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Archive for the ‘Lyme’ Category

The Desperate Need for an Accurate Lyme Disease Test

https://www.linkedin.com/pulse/desperate-need-accurate-lyme-disease-test-rosie-milsom/

The desperate need for an accurate Lyme disease test

1607078449009Stephen Bullough before and after Lyme disease

Published on December 4, 2020

Rosie Milsom

Fundraising & Comms Manager | Helping charities to diversify and increase their income, engage with their supporters, and make a difference

Yesterday, as part of our Big Give Christmas Challenge, we got a very strong reaction and boost to the campaign when we shared the story of Stephen Bullough. I’d like to share that with you now, and the best way is within an article because it’s too long to fit into a LinkedIn post.

His story helps demonstrate the importance of having an accurate test available on the NHS – and a better understanding of the disease from the medical profession.

An 8th Dan in karate and World, European and British champion, Stephen fell ill 2016 after recalling rash in 2015. He had neurological symptoms including seizures, and later vision problems.

He saw several consultants, but no one joined up the dots between the symptoms, and he was diagnosed with Functional Neurological Disorder (FND).

Feeling failed by the NHS, Stephen’s wife Angela began doing her own research and sent his bloods to a lab in Europe, which showed positive for Lyme. Tests done on the NHS had returned as negative.

The positive test was dismissed by Stephen’s neurologist, who said not wanting to believe he had FND was another symptom of the illness.

In 2018, Stephen suffered a series of seizures that resulted in him losing his sight and use of his legs. Still, he got no treatment.

He was certified as blind by a top local ophthalmologist, but again his neurology consultants didn’t accept this as true.

On Father’s Day this year, Stephen was blue lighted to hospital with a Glasgow Coma Scale 3 after series of back to back seizures. He was referred to ICU, but once in ward a doctor refused to treat him, saying that his medical notes suggested the seizures were fake. Luckily, a nurse’s son had epilepsy. She recognised the seizures and subsequently reported the doctor.

Stephen now has severe issues with his heart and nervous system, and is unlikely to ever walk again. He needs round the clock care.

After a recent stay in hospital, a community response doctor was sent to visit Stephen at his home. He happened to be a member of Global Lyme Alliance and listened to Angela’s story in shock.

He consequently carried out a thorough examination, confirming that Stephen has late stage Lyme with secondary and extensive damage to the central nervous system.

He is now on extensive medication and vitamins to help manage his condition.

Angela says:

“To say we’ve been living through four years of hell is an understatement.  If there was a more accurate test on the NHS, we could have gotten Stephen diagnosed and treated more quickly. Now, our lives have been devastated by this illness, and the stress has impacted my health too.”

At the time of writing this, we’re just £138 away from our Big Give Christmas Challenge target. Funds raised are going towards our Innovation Fund for Lyme disease, which will see us give grants to research projects which aim to find a truly accurate test and effective treatments for Lyme disease.

The campaign is accepting donations until Tuesday 8th December at 12pm, but will only be doubled up to £6,000. If you’re moved to support us, please donate via the link below, or get in touch with me if you’d like to talk about other opportunities for support after this time.

Thank you

https://donate.thebiggive.org.uk/campaign/a051r00001fHSDfAAO

  • For more on Caudwell LymeCo Charity’s research mission:  https://caudwelllyme.com/lyme-disease-research/
  • Their scientific advisory committee:  https://caudwelllyme.com/our-scientific-advisory-committee/

___________________

**Comment**

While COVID testing is purposely designed to show mostly ALL positives, Lyme/MSIDS testing is designed to show nearly ALL negatives:

  • https://madisonarealymesupportgroup.com/2020/03/01/study-cdcs-2-tier-lyme-testing-inaccurate-in-more-than-70-of-cases/
  • https://madisonarealymesupportgroup.com/2018/01/16/2-tier-lyme-testing-missed-85-7-of-patients-milford-hospital/
  • https://madisonarealymesupportgroup.com/2020/11/05/your-lyme-disease-test-results-are-negative-but-your-symptoms-say-otherwise/
  • https://madisonarealymesupportgroup.com/2020/02/10/the-bitter-feud-over-lymerix/  Similarly to how COVID testing has created a ‘casedemic’ due to all the false positives, Lyme/MSIDS testing has created a false perception that tick-borne illness isn’t that big of a deal, when it is.

