been done and https://www.dovepress.com/lyme-borreliosis-a-review-of-data-on-transmission-time-after-tick-atta-peer-reviewed-article-IJGM no studies have determined the minimum time it takes for transmission.
There’s also the issue of partially fed ticks transmitting more quickly: http://iai.asm.org/content/61/6/2396.full.pdf Ticks can spontaneously detach – and the authors of this study found that they did so 15% of the time in mice. They also state that about a tenth of questing nymphs appear distended with partially fed sub-adult ticks being common. This quicker transmission is due to spirochetes presiding in the salivary glands rather than the mid-gut.

https://madisonarealymesupportgroup.wordpress.com/2016/12/07/igenex Bob Giguere of IGeneX states a case of a little girl who went outside to play about 8:30a.m. and came inside at 10:30 with an attached tick above her right eye. By 2 o’clock, she had developed the facial palsy. At the hospital she was told it couldn’t be Lyme as the tick hadn’t been attached long enough. They offered a neuro-consult…..By 4pm she couldn’t walk or talk.
A Lyme literate doctor trained by ILADS met the family in his office on a Saturday, gave her an intramuscular injection of antibiotics and within 2 hours the palsy was gone. He continued her treatment for approximately 4 weeks.

Do NOT take a “wait and see” approach when it comes to this plague.  Get on it and get on it now.  The longer you wait the greater the potential for it to embed deep within the body including the brain.  Every SINGLE attached tick should be taken as seriously as a heart attack.  Please spread the word about this.  The myths must END!