Archive for the ‘Activism’ Category

Dear Lyme Warrior….Help!

https://globallymealliance.org/dear-lyme-warriorhelp-9/

lyme warrior

by Jennifer Crystal

Every few months, Jennifer Crystal devotes a column to answering your questions. Here she answers some questions she recently received. Do you have a question for Jennifer? If so, email her at lymewarriorjennifercrystal@gmail.com.

Did your pain move sometimes? My worst pain is near some scar tissue.

Yes! One of the defining features of Lyme pain is that it’s migratory. This distinguishes it from, say, the pain of Rheumatoid Arthritis (RA), which is more symmetrical (both knees instead of just one), and which doesn’t tend to move around like Lyme pain. While RA affects most of the joints, Lyme can affect one, two, or many.

I felt pain mostly in my forearms and shins, but also sometimes in my back, neck, and head. Sometimes my fingers ached so much I couldn’t type, and other days they felt okay. Now that I’m in remission, I know when I’m having a Lyme flare-up because my forearms and shins start to ache. When I’m overtired or I’ve over-exerted myself, I always get a headache on the left side of my head. (This is due to babesia, which eats oxygen in the red blood cells. When I over-exert myself, I don’t get enough  oxygen to that side of my brain, causing inflammation and subsequent pain).

Moreover, Lyme loves to hide in scar tissue, so it makes perfect sense that’s where you’re having the worst pain. I had the anterior cruciate ligament of my left knee repaired before I was aware I had Lyme, and it took much longer for that knee to heal than it should have; this is likely because there was Lyme bacteria in the scar tissue. I’ve also had multiple eye surgeries, and my doctor suspects scar tissue over my left eye is why my headaches often start there.

Is the word “cured” ever used with tick-borne illness?

Yes and no. It depends which illness you have, how long you’ve had it, how quickly you got treatment, and how well you’ve responded to treatment. If Lyme is caught early and treated adequately with two to four weeks of antibiotics—and if it is not complicated by co-infections—it can conceivably be cured. However, even in those cases, some 20% of patients still experience ongoing symptoms called Post Treatment Lyme Disease Syndrome (PTLDS), and they can require additional treatment.

My own Lyme is in remission, not cured because I went eight years undiagnosed. By then the bacteria had crossed the blood-brain barrier. Once it’s in the central nervous system, it becomes very difficult to fully eradicate it. I’m probably 80% restored to full health, a percentage that has continually improved (with brief periods of flare-up).
There are others who have had PTLDS who claim to have been cured, but some of these have subsequently relapsed. It really depends on each individual case.

I was originally diagnosed with the co-infection Ehrlichia, and that is now considered to be cured. I no longer test positive for it or show specific symptoms. The co-infection that still gives me the most trouble is babesia. I was not surprised to hear doctors at this year’s ILADS conference say that babesia can be treated to an extent—symptoms can be alleviated and held at bay for a while—but that it often rebounds. Currently, babesia has no cure.

But don’t despair. Researchers are getting closer to using that coveted word “cure” every day. See my “Highlights From ILADS 2019” post that provides information on new drugs like Dapsone and Disulfiram, the latter of which has some patients, as Dr. Kenneth Liegner stated, “enjoying enduring remission,” that is, feeling well for six months or longer. It’s too early to use the word “cure” decisively.

Do you think I’m going down the right path, being treated for tick-borne disease?

I know it can be confusing when so many doctors give you different diagnoses and treatment options. You don’t know who or what to believe, and that is scary. Even two different LLMDs might give you two different protocols (and that’s because they each have a personal opinion on what might work best for you, since there is no single set protocol for treating tick-borne disease).

If you trust the LLMD who has made a clinical diagnosis of Lyme with or without co-infections, and your symptoms corroborate those infections, and/or your blood work confirms those infections, then yes, I absolutely think you are going down the right path. Remember that having Lyme is not a choice.

Once you begin treatment, you’ll know for sure if you’re on the right path. If you do have Lyme, you’ll likely have a Herxheimer reaction (when the antibiotics kill off the Lyme bacteria at a rate faster than your body can eliminate them, making you feel worse before you feel better). That could be a good indication that you should stay the course.

