Author Archives: Gregg Banse

Two Frogs Has Moved to a New Office as of January 1st!

moving_van

Two Frogs has moved into a larger office!

We are open at our new location inside the:

Frederick Innovative Technology Center (FITCI) at
4539 Metropolitan Court
Frederick, MD 21704

fitci_front

 

There are multiple visitor spaces (highlighted in yellow) across from the front entrance of the FITCI.
If all the visitor spaces are taken, you can park in any open parking space.

 

fitci_above

Here is what the lobby looks like:

fitci_lobby

Have a seat in the waiting area.

Tell the receptionist you are here to see Greg Lee.
Restrooms are right behind the reception desk.
Water is available upon request.

Question? Call us at 301-228-3764 or email at TwoFrogsHealingCenter@gmail.com.
We look forward to seeing you in our new space!

Thanks,

Greg

How These Essential Oils Help People with Lyme Disease to Fight Drug Resistant Candida

english_ivy

For people receiving antibiotic treatment for Lyme disease that have impaired brain function, fatigue, and intestinal bloating due to a drug-resistant Candida infection
by Greg Lee

While clearing space for a new flower garden, I found a tangled mass of vines. English ivy had overgrown a large area. Pulling up one vine unearthed four more. After thirty minutes of pulling and digging, most of the vines were cleaned up.

How is a tangled mass of ivy similar to a person with Lyme disease that is fighting a Candida infection?

Just like a bed of fast growing ivy, Candida can quickly spread in patients receiving antibiotics for Lyme disease
There are over twenty species of Candida that can infect humans1. Candida is a yeast that can be ingested on contaminated food. Candida can normally be found along with healthy microbes in the digestion tract. Both exposure to environmental mold which suppresses the immune system and excess consumption of alcohol, sugar, and carbohydrates can increase the growth of Candida. People who have chronic medical conditions, like Lyme disease, are a greater risk of a systemic Candida infection2. Antibiotic therapy for Lyme disease, can kill off healthy gut microbes, which can create more areas in the intestines for Candida to spread into. In some cases, antibiotic therapy in Lyme patients may be combined with steroid3 or immuno-suppressive4 treatment. Studies have shown that people undergoing antibiotic, steroid, or immuno-suppressive treatment are more at risk of a Candida infection5. A chronic Lyme infection can also suppress the immune system, which may also enable Candida to spread deeper6. A systemic Candida infection can mimic the symptoms of Lyme disease.

There is a significant overlap between symptoms of a systemic Candida and Lyme disease infection
A systemic Candida infection can produce similar symptoms as found in patients with Lyme disease. Symptoms which overlap are:

  • Fever and chills7
  • Chronic fatigue8
  • Digestion pain, bloating, and nausea9
  • Meningitis10
  • Headache11
  • Arthritis12
  • Heart arrhythmia13
  • Cognitive decline and memory recall problems14
  • ADHD15
  • Depression16
  • Urinary tract infections17
  • Systemic inflammatory response18
  • Seizures19
  • Death20

Not surprisingly, both Lyme and Candida can trigger the release of similar inflammatory compounds which are associated with increased symptoms.

Both Lyme and Candida infections can trigger the increase of multiple inflammatory compounds
Candida21 and Lyme disease22 infections have been shown to trigger the release of Interleukin-1β (IL-1β), Interleukin-6 (IL-6), Interleukin-8 (IL-8)23, and Interleukin-10 (IL-10)24. IL-1β is implicated in patients with depression25 and joint inflammation26. IL-6 is strongly associated with rheumatoid arthritis27, depression28, hostility29, fatigue30, flu-like symptoms and fever31, and cognitive impairment32. IL-8 is implicated in patients with anxiety33, meningitis34, and spirochete (leptospira) induced liver inflammation35. IL-10 is associated with irritable bowel disease36 and fatigue37. Unfortunately, these infections also employ other mechanisms to help them survive in their hosts.

Candida and Lyme employ multiple mechanisms to survive longer
Both infections are capable of hiding inside of cells38, and infecting the brain39. They can producing biofilms40, which are a slime produced to protect against antimicrobial drugs41, the killer cells of the immune system, and against other pathogens. Biofilms can increase drug resistance by a factor of ten to a thousand fold42. Biofilms are believed to be a main cause of recurring Candida or Lyme disease symptoms that persist despite multiple rounds of antibiotics43 or antifungal medications44. In addition to increased resistance from biofilms, Candida has also developed intrinsic and acquired resistance to multiple antifungal drugs45. In addition to biofilms, Lyme bacteria and Candida are capable of producing proteins that lower the activation of the complement immune response46. The complement immune system is a primary coordinator of the innate and adaptive immune responses for killing invading pathogens47.

What else can help people with Lyme disease to fight a drug-resistant, biofilm forming, immune system manipulating, systemic Candida infection?

Here are four essential oils that are effective at inhibiting stubborn Candida infections
Fortunately, there are essential oils that have been found to inhibit drug resistant Candida, cut through biofilms, and enhance the immune response to invading infections. Some of these oils also help with reducing inflammatory compounds that are elevated in a Lyme and Candida infection. Preparing the remedies in a micronized form called a liposome increases their antimicrobial and antibiofilm properties. High dose liposomal antifungal medications have been safe and effective at treating systemic Candida infections in premature infants48. Since liposomes are so small and are surrounded by a lipid, they have a greater ability to penetrate into cells where these infections can hide. Which is why liposomal remedies may be highly effective at helping patients with eliminating a resistant Candida infection.

Anti-Candida Essential Oil #1: Eucalyptus Essential Oil
In multiple lab studies, eucalyptus essential oil was highly effective at inhibiting the growth of fluconazole resistant Candida biofilms49, inhibited the growth of hospital acquired drug resistant strains of Candida50 and inducing innate cell mediated immune response against infections51. In other studies, eucalyptus oil was effective in relieving post-operative pain52 and inhibiting nitric oxide inflammatory production53. In addition to eucalyptus oil, cinnamon has excellent anti-Candida properties.

Anti-Candida Essential Oil #2: Cinnamon Bark Essential Oil
In multiple studies, cinnamon essential oil is effective at inhibiting Candida albicans54, Candida biofilms55, hospital acquired strains of Candida56, respiratory tract Candida57, and fluconazole-resistant Candida58. When combined in a capsule with patchouli essential oil, 71% of patients infected with an intestinal infection of multiple species of Candida were cured59. Liposomal cinnamon oil was effective at inhibiting drug resistant staphylococcus and it’s biofilms60. Cinnamon oil was effective in lab studies at inhibiting these inflammatory compounds: neurological inducible nitric oxide synthase (iNOS), Cyclooxygenase-2 (COX-2) expression, and nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) inflammation61. Caution: cinnamon oil has produced allergic dermatitis in some cases when placed on the skin. This oil may interfere with blood clotting. In one case, a boy drank 60 ml of cinnamon oil upon a dare and experienced symptoms of burning sensation in the mouth, chest and stomach, dizziness, double vision, nausea, vomiting and later collapsed62. Another promising anti-Candida essential oil is lemongrass.

Anti-Candida Essential Oil #3: Lemongrass Essential Oil
Vaporized Lemongrass oil was 100% effective at inhibiting Candida albicans in a lab study63. In other studies, lemongrass essential oil inhibited multi-drug resistant Candida albicans64, multi-drug resistant strains of Streptococcus and Candida65, and multiple species of Candida66. Lemongrass essential oil has an enhanced killing effect against two species of Candida when combined with silver ions67. Lemongrass oil followed by clove oil was highly effective against Candida albicans and its biofilms68. In one lab study, lemongrass oil inhibited the production of IL-1beta and IL-669. In a human study, lemongrass oil reduced anxiety and tension70. Another spice oil with anti-Candida properties is oregano.

Anti-Candida Essential Oil #4: Oregano Essential Oil
In multiple studies, oregano essential oil was highly effective at inhibiting multiple drug resistant species of Candida71, stopping germination and mycelial growth of Candida albicans in a dose dependent manner72, and inducing cell wall and membrane damage in thirty different strains of Candida albicans73. Oregano oil inhibited IL-1beta, IL-6, GM-CSF, and TNF-alpha inflammatory compounds in a mouse experiment74. Using multiple essential oils in combination can help with reducing systemic Candida infection symptoms and inflammation.

Essential oils in combination can help to resolve systemic Candida infection symptoms in people with Lyme
Similar to clearing out a tangled mass of ivy, essential oils can help people with Lyme to weed out systemic Candida symptoms. Combining these oils together may enhance their anti-Candia and anti-biofilm properties. Patients that have taken these oils combined with a carrier oil under their tongue have reported reduced symptoms of inflammation, improved sleep, and less brain fog.

When encapsulated into a micronized particle called a liposome, these oils may be capable of even greater penetration into the cells, nervous system, and into biofilms where Candida can hide. Through inhibiting the production of inflammatory compounds, these oils may also help with relieving physical symptoms and uncomfortable emotions that are associated with Candida toxins and inflammation. Since some of these essential oils have cautions on their use, work with a Lyme literate essential oil practitioner to develop a proper, safe, and effective strategy for your condition.

– Greg

Next step: Come to the Getting Rid of Lyme Disease evening lecture on Monday November 7th at 6pm in Frederick, Maryland to learn more about essential oils, herbs, and treatments for healing Lyme disease, co-infection, and Candida symptoms.

https://goodbyelyme.com/events/get_rid_lyme

Also learn about effective remedies and treatments for relieving persistent symptoms of Lyme and co-infections including: cold laser, Frequency Specific Microcurrent, cupping, LED therapy, moxabustion, acupuncture, liposomal herbs, essential oils, bee venom, and more!

P.S. Do you have experiences where remedies or treatments helped you to clear a resistant Candida infection? Tell us about it.


