Showing posts with label Products. Show all posts
Showing posts with label Products. Show all posts

Sunday, February 23, 2020

Hibiscus Flower

The first book in my new series is now available!  If you have an Amazon Kindle Unlimited account you can read it for free here: https://www.amazon.com/dp/B0852B569X/ 
More information on the book is available on the Rain-Tree Publisher's page.

Additionally you can:

BUY eBook
Buy Paperback
Buy Wholesale



Please use this blog page to comment, ask questions, discuss the many wonderful uses of Hibiscus Flowers and share your results using it.

Enjoy!


Thursday, February 20, 2020

The Rainforest Medicinal Plant Guide Series

I am excited to present my new series of books featuring the important medicinal plants of the rainforest that I've  studied and used for more than 20 years. These new plant guides provide up-to-date factual, scientific, and vital information on how to use these powerful medicinal plants effectively to improve your health. I struggled with whether to update my big rainforest plant book, The Healing Power of Rainforest Herbs, since it really needed updating with all the new research that has been conducted on all these wonderful rainforest plants. There was just too much new information on all the plants in the book to do a second edition.  It would be huge and probably necessary to print in two volumes.

Instead, I am doing individual plant guides books on each plant. This will allow me to provide much more information on each plant, provide disease-specific dosages, and more fully explain the main uses that I recommend the plant for, and how the plant can address these uses in much greater detail. These books are between 80 to 150 pages in length.  All will be available through amazon.com as both eBooks and printed books.

Keep in mind, I don't sell herbal supplements or herb products other than books. The books in this series do not promote any specific brands or herbal supplement products however, I'll share my insider information and my research on the plants in a comprehensive consumer guide to help you choose a good product, prepare it correctly, and take it in the proper dosages. These definitive medicinal plant guides concern the plants and their researched effective actions and uses. The information in these guides is more extensive, complete, and unbiased than natural product companies who sell these plants as supplements can provide.  They will contain all the information that you need to use the plants effectively which companies who sell these plants simply cannot legally provide.

The first books in this new series include:


HIBISCUS FLOWER: Nature's Secret for a Healthy Heart

Learn how to address high blood pressure, high cholesterol and clogged arteries, and more naturally without the negative side effects of prescription drugs.
More Information
BUY eBook
Buy Paperback
Buy Wholesale



ACEROLA:  Nature's Secret to Fight Free Radicals

Discover how fighting free radicals with acerola promotes healthy aging and weight loss,  prevents many chronic diseases, and more.
Available March 2020



CAMU-CAMU: Nature's Secret for Disease Prevention

The highest source of natural vitamin C combined with the “Power of Polyphenols” in this Amazon super-fruit provides amazing health benefits
Available March 2020

CHANCA PIEDRA: Nature's Secret for Kidney Stones

Discover how to use this powerful and effective rainforest plant for kidney stones, gout, viruses, and more.
Available April 2020


GRAVIOLA: Nature's Secret for Cancer

Learn about exciting new research that reports this power plant of the Amazon may well be the most powerful natural aid in the battle against cancer. 
Available May 2020



PAU D'ARCO: Nature's Secret to Fight Infections

Learn about the infection-fighting actions of this powerful rainforest plant to kill bacteria, yeast, mold, candida, viruses, and more.
Available July 2020

CAT'S CLAW: Nature's Secret for the Immune System

Learn how to boost your immune system, reduce inflammation, and protect your brain with this effective rainforest vine.
Available June 2020




Tuesday, January 8, 2019

Autoimmune Diseases and Mycoplasmas

I wrote the below article about Mycoplasmas in 2001.  From that date and until Raintree Nutrition closed it's doors at the end of 2012, we were able to help tens of thousands of people with autoimmune diseases, maybe even more.  I created a specific formula called MYCO (which is short for mycoplasmas) that contained rainforest plants that were tested to be able to kill a mycoplasma bacteria.

Many of Raintree's formulas (mostly those named "Amazon Support") were sold only by practitioners and  half of our product sales were to practitioners who tested their patients on and sold our formulas to their patients.   The Myco formula started out as a practitioner-only formula and the results reported by these practitioners who were treating many types of autoimmune diseases with it were incredible.  Demand for the product, spread by word of mouth by these patients who were helped, made us move the product into the retail line of products because our practitioner accounts couldn't keep up with sales.  We never advertised the product, we never attempted to really market it in any way, and we couldn't really even say what to take it for based on the FDA regulations.  These sales were achieved by one person telling another, by a practitioners sharing results with other colleagues and because we had a product and a protocol that really worked.