Category:

Lyme, research, Testing, Treatment

How Many “Negative” Lyme Tests Are Due to B. Miyamotoi?

https://www.lymedisease.org/lyme-sci-miyamotoi-or-lyme/

LYME SCI: How many “negative” Lyme tests are due to B. miyamotoi?

By Lonnie Marcum

July 20, 2020

is it lyme or something else
Do you have all the symptoms of Lyme disease but test negative? Besides the fact the standard test for Lyme misses half the cases, there may be another reason—Borrelia miyamotoi.

A new study out of San Francisco State University (SFSU) has found more Borrelia miyamotoi than Borrelia burgdorferi (Lyme disease) in Ixodes pacificus ticks in some areas of Northern California.

Borrelia miyamotoi disease poses a difficult problem for patients and doctors who are unfamiliar with it. Its symptoms may present as viral-like or Lyme-like and there is currently no FDA-approved test.

What is Borrelia miyamotoi?

The family of tick-borne Borrelia is divided into two broad groups that correspond to the disease manifestations they cause in humans: Lyme disease or relapsing fever. Borrelia miyamotoi is in the tick-borne relapsing fever group (TBRF).

Unlike B. miyamotoi, most North American TBRF species (B. hermsii, B. turicatae, B. parkeri), are transmitted by soft-bodied ticks.

B. miyamotoi is different. It’s transmitted by the same blacklegged tick that carries Lyme disease and several other pathogens.

Furthermore, B. miyamotoi can be transmitted from the adult female tick to her eggs. This is called transovarial transmission. It means that baby ticks can be infected with B. miyamotoi from the get-go.

In contrast, blacklegged ticks don’t start out being infected with Lyme. They must acquire the infection by feeding on an animal that carries it—such as a mouse or squirrel.

The research and findings

For the SFSU study, researchers collected 1,358 Ixodes pacificus ticks and 370 rodents from eight different sites in Northern California from April to May 2018. The ticks included 894 larvae, 281 nymphs and 183 adults.

On average the following tested positive for B. miyamotoi:

  • 0.11% of the larvae
  • 4.98% of nymphs
  • 8.74% of the adult ticks

With the prevalence of infection increasing at each life stage of the tick, and each stage including one blood meal, the researchers estimate that horizontal transmission (from mammal to tick) accounts for 97% of B. miyamotoi infection in nymphal ticks and 43% of infection in adult ticks.

Interestingly, the researchers detected B. burgdorferi in 9.86% of nymph and 2.33% of the adult I. pacificus ticks—a decrease in prevalence of 76% from one life stage to the next. In addition, an average of 5.21% of the mice had blood that tested positive for B. miyamotoi.

During the same time, researchers also took skin biopsies from the ears of the rodents they had collected, and examined them for the presence of miyamotoi infection and Lyme.  They found more B. miyamotoi in the blood samples and more B. burgdorferi in the skin.

This matches with other types of TBRF, which are more easily detected in human blood samples, especially when the person is symptomatic. In contrast, Lyme disease is harder to detect in blood samples after it disseminates throughout the body.

The SFSU authors conclude, “the human risk of B. miyamotoi in the western USA may be even greater than B. burgdorferi in certain disease hot spots.”
How this study compares

The SFSU study only included counties around the San Francisco Bay Area. However, a prior California Department of Public Health 12-year study found B. miyamotoi in I. pacificus ticks in 24 out of 48 California counties.

Another study published in 2018 by Professor Robert Lane, along with researchers at UC Berkeley and Yale, examined a biobank of frozen blood samples. The results showed that 26 out of 101 samples collected from residents of Mendocino County, California, in the 1980s were reactive for relapsing fever borreliosis, including B. miyamotoi.