1 “Candidiasis | Types of Diseses | Fungal Diseases | CDC.” Accessed October 10, 2016. https://www.cdc.gov/fungal/diseases/candidiasis/.
2 “Symptoms | Invasive Candidiasis | Candidiasis | Types of Diseases | Fungal Diseases | CDC.” Accessed October 10, 2016.
https://www.cdc.gov/fungal/diseases/candidiasis/invasive/symptoms.html.
3 Takado, Yuhei, Takayoshi Shimohata, Izumi Kawachi, Keiko Tanaka, and Masatoyo Nishizawa. “[Successful treatment of neuroborreliosis with combined administration of
antibiotics and steroids: a case report].” Rinshō Shinkeigaku = Clinical Neurology 52, no. 6 (2012): 411–15. https://www.ncbi.nlm.nih.gov/pubmed/22790802
4 Singh, S. K., and H. J. Girschick. “Lyme Borreliosis: From Infection to Autoimmunity.” Clinical Microbiology and Infection: The Official Publication of the European Society of Clinical Microbiology and Infectious Diseases 10, no. 7 (July 2004): 598–614.doi:10.1111/j.1469-0691.2004.00895.x. https://www.ncbi.nlm.nih.gov/pubmed/15214872
5 Mitrović, S., D. Milosević, D. Dankuc, and R. Jović. “[Mycotic disease of the mucous membranes of the head and neck].” Medicinski Pregled 53, no. 1–2 (February 2000):
85–88. https://www.ncbi.nlm.nih.gov/pubmed/10953558
6 Diterich, Isabel, Carolin Rauter, Carsten J. Kirschning, and Thomas Hartung. “Borrelia Burgdorferi-Induced Tolerance as a Model of Persistence via Immunosuppression.”
Infection and Immunity 71, no. 7 (July 2003): 3979–87. https://www.ncbi.nlm.nih.gov/pubmed/12819085
7 “Symptoms | Invasive Candidiasis | Candidiasis | Types of Diseases | Fungal Diseases | CDC.” Accessed October 10, 2016.
https://www.cdc.gov/fungal/diseases/candidiasis/invasive/symptoms.html.
8 Evengård, Birgitta, Hanna Gräns, Elisabeth Wahlund, and Carl Erik Nord. “Increased Number of Candida Albicans in the Faecal Microflora of Chronic Fatigue Syndrome
Patients during the Acute Phase of Illness.” Scandinavian Journal of Gastroenterology 42, no. 12 (December 2007): 1514–15. doi:10.1080/00365520701580397.
https://www.ncbi.nlm.nih.gov/pubmed/17886123
9 Cater, R. E. “Chronic Intestinal Candidiasis as a Possible Etiological Factor in the Chronic Fatigue Syndrome.” Medical Hypotheses 44, no. 6 (June 1995): 507–15.
https://www.ncbi.nlm.nih.gov/pubmed/7476598
10 Voice, R. A., S. F. Bradley, J. A. Sangeorzan, and C. A. Kauffman. “Chronic Candidal Meningitis: An Uncommon Manifestation of Candidiasis.” Clinical Infectious Diseases:
An Official Publication of the Infectious Diseases Society of America 19, no. 1 (July 1994): 60–66. https://www.ncbi.nlm.nih.gov/pubmed/7948559
11 Yampolsky, Claudio, Marcelo Corti, and Ricardo Negroni. “Fungal Cerebral Abscess in a Diabetic Patient Successfully Treated with Surgery Followed by Prolonged
Antifungal Therapy.” Revista Iberoamericana De Micología 27, no. 1 (March 31, 2010): 6–9. doi:10.1016/j.riam.2009.12.001. https://www.ncbi.nlm.nih.gov/pubmed/20189857
12 Gamaletsou, Maria N., Blandine Rammaert, Marimelle A. Bueno, Nikolaos V. Sipsas, Brad Moriyama, Dimitrios P. Kontoyiannis, Emmanuel Roilides, et al. “Candida Arthritis: Analysis of 112 Pediatric and Adult Cases.” Open Forum Infectious Diseases 3, no. 1 (January 2016): ofv207. doi:10.1093/ofid/ofv207.
https://www.ncbi.nlm.nih.gov/pubmed/26858961
13 Franklin, W. G., A. B. Simon, and T. M. Sodeman. “Candida Myocarditis without Valvulitis.” The American Journal of Cardiology 38, no. 7 (December 1976): 924–28.
https://www.ncbi.nlm.nih.gov/pubmed/998527
14 Severance, Emily G., Kristin L. Gressitt, Catherine R. Stallings, Emily Katsafanas, Lucy A. Schweinfurth, Christina L. Savage, Maria B. Adamos, et al. “Candida Albicans
Exposures, Sex Specificity and Cognitive Deficits in Schizophrenia and Bipolar Disorder.” NPJ Schizophrenia 2 (2016): 16018. doi:10.1038/npjschz.2016.18.
https://www.nature.com/articles/npjschz201618
15 Rucklidge, Julia J. “Could Yeast Infections Impair Recovery from Mental Illness? A Case Study Using Micronutrients and Olive Leaf Extract for the Treatment of ADHD and Depression.” Advances in Mind-Body Medicine 27, no. 3 (2013): 14–18. https://www.ncbi.nlm.nih.gov/pubmed/23784606
16 Irving, G., D. Miller, A. Robinson, S. Reynolds, and A. J. Copas. “Psychological Factors Associated with Recurrent Vaginal Candidiasis: A Preliminary Study.” Sexually
Transmitted Infections 74, no. 5 (October 1998): 334–38. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1758140/
17 Dyess, D. L., R. N. Garrison, and D. E. Fry. “Candida Sepsis. Implications of Polymicrobial Blood-Borne Infection.” Archives of Surgery (Chicago, Ill.: 1960) 120, no. 3
(March 1985): 345–48. https://www.ncbi.nlm.nih.gov/pubmed/3970669
18 Liao, Xuelian, Haibo Qiu, Ruoyu Li, Fengmei Guo, Wei Liu, Mei Kang, Yan Kang, and China-SCAN Team. “Risk Factors for Fluconazole-Resistant Invasive Candidiasis in
Intensive Care Unit Patients: An Analysis from the China Survey of Candidiasis Study.” Journal of Critical Care 30, no. 4 (August 2015): 862.e1-5.
doi:10.1016/j.jcrc.2015.04.002. https://www.ncbi.nlm.nih.gov/pubmed/26002430
19 Queiroz, L. S., A. Nucci, and J. L. De Faria. “[Systemic candidiasis with localization in the brain. Anatomo-clinical study of 5 cases].” Arquivos De Neuro-Psiquiatria 34, no. 1 (March 1976): 18031. https://www.ncbi.nlm.nih.gov/pubmed/1267947
20 Leroy, Olivier, Jean-Pierre Gangneux, Philippe Montravers, Jean-Paul Mira, François Gouin, Jean-Pierre Sollet, Jean Carlet, et al. “Epidemiology, Management, and Risk
Factors for Death of Invasive Candida Infections in Critical Care: A Multicenter, Prospective, Observational Study in France (2005-2006).” Critical Care Medicine 37, no.
5 (May 2009): 1612–18. doi:10.1097/CCM.0b013e31819efac0. https://www.ncbi.nlm.nih.gov/pubmed/19325476
21 Whiley, Robert A., Alan T. Cruchley, Carelyn Gore, and Eleni Hagi-Pavli. “Candida Albicans Strain-Dependent Modulation of pro-Inflammatory Cytokine Release by in Vitro
Oral and Vaginal Mucosal Models.” Cytokine 57, no. 1 (January 2012): 89–97. doi:10.1016/j.cyto.2011.10.017. https://www.ncbi.nlm.nih.gov/pubmed/22129624
22 Jablonska, Ewa, and Magdalena Marcinczyk. “TLR2 Expression in Relation  to IL-6 and IL-1beta and Their Natural Regulators Production by PMN and PBMC in Patients
with Lyme Disease.” Mediators of Inflammation 2006, no. 1 (2006): 32071. doi:10.1155/MI/2006/32071. https://www.ncbi.nlm.nih.gov/pubmed/16864901
23 Grygorczuk, S., S. Pancewicz, J. Zajkowska, M. Kondrusik, R. Rwierzbińska, and T. Hermanowska-Szpakowicz. “Concentrations of Macrophage Inflammatory Proteins MIP-1alpha and MIP-1beta and Interleukin 8 (Il-8) in Lyme Borreliosis.” Infection 32, no. 6 (December 2004): 350–55. doi:10.1007/s15010-004-3110-4.
https://www.ncbi.nlm.nih.gov/pubmed/15597225
24 Lilic, Desa, Ian Gravenor, Neil Robson, David A. Lammas, Pam Drysdale, Jane E. Calvert, Andrew J. Cant, and Mario Abinun. “Deregulated Production of Protective
Cytokines in Response to Candida Albicans Infection in Patients with Chronic Mucocutaneous Candidiasis.” Infection and Immunity 71, no. 10 (October 2003): 5690–
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25 Rosa, Araceli, Victor Peralta, Sergi Papiol, Manuel J. Cuesta, Fermín Serrano, Alfredo Martínez-Larrea, and Lourdes Fañanás. “Interleukin-1beta (IL-1beta) Gene and
Increased Risk for the Depressive Symptom-Dimension in Schizophrenia Spectrum Disorders.” American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics:
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26 van Vulpen, Lize F. D., Roger E. G. Schutgens, Katja Coeleveld, Els C. Alsema, Goris Roosendaal, Simon C. Mastbergen, and Floris P. J. G. Lafeber. “IL-1β, in Contrast
to TNFα, Is Pivotal in Blood-Induced Cartilage Damage and Is a Potential Target for Therapy.” Blood 126, no. 19 (November 5, 2015): 2239–46. doi:10.1182/blood-2015-03-
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27 Cronstein, Bruce N. “Interleukin-6–a Key Mediator of Systemic and Local Symptoms in Rheumatoid Arthritis.” Bulletin of the NYU Hospital for Joint Diseases 65 Suppl 1
(2007): S11-15. https://www.ncbi.nlm.nih.gov/pubmed/17708739
28 Spalletta, Gianfranco, Luca Cravello, Francesca Imperiale, Francesca Salani, Paola Bossù, Livio Picchetto, Marina Cao, et al. “Neuropsychiatric Symptoms and Interleukin-6
Serum Levels in Acute Stroke.” The Journal of Neuropsychiatry and Clinical Neurosciences 25, no. 4 (2013): 255–63. doi:10.1176/appi.neuropsych.12120399.
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29 Suarez, Edward C. “Joint Effect of Hostility and Severity of Depressive Symptoms on Plasma Interleukin-6 Concentration.” Psychosomatic Medicine 65, no. 4 (August 2003): 523–27. https://www.ncbi.nlm.nih.gov/pubmed/12883100
30 Udina, Marc, José Moreno-España, Ricard Navinés, Dolors Giménez, Klaus Langohr, Mònica Gratacòs, Lucile Capuron, Rafael de la Torre, Ricard Solà, and Rocío Martín-
Santos. “Serotonin and Interleukin-6: The Role of Genetic Polymorphisms in IFNInduced Neuropsychiatric Symptoms.” Psychoneuroendocrinology 38, no. 9 (September
2013): 1803–13. doi:10.1016/j.psyneuen.2013.03.007. https://www.ncbi.nlm.nih.gov/pubmed/23571152
31 Kaiser, L., R. S. Fritz, S. E. Straus, L. Gubareva, and F. G. Hayden. “Symptom Pathogenesis during Acute Influenza: Interleukin-6 and Other Cytokine Responses.”
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6: The Missing Element of the Neurocognitive Deterioration in Schizophrenia? The Focus on Genetic Underpinnings, Cognitive Impairment and Clinical Manifestation.”
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36 Shulman, Robert J., Monica E. Jarrett, Kevin C. Cain, Elizabeth K. Broussard, and Margaret M. Heitkemper. “Associations among Gut Permeability, Inflammatory Markers, and Symptoms in Patients with Irritable Bowel Syndrome.” Journal of Gastroenterology 49, no. 11 (November 2014): 1467–76. doi:10.1007/s00535-013-0919-6.
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Pure Chronic Fatigue: Psychophysical, Cognitive and Biological Correlates in the Chronic Fatigue Syndrome.” European Journal of Applied Physiology 114, no. 9
(September 2014): 1841–51. doi:10.1007/s00421-014-2910-1. https://www.ncbi.nlm.nih.gov/pubmed/24878689
38 Bopp, Lawrence H., Aldona L. Baltch, William J. Ritz, Phyllis B. Michelsen, and Raymond P. Smith. “Antifungal Effect of Voriconazole on Intracellular Candida Glabrata,
Candida Krusei and Candida Parapsilosis in Human Monocyte-Derived Macrophages.” Journal of Medical Microbiology 55, no. Pt 7 (July 2006): 865–70.
doi:10.1099/jmm.0.46393-0. https://www.ncbi.nlm.nih.gov/pubmed/16772413
39 Black, Joseph T. “Cerebral Candidiasis: Case Report of Brain Abscess Secondary to Candida Albicans, and Review of Literature.” Journal of Neurology, Neurosurgery, and
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40 Sapi, Eva, Scott L. Bastian, Cedric M. Mpoy, Shernea Scott, Amy Rattelle, Namrata Pabbati, Akhila Poruri, et al. “Characterization of Biofilm Formation by Borrelia
Burgdorferi in Vitro.” PloS One 7, no. 10 (2012): e48277. doi:10.1371/journal.pone.0048277. https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0048277
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Canadian Journal of Veterinary Research 66, no. 2 (April 2002): 86–92. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC226988/
43 Sapi, Eva, Navroop Kaur, Samuel Anyanwu, David F. Luecke, Akshita Datar, Seema Patel, Michael Rossi, and Raphael B. Stricker. “Evaluation of in-Vitro Antibiotic
Susceptibility of Different Morphological Forms of Borrelia Burgdorferi.” Infection and Drug Resistance 4 (2011): 97–113. doi:10.2147/IDR.S19201.
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Drugs (London, England: 2000) 5, no. 2 (February 2004): 186–97. https://www.ncbi.nlm.nih.gov/pubmed/15043393
45 Sanguinetti, Maurizio, Brunella Posteraro, and Cornelia Lass-Flörl. “Antifungal Drug Resistance among Candida Species: Mechanisms and Clinical Impact.” Mycoses 58
Suppl 2 (June 2015): 2–13. doi:10.1111/myc.12330. https://www.ncbi.nlm.nih.gov/pubmed/26033251
46 Meri, T., H. Amdahl, M. J. Lehtinen, S. Hyvärinen, J. V. McDowell, A. Bhattacharjee, S. Meri, R. Marconi, A. Goldman, and T. S. Jokiranta. “Microbes Bind Complement
Inhibitor Factor H via a Common Site.” PLoS Pathogens 9, no. 4 (April 2013). doi:10.1371/journal.ppat.1003308. https://www.ncbi.nlm.nih.gov/pubmed/23637600
47 Dunkelberger, Jason R., and Wen-Chao Song. “Complement and Its Role in Innate and Adaptive Immune Responses.” Cell Research 20, no. 1 (December 15, 2009): 34–
50. doi:10.1038/cr.2009.139.
48 Juster-Reicher, A., O. Flidel-Rimon, M. Amitay, S. Even-Tov, E. Shinwell, and E. Leibovitz. “High-Dose Liposomal Amphotericin B in the Therapy of Systemic Candidiasis
in Neonates.” European Journal of Clinical Microbiology & Infectious Diseases: Official Publication of the European Society of Clinical Microbiology 22, no. 10 (October 2003):603–7. doi:10.1007/s10096-003-0993-4. https://www.ncbi.nlm.nih.gov/pubmed/13680398
49 Agarwal, Vishnu, Priyanka Lal, and Vikas Pruthi. “Prevention of Candida Albicans Biofilm by Plant Oils.” Mycopathologia 165, no. 1 (January 2008): 13–19.
doi:10.1007/s11046-007-9077-9. https://www.ncbi.nlm.nih.gov/pubmed/17968673
50 Warnke, Patrick H., Stephan T. Becker, Rainer Podschun, Sureshan Sivananthan, Ingo N. Springer, Paul A. J. Russo, Joerg Wiltfang, Helmut Fickenscher, and Eugene
Sherry. “The Battle against Multi-Resistant Strains: Renaissance of Antimicrobial Essential Oils as a Promising Force to Fight Hospital-Acquired Infections.” Journal of
Cranio-Maxillo-Facial Surgery: Official Publication of the European Association for Cranio-Maxillo-Facial Surgery 37, no. 7 (October 2009): 392–97. doi:10.1016/j.jcms.2009.03.017.
51 Serafino, Annalucia, Paola Sinibaldi Vallebona, Federica Andreola, Manuela Zonfrillo, Luana Mercuri, Memmo Federici, Guido Rasi, Enrico Garaci, and Pasquale Pierimarchi. “Stimulatory Effect of Eucalyptus Essential Oil on Innate Cell-Mediated Immune Response.” BMC Immunology 9 (2008): 17. doi:10.1186/1471-2172-9-17.
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52 Jun, Yang Suk, Purum Kang, Sun Seek Min, Jeong-Min Lee, Hyo-Keun Kim, and Geun Hee Seol. “Effect of Eucalyptus Oil Inhalation on Pain and Inflammatory
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53 Vigo, E., A. Cepeda, O. Gualillo, and R. Perez-Fernandez. “In-Vitro Anti-Inflammatory Effect of Eucalyptus Globulus and Thymus Vulgaris: Nitric Oxide Inhibition in J774A.1 Murine Macrophages.” The Journal of Pharmacy and Pharmacology 56, no. 2 (February 2004): 257–63. doi:10.1211/0022357022665.
54 Carvalhinho, Sara, Ana Margarida Costa, Ana Cláudia Coelho, Eugénio Martins, and Ana Sampaio. “Susceptibilities of Candida Albicans Mouth Isolates to Antifungal Agents, Essentials Oils and Mouth Rinses.” Mycopathologia 174, no. 1 (July 2012): 69–76. doi:10.1007/s11046-012-9520-4. https://www.ncbi.nlm.nih.gov/pubmed/22246961
55 Pires, Regina Helena, Lilian Bueno Montanari, Carlos Henrique G. Martins, José Eduardo Zaia, Ana Marisa Fusco Almeida, Marcelo T. Matsumoto, and Maria José S.
Mendes-Giannini. “Anticandidal Efficacy of Cinnamon Oil against Planktonic and Biofilm Cultures of Candida Parapsilosis and Candida Orthopsilosis.” Mycopathologia 172, no. 6 (December 2011): 453–64. doi:10.1007/s11046-011-9448-0. https://www.ncbi.nlm.nih.gov/pubmed/21761153
56 Warnke, Patrick H., Stephan T. Becker, Rainer Podschun, Sureshan Sivananthan, Ingo N. Springer, Paul A. J. Russo, Joerg Wiltfang, Helmut Fickenscher, and Eugene
Sherry. “The Battle against Multi-Resistant Strains: Renaissance of Antimicrobial Essential Oils as a Promising Force to Fight Hospital-Acquired Infections.” Journal of
Cranio-Maxillo-Facial Surgery: Official Publication of the European Association for Cranio-Maxillo-Facial Surgery 37, no. 7 (October 2009): 392–97.
doi:10.1016/j.jcms.2009.03.017. https://www.ncbi.nlm.nih.gov/pubmed/19473851
57 Singh, H. B., M. Srivastava, A. B. Singh, and A. K. Srivastava. “Cinnamon Bark Oil, a Potent Fungitoxicant against Fungi Causing Respiratory Tract Mycoses.” Allergy 50, no. 12 (December 1995): 995–99. https://www.ncbi.nlm.nih.gov/pubmed/8834832
58 Soares, I. H., É S. Loreto, L. Rossato, D. N. Mario, T. P. Venturini, F. Baldissera, J. M. Santurio, and S. H. Alves. “In Vitro Activity of Essential Oils Extracted from
Condiments against Fluconazole-Resistant and -Sensitive Candida Glabrata.” Journal De Mycologie Médicale 25, no. 3 (September 2015): 213-17.
doi:10.1016/j.mycmed.2015.06.003. https://www.ncbi.nlm.nih.gov/pubmed/26281965
59 Wang, Gang-Sheng, Jie-Hua Deng, Yao-Hui Ma, Min Shi, and Bo Li. “Mechanisms, Clinically Curative Effects, and Antifungal Activities of Cinnamon Oil and Pogostemon Oil Complex against Three Species of Candida.” Journal of Traditional Chinese Medicine = Chung I Tsa Chih Ying Wen Pan / Sponsored by All-China Association of Traditional Chinese Medicine, Academy of Traditional Chinese Medicine 32, no. 1 (March 2012): 19–24. https://www.ncbi.nlm.nih.gov/pubmed/22594097
60 Cui, Haiying, Wei Li, Changzhu Li, Saritporn Vittayapadung, and Lin Lin. “Liposome Containing Cinnamon Oil with Antibacterial Activity against Methicillin-Resistant
Staphylococcus Aureus Biofilm.” Biofouling 32, no. 2 (2016): 215–25. doi:10.1080/08927014.2015.1134516. https://www.ncbi.nlm.nih.gov/pubmed/26838161
61 Chen, Yuh-Fung, Yu-Wen Wang, Wei-Shih Huang, Ming-Ming Lee, W. Gibson Wood, Yuk-Man Leung, and Huei-Yann Tsai. “Trans-Cinnamaldehyde, An Essential Oil in
Cinnamon Powder, Ameliorates Cerebral Ischemia-Induced Brain Injury via Inhibition of Neuroinflammation Through Attenuation of iNOS, COX-2 Expression and NFκ-B
Signaling Pathway.” Neuromolecular Medicine 18, no. 3 (September 2016): 322–33. doi:10.1007/s12017-016-8395-9. https://www.ncbi.nlm.nih.gov/pubmed/27087648
62 Tisserand, Robert, and Rodney Young. Essential Oil Safety: A Guide for Health Care Professionals. Elsevier Health Sciences, 2013. p. 890.
63 Tyagi, Amit K., and Anushree Malik. “Liquid and Vapour-Phase Antifungal Activities of Selected Essential Oils against Candida Albicans: Microscopic Observations and
Chemical Characterization of Cymbopogon Citratus.” BMC Complementary and Alternative Medicine 10 (2010): 65. doi:10.1186/1472-6882-10-65.
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64 Khan, Mohd Sajjad Ahmad, Abida Malik, and Iqbal Ahmad. “Anti-Candidal Activity of Essential Oils Alone and in Combination with Amphotericin B or Fluconazole against
Multi-Drug Resistant Isolates of Candida Albicans.” Medical Mycology 50, no. 1 (January 2012): 33–42. doi:10.3109/13693786.2011.582890.
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65 Warnke, Patrick H., Stephan T. Becker, Rainer Podschun, Sureshan Sivananthan, Ingo N. Springer, Paul A. J. Russo, Joerg Wiltfang, Helmut Fickenscher, and Eugene
Sherry. “The Battle against Multi-Resistant Strains: Renaissance of Antimicrobial Essential Oils as a Promising Force to Fight Hospital-Acquired Infections.” Journal of
Cranio-Maxillo-Facial Surgery: Official Publication of the European Association for Cranio-Maxillo-Facial Surgery 37, no. 7 (October 2009): 392–97.
doi:10.1016/j.jcms.2009.03.017. https://www.ncbi.nlm.nih.gov/pubmed/19473851
66 Silva, Cristiane de Bona da, Sílvia S. Guterres, Vanessa Weisheimer, and Elfrides E. S. Schapoval. “Antifungal Activity of the Lemongrass Oil and Citral against Candida
Spp.” The Brazilian Journal of Infectious Diseases: An Official Publication of the Brazilian Society of Infectious Diseases 12, no. 1 (February 2008): 63–66.
67 Ahmad, Aijaz, and Alvaro Viljoen. “The in Vitro Antimicrobial Activity of Cymbopogon Essential Oil (Lemon Grass) and Its Interaction with Silver Ions.” Phytomedicine:
International Journal of Phytotherapy and Phytopharmacology 22, no. 6 (June 1, 2015): 657–65. doi:10.1016/j.phymed.2015.04.002.
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68 Khan, Mohd Sajjad Ahmad, and Iqbal Ahmad. “Biofilm Inhibition by Cymbopogon Citratus and Syzygium Aromaticum Essential Oils in the Strains of Candida Albicans.”
Journal of Ethnopharmacology 140, no. 2 (March 27, 2012): 416–23. doi:10.1016/j.jep.2012.01.045. https://www.ncbi.nlm.nih.gov/pubmed/22326355
69 Sforcin, J. M., J. T. Amaral, A. Fernandes, J. P. B. Sousa, and J. K. Bastos. “Lemongrass Effects on IL-1beta and IL-6 Production by Macrophages.” Natural Product
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70 Goes, Tiago Costa, Fábio Reis Carvalho Ursulino, Thiago Henrique Almeida-Souza, Péricles Barreto Alves, and Flavia Teixeira-Silva. “Effect of Lemongrass Aroma on
Experimental Anxiety in Humans.” Journal of Alternative and Complementary Medicine (New York, N.Y.) 21, no. 12 (December 2015): 766–73. doi:10.1089/acm.2015.0099.
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71 Pozzatti, Patrícia, Liliane Alves Scheid, Tatiana Borba Spader, Margareth Linde Atayde, Janio Morais Santurio, and Sydney Hartz Alves. “In Vitro Activity of Essential
Oils Extracted from Plants Used as Spices against Fluconazole-Resistant and Fluconazole-Susceptible Candida Spp.” Canadian Journal of Microbiology 54, no. 11
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72 Manohar, V., C. Ingram, J. Gray, N. A. Talpur, B. W. Echard, D. Bagchi, and H. G. Preuss. “Antifungal Activities of Origanum Oil against Candida Albicans.” Molecular and
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How These Four Herbs Help to Stop Bartonella Rage and Obsessive Compulsive Disorder (OCD)