Our practitioner protocols were to combine the Myco formula with a good antifungal formula (we recommended our Amazon A-F formula but others were used as well) and a third formula to increase immune function (again, we recommended our Amazon Immune Support Formula) based on the information that is shared in the below article.  The Myco formula was one of Raintree's most popular products and was 4th in highest number of sales of all Raintree formulas.

Toward the end of the below article, you'll find links to all three products we used in our protocols  that will go to the Raintree website.  From those product pages you'll find product search links to find these formulas... they are still available but under other companies' labels.



 Mycoplasmas - Stealth Pathogens

Mycoplasmas are a specific and unique species of bacteria - the smallest free-living organism known on the planet. The primary differences between mycoplasmas and other bacteria is that bacteria have a solid cell-wall structure and they can grow in the simplest culture media. Mycoplasmas however, do not have a cell wall, and like a tiny jellyfish with a pliable membrane, can take on many different shapes which make them difficult to identify, even under a high powered electron microscope. Mycoplasmas can also be very hard to culture in the laboratory and are often missed as pathogenic causes of diseases for this reason.

The accepted name was chosen because Mycoplasmas were observed to have a fungi-like structure (Mycology is the study of fungi - hence "Myco") and it also had a flowing plasma-like structure without a cell wall - hence "plasma". The first strains were isolated from cattle with arthritis and pleuro-pneumonia in 1898 at the Pasteur Institute. The first human strain was isolated in 1932 from an abscessed wound. The first connection between mycoplasmas and rheumatoid diseases was made in 1939 by Drs. Swift and Brown. Unfortunately, mycoplasmas didn't become part of the medical school curriculum until the late 1950's when one specific strain was identified and proven to be the cause of atypical pneumonia, and named Mycoplasma pneumonia. 

The association between immunodeficiency and autoimmune disorders with mycoplasmas was first reported in the mid 1970s in patients with primary hypogammaglobulinemia (an autoimmune disease) and infection with four species of mycoplasma that had localized in joint tissue. Since that time, scientific testing methodologies have made critical technological progress and along with it, more mycoplasma species have been identified and recorded in animals, humans and even plants.

While Mycoplasma pneumonia is certainly not the only species causing disease in humans, it makes for a good example of how this stealth pathogen can move out of it's typical environment and into other parts of the body and begin causing other diseases. While residing in the respiratory tract and lungs, Mycoplasma pneumonia remains an important cause of pneumonia and other airway disorders, such as tracheobronchitis, pharyngitis and asthma.

When this stealth pathogen hitches a ride to other parts of the body, it is associated with non-pulmonary manifestations, such as blood, skin, joint, central nervous system, liver, pancreas, and cardiovascular syndromes and disorders. Even as far back as 1983, doctors at Yale noted:
"Over the past 20 years the annual number of reports on extrapulmonary symptoms during Mycoplasma (M.) pneumoniae disease has increased. Clinical and epidemiological data indicate that symptoms from the skin and mucous membranes, from the central nervous system, from the heart, and perhaps from other organs as well are not quite uncommon manifestations of M. pneumoniae disease."

This single stealth pathogen has been discovered in the urogenital tract of patients suffering from inflammatory pelvic disease, urethritis, and other urinary tract diseases. It has been discovered in the heart tissues and fluid of patients suffering from cardititis, pericarditis, tachycardia, hemolytic anemia, and other coronary heart diseases. It has been found in the cerebrospinal fluid of patients with meningitis and encephalitis, seizures, ALS, Alzheimer's and other central nervous system infections, diseases and disorders.It has even been found regularly in the bone marrow of children with leukemia. It is amazing that one single tiny bacteria can be the cause of so many seemingly unrelated diseases in humans. But as with all mycoplasma species, the disease is directly related to where the mycoplasma resides in the body and which cells in the body it attaches to or invades.

Today, over 100 documented species of mycoplasmas have been recorded to cause various diseases in humans, animals, and plants. Mycoplasma pneumonia as well as at least 7 other mycoplasma species have now been linked as a direct cause or significant co-factor to many chronic diseases including, rheumatoid arthritis, Alzheimer's, multiple sclerosis, fibromyalgia, chronic fatigue, diabetes, Crohn's Disease, ALS, nongonoccal urethritis, asthma,lupus, infertility, AIDS and certain cancers and leukemia, just to name a few. In 1997, the National Center for Infectious Diseases, Centers for Disease Control and Prevention's journal, Emerging Infectious Diseases, published the article, Mycoplasmas: Sophisticated, Reemerging, and Burdened by Their Notoriety, by Drs. Baseman and Tully who stated:

"Nonetheless, mycoplasmas by themselves can cause acute and chronic diseases at multiple sites with wide-ranging complications and have been implicated as cofactors in disease. Recently, mycoplasmas have been linked as a cofactor to AIDS pathogenesis and to malignant transformation, chromosomal aberrations, the Gulf War Syndrome,
and other unexplained and complex illnesses, including chronic fatigue syndrome, Crohn's disease, and various arthritides."