The real question is, do you feel like you are going down the right path? No one knows your body better than you do. You know you are sick. You know what your symptoms are. You know they are not all in your head. If you’ve seen an LLMD and feel in your gut that the doctor is right for you, then trust that feeling, and don’t worry what anyone else says.


jennifer crystal_2

Opinions expressed by contributors are their own.

Jennifer Crystal is a writer and educator in Boston. Her memoir One Tick Stopped the Clock is forthcoming. Contact her at lymewarriorjennifercrystal@gmail.com.

Trump Smashes Hospital Bill Secrecy Sham, Forces Hospitals to Publicly Publish Secret Prices So That Consumers Can Make Informed Choices

https://www.naturalnews.com/2019-11-19-trump-smashes-hospital-bill-secrecy-sham.html

Trump smashes hospital bill secrecy sham, forces hospitals to publicly publish secret prices so that consumers can make informed choices

Image: Trump smashes hospital bill secrecy sham, forces hospitals to publicly publish secret prices so that consumers can make informed choices

(Natural News) The Trump administration is currently in the process of finalizing a new price transparency rule that, once it comes into effect in January 2021, will force all hospitals to publish their service prices publicly for the benefit of consumers.

Currently, hospitals are allowed to charge whatever prices they want to for services, typically in secret, burdening patients with exorbitant bills after they’ve already received medical care. But Trump’s new rule will ensure that customers know right upfront what the charges will be before they opt for oftentimes very expensive hospital services.

“For decades, hospitals, insurance companies, lobbyists, and special interests have hidden prices from consumers so they could drive up costs for you,” the president stated in an announcement to the nation. “And you had no idea what was happening. You’d get bills that were unbelievable and you have no idea why.”

President Trump cited several examples, including hospital patients who have been charged obscene prices for MRI (magnetic resonance imaging) tests and pregnancy services. Even simple blood tests are often billed at absurd rates by hospitals, which have gotten used to bilking consumers by charging insurance companies unrealistically high prices for medical services.

“We’re stopping American patients from just getting, pure and simple – two words, very simple words: ripped off,” Trump is quoted as saying. “Because they’ve been ripped off for years.”

Trump also wants insurance companies to discloses expected costs to policyholders before they receive treatment

Hospitals aren’t the only bad players in the American medical paradigm, as insurance companies themselves are notorious for withholding price information from policyholders until after the medical bills come. This places an enormous burden on patients who oftentimes don’t know what they’re getting themselves into until it is already too late.

“This is the biggest revolution I’ve seen in generations,” stated Dr. Art Laffer, who was recently invited by President Trump to the White House to discuss the significance of the new hospital rule, and its associated proposed insurance rule.

“As opposed to most revolutions, this revolution saves lives; it doesn’t cost lives,” Dr. Laffer went on to explain.

According to Dr. Laffer, the health care industry is in desperate need of transparency reform. Not only do patients deserve to know precisely how much they will be expected to pay before receiving medical care, but they also deserve improved medical care, which simply can’t happen unless the medical industry is forced to be transparent.

Even though President Trump was unsuccessful in fully repealing and replacing Obamacare as he promised to do while on the campaign trail, POTUS has been able to work within this corrupt system to implement important regulatory reforms like this that will at least help to make the process smoother and more pleasant for consumers.

“The changes you described, what we’re doing at HHS (Department of Health and Human Services), will be revolutionary to our health care system – perhaps the biggest single change that President Trump has made to Americans’ health care experience,” added Alex Azar, Secretary of HHS.

Azar, as you may recall, isn’t exactly a revolutionary when it comes to fighting the health care status quo, seeing as how he’s the former president of drug giant Lilly USA, a division of Eli Lilly and Company. Azar has other ties to the drug industry as well, having worked as general counsel and then-deputy secretary of the HHS during the George W. Bush administration.

Still, Azar seems to be cooperating with the agenda of President Trump, which in this case appears to be for the benefit of consumers rather than special interests.

For more related news about President Trump that the mainstream media isn’t telling you, be sure to check out Trump.news.

Sources for this article include:

Breitbart.com

NaturalNews.com

Surviving the Holidays When You’re Chronically Ill

https://www.psychologytoday.com/us/blog/turning-straw-gold/201411/surviving-the-holidays-when-you-re-chronically-ill

Surviving the Holidays when You’re Chronically Ill

Four suggestions for making the holidays as stress-free as possible

Posted Nov 23, 2014

Toni Bernhard J.D.