For people who have been diagnosed with Bartonella that have severe anger and obsessive compulsive behaviors
by Greg Lee

A few months ago I got a surprise call from my credit card provider who asked if I had made a recent $900 purchase from a clothing store in New York. I told them that I didn’t. They also asked about other charges made in shops and restaurants in the same area. Somehow my credit card number was stolen and being used. Several charges had accumulated in a short period of time before the card was canceled.

How is a thief that buys stuff on your credit card just like anger and obsessive behaviors caused by a Bartonella infection?

Just like fraudulent credit card charges that are made without your knowledge, Bartonella can quietly infect organs and tissues throughout the body

Bartonella is a Gram-negative bacterial infection that can be transmitted by insect bites, including fleas, lice, sand flies[1], flea feces,[2] mites[3], and possibly by ticks[4], spiders[5], or bed bugs[6]. This infection may also be transmitted by infected animal bites[7], scratches[8], or possibly by blood transfusion[9] or organ transplant[10].  There are over thirty species of Bartonella, and seventeen of these can infect humans[11]. This bacteria has been found to infect the liver, lymph nodes, skin[12], teeth[13], bones, heart, spleen, eyes, kidney, and brain[14]. This infection manipulates the circulatory system to spread through the body.

Bartonella stimulates the production of vascular endothelial growth factor (VEGF) to invade the body

VEGF is produced in the body to stimulate the production of new blood vessels[15]. In one study that looked at two species of Bartonella henselae, genotype I, aka Houston-1, and II, aka Marseille strain, genotype I was more virulent in human cells due to it’s ability to increase VEGF production and it’s receptor VEGFR-2 in human microvascular endothelial cells[16]. As new blood vessels grow due to VEGF production, Bartonella is then able to infect and spread through the endothelial cell lining of these new vessels[17]. Antibiotics are often the first course of treatment.

Antibiotics are highly effective in killing Bartonella in the lab but not as effective in people

In multiple lab studies, Bartonella was successfully eliminated using these antibiotics: amoxycillin and ceftriaxone, aminoglycosides, doxycycline, rifampicin, erythromycin doxycycline, and ciprofloxacin[18]. However, treatment failures and relapses have been reported with rifampin, ciprofloxacin, gentamicin, co-trimoxazole, and azithromycin[19]. One reason for these failures may be due to resistant strains of Bartonella to antibiotics: quinolones[20], rifampin[21], macrolides[22], fluoroquinolones[23], and gentamicin[24]. Another reason for antibiotic treatment failure may be due to this bacterias ability to produce or to hide within a protective slime called a biofilm. In one study, B. quintana was discovered in a exopolysaccharide (EPS)-like matrix, i.e. bioflm, in lice feces[25]. Biofilms are believed to increase drug resistance up to a thousand times[26]. This infection can produce a wide variety of physical and emotional symptoms.

Bartonella can produce many symptoms including anger, rage and obsessive compulsive disorder (OCD) behaviors
A Bartonella infection can produce symptoms of anemia[27], frequent headaches, visual and auditory hallucinations, anxiety, vision loss, paralysis, facial palsy, chronic insomnia, seizures, dizziness, cognitive dysfunction, and memory loss[28]. It has been found to mimic symptoms of multiple sclerosis (MS)[29], stroke[30], vasculitis[31], breast tumors, pancreatic, biliary or pharyngeal cancer[32], and rheumatic disease[33]. One Lyme literate specialist reports anger, rage and obsessive compulsive behavior in her Bartonella patients[34]. Obsessive behavior may be associated with a reaction in a specific area of the brain.

A specific region of the brain called the basal ganglia is associated with obsessive compulsive behavior

Obsessive compulsive behaviors are a signature symptom in children diagnosed with Pediatric Autoimmune Disorders Associated with Strep (PANDAS). In children with PANDAs, an infection by group A beta-hemolytic streptococcus (GABHS), toxins, or inflammation stimulates an autoimmune reaction in the basal ganglia area of the brain[35]. This reaction produces obsessive compulsive disorder (OCD) behaviors[36]. In one study, 19% of Bartonella patients showed lesions on brain MRIs in the cerebral white matter, basal ganglia, thalamus, and gray matter[37]. If Bartonella can produce abnormal MRI lesions in the basal ganglia, then it may be capable of producing OCD behaviors similar to a PANDAS infection.

What else can help you to stop a resistant Bartonella infection that produces angry outbursts, rage, or obsessive compulsive behaviors?

In Chinese medicine, anger, rage, and compulsive behaviors are associated with an imbalance in the liver

In Chinese medicine, when the liver becomes too hot or too dry due to excess toxins, a person may exhibit symptoms of sudden anger or rage[38]. A Chinese medicine diagnosis of liver stagnation, also known as congestion, along with a spleen deficiency is associated with OCD behaviors[39]. Obsessive compulsive behaviors have also been identified in people with toxic parasitic infections called Gu Syndrome in Chinese medicine texts[40]. Some patients with obsessive behaviors report a need to have their environment in a precise order by putting things in a specific place, extreme anxiety over unexpected surprises that disrupt daily rituals, or thoughts like, “Did I lock the door?” that they worry about over and over again. Fortunately, there are four herbs which may help to reduce obsessive behaviors, inhibit VEGF production, and lower rage by cooling and moistening the liver.

