Lyme Wars – Part 4

http://www.nbcnewyork.com/on-air/as-seen-on/Lyme-Wars-Part-IV-Invasive-Plant-Contributes-to-Problem_New-York-453449133.html  (News video in link) Oct. 26, 2017

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Japanese barberry, an invasive plant species banned for sale in New York and Connecticut, could be making an already bad Lyme disease problem in the tri-state worse. Brian Thompson reports in the fourth edition of a five-part series on the fight against Lyme disease.

Park Police Officer, Margie Raimondi, picked ticks off of her daily as if they were mosquitoes.  She was 4.5 months bed bound from Lyme Disease and is now recovering and on disability.

Dr. Scott Williams, an expert on the Japanese Barberry, states the shrub is a perfect habitat for ticks by creating a higher humidity.  Six states have banned or limit the shrub.

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**Comment**

For more on the Japanese Barberry:  https://madisonarealymesupportgroup.com/2015/09/30/barberry-friend-or-foe/

Barberry has a stronger form of Berberine, according to some experts, than what’s found in Goldenseal, Coptis, or golden thread and the Oregon Grape and is used in both Indian and Chinese medicine.  Master herbalist, Steven Buhner states it is active against a large number of resistant bacteria and numerous strains of Mycoplasma, a common coinfection of Lyme.

I’m so glad Ms. Raimondi spoke up about being infected as I often worry about our public servants who work outside.  Please warn these workers about tick prevention as they are in harm’s way.  Please share this info with them:  https://madisonarealymesupportgroup.com/2017/05/11/tick-prevention-and-removal-2017/ (Great info plus Consumer Report review on tick repellents & how to remove ticks)

Unfortunately, public servant uniforms are nearly always dark which is going to make seeing ticks nearly impossible; however, they should definitely spray their clothing and shoes with Permethrin and keep Picaridin repellent in their vehicle to spray on skin if they have to go into tick infested areas.  Please read info in blue link for more helpful tips.

http://soundchoice.org/wp-content/uploads/Dawson_2017_Autism_autoUCB.pdf  Stem Cells Translational Medicine

GERALDINE DAWSON, JESSICA M. SUN, KATHERINE S. DAVLANTIS, MICHAEL MURIAS, LAUREN FRANZ, JESSE TROY,  RYAN SIMMONS, MAURA SABATOS-DEVITO, REBECCA DURHAM, JOANNE KURTZBERG

Autologous Cord Blood Infusions Are Safe and Feasible in Young Children with Autism Spectrum Disorder: Results of a Single-Center Phase I Open-Label Trial

ABSTRACT

Despite advances in early diagnosis and behavioral therapies, more effective treatments for children with autism spectrum disorder (ASD) are needed. We hypothesized that umbilical cord blood derived cell therapies may have potential in alleviating ASD symptoms by modulating inflammatory processes in the brain. Accordingly, we conducted a phase I, open-label trial to assess the safety and feasibility of a single intravenous infusion of autologous umbilical cord blood, as well as sensitivity to change in several ASD assessment tools, to determine suitable endpoints for future trials.

Twenty-five children, median age 4.6 years (range 2.26–5.97), with a confirmed diagnosis of ASD and a qualified banked autologous umbilical cord blood unit, were enrolled. Children were evaluated with a battery of behavioral and functional tests immediately prior to cord blood infusion (baseline) and 6 and 12 months later. Assessment of adverse events across the 12-month period indicated that the treatment was safe and well tolerated.

Significant improvements in children’s behavior were observed on parent-report measures of social communication skills and autism symptoms, clinician ratings of overall autism symptom severity and degree of improvement, standardized measures of expressive vocabulary, and objective eye-tracking measures of children’s attention to social stimuli, indicating that these measures may be useful endpoints in future studies. Behavioral improvements were observed during the first 6 months after infusion and were greater in children with higher baseline nonverbal intelligence quotients. These data will serve as the basis for future studies to determine the efficacy of umbilical cord blood infusions in children with ASD.

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**Comment**

**UPDATE July, 2022**

Roughly 1 in 30 children and adolescents ages 3-17 were diagnosed with an autism spectrum disorder in 2020, according to a JAMA Pediatrics research letter, which referenced a new study showing a 53% increase in ASD in young Americans since 2017.

According to the documentary Trace Amounts as of 2014, 1 in 68 children have Autism. That’s 1 Million US children.

http://soundchoice.org/wp-content/uploads/notbornwithit-2.pdf According to Sound Choice Pharmaceutical Institute, the Duke study is remarkable in that 60-70% or more of children with Autism have de novo gene mutations (not found in either parent) that must have occurred after birth according to the results, not in the egg, sperm or early utero development as previously, and erroneously assumed.