Mycoplasmas, unlike viruses, can grow in tissue fluids (blood, joint, heart, chest and spinal fluids) and can grow inside any living tissue cell without killing the cells, as most normal bacteria and viruses will do. Mycoplasmas are frequently found in the oral and genito-urinary tracts of normal healthy people and are found to infect females four times more often than males, which just happens to be the same incidence rate in rheumatoid arthritis, fibromyalgia, Chronic Fatigue and other related disorders. 

Mycoplasmas are parasitic in nature and can attach to specific cells without killing the cells and thus their infection process and progress can go undetected. In some people the attachment of mycoplasmas to the host cell acts like a living thorn; a persistent foreign substance, causing the host's immune defense mechanism to wage war. This allergic type of inflammation often results in heated, swollen, and painful inflamed tissues, like those found in rheumatoid diseases, fibromyalgia and many other autoimmune disorders like lupus and MS, Crohn's and others. In such cases the immune system begins attacking itself and/or seemingly healthy cells. Some species of mycoplasmas also have the unique ability to  completely evade the immune system. Once they attach to a host cell in the body, their unique plasma and protein coating can then mimic the cell wall of the host cell and the immune system cannot differentiate the mycoplasma from the body's own host cell.


Mycoplasmas are parasitic in nature because they rely on the nutrients found in host cells including cholesterol, amino acids, fatty acids and even DNA. They especially thrive in cholesterol rich and arginine-rich environments. Mycoplasmas can generally be found in the mucous membrane in the respiratory tract. They need cholesterol for membrane function and growth, and there is an abundance of cholesterol in the bronchial tubes of the respiratory tract. Once attached to a host cell, they then begin competing for nutrients inside the host cells. As nutrients are depleted, then these host cells can begin to malfunction, or even change normal functioning of the cell, causing a chain reaction with other cells (especially within the immune and endocrine systems). Mycoplasmas can even cause RNA and DNA mutation of the host cells and have been linked to certain cancers for this reason.

Mycoplasmas can also invade and live inside host cells which evade the immune system, especially white blood cells. Once inside a white blood cell, mycoplasmas can travel throughout the body and even cross the blood/brain barrier, and into the central nervous system and spinal fluid.

FOOTNOTES
  1. Baseman, Joel, et.al., Mycoplasmas: Sophisticated, Reemerging, and Burdened by Their Notoriety, CDC, Journal of Infectious Diseases, Vol 3, No.1, Feb 1997
  2. S-C. Mycoplasmas and AIDS. In: Maniloff J, McElhaney RN, Finch LR, Baseman JB, editors. Mycoplasmas: molecular biology and pathogenesis. Washington (DC): American Society for Microbiology, 1992:525-45.
  3. Nicolson G, Nicolson NL. Diagnosis and treatment of mycoplasmal infections in Gulf War illness-CFIDS patients. Intl J Occup Med Immunol Toxicol 1996;5:69-78.
  4. Wear DJ, et.al. Mycoplasmas and oncogenesis:persistent infection and multistage malignant transformation. Proc Natl Acad Sci USA 1995;92:10197-201.
  5. Ekbom A, Daszak P, Kraaz W, Wakefield AJ. Crohn's disease after in-utero measles virus exposure. Lancet 1996;348:516-7.
  6. Taylor-Robinson D. Mycoplasmas in rheumatoid arthritis and other human arthritides. J Clin Pathol 1996;49:781-2.
  7. Dr.Harold Clark, The Intercessor, June 1993, The Road Back Foundation, Delaware OH.
  8. Goulet M, et.al., Isolation of Mycoplasma pneumoniae from the human urogenital tract. J Clin Microbiol 1995;33:2823-5
  9. Daxbock F, et.al., Severe hemolytic anemia and excessive leukocytosis masking mycoplasma pneumonia. Ann Hematol. 2001 Mar;80(3):180-2.
  10. Higuchi ML, et.al., Detection of Mycoplasma pneumoniae and Chlamydia pneumoniae in ruptured atherosclerotic plaques. Braz J Med Biol Res. 2000 Sep;33(9):1023-6.
  11. Socan M, Neurological symptoms in patients whose cerebrospinal fluid is culture- and/or polymerase chain reaction-positive for Mycoplasma pneumoniae. Clin Infect Dis. 2001 Jan 15;32(2):E31-5.
  12. Bencina D, et.al., Intrathecal synthesis of specific antibodies in patients with invasion of the central nervous system by Mycoplasma pneumoniae. Eur J Clin Microbiol Infect Dis. 2000 Jul;19(7):521-30
  13. Smith R, et.al., Neurologic manifestations of Mycoplasma pneumoniae infections: diverse spectrum of diseases. A report of six cases and review of the literature. Clin Pediatr (Phila). 2000 Apr;39(4):195-201.
  14. Umemoto M, Advanced atrioventricular block associated with atrial tachycardia caused by Mycoplasma pneumoniae infection.  Acta Paediatr Jpn. 1995 Aug; 37(4): 518-20.
  15. Lind K. Manifestations and complications of Mycoplasma pneumoniae disease: a review.Yale J Biol Med. 1983 Sep-Dec; 56(5-6): 461-8.
  16. Alexander FE. Is Mycoplasma Pneumonia associated with childhood acute lymphoblastic leukemia? Cancer Causes Control. 1997 Sep;8(5):803-11.
  17. Hall JE, Mycoplasma pneumonia in acute childhood leukemia. Pediatr Pulmonol. 1985 Nov-Dec;1(6):333-6.
  18. Murphy WH, Gullis C, Dabich L, Heyn R, Zarafonetis CJD. Isolation of Mycoplasma from leukemic and nonleukemia patients. J Nat Cancer Inst 1970;45:243-51.