Here are four herbs for stopping Bartonella from spreading and causing painful emotions

Limiting VEGF production may help to stop Bartonella from spreading. Harmonizing the liver is a Chinese medicine strategy for lowering rage and obsessive compulsive behaviors. Formulating remedies into microparticles called liposomes increases their penetration into endothelial cells[41] where Bartonella hides out, the liver[42], and the basal ganglia[43] Liposomal remedies have also been effective at reducing the production of VEGF[44] and its receptor VEGFR2[45], which may help to limit the virulence of Bartonella. These herbs have been used for centuries in traditional medicine formulas for treating angry outbursts, rage, and obsessive compulsive disorder (OCD) behavior.

Stopping Bartonella Rage and OCD Herb #1: Angelica sinensis

Angelica sinensis, Chinese name Dang Gui, has antimicrobial, neuro-protective, anticancer, anticoagulant, and liver-protective properties. In Chinese medicine, angelica is used to strengthen and replenish the blood and it’s used to treat anemia, pale complexion, dry hair, dizziness, blurred vision, fatigue and weakness, palpitations and pain[46]. It is a primary ingredient in multiple Chinese herbal formulas for reducing angry outbursts or rage due to a liver imbalance[47] called liver yin deficiency or liver fire blazing.

In a lab study, angelica was effective at reducing VEGF[48]. In another study, angelica was effective at increasing cognitive abilities and brain plasticity of rats when under chronic stress[49]. Angelica also has demonstrated anti-endotoxin properties in multiple animal studies[50]. This herb has demonstrated an inhibitory effect on Salmonella typhi, E. coli, Corynebacterium diptheriae, Vibrio cholerae, alpha-hemolytic streptococcus, and beta-hemolytic streptococcus[51]. Another herb that is often used with angelica is peony.

Stopping Bartonella Rage and OCD Herb #2: White peony root

White peony root, Chinese name Bai Shao, has anti-inflammatory, antibiotic, CNS calming, and digestion healing properties. In Chinese medicine, white peony is used to nourish the blood, treat anemia, regulate menstrual disorders, relieve pain, reduce night sweats, nourish, cool and soften the liver[52]. A compound found in white peony called total glucosides was effective in reducing the abnormal proliferation of VEGF in a rat study[53]. Paeoniflorin, another component of white peony, demonstrated liver protective[54] and anti-endotoxin[55] properties in multiple animal studies. Albiflorin, another compound in white peony, demonstrated similar anti-inflammatory properties compared to paeoniflorin[56].

This herb has shown to have an inhibitory effect against Bacillus dysenteriae, E. Coli, Salmonella typhi, Pseudonomas aeruginosa, Staphyloccus aureus, beta-hemolytic streptococcus, and Diplococcus pneumoniae[57]. Peony is often paired with angelica in herbal formulas for treating liver imbalances, including those that are marked by irritation, rage, and angry outbursts[58]. Bupleurum is another herb used in traditional Chinese medicine for supporting the liver.

Stopping Bartonella Rage and OCD Herb #3: Bupleurum

Bupleurum, Chinese name Chai Hu, has pathogen expelling, anti-malarial, liver harmonizing, and yang lifting properties. In Chinese medicine, bupleurum is used to treat infections with symptoms of fever, chills, fullness in the chest, bitter taste in the mouth, dry throat, poor appetite, nausea, vertigo, and irritability. This herb is often used to treat malaria, emotional distress, eye disorders, breast swelling and pain, irregular menstruation, jaundice, migraines, and prolapsed organs[59]. In Chinese herbal formulas, this herb is used to release anger and frustration that is inexpressible[60].

This herb has an inhibitory effect on B-hemolytic streptococcus, Vibrio cholerae, Mycobacterium tuberculosis, leptospirosis (a spirochete infection), influenza viruses, and hepatitus viruses Buplerum is cautioned in patients with excessive dryness and heat symptoms. There may an increased risk of acute pneumonitis when this herb is used with interferon[61]. Polysaccharides found in this herb have anti-toxin properties[62]. Bupleurum reduced depression in one human study by increasing Nerve Growth Factor (NGF) and Brain Derived Neurotrophic Factor (BDNF)[63]. In a rat study, an herbal formula with bupleurum was effective at reducing inflammatory cytokines causing jaundice and liver hepatitis[64]. Bupleurum is a component with angelica and white peony in a famous formula called “Rambling Powder” to treat liver stagnation[65]. Withania somnifera is another herb for calming the emotions.

Stopping Bartonella Rage and OCD Herb #4: Withania somnifera

Withania somnifera, also called ashwagandha, has a very revered place in ayurvedic medicine. It’s properties are tonifying, replenishing, longevity enhancing, adaptogenic, stress reducing, anti-tumor, neuroregenerative, anti-arthritic, aphrodisiac, narcotic, diuretic, anthelmintic, astringent, thermogenic, and stimulant[66].

Withania somnifera has been used to treat the following conditions: arthritis, inflammatory conditions, anxiety, insomnia, respiratory disorders, asthma, and bronchitis. It is also used to treat disorders of the nervous, immune, and the reproductive system. It is especially used to treat nervousness, depression, digestion problems, and low libido[67]. This herb has also been used to treat gastric ulcers, uterine fibroids, dementia, memory problems, Parkinson’s, Huntington’s, Alzheimer’s disease, mitochondrial energy depletion, rheumatoid, and osteoarthritis[68].

In one mouse study, Withania somnifera was effective at inhibiting obsessive compulsive behavior[69]. In a rat study, Withania somnifera demonstrated liver protective and anti-inflammatory effects against gentamicin liver damage[70]. This herb was also effective in multiple studies against Staphylococcus aureus, Methicilin Resistance Staphylococcus aureus (MRSA)[71], Enterococcus spp.[72], Escherichia coli, Salmonella typhi, Citrobacter freundii, Pseudomonas aeruginosa, Klebsiella pneumoniae[73], Aeromonas hydrophila[74], Plasmodium berghei[75], Linoleic and oleic acids from Withania somnifera were effective at inhibiting streptococcus mutans biofilms[76]. Withaferin A and withanone are compounds found in this herb that show inhibitiatory potential against leshmania protozoa[77]. Withaferin A also inhibited the production of H. pylori induced inflammatory compound IL-1beta[78], MMP-9[79] produced by metastatic cancer cells, and VEGF produced by brain cancer cells[80] in lab experiments. Using a combination of these herbs can help to fight the uncomfortable emotions triggered by a Bartonella infection.

These four herbs can help to reduce painful emotions of rage and obsessive compulsive behaviors from a Bartonella infection

People with Lyme disease that have uncontrolled anger, rage and obsessive behaviors may have a stealthy Bartonella infection affecting their liver and nervous system. Similar to canceling a credit card with fraudulent charges, these herbs may help to stop the spread of Bartonella through inhibiting VEGF. By harmonizing and decongesting the liver, these herbs may help to reduce angry outbursts and obsessive compulsive behaviors. Using liposomal anti-Bartonella herbs may be more effective in stopping Bartonella inside the liver, the basal ganglia in the brain, and in endothelial cells. Since some of these herbs have cautions on their use, work with a Lyme literate natural remedy practitioner to develop a proper, safe, and effective strategy for your condition.

– Greg

Next step: Come to the Getting Rid of Lyme Disease evening lecture on Monday August 1st at 6pm in Frederick, Maryland to learn more about essential oils, herbs, and treatments for healing from Lyme disease and co-infection symptoms.

https://goodbyelyme.com/events/get_rid_lyme

Also learn about effective remedies and treatments for relieving persistent symptoms of Lyme and co-infections including: cold laser, Frequency Specific Microcurrent, cupping, LED therapy, moxabustion, acupuncture, liposomal herbs, essential oils, bee venom, and more!

P.S. Do you have experiences where remedies or treatments helped you to stop angry outbursts, rage, or obsessive compulsive behaviors due to a Bartonella infection? Tell us about it.


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[9]Diniz, Pedro Paulo Vissotto de Paiva, Paulo Eduardo Neves Ferreira Velho, Luiza Helena Urso Pitassi, Marina Rovani Drummond, Bruno Grosselli Lania, Maria Lourdes Barjas-Castro, Stanley Sowy, Edward B. Breitschwerdt, and Diana Gerardi Scorpio. “Risk Factors for Bartonella Species Infection in Blood Donors from Southeast Brazil.” PLoS Neglected Tropical Diseases 10, no. 3 (March 2016): e0004509. doi:10.1371/journal.pntd.0004509. https://www.ncbi.nlm.nih.gov/pubmed/26999057

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Is Memory Loss Caused by Neurological Lyme Disease or Brain Eating Parasites?

wasp_nest

For people with neurological Lyme disease that have dementia, multiple sclerosis, or Alzheimer’s disease
by Greg Lee
.
One afternoon, I heard one of my daughters cry out with a huge scream after a wasp stung her arm. After she was taken care of, I got out my wasp fighting gear: electric bug zapper, thick gloves, hat, and a bottle of hair spray. You may be asking, “Why hair spray?” It sticks like glue to the wasp’s wings so they can’t fly and I don’t like pesticides. Once they hurt my girl, then it got personal and they had to go!

So it was me against over a dozen wasps. After zapping and spraying them into submission, I saw one of the wasps crawl into a slot between two deck boards. And then another wasp followed. I cautiously peered into the slot and saw the nest. I got out the garden hose and sprayed that nest until no wasp remained. Then I quickly pried it out and threw it down the sewer. Once the nest was gone, the rest got the message and didn’t return.

How is being stung by angry wasps defending their nest similar to nematodes that infect the brain?

Just like a wasp nest that swarms you, nematodes can infect and damage the brain
Recent research by Dr. Alan MacDonald has found worms called nematodes in autopsy brain tissue samples from patients with neurological Lyme disease who were also diagnosed with Multiple Sclerosis, dementia, brain tumors, and Alzheimer’s Disease[1]. Lyme disease bacteria were actually detected within some of the nematodes. Similar to how wasps can hide in their nest, Lyme bacteria can hide from antibiotic treatment when they are inside of larger parasitic worms. Unfortunately, nematodes have also been detected in ticks.

In deer ticks and lone star ticks, nematodes have been detected
In multiple tick studies, nematodes have been detected in lone star ticks found in Maryland[2] and Virginia[3], and in deer ticks from Connecticut[4]. Ticks are capable of transmitting nematodes when they feed on a host[5]. Other vectors that can transmit nematodes are mosquitoes and black flies[6]. Once they infect a host, adult nematodes mate and then release thousands of very small larva called “microfilariae” into the blood. Microfilariae circulate throughout the host and can end up in the nervous system[7]. These microfilariae evolve into larvae which can eat through the brain and can cause a wide range of symptoms.

Nematodes produce many symptoms when they infect the brain and spinal fluid
Larval nematodes in the nervous system can damage tissues and produce masses called granulomas. They can also cause fibrosis, blockages in cerebral blood vessels, or inflammation resulting in meningitis, encephalitis or localized inflammation[8], weakness, blurred vision, stomach flu[9], and even death. In a Taiwan study, patients infected with nematodes reported meningitis, brain inflammation, fever, vomiting, headache, and neuropathy. Two patients died from their infection. In some patients, nematodes were recovered from their cerebral-spinal fluid (CSF). Elevated levels of inflammatory markers vascular endothelial growth factor (VEGF), hepatocyte growth factor (HGF), and matrix metalloproteinase 9 (MMP-9) were also detected in patient’s CSF fluid[10]. Research shows that nematodes can also manipulate the immune system response.

Nematodes produce compounds to deflect how the immune system attacks parasites
One research study on a nematode called B. Malayi, identified proteins that it releases to manipulate the immune response in favor of a parasitic infection[11]. Another study on a filarial nematode infection illustrated how these parasites inhibit the inflammatory response by the immune system[12]. In most cases, anti-parasitic medications are used to treat nematode infections in the nervous system.

Anti-parasitic medications help to kill nematode infections in the brain and spinal fluid
Anti-parasitic medications called antihelminthics are used to treat nematodes in the nervous system including: Mebendazole, Pyrantel pamoate, Thiabendazole, Diethylcarbamazine (DEC), Ivermectin[13], Moxidectin[14], and Alinia[15]. Ivermectin and moxidectin are the most widely administrated antihelminthic medications for nematode infections and unfortunately, their widespread and frequent use has led to high level of resistance to these drugs[16]. Ivermectin only kills the microfilariae, not the adult nematode[17]. DEC can worsen onchocercal nematode eye infections. In patients with a nematode infection called loiasis, DEC can cause serious adverse reactions, including encephalopathy and death, depending upon the density of the parasites. DEC is only available in the US from the CDC upon submitting positive lab results[18]. A mechanism within nematodes called a “drug effux pump” is believed to enable these parasites to develop drug resistance[19]. Killing nematodes can lead to significant Herxheimer reactions.