This new finding reveals research should now be geared to finding out what environmental damage after birth leads to these mutations and/or what pathogens are acting as triggers.

Autism like Lyme/MSIDS is an epidemic and according to one Wisconsin LLMD, 80% of his Autistic patients are also infected with Lyme/MSIDS.

For more:  https://madisonarealymesupportgroup.com/2017/09/19/autism-aluminum-adjuvant-link-corroborated/

https://madisonarealymesupportgroup.com/2017/09/21/aluminum-flawed-assumptions-fueling-autoimmune-disease-and-lyme/

https://madisonarealymesupportgroup.com/2016/12/08/mercury-and-autism/

https://madisonarealymesupportgroup.com/2017/03/27/vaccines-revealed-8-watch-trace-amounts-for-free-until-9pm-tonight/  I highlight the documentary Trace Amounts

http://www.nbcnewyork.com/on-air/as-seen-on/Lyme-Wars-Part-III-How-Science-Could-Overcome-Lyme_New-York-453167163.html  (Click on link for news video)

Erica Byfield reports on a Johns Hopkins University research center dedicated to curing the tick-borne illness. This is the third in our five-part series on Lyme disease and the debate over the controversial diagnosis of chronic Lyme.

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**Comment**

Christine Heidt of the University of Alberta has written a clear treatise on the issue of the persistence of Lyme (borrelia) TheCaseforthePersistenceofLymeDiseaseAfterAntibioticTherapy

In a study published over 20 years ago, it was reported that “Antibiotic therapy with penicillin, doxycycline, and ceftriaxone has proven to be effective for the treatment of Lyme borreliosis. In some patients, however, it was noticed that borreliae can survive in the tissues in spite of seemingly adequate therapy.”(14) Interestingly, recent studies support this same conclusion. Additionally, researchers have observed that either of the two antibiotics that were administered in the IDSA studies were found to initiate the transformation of the LD spirochete into treatment resistant persister cells and other bacterial forms.(5,6,9,10,11,12,13,14,15,16) Ironically, the four clinical trials meant to support the IDSA’s PTLDS model actually serve to support this recent research, which in turn supports ILADS assertion of reversion to persistent bacteremia causing ongoing symptoms, rather than the IDSA’s expert opinion that the infection has been eradicated and residual symptoms remain indefinitely….

A recent research article co-authored by, Dr Paul Auwaerter (President-elect of the IDSA), entitled “Drug Combinations against Borrelia burgdorferi Persisters In Vitro: Eradication Achieved by Using Daptomycin, Cefoperazone and Doxycycline” suggests that perhaps even the IDSA’s own members are not fully convinced of the IDSA’s version of chronic Lyme disease.(10) While Auwaerter asserts that the cause of PTLDS is unknown, he admits that “findings that suggest the continued presence of B. burgdorferi in some form indicate that current Lyme disease treatment may not sufficiently eliminate B. burgdorferi persisters or that the immune system fails to clear persisting organisms or bacterial debris, which may be the underlying cause for those who suffer from unresolved Lyme disease symptoms.”

Prior to this publication, Dr Auwaerter co-authored a publication with IDSA LD Guidelines members entitled “ Antiscience and ethical concerns associated with advocacy of Lyme disease” where he and the other authors attempt to discredit any research that does not support the IDSA’s PTLDS theories, with statements such as “Some activists portray Lyme disease, a geographically limited tick-borne infection, as a disease that is insidious, ubiquitous, difficult to diagnose, and almost incurable; they also propose that the disease causes mainly non-specific symptoms that can be treated only with long-term antibiotics and other unorthodox and unvalidated treatments. Similar to other antiscience groups, these advocates have created a pseudoscientific and alternative selection of practitioners, research, and publications and have coordinated public protests, accused opponents of both corruption and conspiracy, and spurred legislative efforts to subvert evidence-based medicine and peer-reviewed science.”(21)  

The truth is that over 50% of the IDSA’s guidelines are based on “expert opinion” rather than “evidence-based medicine” as their publication suggests. A further 31% of the IDSA guidelines are based on observational studies. Only a meagre 29% of the IDSA Guidelines fit into “evidence-based medicine”.(22,23,24,25,27) Importantly, the IDSA’s own research supports these very findings.(22) Furthermore, various IDSA members that co-authored the “Antiscience and ethical concerns” publication(21) were also involved with the creation of the Lyme Guidelines although they, themselves hold competing interests. Some members hold patents for LD products, some own shares in companies that have vested interests with the diagnosis and treatment of LD and some act as “expert witnesses in malpractice litigation” against any Dr that dares to question their “expert opinion”.(22,26) Rather than sharing information and learning from others, the IDSA continues to belittle, publicly attack and/or attempt to jail any Dr or researcher that does not endorse their Lyme disease Guidelines and policies.(22) 