Similarly, another study published in 2018 looked at blood samples drawn from patients in 25 California counties. The results showed positive testing for TBRF in 16 of those counties, with the highest rates of positivity coming from Santa Clara, Alameda, Marin and San Francisco.

That study used a novel laboratory technique that can detect multiple species of TBRF. Co-author Jyotsna Shaw, of IGeneX, Inc., says “we hope that these techniques can be used to develop accurate FDA-approved tests for the future.”

A hidden epidemic?

B. miyamotoi was discovered in ticks more than 20 years ago in Japan. But it wasn’t proven to cause illness in humans until 2011, when the first human cases were reported in Russia.

It is now known to be widespread in North America, wherever Ixodes scapularis ticks and Ixodes pacificus ticks are found.

Unfortunately, Borrelia miyamotoi disease (BMD) is not reportable to the CDC, and the standard test for Lyme disease will not detect it. Because of this, many patients are likely going undiagnosed, and therefore we really have no idea how widespread the illness is.

The symptoms of Borrelia Miyamotoi Disease (BMD)

(according to the CDC)

Symptoms

  • Fever
  • Chills
  • Fatigue
  • Severe headache
  • Muscle or joint pain
  • Dizziness, confusion, vertigo (uncommon)
  • Rash (uncommon)
  • Shortness of breath (uncommon)
  • Nausea, abdominal pain, diarrhea, and anorexia (uncommon)

A recent feature in the New York Times discusses a difficult case where a patient tested negative for Lyme and many other conditions. Medical detective work by Dr. Brian Fallon of the  Columbia Lyme and Tick-Borne Disease Center eventually determined that she suffered from B. miyamotoi. (She tested negative for Lyme disease. So what was wrong?)

LymeSci is written by Lonnie Marcum, a Licensed Physical Therapist and mother of a daughter with Lyme. Follow her on Twitter: @LonnieRhea  Email her at: lmarcum@lymedisease.org .

References

Sambado, S., J. Salomon, A. Crews, and A. Swei. (2020) Mixed transmission modes promote persistence of an emerging tick-borne pathogen. Ecosphere 11(6):e03171. 10.1002/ecs2.3171

Krause PJ, Carroll M, Fedorova N, Brancato J, Dumouchel C, Akosa F, et al. (2018) Human Borrelia miyamotoi infection in California: Serodiagnosis is complicated by multiple endemic Borrelia species. PLoS ONE 13(2): e0191725. https://doi.org/10.1371/journal.pone.0191725

Padgett K, Bonilla D, Kjemtrup A, Vilcins I-M, Yoshimizu MH, Hui L, et al. (2014) Large Scale Spatial Risk and Comparative Prevalence of Borrelia miyamotoi and Borrelia burgdorferi Sensu Lato in Ixodes pacificus. PLoS ONE 9(10): e110853. https://doi.org/10.1371/journal.pone.0110853

Jeomhee Mun, Rebecca J. Eisen, Lars Eisen, Robert S. Lane (2006) Detection of a Borrelia miyamotoi Sensu Lato Relapsing-Fever Group Spirochete from Ixodes pacificus in California , Journal of Medical Entomology, 43 (1) 120–123, https://doi.org/10.1093/jmedent/43.1.120

Geoffrey E Lynn, Christine B Graham, Kalanthe Horiuchi, Lars Eisen, Tammi L Johnson, Robert S Lane, Rebecca J Eisen (2018) Prevalence and Geographic Distribution of Borrelia miyamotoi in Host-Seeking Ixodes pacificus (Acari: Ixodidae) Nymphs in Mendocino County, California, Journal of Medical Entomology, 55(3), 711–716, https://doi.org/10.1093/jme/tjx258

Borrelia miyamotoi Disease | Tick-borne Diseases | Ticks | CDC https://www.cdc.gov/ticks/tickbornediseases/borrelia-miyamotoi.html

Test Order | Submitting Specimens to CDC | Infectious Diseases Laboratories | CDC https://www.cdc.gov/laboratory/specimen-submission/detail.html?CDCTestCode=CDC-10532 via @CDCgov

__________________
 
**Comment**
 
This is another great read:  https://madisonarealymesupportgroup.com/2020/11/05/your-lyme-disease-test-results-are-negative-but-your-symptoms-say-otherwise/
 
Since Borrelia miyamotoi is not a reportable illness to the CDC, no one has any clue about prevalence but reports are coming in continually that it’s highly likely to be a much bigger problem than ‘authorities’ believe.
 