A symbiotic bacteria within nematodes is the source of Herxheimer toxins
Wolbachia is a symbiotic bacteria which enables normal development and fertility of nematodes[20]. Wolbachia belong to the order Rickettsiales and is closely related to Anaplasma, Ehrlichia and Rickettsia[21]. Fortunately, this bacteria does not infect people. When nematodes are killed off by anti-parasitic drugs, Wolbachia cannot survive without their host and are killed, which releases their endotoxins. Wolbachia toxins stimulate the production of pro-inflammatory compounds including tumor necrosis factor alpha (TNF)-alpha, Interleukin-1 (IL-1), and Interleukin-12 (IL-12)[22]. In an animal study, Wolbachia surface protein upregulated (IL)-1beta, IL-6, and tumor necrosis factor[23]. These endotoxins and inflammatory compounds can produce painful symptoms associated with a Herxheimer reaction. A combination of anti-parasitic and antibiotic medications is more effective at reducing adult and microfilariae forms of nematodes.

A combination of medications which kill both the adult and microfilariae forms is more effective
Recent drug strategies combine Ivermectin for microfilariae and doxycycline to kill Wolbachia which eventually kills the adult nematodes in the nervous system. This combination drug treatment is recommended for six weeks[24]. Another animal study combined DEC with liposomal doxycycline and liposomal rifampin resulting in significant increase in microfilariae die off and a marginal increase in the die off of adult nematodes[25]. Other studies demonstrate the inhibitory effect of anti-Rickettsia antibiotics like tetracycline, rifampin, and azithromyacin on adult nematodes[26].

What else can help people to expel brain-eating nematodes from their central nervous system who have persistent neurological Lyme disease, multiple sclerosis, dementia, brain tumors, or Alzheimer’s disease?

Here are four strategies for expelling brain-eating nematodes from the central nervous system
A combination of remedies for attacking both the adult and microfilariae forms is the most effective at reducing the overall numbers of parasites. Formulating remedies into microparticles called liposomes enhances the efficacy of anti-parasitic herbs and essential oils for killing the different life stages of nematodes[27] and possibly their symbiotic bacteria.

Clearing Brain-Eating Nematodes Strategy #1: Essential Oils
Essential oils have been found to inhibit different species of nematodes.

Thyme essential oil was effective at inhibiting Meloydogine javanica[28] and larvae from the Anisakis nematode[29]. Thyme essential oil was also effective against gram negative bacteria: Pseudomonas aeruginosa[30], Salmonella spp.[31], and E. Coli[32]. Thyme combined with oregano oil reduced mRNA levels of pro-inflammatory cytokines IL-1beta, IL-6, GM-CSF, and TNFalpha[33].

Palmarosa essential oil was effective against Caenorhabditis elegans[34] and Haemonchus contortus[35] in separate studies. This oil was also effective at inhibiting E. Coli[36] and Aspergillus fumigatus[37]. Palmarosa oil also reduced pro-inflammatory compounds TNF-α, IL-1β, and IL-8[38] and increased anti-inflammatory IL-10 in lab studies[39].

Clove bud essential oil was highly effective at reducing[40] Meloidogyne incognita egg hatch 50% and killing second stage juveniles (J2) as much as 100% in a lab study[41]. Eugenol, the primary compound in clove bud oil, in one rat study reduced expression of VEGF, MMP-2, and MMP-9[42], which are elevated in nematode infections. Processing these oils into a liposomal micronized form increases their penetration into the nervous system[43]. Adding nanoparticles of silver to liposomal oils may further enhance their anti-microbial properties.

Clearing Brain-Eating Nematodes Strategy #2: Nanoparticle Silver
In multiple lab studies, nanoparticles of silver were effective at reducing motility and killing microfilariae of Brugia malayi[44], demonstrated antifilarial activity against microfilaria of S. Cervi[45], disrupted metabolism of Caenorhabditis elegans[46], and killed most of Meloidogyne incognita[47]. Encapsulating nanoparticles of silver along with essential oils into a liposomal remedy may increase their anti-parasitic and anti-symbiotic bacterial properties. When nanoparticle silver is combined with tea tree essential oil into a liposome, their antimicrobial efficiency is enhanced against Pseudomonas aeruginosa, Staphylococcus aureus, and Candida albicans[48]. Silver nanoparticles may reduce inflammation from nematodes by inhibiting IL-1beta and VEGF induced permeability as reported in a pig study[49] and reducing MMP-2 and MMP-9 in another rat study[50]. Herbs have also been effective for treating nematode infections for thousands of years.

Clearing Brain-Eating Nematodes Strategy #3: Herbs
In addition to essential oils and silver, herbs have been used for centuries for fighting nematode infections.

Andrographis, Chinese name Chuan Xin Lian, has been effective at inhibiting Haemonchus contortus[51], microfilaricidal activity against Dirofilaria immitis filarids[52], antifilarial activity against adult worms of subperiodic Brugia malayi[53], killing in vitro the microfilaria of Dipetalonema reconditum in dogs[54], and anthelmintic activity against Ascaris lumbricoides[55]. This herb is also used in Chinese medicine against leptospirosis, another spirochete infection[56]. Andrographis was also effective at reducing inflammatory compounds IL-1α, IL-1β, and IL-6 in a lab study[57]. A compound in Andrographis called andrographolide inhibits expression of inflammatory compounds MMP-2, IL-1beta[58] and VEGF[59] in lab studies.

Ajowan, ajwain, or Trachyspermum ammi has been effective against multiple species of nematodes in multiple studies. Methanolic extract of fruits of Trachyspermum ammi were effective against adult bovine filarial Setaria digitata worms and demonstrated macrofilaricidal activity and female worm sterility in vivo against B. Malayi[60].

Lantana camara is an ornamental shrub which is very hardy and is used medicinally through much of the world. This herb contains triterpenoids pomolic acid, lantanolic acid, lantoic acid, camarin, lantacin, camarinin, and ursolic acid which exhibited 100% mortality in 24 – 48 hours against the nematode Meloidogyne incognita[61]. In other studies, a lantana extract killed adult Brugia malayi nematodes and sterilized many of the surviving female worms, and demonstrated strong microfilaricidal and sterilization efficacy with mild macrofilaricidal action against Acanthocheilonema viteae[62]. Not only herbs, but also tiny electrical frequencies can help to stop nematodes that have infected the brain and spinal fluid.

Clearing Brain-Eating Nematodes Strategy #4: Frequency Specific Microcurrent
Frequency Specific Microcurrent uses millionth of an amp electrical currents to reduce parasitic and bacterial infections, toxins and inflammation[63]. Frequencies for inhibiting parasitic worms, symbiotic bacteria, neutralizing toxins and inflammation, reducing tumors, and promoting healing are paired with frequencies to target infected areas of the nervous system: the brain, forebrain, meninges, basal ganglia, spinal cord, spinal fluid, cranial nerves, and eyes[64]. These paired frequencies have also been helpful in reducing symptoms in patients diagnosed with multiple sclerosis, autism, brain inflammation, mold toxicity, and neurological Lyme disease. These four strategies may help people with neurological Lyme to stop an underlying parasitic nematode brain infection.

A combination of anti-parasitic remedies and treatments can help to overcome a chronic neurological Lyme and nematode infection
People diagnosed with multiple sclerosis, Alzheimer’s disease, dementia, or brain tumors may have hidden parasitic nematodes along with Lyme disease in their nervous system. Just like finding and eliminating the wasp nest, expelling parasitic nematodes that harbor Lyme bacteria may help to improve neurological symptoms and memory recall. Using liposomal anti-parasitic and anti-symbiotic bacteria remedies and treatments may be effective in eliminating larger parasites and the Lyme bacteria they contain.

Anti-toxin treatments and remedies may also help with reducing inflammatory compounds which may lower toxic Herxheimer pain and discomfort. Making these remedies into micronized liposomes enhances their delivery into the nervous system and may increase their anti-nematode effectiveness. Since some of these treatments and remedies require specialized training, work with a Lyme literate natural remedy practitioner to develop a proper, safe, and effective strategy for your condition.

– Greg

Next step: Come to the Getting Rid of Lyme Disease evening lecture on Monday July 11th at 6pm in Frederick, Maryland to learn more about essential oils, herbs, and treatments for healing from Lyme disease and co-infection symptoms.

https://goodbyelyme.com/events/get_rid_lyme

Also learn about effective remedies and treatments for relieving persistent symptoms of Lyme and co-infections including: cold laser, Frequency Specific Microcurrent, cupping, LED therapy, moxabustion, acupuncture, liposomal herbs, essential oils, bee venom, and more!

P.S. Do you have experiences where remedies or treatments helped you to overcome memory problems caused by brain-eating parasites or a Lyme disease infection? Tell us about it.


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[50] Liu, Binbin. “In Vitro Cytotoxicity of Silver Nanoparticles in Primary Rat Hepatic Stellate Cells.” Molecular Medicine Reports, September 13, 2013. doi:10.3892/mmr.2013.1683. https://www.spandidos-publications.com/mmr/8/5/1365
[51] Kamaraj, Chinnaperumal, Abdul Abdul Rahuman, Gandhi Elango, Asokan Bagavan, and Abdul Abduz Zahir. “Anthelmintic Activity of Botanical Extracts against Sheep Gastrointestinal Nematodes, Haemonchus Contortus.” Parasitology Research 109, no. 1 (July 2011): 37–45. doi:10.1007/s00436-010-2218-y. https://www.ncbi.nlm.nih.gov/pubmed/21161270
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How These Five Remedies Stop Persistent Gut Problems Caused by Listeria in People with Lyme Disease

hitchhiker_seeds

For people with Lyme disease that have recurring digestion problems, leaky gut, or small intestine bacterial overgrowth (SIBO)
by Greg Lee

I used to play football and baseball with other neighborhood boys at Mr. Johnson’s field. Occasionally we’d have to go looking for one of our balls at the far end of the field which had tall grass and weeds. Sometimes I’d come out with “hitchhiker” weed seeds clinging to my clothes.

How are hitchhiker seeds similar to people with Lyme disease that have chronic digestion problems?

Just like seeds that sneak on to your clothes, Listeria can be a dangerous pathogen which sneaks into the intestines
In several different recalls of food products, Listeria monocytogenes was cited as a contaminant in multiple food processing plants which produce frozen food, fruit, ice cream, cheese, and sunflower seeds. In another incidence, Listeria was found in whole cantaloupes that ended up sickening 147 people and resulted in 43 fatalities[1]. According to one CDC report, Listeria can be fatal in 21% of cases[2] even despite early antibiotic treatment[3]. Fatality may be as high as 40-60% in patients with a central nervous system infection and concurrent debilitating disease[4]. People over 65, pregnant women and especially their unborn children, and immune compromised patients like people with chronic Lyme or co-infections are at greater risk. Fortunately, the risk of getting a Listeria infection is low, about 2-3 people per million in the US. However, the risk is greater in immune compromised people, even at low doses of Listeria contamination on food[5]. This infection usually starts with symptoms in the digestion system.

Listeria often presents with bloating, nausea, and diarrhea
This infection can produce symptoms of fever and muscle aches, sometimes preceded by diarrhea or other gastrointestinal symptoms. In 55-70% of cases, Listeria can affect the central nervous system (CNS)[6].  When Listeria spreads beyond the digestion tract, it can produce symptoms of headache, stiff neck, confusion, loss of balance, convulsions, meningitis, septicemia, and death[7]. Some immune compromised patients may not have any symptoms. Listeria employs multiple methods to spread through unsuspecting people.

Listeria uses multiple methods to help it to spread through the body
The first line of defense against food borne Listeria are the endothelial cells which line the intestines. Listeria employs multiple strategies to invade several different types of cells and spread through the body: intestinal epithelial cells, hepatocytes, placental cytotrophoblasts, endothelial cells, macrophages and other immune cells[8]. In one lab study, listeriolysin O (LLO) is a toxin produced by Listeria which enables it to move freely inside of and to propagate between endothelial cells[9]. This toxin also disables “T” cells which enable this bacteria to evade the immune system and survive longer[10]. Listeria has also developed drug resistance to multiple antibiotics.

Listeria can persist due to drug resistance to many antibiotics
Unfortunately, mutant strains of Listeria have developed resistance to several antibiotics including: ampicillin, cephalothin, penicillin, meticillin, oxacillin[11],  tetracycline, streptomycin, cefotaxime, and gentamicin[12]. Listeria uses a mechanism called an effux pump to sample drug molecules to develop drug-resistance[13]. This bacteria can also produce biofilms under which many species of pathogens may live, which suggests that Listeria is likely capable of long-term infection in the gut[14]. In one study on sanitizers, Listeria under a biofilm demonstrated increased resistance of 1000 times[15]. In another lab study, Listeria has also been shown to be capable of receiving drug resistant genes from other bacteria that contaminate food[16]. Unfortunately, some Lyme disease patients with chronic digestion problems have tested positive for resonant frequencies for Listeria in their intestines.

What else can help people with Lyme disease to fight a drug-resistant, biofilm forming, intracellular Listeria gut and central nervous system infection?

Here are five strategies for stopping Listeria infections in the gut and the central nervous system
Here are four strategies for helping to stop Listeria from spreading. Making remedies into a small particle size can increase their anti-Listeria properties. When anti-Listeria medicines were processed into small particles and wrapped with a lipid or a fat outer layer called a liposome, they had a 90-fold greater effect at killing the intracellular infection in mice[17]. Liposomal remedies have been shown to be more effective at penetrating and delivering remedies into Listeria infected cells than their non-liposomal equivalents[18]. In other studies, herbs, specific frequencies of light, and dietary changes inhibited Listeria.