Animal studies have also shown detectable borrelia DNA:  Straubinger’s dog study (persist & reactivate).pages

B. burgdorferi disseminates through tissue by migration following tick inoculation, produces episodes of acute arthritis, and establishes persistent infection. The spirochete survives antibiotic treatment and disease can be reactivated in immunosuppressed animals.

http://archives.republicans.foreignaffairs.house.gov/112/HHRG-112-FA16-WState-BartholdS-20120717.pdf  by Stephen W. Barthold, DVM, PhD

It’s been demonstrated in dogs, mice, and monkeys that non cultivable spirochetes persist following antibiotic treatment.  So, researchers have been able to detect borrelia DNA but they have not been able to culture it from tissues.  This has led many researchers to conclude that after treatment with antibiotics, spirochetes are viable but not infectious.

http://www.hoajonline.com/infectdis/2052-5958/1/2

Stricker and Johnson state that the Embers et al. monkey study provides animal evidence for persistent infection when three quarters failed antibiotic treatment and had persistent infection showing up in tissues at necropsy using PCR.  It’s also important to note that “small numbers of intact spirochetes were recovered by xenodiagnosis from treated monkeys.”  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3256191/

What this means is researchers put ticks void of infection upon the monkeys after treatment.  After a blood meal they removed the ticks and found spirochetes in them proving there were still spirochetes in the treated monkeys.

This has been done in humans too:  https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3952603/

Dr. Betty Maloney states that the positive xenodiagnostic test in a persistently ill post-treatment subject is highly significant evidence of persistence infection; however, she feels the authors went to great lengths to discount the significance and only questioned whether the recovered DNA was just dead remnants that happened to be in the tick bite site, or due to patient noncompliance with previous therapy, inadequate blood levels of antibiotics, or re-infection.  https://www.lymedisease.org/TheLymeTimes-V26-3/index.html#25/z  The authors concluded there was insufficient evidence.

To read Dr. Horowitz’s comment about episode 3 on his FB page:  https://www.facebook.com/drrichardhorowitz/posts/1524119334343526 He too lists studies as well as the fact treating physicians have found antibiotics to significantly help improve the quality of life of patients and that recent peer-reviewed studies have shown borrelia can persist like TB and leprosy due to biofilms and dormant forms.

https://madisonarealymesupportgroup.com/2017/08/18/drexel-prof-lyme-persists/

https://madisonarealymesupportgroup.com/2016/12/21/dr-zhang-on-persisters/

https://madisonarealymesupportgroup.com/2015/09/19/proof-of-borrelia-persistence/

https://madisonarealymesupportgroup.com/2017/08/25/sleeper-cells-the-stringent-response-and-persistence-in-the-borreliella-burgdorferi-enzootic-cycle/

And so the circle goes round and round without end.  The IDSA states none of this proves infection.  We ALL want to know why folks are still sick.

And the IDSA wants to have us believe Lyme disease is simple.  Really?

 

http://www.nbcnewyork.com/on-air/as-seen-on/Part-II-Child-Makes-Recovery-After-Chronic-Lyme_New-York-452896893.html(News video here)  Published on Oct 24, 2017

Kyra Lerner tells her story of struggle and recovery after contracting chronic Lyme, a controversial diagnosis linked to Lyme disease-carrying ticks. Kyra’s story is the second in our five-part investigative series. Natalie Pasquarella reports.

For more:  https://madisonarealymesupportgroup.com/2017/10/24/lyme-wars-part-1-julias-story/

https://madisonarealymesupportgroup.com/2017/10/24/the-lyme-wars-faces-of-the-health-crisis-a-digital-documentary/

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**Comment**

Lots of great info presented in this story – particularly the polarization of medicine and the fact that if Kyra’s parents would have followed the paradigm of the Infectious Diseases Society of America (IDSA), where they espouse essentially 21 days of doxycycline to be curative in all cases, she would be sicker than a dog with no hope.  Thankfully, she and thousands of others have followed the paradigm of the International Lyme and Associated Diseases Society (ILADS) who believe Lyme is pleomorphic and persistent, requiring much more than 21 days of doxycycline as well as the fact there is often coinfection involvement, requiring different drugs for far longer than a month.  This group also believes that IV treatments can be quite helpful for a subset of patients despite the government’s recent attempt to stop IV therapy for Lyme/MSIDS:  https://madisonarealymesupportgroup.com/2017/06/21/ilads-rebuttal-to-mmwr-article/

https://madisonarealymesupportgroup.com/2017/06/23/no-bias-in-mmwr-for-any-other-infectious-disease-requiring-iv-antibiotics-except-for-lyme/