It was recently discovered that:
  • Among positive ticks, 60% were for B. miyamotoi.
  • Testing on over 2,000 humans (mainly late stage/chronic patients) showed 30% negative results and 70% positive, among which over 60% indicated the presence of specific Borrelia miyamotoi phages.  https://madisonarealymesupportgroup.com/2020/11/30/neglected-infections-gastrointestinal-issues-in-patients-with-late-vector-borne-infections/

Also, Borrelia miyamotoi has been in California ticks for a long time:

https://madisonarealymesupportgroup.com/2018/02/15/b-miyamotoi-in-ca-ticks-for-a-long-time/

The following case shows how you can become infected while traveling:  https://madisonarealymesupportgroup.com/2020/10/24/a-case-of-borrelia-miyamotoi/

For more:  https://madisonarealymesupportgroup.com/2020/11/18/what-you-need-to-know-about-borrelia-miyamotoi/

https://madisonarealymesupportgroup.com/2020/06/17/borrelia-miyamotoi-infection-in-a-highly-endemic-area-of-lyme-disease/

Category:

Borrelia Miyamotoi (Relapsing Fever Group), Lyme, research, Testing

Overcoming NeuroLyme Live Webinar: Dec. 15, 8pm EST

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Watch December 15th, 8pm EST

Chronic Lyme disease can manifest in seemingly endless ways. But neurological symptoms such as brain fog, limb pain, muscle weakness, anxiety, and more can feel especially debilitating, and they’re notoriously difficult to diagnose and overcome.

Why are some people more likely to experience neurological Lyme disease — and what can you do to feel better?

Join a live webinar with Dr. Bill Rawls, author of the best-selling book Unlocking Lyme, who knows firsthand what it’s like to live with chronic Lyme disease and neurological symptoms.

He’ll demystify neurological Lyme and share effective ways to restore your health and get much-needed symptom relief.

PLUS: Don’t miss an exclusive gift for webinar attendees, and have your questions ready for a LIVE Q&A on neurological Lyme disease with Dr. Rawls.

 In this webinar, Dr. Rawls will discuss:
  • Why neurological symptoms such as nerve and limb pain, headache, brain fog, memory loss, and more are so prevalent among Lyme patients
  • What causes neurological symptoms to become chronic and predominant in some people (but not others)
  • What your gut and common Lyme coinfections have to do with it
  • Why go-to and conventional treatments typically don’t work, and the six essential steps to effective recovery
  • The best therapies for easing symptoms and restoring health at the root cause
  • Numerous insights during the live Q&A with Dr. Rawls

RESERVE MY SEAT »

______________________
For more:
  • https://madisonarealymesupportgroup.com/2018/04/21/neurological-lyme-disease-what-you-need-to-know/
  • https://madisonarealymesupportgroup.com/2016/07/10/greg-lee-excellent-article-on-strategies-for-neurological-lyme/
  • https://madisonarealymesupportgroup.com/2020/11/04/opinion-neurologic-problems-in-lyme-disease-also-seen-in-covid-19/
  • https://madisonarealymesupportgroup.com/2019/08/22/lyme-disease-common-in-turkey-patients-with-neurological-symptoms-misdiagnosed-with-ms/
  • https://madisonarealymesupportgroup.com/2020/05/19/chronic-neurological-lyme-disease-or-co-morbid-conditions/

Category:

Activism, Lyme, Psychological Aspects

Unlocking Latency: Treating Microbial Resistance With Natural Medicine – FREE Webinar Dec. 30, 2020

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In the past, Thing has promoted liposomal essential oils. My guess is this will be discussed in this Webinar as well:

https://madisonarealymesupportgroup.com/2019/11/17/liposomal-essential-oil-remedies-a-breakthrough-in-natural-lyme-treatment/