Turning Straw Into Gold

freeimages.com
Source: freeimages.com

For the chronically ill—which includes those who suffer from chronic pain—the holidays can feel like a no-win situation. If we participate at all, there’s likely to be payback later. On the other hand, if we don’t participate, we’ll feel isolated and risk other people not understanding why we haven’t joined in the festivities….(See link for full article)

 

NY Grants Approval for IGeneX’s Newly Developed Tick-Borne Relapsing Fever ImmunoBlot Tests

https://www.prnewswire.com/news-releases/new-york-state-grants-approval-for-igenexs-newly-developed-tick-borne-relapsing-fever-tbrf-immunoblot-tests-300933720.html

New York State Grants Approval for IGeneX’s Newly Developed Tick-Borne Relapsing Fever (TBRF) ImmunoBlot Tests

TBRF ImmunoBlots (IgM and IgG) represent a quantum leap in testing for tick-borne diseases, particularly for patients with Lyme-like symptoms

NEWS PROVIDED BY

IGeneX


MILPITAS, Calif., Oct. 8, 2019 /PRNewswire/ — The Division of Laboratories of the Department of Health of the State of New York has approved IGeneX’s newly developed Tick-Borne Relapsing Fever (TBRF) ImmunoBlots (IgM and IgG), making them immediately available to New Yorkpractitioners.

Until recently, diagnostic tests for TBRF have been grossly insensitive and have not been able to detect many of the ever-growing list of species and strains of TBRF Borrelia carried by hard and soft ticks. The new IGeneX ImmunoBlots overcome these obstacles with the ability to detect antibodies to TBRF Borrelia species including, but not limited to, B. hermsii, B. miyamotoi, and B. turicatae.

TBRF is often considered a Lyme disease imitator because both TBRF and Lyme sufferers display many similar symptoms, such as high fever, chills, and headache, often leading to misdiagnosis. Moreover, some of the Borrelia that cause TBRF are transmitted by the same ticks that transmit B. burgdorferi, the causative agent of Lyme disease. Therefore, it is important for physicians to test for both TBRF and Lyme.

“We are very excited to be able to offer the TBRF ImmunoBlots to physicians in New York State,” said Dr. Jyotsna Shah, President of IGeneX. “Doctors use to call me and say ‘my patients have Lyme-like symptoms. Why are your tests negative?’ We now know that their symptoms might have been due to TBRF Borrelia infection. These new TBRF ImmunoBlot tests will help patients in this group, as well as patients with Lyme and TBRF Borrelia mixed infections.”

The accuracy of the TBRF ImmunoBlot has been established. The specificity is 98.5% for IgM and IgG based on a study performed on 212 well characterized samples, of which 50 were provided by the CDC. Additionally, the TBRF ImmunoBlots can detect the full spectrum of disease: early, active and late-stage disease.

For more information on IGeneX and the TBRF ImmunoBlot tests, please visit http://igenex.com.

About IGeneX
For over 25 years, IGeneX has been at the forefront of research and development of diagnostic testing for Lyme disease, TBRF, Bartonella, and other tick-borne diseases. IGeneX arms its talented scientists with the most cutting-edge technology available to enable them to find new solutions that challenge the status quo of testing for Lyme and associated tick-borne diseases. The mission of IGeneX is to aid practitioners in their diagnosis of tick-borne illnesses by providing the most comprehensive testing possible. Learn more at: www.igenex.com

Media Contact:
Joseph Sullivan
225913@email4pr.com 
408-504-7691

SOURCE IGeneX

Related Links

http://www.igenex.com

___________________

More on Relapsing Fever:  https://madisonarealymesupportgroup.com/2018/12/28/relapsing-fever-spirochete-uniquely-adapted-to-highly-oxidative-salivary-glands-of-soft-bodied-tick/

https://madisonarealymesupportgroup.com/2019/03/22/tick-borne-relapsing-fever-in-arizona/

https://madisonarealymesupportgroup.com/2017/12/22/tbrf-in-texan-dogs-yep-despite-poor-tests-its-there/