How Mycoplasmas Interact in the Body


  • Mycoplasmas are able to hide inside the cells of the host (patient) or to attach to the outside of host cells.
  • Whether they live inside or outside the host cell, they depend on host cells for nutrients such as cholesterol, amino acids, etc. They compete with the host cells for these nutrients which can interfere with host cell  function without killing the host cell.
  • A mycoplasma has very little DNA of its own, but is capable of using DNA from a host cell. When a mycoplasma takes over the DNA of the host cell, anything can happen - including causing that cell to malfunction in many different ways and/or die, or can cause DNA mutation of the host cell.
  • Mycoplasmas attach to host cells with a tiny arm coated in protein which attaches to the protein coating of host cells. For this reason, antibiotics like tetracycline, which are classified as "protein synthesis inhibitors" are often used against mycoplasma infections. While these antibiotics may block this protein attachment and very slowly starve it from the nutrients it needs from host cells to thrive and replicate, it still takes a healthy immune system to actually kill the mycoplasma for good.
  • Mycoplasmas are highly adaptable to changing environments and can move anywhere in the body, attaching to or invading virtually any type of cell in the body.
  • The mycoplasma adhesion proteins are very similar to human proteins. Once adhered to the host cell, the mycoplasma can completely mimic or copy the protein cell of the host cell. This can cause the immune system to begin attacking the body's own cells; an event that happens in all autoimmune diseases.
  • Certain Mycoplasma species can either activate or suppress host immune systems, and they may use these activities to evade host immune responses. Mycoplasmas can turn on the chain reaction called an immune system response. This includes the stimulation of pro-inflammatory cytokines (chemical messengers of the immune system) which is generally found in most autoimmune and inflammatory diseases and disorders.
  • Mycoplasma can also attach to or invade immune system cells, like the very phagocytes (natural killer cells) that are supposed to kill them. Inside these phagocytes, they can be carried to new locations of inflammation or disease - hidden away like a spy who has infiltrated the defending army.
  • When a mycoplasma attaches to a host cell, it generates and releases hydrogen peroxide and superoxide radicals which cause oxidative stress and damage to the surrounding tissues.