Category:

Activism, Herbs, Lyme

Herxheimer Reaction Cause Debunked as New Research Reveals True Cause

https://biologixcenter.com/herxheimer-reactions/herxheimer-reaction-cause-debunked-as-new-research-reveals-true-causes/

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Herxheimer Reaction Cause Debunked as New Research Reveals True Cause

By Dr. David A. Jernigan

Remarkable new research debunks the dominant explanation for why people undergoing antibiotic treatment for Lyme disease very often experience a dramatic worsening of their symptoms, as well as new symptoms, in what is known as a Jarisch-Herxheimer reaction. The dominant explanation has been essentially that the guts or endotoxins of the dying bacteria spill into the body causing this worsening of symptoms. This explanation, though widely held as true is, according to the scientific research, completely incorrect.

A Jarisch-Herxheimer response, otherwise known as a Herx reaction is a worsening of person’s symptoms during and after antibiotic treatment of the spirochetal infections syphilis, Lyme disease, leptospirosis, and relapsing fever (RF), associated with immune cells in the body releasing cytokines that increase inflammation and tissue damage. The popular idea that a herx is due to the direct die off toxins of the bacteria is not supported by the latest research.

This article will present research explaining why natural and prescription antibiotics cause severe herx reactions when compared to the use of induced native bacteriophages, which can completely annihilate the entire population of the targeted bacteria, with virtually no Herx reaction. The article will also present preventive measures to minimize herx reactions if inefficient treatments, such as natural and prescription antibiotics, are utilized.

What Actually Causes a Herx Reaction?

In order to develop effective therapeutic countermeasures to herx reactions, the pathophysiology, or the disordered physiological processes associated with a herx reaction, must be understood.

Many authors have incorrectly proposed that the Herxheimer reaction is caused by the release of toxins (endotoxins) by dying spirochetes, or Mast Cell Activation (MCAS) cytokine-responses causing inflammation in response to spirochete endotoxins. However, according to the most recent understanding, these mechanisms are largely unsupported by the research.

In a review of the research, Thomas Butler states:

“After antibiotic treatment, spirochetes are rendered more susceptible to PMN phagocytosis likely caused by an alteration of the microbial surface to expose antigens and molecular patterns that allow antibody and complement to bind more effectively for phagocytic uptake. Once inside, PMN spirochetes probably provoke more severe inflammation.“

Butler goes on to say:

“Causes of inflammation in the JHR (Herx Reactions) are multi-factorial. When spirochetes are cleared from blood by phagocytosis, rises in concentrations of pro-inflammatory cytokines occur. Spirochetal inflammatory substances include lipoproteins and nonendotoxin pyrogens that cause rises in cytokines such as TNF-a, IL-6, and IL-8, as well as rises in histamine.”

The True Cause of a Herx Reaction in Layman’s Terms

In layman’s terms, a Herx is not just any worsening from any cause while undergoing treatment with antibacterial medication. A Herx occurs with antibiotics and other antibacterial efforts, such as botanicals, due to the fact that while the antibiotics do kill some of the bacteria, they often only injure many of the bacteria and/or cause a slow death, which allows your body’s immune cells, called phagocytes, time to come along and gobble up (PNM phagocytosis) these injured and dying bacteria, much like a Pac-Man from the old video game.

Once gobbled up, these live bacteria release genetic material inside of the phagocyte, causing it (the Pac-Man) to crank out excessive amounts and various types of cytokines, which are biochemicals that promote inflammation. This does not occur when bacteriophages kill the bacteria, since the phages literally kill the bacteria outright and so rapidly, that when the Pac-men of the immune system come along, they only gobble up the dead pieces, and no cytokines are produced, therefore there is no increased inflammation.