Listeria Stopping Strategy #1: Essential Oils
In one lab study, five plant essential oils: bay, clove, cinnamon, nutmeg and thyme significantly reduced the toxin listeriolysin O[19], which can help to prevent Listeria monocytogenes from spreading through the body. In another lab study, nanoemulsions of anise oil were more effective at inhibiting Listeria than anise essential oil[20]. Other lab studies indicated the effectiveness of oregano[21], lemongrass[22], spearmint[23], clove[24], myrtle[25], ajowan[26], orange[27], peppermint[28], geranium[29], artemisia annua[30], cinnamon Chinese cassia, red thyme[31], lemon and cinnamon[32] essential oils against Listeria monocytogenes. In lab experiments, thyme and oregano[33] essential oils were also effective at eliminating the biofilm forms of Listeria. Encapsulation the oils in liposomes, increases their effectiveness at targeting intracellular L. monocytogenes in endothelial cells[34] and the central nervous system[35]. Not only oils can help with stopping Listeria, so can specific wavelengths of light.

Listeria Stopping Strategy #2: Light Therapy
Light Emitting Diode (LED) frequencies of 405 nm[36] and 461 nm[37] inactivated L. monocytogenes in multiple lab experiments. Applying these wavelengths to the skin may help with stopping a cutaneous Listeria[38] infection. In studies on the penetration depth of laser wavelengths of 405 nm, this frequency was able to penetrate to a depth of 0.08 mm with 55% transmission into fair colored skin, and 2.5% in darker skin[39]. In addition to light, herbs can also help with stopping Listeria.

Listeria Stopping Strategy #3: Herbs
In addition to essential oils and light frequencies, these herb extracts have anti-Listeria properties in one study: rosemary, Echinacea angustifolia, thyme, tea tree, and peppermint[40]. In other studies, green tea was effective at inhibiting Listeria in food[41]. A green tea compound called epigallocatechin gallate (ECGC) was also effective at inhibiting the intracellular growth of L. Monocytogenes in a macrophage study[42]. Processing these herbs into small particle liposomes enhances their ability to penetrate and stop intracellular Listeria[43] and potentially disrupt it’s biofilms[44]. Not only herbs, but also tiny electrical frequencies can help to stop a Listeria infection.

Listeria Stopping Strategy #4: Frequency Specific Microcurrent
Frequency Specific Microcurrent uses millionth of an amp electrical currents to reduce bacterial infections, toxins and inflammation[45]. Frequencies for reducing pathogens, neutralizing toxins and inflammation, and promoting healing are combined with frequencies to target Listeria hiding inside blood cells[46], and organs like the intestines[47], liver, spleen[48], and the central nervous system[49]. These paired frequencies have been helpful in reducing symptoms in patients with meningitis, headaches, and confusion. In addition to microcurrent, dietary changes can also help to fight Listeria.

Listeria Stopping Strategy #5: Dietary Changes
In multiple studies, these foods and supplements inhibited the growth of Listeria: virgin olive oil[50], zinc and isomeric vitamin A[51], feijoa fruit extract from New Zealand[52], Lactobacilus[53] and Bifidobacterium[54] probiotics. Eliminating alcohol intake may also help with boosting the strength of your innate immunity against Listeria[55]. Multiple strategies can help people with Lyme to stop a persistent Listeria gut or brain infection.

A combination of anti-Listeria strategies can help to resolve a chronic gastrointestinal problems or infections in people with Lyme disease
Similar to taking the hitchhiking seeds off your clothes, anti-Listeria remedies and treatments may help to resolve chronic digestion problem, gut infections and meningitis. Processing these oils and herbs into a small particle liposome can enhance their antimicrobial, antibiofilm properties, and ability to penetrate inside cells and into the central nervous system. Some patients will also take these oils or herb extracts in an enema to increase their delivery into the intestines. Since some of these oils and herbs have cautions on their use, work with a Lyme literate natural remedy practitioner to develop a proper, safe, and effective strategy for your condition.

– Greg

Next step: Come to the Getting Rid of Lyme Disease evening lecture on Monday June 6th at 6pm in Frederick, Maryland to learn more about essential oils, herbs, and treatments for healing from Lyme disease and co-infection symptoms.

https://goodbyelyme.com/events/get_rid_lyme

Also learn about effective remedies and treatments for relieving persistent symptoms of Lyme and co-infections including: cold laser, Frequency Specific Microcurrent, cupping, LED therapy, moxabustion, acupuncture, liposomal herbs, essential oils, bee venom, and more!

P.S. Do you have experiences where remedies or treatments helped you to overcome chronic gut problems caused by a toxic Listeria infection? Tell us about it.



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[36] Kim, Min-Jeong, Marta Mikš-Krajnik, Amit Kumar, Vinayak Ghate, and Hyun-Gyun Yuk. “Antibacterial Effect and Mechanism of High-Intensity 405 ± 5 Nm Light Emitting Diode on Bacillus Cereus, Listeria Monocytogenes, and Staphylococcus Aureus under Refrigerated Condition.” Journal of Photochemistry and Photobiology. B, Biology 153 (December 2015): 33–39. doi:10.1016/j.jphotobiol.2015.08.032. https://www.ncbi.nlm.nih.gov/pubmed/26398810

[37] Ghate, Vinayak, Ai Ling Leong, Amit Kumar, Woo Suk Bang, Weibiao Zhou, and Hyun-Gyun Yuk. “Enhancing the Antibacterial Effect of 461 and 521 Nm Light Emitting Diodes on Selected Foodborne Pathogens in Trypticase Soy Broth by Acidic and Alkaline pH Conditions.” Food Microbiology 48 (June 2015): 49–57. doi:10.1016/j.fm.2014.10.014. https://www.ncbi.nlm.nih.gov/pubmed/25790991

[38] Godshall, Casey E., Gina Suh, and Bennett Lorber. “Cutaneous Listeriosis.” Journal of Clinical Microbiology 51, no. 11 (November 2013): 3591–96. doi:10.1128/JCM.01974-13. https://www.ncbi.nlm.nih.gov/pubmed/23966491

[39] F. H. Mustafa, M. S. Jaafar. “Comparison of Wavelength-Dependent Penetration Depths of Lasers in Different Types of Skin in Photodynamic Therapy.” Indian Journal of Physics 87, no. 3 (2012). doi:10.1007/s12648-012-0213-0. https://www.researchgate.net/publication/234720204_Comparison_of_wavelength-dependent_penetration_depths_of_lasers_in_different_types_of_skin_in_photodynamic_therapy

[40] M Sandasi, C. M. Leonard. “The in Vitro Antibiofilm Activity of Selected Culinary Herbs and Medicinal Plants against Listeria Monocytogenes.” Letters in Applied Microbiology 50, no. 1 (2009): 30–35. doi:10.1111/j.1472-765X.2009.02747.x. https://www.researchgate.net/publication/38052994_The_in_vitro_antibiofilm_activity_of_selected_culinary_herbs_and_medicinal_plants_against_Listeria_monocytogenes

[41] Lee, Sun-Young, So-Young Gwon, Seung-Ju Kim, and Bo Kyung Moon. “Inhibitory Effect of Commercial Green Tea and Rosemary Leaf Powders on the Growth of Foodborne Pathogens in Laboratory Media and Oriental-Style Rice Cakes.” Journal of Food Protection 72, no. 5 (May 2009): 1107–11. https://www.ncbi.nlm.nih.gov/pubmed/19517743

[42] Kohda, Chikara, Yoko Yanagawa, and Tadakatsu Shimamura. “Epigallocatechin Gallate Inhibits Intracellular Survival of Listeria Monocytogenes in Macrophages.” Biochemical and Biophysical Research Communications 365, no. 2 (January 11, 2008): 310–15. doi:10.1016/j.bbrc.2007.10.190. https://www.ncbi.nlm.nih.gov/pubmed/17996193

[43] Ito, M., et al. “Inhibitory Effect of Liposome-Encapsulated Penicillin G on Growth of Listeria Monocytogenes in Mouse Macrophages.”  https://www.ncbi.nlm.nih.gov/pubmed/3103258

[44] Sadekuzzaman, M., S. Yang, M.f.r. Mizan, and S.d. Ha. “Current and Recent Advanced Strategies for Combating Biofilms.” Comprehensive Reviews in Food Science and Food Safety 14, no. 4 (July 1, 2015): 491–509. doi:10.1111/1541-4337.12144. https://onlinelibrary.wiley.com/doi/10.1111/1541-4337.12144/pdf

[45] DC, Carolyn McMakin MA. Frequency Specific Microcurrent in Pain Management, 1e. 1 Pap/Dvdr edition. Edinburgh ; New York: Churchill Livingstone, 2011.

[46] Kose, Adem, and Yusuf Yakupogullari. “A Rapidly Fatal Sepsis Caused by Listeria Monocytogenes Type-4b in a Patient with Chronic Renal Failure.” Jundishapur Journal of Microbiology 8, no. 3 (March 2015): e19980. doi:10.5812/jjm.19980. https://www.ncbi.nlm.nih.gov/pubmed/25969704

[47] Regan, Tim, Ken Nally, Ruaidhri Carmody, Aileen Houston, Fergus Shanahan, John Macsharry, and Elizabeth Brint. “Identification of TLR10 as a Key Mediator of the Inflammatory Response to Listeria Monocytogenes in Intestinal Epithelial Cells and Macrophages.” Journal of Immunology (Baltimore, Md.: 1950) 191, no. 12 (December 15, 2013): 6084–92. doi:10.4049/jimmunol.1203245. https://www.ncbi.nlm.nih.gov/pubmed/24198280

[48] Kernbauer, Elisabeth, Verena Maier, Isabella Rauch, Mathias Müller, and Thomas Decker. “Route of Infection Determines the Impact of Type I Interferons on Innate Immunity to Listeria Monocytogenes.” PloS One 8, no. 6 (2013): e65007. doi:10.1371/journal.pone.0065007. https://www.ncbi.nlm.nih.gov/pubmed/23840314

[49] Vázquez-Boland, et al. “Listeria Pathogenesis and Molecular Virulence Determinants.” https://www.ncbi.nlm.nih.gov/pmc/articles/PMC88991/#

[50] Medina, Eduardo, Concepción Romero, Manuel Brenes, and Antonio De Castro. “Antimicrobial Activity of Olive Oil, Vinegar, and Various Beverages against Foodborne Pathogens.” Journal of Food Protection 70, no. 5 (May 2007): 1194–99. https://www.ncbi.nlm.nih.gov/pubmed/17536679

[51] Castillo, Yussaira, Masato Tachibana, Yukiko Nakatsu, Kenta Watanabe, Takashi Shimizu, and Masahisa Watarai. “Combination of Zinc and All-Trans Retinoic Acid Promotes Protection against Listeria Monocytogenes Infection.” PloS One 10, no. 9 (2015): e0137463. doi:10.1371/journal.pone.0137463. https://www.ncbi.nlm.nih.gov/pubmed/26351852

[52] Hap, S., and N. A. Gutierrez. “Functional Properties of Some New Zealand Fruit Extracts towards Selected Probiotic and Pathogenic Bacteria.” Beneficial Microbes 3, no. 4 (December 1, 2012): 309–18. doi:10.3920/BM2012.0004. https://www.ncbi.nlm.nih.gov/pubmed/22968373

[53] Uymaz, Başar, Nefise Akkoç, and M. Akçelik. “Partial Characterization of Bacteriocins Produced by Two Lactobacilus Strains with Probiotic Properties.” Acta Biologica Hungarica 62, no. 1 (March 2011): 95–105. doi:10.1556/ABiol.61.2011.1.10. https://www.ncbi.nlm.nih.gov/pubmed/21388923

[54] Corr, Sinead C., Cormac G. M. Gahan, and Colin Hill. “Impact of Selected Lactobacillus and Bifidobacterium Species on Listeria Monocytogenes Infection and the Mucosal Immune Response.” FEMS Immunology and Medical Microbiology 50, no. 3 (August 2007): 380–88. doi:10.1111/j.1574-695X.2007.00264.x. https://www.ncbi.nlm.nih.gov/pubmed/17537177

[55] Pavia, Charles S., Cynthia M. Harris, and Marie Kavanagh. “Impaired Bactericidal Activity and Host Resistance to Listeria Monocytogenes and Borrelia Burgdorferi in Rats Administered an Acute Oral Regimen of Ethanol.” Clinical and Diagnostic Laboratory Immunology 9, no. 2 (March 2002): 282–86. doi:10.1128/CDLI.9.2.282-286.2002. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC119923/

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Why You Need These Four Essential Oils for Relieving Lyme Disease Insomnia and Brain Fog caused by Toxic Sinuses

Ernie_Banks_gum

For people with Lyme disease who have brain fog and insomnia due to toxic sinus infections
by Greg Lee

 

I loved collecting baseball cards as a kid. When I opened a new pack of cards, I was always filled with excited thoughts of, “Will I get a Willie Mays or a Hank Aaron?” And sometimes I only got cards that I already had multiple copies of, bless you Bob Burda. After finding out which cards I received, I got to enjoy a big pink stick of bubble gum. I got in big trouble once, when I put the gum in my pocket and it ended up going through the washer. Many of the other clothes ended up being stuck to pink gooey gum.

 

How is melted bubble gum that sticks to your clothes similar to toxic sinus infections in people with Lyme?

 

Just like gooey bubble gum, toxic infections can get stuck in the sinuses
In multiple studies, people with chronic sinus irritation have tested positive for a variety of different infections including: Staphylococcus aureus[1], Staphylococcus epidermidis[2], Streptococcus intermedius[3], Chlamydia[4], Clostridia[5], Mycoplasma[6], Nocardia nova[7], Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis, and Streptococcus pyogenes, and anaerobic organisms: Prevotella and Porphyromonas, Fusobacterium, and Peptostreptococcus spp.[8] In immune compromised patients, multiple infections have detected including: Alternaria alternata[9], Aspergillus flavus[10], Mucormycetes[11], Fusarium[12], Cytomegalovirus[13], Bordetella petrii[14], Escherichia coli, Stenotrophomonas maltophilia, and basidiomycetous fungi (Schizophyllum commune)[15]. In rare cases, unusual infections that are mostly found in animals or soil have also been detected in sinus infections like: Staphylococcus pseudintermedius[16], and Paecilomyces variotii[17]. In other studies, dental infections have also been found to invade the sinuses[18]. Inflammatory markers can help to identify the types of infections in the sinus.