For a great article explaining the tug of war:  TheCaseforthePersistenceofLymeDiseaseAfterAntibioticTherapy  The truth is that over 50% of the IDSA’s guidelines are based on “expert opinion” rather than “evidence-based medicine” as their publication suggests. A further 31% of the IDSA guidelines are based on observational studies. Only a meagre 29% of the IDSA Guidelines fit into “evidence-based medicine”.(22,23,24,25,27) Importantly, the IDSA’s own research supports these very findings.(22

Please understand for those of you just tuning in – THIS IS A WAR of epic proportions.

The reason we find ourselves here even 40 years after Lyme was “officially” discovered is due to money, power, and collusion at the highest level of government.  The government holds the patents on Borrelia burgdorferi (Bb), Lyme testing, the Lyme vaccine, and has been controlling the narrative for decades, even taking specific bands out of Lyme testing that show infection due to their patent on the Lyme vaccine.  

https://www.google.com/patents/US8680236 Gov. patent on OspA (outer surface protein) of Borrelia Burgdorferi (Bb).

https://www.google.com/patents/US6087097  Gov. patent on Lyme test based on OspA (outer surface protein) which causes the same disease it was meant to prevent which is the real reason it was yanked from the market.

https://www.google.com/patents/US4721617 Gov. patent on Lyme Vaccine

https://crymedisease.wordpress.com/2016/02/28/the-conspirators-they-own-the-patents-and-changed-the-testing/  A lengthy expose on all shenanigans for the stout of heart.

Please, don’t allow yourself to be fooled.  The powers that be have been controlling research and the narrative on Tick borne illness from the start.  Nothing about this is new. It’s as old as the hills.  In fact, one researcher has filed an anti-trust law-suit due to government suppression of a more accurate and cheaper Lyme test:  https://madisonarealymesupportgroup.com/2017/09/25/speaking-of-fake-science-fifty-seven-million-anti-trust-lawsuit-against-cdc-lyme-tests/

This same researcher and others have also complained of how the CDC is controlling the research being done:  https://madisonarealymesupportgroup.com/2017/01/13/lyme-science-owned-by-good-ol-boys/.  This article explains how they do it on a practical level: https://madisonarealymesupportgroup.com/2017/01/02/fake-science/

So while I’m extremely happy for these news stories, this abusive treatment of Lyme/MSIDS patients and the doctors who dare to treat them has been going on since it was formally given a name in the 80’s.

https://www.nbcnewyork.com/on-air/as-seen-on/Debate-Over-Chronic-Lyme-Disease-Affects-Brooklyn-Teen_New-York-452584583.html Oct. 23, 2017 (News Video in link)

The Lyme Wars Part 1

Julia’s Story:  Teen’s Health Affected in Fight Over Chronic Lyme

The life of a Brooklyn teenager who once danced and played sports changed in nearly an instant. Now she takes more than 70 pills a day and is unable to walk as her doctor tries to treat what he calls chronic Lyme, a controversial diagnosis linked to Lyme disease-carrying ticks. Julia’s story is the first in our five-part investigative series. Stefan Holt reports.

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A 2015 report reveals Emblem Health stopped paying for Julia’s treatment which was giving her feeling back in her feet:  http://www.nbcnewyork.com/investigations/Lyme-Disease-Insurance-Fight-Investigation-360476931.html  Insurance companies have been hiding behind the outdated and unscientific CDC guidelines for decades, denying coverage for Lyme patients.  Since the testing misses over half of all cases and since the antiquated 2006 guidelines recommend 21 days of doxycycline for everyone, regardless of persisting symptoms, insurance companies get away with it.  One key point here is that treatment was working for Julia.  

Dr. Wormser and others who affiliate with the IDSA guidelines theorize & believe there should be antibodies present – but herein lies the problem which is two-fold; 1) the CDC has set up arbitrary levels of needed antibody presence and taken out key bands of the test (band 31 OspA & band 34 OspB) that are specific to infection due to their patent on the Lyme vaccine which also uses those bands, and while many patients do have antibodies they don’t have enough, and 2) it’s been proven some folks never mount an appropriate immune response to reveal these antibodies.  It’s a Catch-22 with multitudes not meeting the Lyme Cabal’s subjective criteria.

More on testing:  https://www.lymedisease.org/lyme-basics/lyme-disease/diagnosis/

For more on the Lyme Wars:  https://madisonarealymesupportgroup.com/2017/10/24/the-lyme-wars-faces-of-the-health-crisis-a-digital-documentary/