A Herx reaction:

  • Is not a desirable event.
  • Serves no therapeutic benefit.
  • Is a sign that the antibacterial medication is increasing inflammation and damage in the body.
  • Is a sign of inefficient medication is being utilized, causing live and damaged bacteria to be engulfed by phagocyte immune cells.
  • Should be avoided

Lessons from Bacteriophages: Less Herx From Bacteriophages Than Antibiotics:

Much of what we now understand about a Herx reaction is through the science of bacteriophages, which are viruses that only infect bacteria. When induced, or stimulated, bacteriophages can completely and rapidly kill all of the bacteria they infect, annihilating the entire target bacteria population. When the last of the bacterial population is dead, the bacteriophages themselves die within four days.

Bacteriophages kill bacteria by a process called lysis, the disintegration of the bacteria by rupture of the cell wall or membrane. To see this in action, watch the National Institute of Health video on this link. Research has demonstrated that Borrelia burgdorferi which were killed by lysis, did not cause nearly as much cytokine release, nor increased inflammosomes. Conversely, antibiotics often cause increased phagocytosis of the bacteria, resulting in significantly greater transcription of proinflammatory cytokine genes than do lysates.

Anti-Herx Therapeutic Measures: (If antibiotics and botanicals are being used to kill bacteria )

  • Botanical/Nutitional/Homeopathic/Fatty Acid: Doctor recommended anti-inflammatory and anti-cytokine support
  • I.V. Hydration has been shown to reduce the occurrence and severity of herx reactions
  • Hyperbaric Oxygen therapy (HBOT), and other oxygen therapies have been shown to reduce the severity of herx reactions
  • BEMER mat therapy
  • Near/Mid/Far Infrared Sauna therapy
  • Antihistamines and enhance the optimum histamine clearance via enzyme activation in the metabolic pathway.
  • NSAID’s can have a beneficial effect on acute herx reactions
  • Note: Toxin-binder supplements used to bind up and eliminate bacterial endotoxins are understood now to not be of therapeutic benefit in that there are no bacterial endotoxins to bind. These binder products can often be beneficial for other environmental toxins.

Conclusion:

Antibiotics have dominated the medical treatment of infections for almost a century, are an inefficient approach to dealing with infections, especially in light of the more rapid and precise actions of therapeutic bacteriophage treatments.

Many people who believe they are feeling worse due to the medication working, are actually being injured by the clumsy manner in which antibiotics work, not to mention their direct pharmaco-toxic effects. Many people report having to ramp up to a therapeutic dose of the more popular antibiotics, such as Disulfiram, often experiencing horrible symptoms, leaving the patient to wonder if they should tough it out and continue the drug, risking being permanently injured by the process, or to discontinue altogether.

Patients are often left on their own, searching the social media groups for guidance and encouragement, since their physician offered no advice on dealing with the very predictable problems they will face.

In the article by Thomas Butler states, “Physicians need to anticipate a JHR when treating spirochetal diseases to provide supportive care of monitoring vital signs and administering fluids.” The prognosis according to the research linking in this article, is favorable for full recovery even if a herx reaction occurs, usually resolving in a few hours in most patients given supportive care and adequate weekly IV nutritional fluids, such as a Myers Cocktail, or High-dose Vitamin C with Glutathione.

Although for many years it was thought that a Herxheimer reaction was caused by the toxins released as bacteria die and break apart, we now know this is incorrect. A Herxheimer reaction the result of the ingesting of the live, antibiotic-weakened bacteria, by immune cells, specifically polymorphonuclear leukocytes, white blood cells, such as neutrophils, which eat the live bacteria and eventually digest them, but in the meantime the bacteria, through genetic transcription cause the production of highly proinflammatory cytokines, TNF-a, IL-6, IL-8, and histamine.

When the target bacteria die from phages causing their death by lysis, as is the case with INPT bacteriophage therapy, the bacteria burst and the polymorphonuclear cells gobble up the dead pieces. In that there are no live bacteria essentially being eaten by these immune cells, very little cytokines are produced.

Bacteriophages kill the targeted bacteria extremely quickly, killing all of the target bacterial population usually in less than seven days, which means that by the time the immune system can begin to respond, the war is over. This means that when neutrophils arrive at the scene to start the cleanup, there is only remnants of the dead bacterial, and no live bacteria are being engulf, therefore the bacteria cannot cause genetic transcription and thus cannot cause the production of excessive proinflammatory cytokine substances…thereby there is minimal if any Herx reaction. All of this translates into phages cause much less herx symptoms than do antibiotics.