 

Inflammatory markers can give a clue to bacterial and fungal sinus infections
In sinus patients infected with Aspergillus and Alternaria, interleukin (IL)- 2, IL-4, IL-5, IL-10, tumor necrosis factor α, and interferon-γ were elevated[19]. Another study on chronic bacterial sinus infection patients showed that inflammatory markers IL-4, IL-8, IL-13 and Myeloperoxidase (MPO) were higher in the upper airway compared to the lower airway[20]. Sinus infections can also produce chronic physical problems and difficult emotions.

 

Sinus infections can affect physical as well as emotional symptoms
Severe sinus infections produce toxins which triggers inflammation and can lead to complications like irritability, decreased attention, anxiety, insomnia, depression[21], meningitis, abscesses in the brain[22], paralysis, tremors, weakness, blindness[23], sepsis[24], cerebral aneurysm[25], stroke[26], and death[27]. Elevated inflammatory compounds: IL-1β, IL-6, IL-8, and IL-13 were correlated with sleep disturbance and depression and may be an indicator of the severity of a sinus infection[28]. Unfortunately, these infections have multiple defense mechanisms to help them persist in the sinuses.

 

Toxic sinus infections can survive longer by hiding under multiple defenses
Sinus infections can be characterized by local inflammation, mucus discharge, immunoglobulin deficiency[29], pus, cysts, or polyps[30]. Sinus polyps have been found to have high levels of fibrin[31], which can isolate infections from your immune system and medications. Biofilms[32] are a slime produced by many different infections to protect against antimicrobial drugs, the killer cells of the immune system, and against other pathogens. Biofilms can increase drug resistance by a factor of ten to a thousand fold[33]. Biofilms are believed to be a main cause of recurring sinus infections that persist despite surgeries, multiple rounds of antibiotics or antifungals[34]. One study identifies nasal cysts, polyps, and mucus as likely places where infections can survive despite intravenous antibiotic treatment[35]. Unfortunately, patients with Lyme disease have also been found to have drug-resistant Staph bacteria.

 

Drug resistant Staph bacterial have been detected in the sinuses of Lyme patients receiving antibiotic treatment
Dr. Ritchie Shoemaker has found Multiple Antibiotic Resistant Coagulase Negative Staph (MARCoNS) infections in the sinuses of his patients receiving antibiotic treatment[36]. His protocol uses a nasal spray consisting of antibiotics along with biofilm dissolving EDTA. Unfortunately, the majority of health care providers treating Lyme patients are not following Dr. Shoemaker’s protocol.

 

What else can help people with Lyme disease to fight drug-resistant, biofilm forming, multi-species sinus infections?

 

Here are four essential oils that are effective at inhibiting infections and inflammatory compounds found in sinus infections
Fortunately, there are essential oils that have been found to inhibit many of the infections and biofilms that infect the sinuses and have also been effective at relieving pain, sleep problems, and difficult emotions. Preparing the remedies in a micronized form called a liposome, which are microscopic particles of medicinal oils that are wrapped in a lipid, increases their penetration into tissues and their antimicrobial, antibiofilm properties[37]. Which is why liposomal remedies may be highly effective at helping patients with penetrating into and eliminating persistent sinus infections and accompanying symptoms.

 

Sinus Infection Essential Oil #1: Tea Tree
In one wound study, liposomal tea tree oil combined with silver ions was effective at inhibiting Pseudomonas aeruginosa, Staphylococcus aureus, and Candida albicans[38]. Tea Tree essential oil was also effective a reducing the size of wounds caused by methicillin-resistant Staphylococcus aureus (MRSA)[39]. Tea tree oil was also effective against Staphylococcus epidermidis, Escherichia coli, Saccharomyces cerevisiae[40], antibiotic resistant Candida spp.[41], Pseudomonas aeruginosa and its biofilm,[42] Aspergillus niger, Aspergillus flavus[43], Aspergillus fumigatus, Penicillium chrysogenum[44], Mycoplasma pneumoniae, Mycoplasma hominis and Mycoplasma fermentans[45], group A streptococcus[46], Fusarium graminearum, Fusarium culmorum, Pyrenophora graminea[47], Alternaria alternata, Botrytis cinerea and Fusarium oxysporum[48] in lab and animal studies.

 

In response to bacterial endotoxins, tea tree essential oil was effective at lowering inflammatory compounds IL-1β, IL-6 and IL-10[49]. In another lab study, tea tree oil decreased IL-2 and increased anti-inflammatory compound IL-4[50]. Caution: some cases have been reported where tea tree oil caused allergic dermatitis when placed on the skin[51]. In five cases, high doses of this oil internally, 0.5-1.0 ml/kg, have produced central nervous system symptoms of loss of coordination, drowsiness, unconsciousness, diarrhea, and abdominal pain[52]. In addition to tea tree oil, cinnamon has excellent antimicrobial properties.

 

Sinus Infection Essential Oil #2: Cinnamon Bark 
In unpublished lab research, cinnamon essential oil was effective at cutting through the Lyme biofilm and killing the bacteria. This oil is also effective at inhibiting: multi-drug resistant Pseudomonas aeruginosa and Escherichia coli toxin production and biofilms[53], multi-drug resistant strains of Salmonella typhi, Salmonella paratyphi A, Escherichia coli, Staphylococcus aureus, Pseudomonas fluorescens and Bacillus licheniformis[54], methicillin-resistant Staphylococcus aureus (MRSA)[55], Candida albicans[56], quorum sensing communication in drug resistant Chromobacterium violaceum and Pseudomonas aeruginosa[57], Haemophilus influenzae, Streptococcus pneumoniae, Streptococcus pyogenes[58], Campylobacter jejuni, Salmonella enteritidis, Listeria monocytogenes[59], Penicillium commune, P. roqueforti, Aspergillus flavus and Endomyces fibuliger[60].

 

In other studies which combine this oil and antibiotics, cinnamon bark essential oil helped to reduce drug resistance in multiple bacterial strains when combined with a beta-lactam antibiotic[61] and had a synergistic effect with gentamicin against multidrug-resistant Acinetobacter spp.[62]. Cinnamon oil has produced allergic dermatitis in some cases when placed on the skin. This oil may interfere with blood clotting. In one case, a boy drank 60 ml of cinnamon oil upon a dare and experienced symptoms of burning sensation in the mouth, chest and stomach, dizziness, double vision, nausea, vomiting and later collapse[63]. Another promising sinus antimicrobial remedy is thyme oil.

 

Sinus Infection Essential Oil #3: Thyme 
Thyme essential oil has been shown to inhibit Methicillin resistant Staphylococcus aureus (MRSA)[64], Staphylococcus aureus biofilms[65], Antibiotic-Resistant Candida spp.[66], Vancomycin-Resistant Enterococci[67], drug-resistant strains of Aspergillus spp. and Trichophyton rubrum[68],  Clostridium perfringens, Campylobacter jejuni[69], Listeria monocytogenes, Salmonella Typhimurium, enterohemorrhagic Escherichia coli, Brochothrix thermosphacta, Pseudomonas fluorescens[70], Zygosaccharomyces bailii[71], Staphylococcus, Enterococcus, Escherichia, Pseudomonas genera[72], Aeromonas species[73], Haemophilus influenzae, Streptococcus pneumoniae, and Streptococcus pyogenes[74].

 

In one mouse colitis experiment, thyme oil combined with oregano essential oil was effective at lowering IL-1beta, IL-6, GM-CSF, and TNFalpha[75]. Caution: thyme oil (geraniol chemotype) should not be taken in people with obstructed bile flow[76]. In addition to thyme, lemongrass has antimicrobial and antibiofilm properties.

 

Sinus Infection Essential Oil #4: Lemongrass 
Lemongrass essential oil has inhibited Staphylococcus aureus biofilms[77], drug-resistant strains of Actinomyces naeslundii, Porphyromonas gingivalis[78], methicillin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant Enterococcus (VRE), multi-drug resistant Pseudomonas aeruginosa, ESBL-producing Escherichia coli, Klebsiella pneumoniae[79], multi-drug resistant Candida albicans[80], multi-drug resistant strains of Streptococcus and Candida[81], and the Aeromonas hydrophyla biofilm[82].

 

Vaporized lemongrass oil combined with geranium oil inhibited MRSA, vancomycin-resistant Enterococci (VRE), Acinetobacter baumanii and Clostridium difficile[83]. Lemongrass oil followed by clove oil was highly effective against Candida albicans and its biofilms[84]. In one lab study, lemongrass oil inhibited the production of IL-1beta and IL-6[85]. Using multiple essential oils in combination can help with reducing chronic sinus infection symptoms.

 

Essential oils in combination can help to resolve chronic sinus infection symptoms in people with Lyme
Similar to getting sticky bubble gum off a bunch of clothes, essential oils can help people with Lyme to reduce sinus infection symptoms. Combining these oils can enhance their antimicrobial and antibiofilm properties. Patients that take these oils in a carrier oil under their tongue report reduced inflammation, improved sleep, and less brain fog. When encapsulated into a micronized particle called a liposome, these oils may be capable of even greater penetration into the sinus tissues when held in the mouth. In addition to inhibiting multiple harmful bacteria and fungi, these oils may also help with relieving uncomfortable emotions that are associated with elevated toxins and inflammation. Since some of these essential oils have cautions on their use, work with a Lyme literate essential oil practitioner to develop a proper, safe, and effective strategy for your condition.

 

– Greg

Next step: Come to the Getting Rid of Lyme Disease evening lecture on Monday June 6th at 6pm in Frederick, Maryland to learn more about essential oils, herbs, and treatments for healing from Lyme disease and co-infection symptoms.

https://goodbyelyme.com/events/get_rid_lyme

Also learn about effective remedies and treatments for relieving persistent symptoms of Lyme and co-infections including: cold laser, Frequency Specific Microcurrent, cupping, LED therapy, moxabustion, acupuncture, liposomal herbs, essential oils, bee venom, and more!

P.S. Do you have experiences where remedies or treatments helped you to overcome insomnia and brain fog caused by a toxic sinus infection? Tell us about it.