The Main Human Mycoplasma Pathogens



PathogenImplicated Disease
Mycoplasma genitalium Arthritis, chronic nongonococcal urethritis, chronic pelvic inflammatory disease, other urogenital infections and diseases, infertility, AIDS/HIV
Mycoplasma fermentans Arthritis, Gulf War Syndrome, Fibromyalgia, Chronic Fatigue Syndrome, Lupus, AIDS/HIV, autoimmune diseases, ALS, psoriasis and Scleroderma, Crohn's and IBS, cancer, endocrine disorders, Multiple Sclerosis, diabetes
Mycoplasma salivarium Arthritis, TMJ disorders, Eye and ear disorders and infections, gingivitis, periodontal diseases including even cavities.
Mycoplasma hominis and Ureaplasma urealyticum Pelvic inflammatory disease, infertility, non-gonococcal urethritis, vaginitis, cervicitis, amnionitis, pyelonephritis, post-partum septicemia, neonatal pneumonia, neonatal conjunctivitis, Reiter's syndrome, peritonitis, wound infection(C-section), low birth weight infants, and premature rupture of membranes.
Mycoplasma pneumoniaPneumonia, asthma, upper and lower respiratory diseases, heart diseases, leukemia, Steven-Johnson syndrome, polyarthritis or septic arthritis, CNS disorders and diseases, urinary tract infections, Crohn's and Irritable Bowel Syndrome, Guillain-Barr syndrome, polyradiculitis, encephalitis, and septic meningitis, autoimmune diseases.
Mycoplasma pirumUrogenital infections and diseases, AIDS/HIV
Mycoplasma incognitus and
Mycoplasma penetrans
AIDS/HIV, urogenital infections and diseases, Autoimmune disorders and diseases
Mycoplasma faucium, M. lipophilum and M. buccale
Diseases of the gingival crevices and respiratory tract



Treatment Options For Mycoplasmal Infections

The negative impact of a mycoplasmal infection on the human immune system is undisputed. Due to it's ability to either activate or suppress the immune system, it is now being considered one of the culprits of many autoimmune diseases. Yet, scientists still argue over the "chicken or egg first" type of sequence of events. Do the mycoplasmas begin growing and replicating first and then weaken or deregulate the immune system? Or does a weakened immune system (caused by stress, poor diet or other illness) allow the mycoplasmas to take hold and begin their opportunistic growth resulting in chronic disease and to weaken and deregulate the immune system even further? The answer is probably both, and it becomes one of the most critical treatment aspects of mycoplasmal infections. In immunodeficient patients it can be very difficult to treat these mycoplasma infections with appropriate broad spectrum antibiotics which are immunosuppressive themselves. Although the tetracycline and erythromycin types of antibiotics are effective for some mycoplasmal infections, M. fermentans, M. hominis and M. pirum strains are usually resistant to erythromycin, and tetracycline-resistant strains of M. hominis and U. urealyticum have been reported. However, these antibiotics have a very limited ability to directly kill these mycoplasmas, and their efficacy eventually depends on an intact host immune system to eliminate the mycoplasmas. These types of protein inhibiting antibiotics will stop the protein adhesion of the mycoplasma to host cells but won't directly kill the mycoplasma itself. With an already weaken immune system, many patients lack the ability to mount a strong antibody response against these deadly stealth pathogens to kill them effectively.

Regardless, many physicians and rheumatologists are treating their arthritis, CFISD, fibromyalgia and other mycoplasma infections with long term antibiotic therapy. One of the more popular conventional protocols involves rotating multiple 6 week cycles of Minocycline or Doxycycline (200-300 mg/day), Ciprofloxacin (1,500 mg/day), Azithromycin (250-500 mg/day, and/or Clarithromycin (750-1,000 mg/day) among others.(1) Sometimes the side effects of these strong antibiotics can be as bad as the symptoms of the diseases they are treating since a minimum of 6 months and up to two years of antibiotic therapy may be required. Many doctors now believe that antibiotics should not be used solely or exclusively to treat mycoplasmal infections, without addressing rebuilding the immune system which is imperative for a complete recovery and eradication of infection. Others are using more natural antibiotics found in plants which can be as effective or more effective with fewer side effects or negative impact on the body. These include olive leaf extract products, urva ursi, and Neem leaf or seed extracts. Also see Raintree's Myco herbal formula.

One of the main side effects of antibiotics, whether it is a natural plant antibiotic or a chemical antibiotic, is the loss of friendly bacteria that is needed in the gastrointestinal system for proper digestion and elimination. No antibiotic can differentiate a friendly bacteria from a harmful one. Therefore, any time an antibiotic must be taken, especially long term, taking a probiotic formula to replace friendly bacteria is indicated and helpful in avoiding side effects like candida and fungi overgrowth which can cause digestive and elimination difficulties and other side effects. Several probiotic products are widely available over-the-counter which combine these friendly bacteria - live cultures of Lactobacillus acidophilous, Lactobacillus bifidus and other bacteria with FOS (fructoologosaccharides) to promote growth in the gastrointestinal system. It's important to take this type of supplement when taking antibiotics of any kind and best to be taken either 3-4 hours prior to, or after taking the antibiotic dosage. Full live-cultured yogurt contains acidophilous and is a good food source for these friendly bacteria. Also see Raintree's Amazon A-F.