Conversely, many of the worsening symptoms experienced with natural or prescription antibiotics, including the latest trending antibiotic, Disulfiram, are due to the disruptive nature of the medication on the patient’s metabolic processes and frank antibiotic toxicity. These antibiotic-induced Herxheimer reactions are often the cause of poor patient compliance, often causing the patient to self-reduce the therapeutic dosage, enabling improved tolerance but greater risk of bacterial mutations rendering the drug ineffective. Antibiotic treatment can also result in new symptoms that can last months or be permanent.

Bacteriophage therapies are a superior form of treatment in the fight of treatment-resistant microbial infections.

Ongoing Development of INPT at the Biologix Center

INPT was developed by Phagen Corp. and is being used at the Biologix Center for Optimum Health, as a part of an IRB study, to go beyond Borrelia and target any microbial issue, including all of the co-infections associated with Lyme disease, as well as Candida sp., mold, and parasite infections, however at this time the only lab test for detecting bacteria-specific phages is for Borrelia strains.

The future of INPT includes intravenous and injectable forms of application, in addition to the present oral medication, available through doctors only. INPT is not projected to be sold directly to the public at this time.

To Get Treatment:

If you would like to participate in our one to two week INPT programs please contact us at www.biologixcenter.com/get-treatment/ or call our Patient Care Department at 615-398-6196 Financial assistance is available for those with chronic illness of any type, who desire treatment at Biologix Center and are struggling financially.

A more detailed report of these findings are presently being edited for publication in peer-reviewed article submission.

______________________

**Comment**

I don’t pretend to understand everything about phage therapy for Lyme disease.  While interesting, I have no experience with it.  For more:  https://biologixcenter.com/inpt-phage-therapy/new-lyme-phage-treatment-appears-to-eliminate-borrelia-in-two-weeks/

I know practitioners are all quite biased in their approach to Lyme/MSIDS based upon their own experiences and preferences.  Some promote herbal therapy, some ozone therapy, some have used antibiotics for decades, some hyperthermia with antibiotics, and so on.  Here we read of a practitioner using phage therapy, so his experiences are going to be viewed through that lens.

To my knowledge there is still no magic bullet treatment for Lyme/MSIDS.  The jury’s out for me on phage therapy until I learn more and hear of actual patient success with it, but in my experience, the axiom “If it’s too good to be true, it usually is,” has proven true again and again. I think we would all give our left arms to eradicate Lyme/MSIDS quickly , inexpensively, and without pain, but alas, I’ve yet to discover this secret elixir.  I remember the promised Stem Cell Therapy which turned out to be a big, fat dud for tick-borne illness. This stem-cell documentary was eye-opening to say the least:  https://madisonarealymesupportgroup.com/2020/07/27/free-documentary-from-jail-cell-to-stem-cell-the-next-con-for-the-ex-con-documentary/  (You can probably still find it on another platform for free)

The information on the cause of herxheimer reactions is also interesting – but the result is somewhat the same: inflammation and pain.  Patients really don’t care why.  This inflammation and pain can make many patients question their treatment and even quit – or mistakenly believe if they just change doctors all will be well.  I’ve experienced this myself too many times to count, but slow and steady – utilizing a multi-pronged approach (treat, detox, support) with numerous antimicrobials (antibiotic, ozone, herbs, EO’s, and more) won the race for my husband and I.  We relapsed twice, requiring 2-3 month stints which brought us to our current remission.  I’m also hearing good reports of Disulfiram.  Go here for Lyme treatments:  https://madisonarealymesupportgroup.com/2016/02/13/lyme-disease-treatment/  (Numerous sources for treatment outcomes within link as well)

I think there are still many ways to skin a cat, and I truly hope phage therapy actually works as we definitely need more tools in our toolbox for this beast that ‘authorities’ continue to under appreciate.

But, I’m not going to hold my breath.

Category:

Detoxing, Lyme, research, Treatment

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