https://madisonarealymesupportgroup.com/2019/01/10/relapsing-fever-found-at-popular-recreation-site-in-ca-ticks/

https://madisonarealymesupportgroup.com/2018/12/20/tick-borne-relapsing-fever-as-a-potential-veterinary-medical-problem/

https://madisonarealymesupportgroup.com/2017/05/04/us-soldier-aquires-tickborne-relapsing-fever-caused-by-b-turicatae-from-a-ornithodoros-turicata-tick/

https://madisonarealymesupportgroup.com/2019/03/17/first-case-of-b-corocidurae-in-native-european-presenting-as-meningitis-with-cranial-polyneuritis-cavernous-sinus-thrombosis/

Wormser’s Junk Science, Deliberate Avoidance of Chronically Ill Patients & A Letter Him Asking Why

Wormser’s junk science and deliberate avoidance of the horribly disabled

NOV 13, 2019 — 

Editorial censorship over the past thirty years has kept the truth from the public as patient testimony all across America (and the globe) is describing a disease that is destroying lives, ending careers while leaving its victim in financial ruin. This petition site is a clearinghouse of evidence to be used in current and future litigation over the deliberate mishandling of Lyme disease by the academics that have controlled the narrative, government health officials who have aligned themselves and financed the deception with US taxpayer dollars and the editors of journals who continue to conceal the truth.

There is no way my letter to the editor below will see the light of day so it is being published here for everyone to see …….

When evidence based medicine has been spun to fit bias agendas and the patient voice has been intentionally ignored who investigates the dishonest science?

-Carl Tuttle

Letter to: Dr. Joerg Heber with copy to The Tick-borne Disease Working Group and Dr. Anthony Fauci who continues to fund Wormser’s “JUNK SCIENCE”
———- Original Message ———-
From: CARL TUTTLE < runagain@comcast.net>
To:  jheber@plos.org,  plosone@plos.org
Cc:  ipuebla@plos.org,  mdohm@plos.org,  gvousden@plos.org,  mbyrne@plos.org,  afauci@niaid.nih.gov
Date: November 12, 2019 at 8:28 AM
Subject: Post-treatment Lyme disease symptoms score: Developing a new tool for research.

PLOS

Post-treatment Lyme disease symptoms score: Developing a new tool for research.

Turk SP, Lumbard K, Liepshutz K, Williams C, Hu L, Dardick K, Wormser GP, Norville J, Scavarda C, McKenna D, Follmann D, Marques A  https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0225012

Excerpt:

“Some patients have residual non-specific symptoms after therapy for Lyme disease, referred to as post-treatment Lyme disease symptoms or syndrome, depending on whether there is functional impairment.”

Nov 12, 2019

PLOS
1160 Battery Street
Koshland Building East, Suite 225
San Francisco, CA 94111
Attn: Joerg Heber, Editor-in-Chief (PhD in Semiconductor Physics)

Dear Dr. Heber,

As the Editor-in-Chief of a scientific journal you should be well aware of the following: (Taken from the attached JAMA letter to the editor published Dec 18, 2018)  https://jamanetwork.com/journals/jama/article-abstract/2718786

“It is well known that untreated streptococcal pharyngitis can progress to rheumatic fever, causing irreversible heart damage. Untreated syphilis leads to progressive disability and dementia, and untreated human immunodeficiency virus infection progresses to AIDS with significant disability and death. What happens to a patient with Lyme disease who goes months, years, or decades before diagnosis because of a false-negative serological test result?”

Wormser et al do not discuss the consequences of untreated Lyme disease in their PLOS published paper. Why do you think that is the case Dr. Heber?

Post Treatment Lyme Disease Syndrome after early treatment and untreated late stage Lyme of months, years or decades are two distinctly different disease states with the later going unrecognized for over three decades. The absence of a bulls-eye rash after tick bite allows patients to progress to severe neurological disease instead of obtaining a prompt diagnosis and early treatment. Purposely avoiding the advanced stage of disease hides the horribly disabled and anyone unable to see this is somewhat naïve. Avoiding the seriously disabled Lyme patient population hides the severity of the disease as exposed in the “Under our Skin” documentary.