Another common side effect when taking antibiotics is called a Herxheimer Reaction. This occurs from the organism die-off and generally is the first indication that the antibiotic therapy is working. Symptoms that are associated with a Herxheimer include: chills, fever, night sweats, muscle aches, joint pains, lymphatic pain, mental fog, and extreme fatigue. Depending on the severity of the infection and resulting die-off, these symptoms can last 1-2 weeks and sometimes longer and can vary in intensity. Drinking at least two quarts of filtered or distilled water every day to flush the organisms from the body is helpful in reducing the length and severity of a Herxheimer reaction. Another natural remedy to reduce Herxheimer reactions and thought to be helpful in helping the lymph glands to filter and remove dying organisms is a Whole Lemon-Olive Oil Drink. To prepare this natural remedy, place one whole unpeeled lemon (washed) in a blender with 1 cup of juice or water and 1 tablespoon of extra virgin olive oil. Blend in blender until smooth, then pour through a wire strainer. Discard pulp and drink liquid.

Once the mycoplasmas are being controlled by some form of effective natural or chemical antibiotic, re-nourishing and replacing the nutrients drained from the infected host cells can help speed recovery and reduce symptoms. A general multi-vitamin supplement plus extra C, D, E, CoQ-10, beta-carotene, quercetin, folic acid, bioflavoids and biotin are necessary and helpful when recovering from a mycoplasmal infection. Supplementing back the depleted amino acids has been reported to be helpful in some recovering from these infections. These include L-cysteine, L-tyrosine, L-glutamine, L-carnitine, and malic acid. Remember, however, that mycoplasmas thrive on arginine! Avoid L-arginine supplements and multi-amino acid formulas containing L-arginine, as well as foods rich in arginine to avoid feeding the mycoplasmas. The richest food sources of arginine (to avoid) are nuts and seeds, including the oils derived from seeds and nuts which should be eliminated or drastically reduced in the diet. Vitamins A, C and E, and other antioxidants found in natural plants, have also been reported to help speed recovery and to minimize the oxidative stress caused by mycoplasmas. One of the most popular antioxidants sold today are various extracts of grape seeds. Remember however, most seeds are rich in arginine, including grape seeds, and should generally be avoided.
Other helpful supplements to replenish drained nutrients from parasitic mycoplasmas are generally indicated based upon which specific cells the mycoplasma might be feeding on and which nutrients are being depleted. Specifically with fibromyalgia patients, leading research indicates that many of the hormones and enzymes produced in the neuroendocrine system and Hypothalamus-Pituitary-Adrenal Axis are depleted or malfunctioning which have the ability to cause many of the symptoms found in these patients.

Finally and most importantly is nutritionally supporting the immune system. There are various natural products sold today which can stimulate and support immune function. There are many natural products available in the market place today which nutritionally support immune function. One of the best from the rainforest is cat's claw. Also see Raintree's Immune Support. Another important consideration is the elimination of drugs that might suppress immunity. Dr. Garth Nicolson, one of the world renown experts on mycoplasmas states: "We have recommended that patients be taken off antidepressants and other potentially immune-suppressing drugs. Some of these drugs are used to help alleviate certain signs and symptoms, but in our opinion they can interfere with therapy, and they should be gradually reduced or eliminated." This of course would be indicated for many fibromyalgia and Chronic Fatigue patients who are routinely prescribed antidepressants.



    TESTING FOR MYCOPLASMAS

    Testing for mycoplasmas is much harder and more complicated than testing for all other bacteria, which is one of the main reasons conventional medical practitioners mis-diagnose or miss these types infections. The most reliable testing method offered today is with a lab test called a PCR test (Polymerase Chain Reaction). Even performing a PCR lab test on a standard whole blood sample may not find the mycoplasma, simply because the mycoplasma may be residing in other fluids and tissues in the body and not the blood (i.e.; the fluid in the joints, in the spinal fluid, or in any tissue cell like heart, liver, pancreas, endocrine organs, etc.). A PCR test is generally performed by specific mycoplasma species. These laboratory tests can be expensive, but are insurance reimburseable if ordered by your primary care physician. Specific mycoplasma PCR tests are available through these companies, both of which have more information on mycoplasmas in general and testing at their websites:

    The Institute for Molecular Medicine
    15162 Triton Lane
    Huntington Beach, CA 92649
    (714) 596-78210
    Website
    Immunosciences Lab, Inc.
    8730 Wilshire Blvd, Suite 305
    Beverly Hill, CA 90211
    310-657-1077
    Website

Sunday, January 6, 2019

Emerging Infectious Diseases - Plants versus Chemicals


It has long been known by doctors and scientists that bacteria, viruses, parasites, fungi and other disease-causing microorganisms can readily develop defense mechanisms against our prescription drugs and become drug resistant. Many have already, as is readily apparent in the news today. The common staph bacteria (Staphylococcus) has gone thru so many mutations over the last thirty years that many different strains have evolved which are now completely resistant to the eight major antibiotic drugs that were once effective against it.  There are also at least five new strains of malaria that have evolved which are now completely resistant to our gold-standard antimalarial drugs. The hepatitis virus has continued to mutate into new types and subtypes and our antiviral drugs are largely ineffective. Could plants hold the answer? Very possibly! 