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[2] Dlugaszewska, Jolanta, Malgorzata Leszczynska, Marcin Lenkowski, Agnieszka Tatarska, Tomasz Pastusiak, and Witold Szyfter. “The Pathophysiological Role of Bacterial Biofilms in Chronic Sinusitis.” European Archives of Oto-Rhino-Laryngology: Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS): Affiliated with the German Society for Oto-Rhino-Laryngology – Head and Neck Surgery, May 30, 2015. doi:10.1007/s00405-015-3650-5. https://www.ncbi.nlm.nih.gov/pubmed/26024693
[3] Yin, Xiuyun, Yuying Liang, Lijun Zeng, and Shuiping Chen. “A Case of Sinusitis Caused by Schizophyllum Commune and Bacteria in Acute Myelocytic Leukemia.” Clinical Laboratory 61, no. 11 (2015): 1799–1801. https://www.ncbi.nlm.nih.gov/pubmed/26722629
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[6] Ciobanu, Adela Magdalena, Tatiana Roşca, Camelia Teodora Vlădescu, Cecilia Tihoan, Mihaela Camelia Popa, Monica Claudia Boer, and Romică Cergan. “Frontal Epidural Empyema (Pott’s Puffy Tumor) Associated with Mycoplasma and Depression.” Romanian Journal of Morphology and Embryology = Revue Roumaine De Morphologie Et Embryologie 55, no. 3 Suppl (2014): 1203–7. https://www.ncbi.nlm.nih.gov/pubmed/25607407
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[9] Pesic, Zoran, Suzana Otasevic, Dragan Mihailovic, Sladjana Petrovic, Valentina Arsic-Arsenijevic, Dragan Stojanov, and Milica Petrovic. “Alternaria-Associated Fungus Ball of Orbit Nose and Paranasal Sinuses: Case Report of a Rare Clinical Entity.” Mycopathologia 180, no. 1–2 (August 2015): 99–103. doi:10.1007/s11046-015-9881-6. https://www.ncbi.nlm.nih.gov/pubmed/25749849
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[11] Mahomed, Sharana, Sujith Basanth, and Koleka Mlisana. “The Successful Use of Amphotericin B Followed by Oral Posaconazole in a Rare Case of Invasive Fungal Sinusitis Caused by Co-Infection with Mucormycosis and Aspergillus.” IDCases 2, no. 4 (2015): 116–17. doi:10.1016/j.idcr.2015.10.001. https://www.ncbi.nlm.nih.gov/pubmed/26793475
[12] Davoudi, S., V. A. Kumar, Y. Jiang, M. Kupferman, and D. P. Kontoyiannis. “Invasive Mould Sinusitis in Patients with Haematological Malignancies: A 10 Year Single-Centre Study.” The Journal of Antimicrobial Chemotherapy 70, no. 10 (October 2015): 2899–2905. doi:10.1093/jac/dkv198. https://www.ncbi.nlm.nih.gov/pubmed/26188039
[13] Sridhar, Siddharth, Iris W. S. Li, Sally C. Y. Wong, and Kwok-Yung Yuen. “Circulating Cytomegalic Cells in a Patient with Advanced HIV Presenting with Cytomegalovirus Rhinosinusitis.” Journal of Clinical Virology: The Official Publication of the Pan American Society for Clinical Virology 65 (April 2015): 87–89. doi:10.1016/j.jcv.2015.02.009. https://www.ncbi.nlm.nih.gov/pubmed/25766996
[14] Nagata, Jason M., Gregory W. Charville, Jenna M. Klotz, Walter R. Wickremasinghe, Dylan C. Kann, Hayden T. Schwenk, and Christopher A. Longhurst. “Bordetella Petrii Sinusitis in an Immunocompromised Adolescent.” The Pediatric Infectious Disease Journal 34, no. 4 (April 2015): 458. doi:10.1097/INF.0000000000000564. https://www.ncbi.nlm.nih.gov/pubmed/25760569
[15] Yin, Xiuyun, Yuying Liang, Lijun Zeng, and Shuiping Chen. “A Case of Sinusitis Caused by Schizophyllum Commune and Bacteria in Acute Myelocytic Leukemia.” Clinical Laboratory 61, no. 11 (2015): 1799–1801. https://www.ncbi.nlm.nih.gov/pubmed/26732008
[16] Kuan, Edward C., Alexander J. Yoon, Tara Vijayan, Romney M. Humphries, and Jeffrey D. Suh. “Canine Staphylococcus Pseudintermedius Sinonasal Infection in Human Hosts.” International Forum of Allergy & Rhinology, February 16, 2016. doi:10.1002/alr.21732. https://www.ncbi.nlm.nih.gov/pubmed/26880481
[17] Swami, T., S. Pannu, Mukesh Kumar, and G. Gupta. “Chronic Invasive Fungal Rhinosinusitis by Paecilomyces Variotii: A Rare Case Report.” Indian Journal of Medical Microbiology 34, no. 1 (March 2016): 103–6. doi:10.4103/0255-0857.174126. https://www.ncbi.nlm.nih.gov/pubmed/26776131
[18] Saibene, Alberto Maria, Christian Vassena, Carlotta Pipolo, Mariele Trimboli, Elena De Vecchi, Giovanni Felisati, and Lorenzo Drago. “Odontogenic and Rhinogenic Chronic Sinusitis: A Modern Microbiological Comparison.” International Forum of Allergy & Rhinology 6, no. 1 (January 2016): 41–45. doi:10.1002/alr.21629. https://www.ncbi.nlm.nih.gov/pubmed/26345711
[19] Kale, Pratibha, Shivaprakash M. Rudramurthy, Naresh K. Panda, Ashim Das, and Arunaloke Chakrabarti. “The Inflammatory Response of Eosinophil-Related Fungal Rhinosinusitis Varies with Inciting Fungi.” Medical Mycology 53, no. 4 (May 2015): 387–95. doi:10.1093/mmy/myv001. https://www.ncbi.nlm.nih.gov/pubmed/25724204
[20] Doht, Franziska, Julia Hentschel, Nele Fischer, Thomas Lehmann, Udo R. Markert, Klas Böer, Wolfgang Pfister, Mathias W. Pletz, Orlando Guntinas-Lichius, and Jochen G. Mainz. “Reduced Effect of Intravenous Antibiotic Treatment on Sinonasal Markers in Pulmonary Inflammation.” Rhinology 53, no. 3 (September 2015): 249–59. doi:10.4193/Rhin14.300. https://www.ncbi.nlm.nih.gov/pubmed/26363166
[21] Ciobanu, Adela Magdalena, Tatiana Roşca, Camelia Teodora Vlădescu, Cecilia Tihoan, Mihaela Camelia Popa, Monica Claudia Boer, and Romică Cergan. “Frontal Epidural Empyema (Pott’s Puffy Tumor) Associated with Mycoplasma and Depression.” Romanian Journal of Morphology and Embryology = Revue Roumaine De Morphologie Et Embryologie 55, no. 3 Suppl (2014): 1203–7. https://www.ncbi.nlm.nih.gov/pubmed/25607407
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[67] Selim, Samy. “Antimicrobial Activity of Essential Oils against Vancomycin-Resistant Enterococci (vre) and Escherichia Coli o157:h7 in Feta Soft Cheese and Minced Beef Meat.” Brazilian Journal of Microbiology: [publication of the Brazilian Society for Microbiology] 42, no. 1 (January 2011): 187–96. doi:10.1590/S1517-83822011000100023. https://www.ncbi.nlm.nih.gov/pubmed/24031620
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[72] Sienkiewicz, Monika, Monika Łysakowska, Julita Ciećwierz, Paweł Denys, and Edward Kowalczyk. “Antibacterial Activity of Thyme and Lavender Essential Oils.” Medicinal Chemistry (Shāriqah (United Arab Emirates)) 7, no. 6 (November 2011): 674–89. https://www.ncbi.nlm.nih.gov/pubmed/22313307
[73] Uyttendaele, M., K. Neyts, H. Vanderswalmen, E. Notebaert, and J. Debevere. “Control of Aeromonas on Minimally Processed Vegetables by Decontamination with Lactic Acid, Chlorinated Water, or Thyme Essential Oil Solution.” International Journal of Food Microbiology 90, no. 3 (February 1, 2004): 263–71. https://www.ncbi.nlm.nih.gov/pubmed/14751681
[74] Inouye, S., H. Yamaguchi, and T. Takizawa. “Screening of the Antibacterial Effects of a Variety of Essential Oils on Respiratory Tract Pathogens, Using a Modified Dilution Assay Method.” https://www.ncbi.nlm.nih.gov/pubmed/11810593
[75] Bukovská, Alexandra, Stefan Cikos, Stefan Juhás, Gabriela Il’ková, Pavol Rehák, and Juraj Koppel. “Effects of a Combination of Thyme and Oregano Essential Oils on TNBS-Induced Colitis in Mice.” Mediators of Inflammation 2007 (2007): 23296. doi:10.1155/2007/23296. https://www.ncbi.nlm.nih.gov/pubmed/18288268
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Essential Oils for Healing Persistent Lyme Symptoms Online Six Week Training

herbs_essential_oils
ONLINE Live Six Week Training: Essential Oils for Healing Persistent Lyme Symptoms for Medical Providers

Learn to Reduce Persistent Symptoms Faster in Your Lyme Disease Patients Through Essential Oils

– Do you have Lyme patients that continue to report recurring pain, fatigue and mental fog?

– Are you frustrated by the lack of patient improvement with
Lyme protocols?

– Learn about safe amounts of essential oils for internal use
to treat stubborn Lyme symptoms.

Sign up by April 28th and receive a BONUS cold laser and an essential oil remedy laser kit for Lyme and other infection symptoms worth $100.

Participants will get six one-hour live training sessions every Friday 3pm – 4pm EST from April 29th – June 3rd. All sessions are recorded and available for replay 24/7. Participants will also get bonus videos on using cold laser essential oils and making liposomal essential oil remedies for resolving persistent Lyme symptoms.

You can see two videos, one on specific essential oils for Lyme and co-infections and a second of an indepth case study on how oils helped heal neurological Lyme disease and co-infections here:

JASA / Acupuncture Today Free Report on Essential Oils and Herbs for Lyme Disease

Registration closes Thursday April 28th. Space is limited…
This training costs $900, which is 25% off the cost of the live event.

Questions about the training?
Please email me at TwoFrogsHealingCenter at gmail.com

– Greg

Can These Three Sweets Help You to Heal Lyme Disease?

house_of_cards
For people with Lyme disease and co-infections who crave sweets and carbohydrates
by Greg Lee

Have you ever been glued to watching your favorite TV series? I’m often left with more questions at the end of an episode of House of Cards. Has Frank gone to far? Will this finally be his downfall? What will be the backlash of losing a hostage? My brain goes round and round with what might happen next season.

How is thinking about a captivating TV series similar to food cravings in people with Lyme disease?

Just like the drama in a popular TV series, people with Lyme disease can have unstoppable cravings for sweets
Many patients diagnosed with Lyme disease report craving carbohydrates, gluten-rich foods, sugar, and sweet fruits. They go back and forth with thoughts like, “Eat the ice cream, you deserve a treat!” “Don’t eat the ice cream, it’s bad for you.” Many of these people report an increase in their symptoms after giving in to the “EAT IT!” voice. Multiple studies correlate similar types of cravings with decreased levels of serotonin[1], melatonin[2], leptin[3], or dopamine[4]. Patients diagnosed with Lyme, co-infections, or mold can have lowered levels of serotonin[5], melatonin[6], or dopamine[7]. Unfortunately, these people can have difficulty overcoming their cravings.

People with Lyme disease often need more than dietary restrictions to overcome cravings
Most Lyme diet guideline tell people to avoid dairy, gluten, and refined sugars. These foods can increase inflammation which may increase symptoms of fatigue, brain fog, and pain. However, these restrictive diets often increase the intensity of cravings in patients which often leads to an inability to stick to the “recommended” foods. If the craving for carbs and sweets is related to an underlying deficiency, then increasing the deficient compound(s) could effectively reduce or eliminate the cravings.

What else beside dietary recommendations can help people with Lyme disease to stop cravings and fight infections?

These three sweets help reduce cravings and support the immune system to fight Lyme disease
Studies on obesity often recommend healthier replacements like stevia and xylitol in place of artificial sweeteners or refined sugars which people have become addicted to[8]. Fortunately, these sweeteners can reduce cravings and can help people to fight infections. These and other sweeteners can protect vital organs from toxic compounds and enhance the neurological functioning. Processing these sweeteners into a micronized particle called a liposome, enhances their delivery inside cells[9], into the nervous system[10], and into biofilms[11].

Lyme Healing Sweetener #1: Stevia
A big challenge in experiments is how to kill persistent “antibiotic resistant” forms of the Lyme bacteria. In one experiment, whole leaf extract of stevia was effective in eliminating persistent forms of Lyme as well as biofilms that they hide under[12]. In another study, it lowers blood glucose and serum triglyceride levels[13]. Other studies indicate that stevia has anti-hypertensive, anti-inflammatory, anti-tumor, anti-diarrheal, diuretic, and immunomodulatory effects[14]. In addition to stevia, xylitol is a natural sweetener with additional healing properties for people with Lyme.

Lyme Healing Sweetener #2: Xylitol
Xylitol has shown in multiple animal and lab studies to inhibit different microbes including: H1N1[15], Streptococcus mutans and it’s biofiims[16], and Streptococcus pneumoniae[17]. It also has a bacteriostatic effect on Listeria Monocytogenes[18]. This sweetener also had a protective effect against Clostridium difficile in a mouse study[19]. Xylitol inhibits multiple oral biofilms in lab studies[20]. When combined with lactoferrin and silver, xylitol has enhanced anti-biofilm properties in wound healing studies[21]. A third sweetener, royal jelly can help with healing the damaging effects of Lyme.

Lyme Healing Sweetener #3: Royal Jelly
Royal jelly (RJ) is the food that is given to queen honey bees and larvae. Since the only way to develop queen bees is to continually feed them RJ, this sweetener enhances the genetic expression of larvae[22]. In one study, RJ had antifungal activity against Candida species[23]. In another study, RJ has been demonstrated to possess numerous functional properties such as antibacterial activity, anti-inflammatory activity, vasodilative and hypotensive activities, disinfectant action, antioxidant activity, antihypercholesterolemic activity, and antitumor activity[24].

In one study, RJ protected mice embryos from toxic oxymetholone[25]. In another mouse study, RJ enhanced bone regeneration[26]. In another rat study, RJ protected the colon against chemically induced colitis[27]. It also protected rats against chemotherapy kidney injury in another study[28].

Another study on rat pup brains showed how RJ increased gamma amino butyric acid (GABA), dopamine, and serotonin levels in response to toxic tartrazine[29]. Bees fed tyrosine, a compound in RJ, had increased levels of dopamine[30]. Rats with chemically induced brain injury, had greater memory recall and spatial learning when fed RJ[31]. In another experiment, RJ facilitated the differentiation of different neural cells and it’s compound HDEA facilitated neural growth[32]. RJ is most commonly mixed with honey. One caution, some people may have an allergic reaction to royal jelly. The sweeteners provide a sweet answer to food cravings in patients with Lyme and co-infections.

These sweeteners can help people with Lyme disease to stop food cravings by increasing deficient neurological compounds
Just like watching the “reveal all” episode that stops the obsessive thinking about the characters in a TV series, these sweeteners can be helpful at resolving food cravings by satisfying the underlying deficiencies in neurological compounds like dopamine and serotonin. These sweeteners can also help people to fight stealthy forms of infections, penetrate biofilms, and reduce the damaging effects of Lyme and co-infections. When encapsulated into a liposome, these sweeteners may have even greater penetration into the places where germs hide and provide deeper protection for the brain and other vital organs. Since some of these sweeteners have cautions on their use, work with a Lyme literate herbal practitioner to develop a proper, safe, and effective strategy for your condition.

– Greg

Next step: Come to our evening lecture Getting Rid of Lyme Disease in Frederick, Maryland on Monday April 4th at 6pm to learn more about sweeteners, herbs, and essential oils for protecting yourself from Lyme disease and co-infections.

https://goodbyelyme.com/events/get_rid_lyme

Also learn about effective remedies and treatments for relieving persistent symptoms of Lyme and co-infections including: cold laser, Frequency Specific Microcurrent, cupping, LED therapy, moxabustion, acupuncture, liposomal herbs, essential oils, bee venom, and more!

P.S. Do you have experiences where sweeteners helped you to fight and heal Lyme disease and co-infections? Tell us about it.


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