Under Our Skin – Extended Trailer (5min, please watch the video)

https://www.youtube.com/watch?v=sxWgS0XLVqw

For the past three decades, Lyme disease has been portrayed as hard to catch and easily treated  [1] while those who control the narrative (Through editorial censorship) refuse to recognize this pathogen as an antibiotic resistant/tolerant superbug by suppressing evidence of persistent infection.  [2] This misclassification has all but eliminated government funding that should have been equal to or greater than AIDS or Zika which are also life-altering/life-threatening infections in need of cures.

For example: (in reference to persistent infection)

I would like to point out the following case study from Stony Brook Lyme Clinic. I understand the patient received thirteen spinal taps, multiple courses of IV and oral meds, and relapsed after each one, proven by CSF antigens and/or PCR. The only way this patient (said to be a physician) remained in remission was to keep her on open ended clarithromycin- was on it for 22 months by the time of publication.

Seronegative Chronic Relapsing Neuroborreliosis.  
https://www.ncbi.nlm.nih.gov/pubmed/7796837

Lawrence C.a · Lipton R.B.b · Lowy F.D.c · Coyle P.K.d  aDepartment of Medicine, bDepartment of Neurology, and cDivision of Infectious Diseases, Albert Einstein College of Medicine, and dDepartment of Neurology, State University of New York at Stony Brook, New York, NY., USA
Eur Neurol 1995; 35:113–117  (DOI:10.1159/000117104)

Abstract

We report an unusual patient with evidence of Borrelia burgdorferi infection  who experienced repeated neurologic relapses despite aggressive antibiotic therapy. Each course of therapy was associated with a Jarisch-Herxheimer-like reaction. Although the patient never had detectable free antibodies to B. burgdorferi in serum or spinal fluid, the CSF was positive on multiple occasions for complexed anti-B. burgdorferi antibodies, B. burgdorferi nucleic acids and free antigen.

Duke University Oncologist Dr. Neil Spector required a heart transplant after his infection was left untreated for four years while serology was repeatedly negative for Lyme disease.
Gone in a Heartbeat – A Physician’s Search for True Healing 

https://www.lymedisease.org/book-review-spector-lyme-disease/

Patient testimony all across America (and the globe) is describing a disease that is destroying lives, ending careers while leaving its victim in financial ruin.

The truth about this devastating disease has been kept from the public for 43 years and there are no  Public Service  Announcements informing the public that you could become horribly disabled  [3]  [4] or die  [5] from Lyme disease.

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 as health agencies across the globe are blindly following what has been deceitfully established here in the U.S. The academics that controlled the narrative for the past three decades have been named as defendants in a Texas District Court racketeering lawsuit and that fact is missing from the conflicts of interest statement in the Wormser published PLOS article.  Why is that Dr. Heber?

Court Document:

https://www.dropbox.com/s/18uyrli878ug51m/LymeDisease%20RICO%20Lawsuit.pdf?dl=0

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 public health disaster.

And once again we see  Wormser fixated on the acute stage of disease after early treatment as he continues to believe that he has pulled the wool over the eyes of the reader and medical community.

When evidence based medicine has been spun to fit bias agendas and the patient voice has been intentionally ignored who investigates the dishonest science?

A response to this inquiry is required.

Respectfully submitted,

Carl Tuttle

Lyme Endemic Hudson, NH
Cc: Iratxe Puebla, Senior Managing Editor
Michelle Dohm, Managing Editor, Editorial Board Services
George Vousden, Senior Editor
Meghan Byrne, Senior Editor, Team Manager
Anthony S. Fauci, M.D., NIAID Director

References: (Please read them!)

1.  Lyme Disease Is Hard to Catch And Easy to Halt, Study FindsNew York Times By GINA KOLATA Published: June 13, 2001

http://www.nytimes.com/2001/06/13/us/lyme-disease-is-hard-to-catch-and-easy-to-halt-study-finds.html

Excerpt: But some who have treated hundreds of patients with long-term antibiotics, like Dr. Sam L. Donta of Boston University Medical Center, were not convinced. The antibiotics in the studies were not given for a long enough time, Dr. Donta said, and he would have chosen different ones. Perhaps all that the studies show, he said, is ”that this particular treatment doesn’t work.”