The rainforests of the world are, and will continue to be, of the most utmost importance and one of the main areas where the search for new antimicrobial drugs will likely take place.  Rainforests hold the highest biodiversity and sheer number of novel chemicals on the planet.  Acre for acre, there are more species of plants, animals, insects, and even microbial species such as bacteria, fungi and viruses than anywhere on earth. It is estimated that one-half of all species on earth are found in tropical rainforests.

Survival instincts are bred in all living things. It is literally part of the cellular makeup of all species on earth. In highly mobile species like humans, animals and insects, the main survival mechanism is  “flee, fight, or hide.”  Even bacteria and virus species are considered mobile and have learned to flee or hide from immune cells and chemical agents attacking them, as well as to fight them by mutating.  With stationary plants rooted to the ground and incapable of physically fleeing from danger, this survival instinct is controlled by wonderfully complex and rich chemical defense mechanisms that have evolved over eons. Living plants have either created a chemical defense mechanism against what might harm them, or they have succumbed and become extinct.

In the species-rich rainforest there are many species of fungi, mold, bacteria, viruses, parasites, and even insects that attack and kill plants.  It is of little wonder that rainforest plants contain so many potent and active plant chemicals—they are in a constant battle for survival in an environment literally teeming with life that is constantly evolving. From the soil-borne root-rot (a virus) that attacks tender herbaceous plants, to the fungi and mold smothering the life out of huge canopy trees or even the incredible amount of insects devouring any defenseless leaf in the forest. . .  rainforest plants have learned to adapt, create chemical defenses against attack and to survive. Within this rich arsenal of defensive chemicals, many rainforest plants have been tested with antibacterial, antiviral, anti-fungal, anti-parasitic, anti-mold and insecticidal chemicals with potent actions. This IS the mechanism they’ve use to survive, grow and flourish as well as to fight the many disease-causing organisms that attack them.   It is likely that within these diverse chemicals created to protect the plants from disease, at least a handful of highly active chemicals can and will be harvested and put to the use of protecting humans and animals from the same types of disease-causing organisms.

A very interesting emerging concept is that many disease-causing microorganisms can pretty easily adapt and mutate to become resistant to a single chemical, but. . . it would be much harder and take much more time for it to create a defense mechanism against numerous different chemicals simultaneously.  Unlike a single chemical drug, a single medicinal plant can contain up to 400 different chemicals or more— many of which can have active biological properties. Could this hold the answer?  Very possibly!.  For example: a rainforest Indian shaman’s “dysentery remedy” was evaluated a few years back by scientists. It was a crude plant extract that contained seven plants.  Now, one must remember; a dysentery diagnosis in the Amazon could be attributed to any number of different bacteria, amebas and even parasites in contaminated and communal food and water supplies found and shared in the close communal living environments of indigenous groups. The Indian shaman doesn’t have the ability to send blood or stool samples to a laboratory to find out which specific organism is causing the dysentery in his village, but he must still select the appropriate plants to treat his patients. Maybe this is why a shaman usually selects a handful of plants (about 4 to 7) to brew into a plant-based remedy, instead of just one.  When the seven different plants in the dysentery remedy were analyzed, at least twelve different known antibacterial chemicals, five anti-amebic chemicals, and seven anti-parasitic chemicals were found between all the plants in the shaman’s formula. Of the twelve different antibacterial chemicals in the extract, there were at least five different biological pathways of action which the plant chemicals possessed to kill bacteria.  Based on just the chemical content of the plant extract and the number of different dysentery-causing microbes that were susceptible to these chemicals. . . the shaman didn’t really need to know which microorganism was the culprit in what main-stream medicine would call his “shot-gun” approach. But... his shotgun was loaded with a thousand or more individual plant chemicals that had at least 31 active chemicals which hit the top 10 or so main microbes that might cause dysentery—and it was effective!  Imagine a conventional practitioner sending his patient home with 31 prescriptions. . . not likely!