2.   Peer Reviewed Evidence of Persistence of Lyme Disease Spirochete Borrelia burgdorferi and Tick-Borne Diseases after the mandated one-size-fits-all IDSA treatment approach:(700 articles)

https://www.dropbox.com/s/n09sk90eo6xz7ua/700%20articles%20LYME%20EvidenceofPersistence-V2.pdf?dl=0

3.   Latent Lyme Disease Resulting in Chronic Arthritis and Early Career Termination in a United States Army Officer(Published: 06 March 2019)

https://academic.oup.com/milmed/advance-article/doi/10.1093/milmed/usz026/5370051?searchresult=1

4.   Nicole Malachowski: Unfit for Duty from Debilitating Tick-Borne Disease

http://cdmrp.army.mil/cwg/stories/2018/nicole_malachowski_profile

5.    Deaths From Lyme Disease Compiled by: John D. Scott, Research Scientist 17 April 2018

https://www.dropbox.com/s/eo794dx7zspc1ln/Ld%20deaths.doc?dl=0

Today’s letter to Dr. Gary Wormser of New York Medical College

NOV 14, 2019 — 

There has never been a response to any of my inquiries addressed to Dr. Wormser….I wonder why? A copy of this letter was sent to the lead attorney of the current Texas RICO lawsuit.

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: gary wormser <gary_wormser@nymc.edu>, jheber@plos.org
Cc: ipuebla@plos.org, mdohm@plos.org, gvousden@plos.org, mbyrne@plos.org, afauci@niaid.nih.gov, amarques@niaid.nih.gov, gwormser@nymc.edu, donna_mckenna@nymc.edu, dean.follmann@nih.gov, gary_wormser@nymc.edu, joshua.norville@tufts.edu, lymestudy@mfpstorrs.com, linden.hu@tufts.edu, plosone@plos.org
Date: November 14, 2019 at 8:48 AM
Subject: Re: Post-treatment Lyme disease symptoms score: Developing a new tool for research.

Nov 14, 2019

Division of Infectious Diseases,
New York Medical College,
Valhalla, NY 10595
Attn: Gary P. Wormser, MD

Dr. Wormser,

As an Infectious Disease Specialist I would like to ask you a few questions that I hope you could take the time to answer:

1. Does untreated strep throat lead to rheumatic fever causing irreversible heart damage?

2. Does untreated human immunodeficiency virus infection progresses to AIDS with significant disability and death?

3. Does untreated syphilis lead to progressive disability and dementia?

4. Does untreated Lyme disease produce sudden death with no warning signs; [1,2,3,] heart damage requiring transplant, [4] paralysis with seizures, [5] lymphoma [6] and persistent infection after antibiotic treatment [7, 8,9,10,11] along with congenital transmission [12] and ability to create wheelchair bound patients [13]?
Your thirty year fixation on the acute stage of disease (with bulls-eye rash) after early treatment gives the impression that you have disregarded the consequences of untreated Lyme disease which leaves the patient horribly disabled similar to the other examples I have presented.

I believe you have coined the phrase “aches and pains of daily living” when patients experience a return of symptoms after the one-size-fits-all IDSA treatment mandate.

“Post Treatment Lyme Disease Syndrome” after early treatment and untreated late stage Lyme of months, years or decades are two distinctly different disease states with the later going unrecognized for over three decades. Patients who have had a prolonged exposure to the pathogen are almost always incapacitated.

5. So what is your motivation for disregarding the consequences of untreated Lyme disease? Is it because the outcome of untreated Lyme doesn’t match the well-established dogma that Lyme is a simple nuisance disease; hard to catch and easily treated, which you helped to establish?

We have a disease that is wreaking havoc all across America (and the world) while you remain focused on the early stage of disease as indicated in your latest PLOS publication; shameful indeed.   

Misclassification has pigeonholed Lyme disease into a low-risk and non-urgent health issue which has all but eliminated adequate government funding for a disease capable of long term disability and death.

A response to this inquiry is requested.

Carl Tuttle

Lyme Endemic Hudson, NH

References: (Tip of the iceberg)

1. 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.”

2. 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

3. 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

4. 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.

5. 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.

6. 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).

7. 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.

8. 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.

9. 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.

10. 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.

11. 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.”

12. Congenital Transmission of Lyme/TBD

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

13. 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.”