But let’s go back to that interesting concept. . . If this particular dysentery-microbe was a easily-mutating bacteria like Staphylococcus; how likely would it be that this one organism could survive long enough to create a defense against 12 different antibacterial chemicals coming at it and in at least 5 different ways simultaneously? Not very likely.  That’s why, sometimes, plants really can be better than drugs.  These drug-resistant strains of bacteria are certainly more prevalent in first world nations which regularly employ single-chemical antibiotics than in poor tropical countries where mainly plant-based remedies are used. Maybe it will take a broadly-scattering “shotgun” to fight these tricky and quickly mutating organisms, instead of single chemical bullet.

As more of our gold-standard single-bullet drugs become less effective to newly developing strains of drug-resistant bacteria, viruses, fungi, and parasites; we will probably see more interest and research on medicinal plants, herbal based drugs and traditional remedies. Much of this research is taking place in the rainforests of the world.  The following rainforest plants (and/or their chemical constituents) have been identified through laboratory research to possess antimicrobial actions. For more information about these rainforest plants and the research conducted on them see the online Tropical Plant Database  or they can be found in my book, The Healing Power of Rainforest Herbs.

Antibacterial:
The rainforest plants documented with antibacterial actions are: abuta, ajos sacha, amor seco, anamu, andiroba, avenca, bellaco caspi, bitter melon, Brazilian peppertree, cat’s claw, clavillia, copaiba, cumaseba, embauba, erva tostão, fedegoso, gervâo, guacatonga, guaco, huacapu, macela, matico, mullaca, mulungu, mutamba, pau d’arco, picão preto, sangre de grado, sarsaparilla,  simarouba, tamamuri, ubos, and vassourinha.

Ten  of the most potent of these rainforest plants were formulated into one product that was sold in capsules and called Amazon C-F. It was also available in non-alcoholic liquid extract formulated for children called Amazon C-F Extract.  This glycerine liquid extract was also used topically on the skin for various skin infections.  Between the ten plants ingredients (cat's claw, amor seco, fedegoso, picão preto, mullaca, clavillia, simarouba, Brazilian peppertree, gervâo, and bitter melon) in these products there are at least 14 known chemicals that have been documented with antibacterial actions. There were also 8 different antiviral plant chemicals between all the plants that were active against common upper respiratory viruses.  C-F stood for Cold-Flu and it has been used for colds and flu effectively for over 15 years.  I've also personally used it for many other types of bacterial infections, here, and in my rainforest travels with remarkable results.

Antiviral:
The rainforest plants documented with antiviral actions include abuta, ajos sacha, amargo, anamu, bitter melon, Brazilian peppertree, carqueja, cat’s claw, chanca piedra, clavillia, erva tostão, huacapu, iporuru, macela, matico, mullaca, mutamba, pau d’arco, picão preto, sangre de grado, simarouba, ubos, and vassourinha.

Nine of these dynamic antiviral rainforest plants were formulated into a product called Amazon A-V  that was once sold by Raintree. Between these plants (which included a blend of bitter melon, clavillia, mullaca, jergon sacha, carqueja, amargo, chanca piedra, mutamba, and anamu) there are at least 11 documented plant chemicals with antiviral actions. The formula was also available in a topical formula for the skin that was called Amazon A-V Topical.

Anticandidal & Antifungal:
The rainforest plants that have been documented as active against fungi, yeast, candida and mold are anamu, avenca, bellaco caspi, Brazilian peppertree, clavillia, copaiba, cumaseba, guaco,  jatoba, matico, mulateiro, pau d’arco, picão preto, piri-piri, sangre de grado, tamamuri, ubos, and vassourinha.  All of these plants can be found in the Tropical Plant Database.

I formulated two products using twelve of these potent rainforest plants called Amazon A-F Capsules and Amazon A-F Topical (used topically on the skin and nails).  They contained jatoba, Brazilian peppertree, anamu, bellaco capsi, matico, piri-piri, pau d'arco, ubos, fedegoso, tamamuri, guaco, and graviola. The liquid topical formula also contained sangre de grado and copaiba oil, both documented with potent antifungal properties.  Between these plants, there are at least 19 documented antifungal and/or anticandidal plant chemicals.

Antiparasitic & Antiprotozoal:
The rainforest plants documented with actions against parasites and protozoa include amargo, anamu, andiroba, bitter melon, boldo, carqueja, epazote, erva tostão, fedegoso, graviola, guaco, huacapu, piri-piri, quinine, simarouba, tamamuri, and ubos.  More information on each plant can be found in my book or in the Tropical Plant Database.

I formulated a blend of ten of these rainforest plants (which include amargo, simarouba, boldo, fedegoso, carqueja, quinine, erva tostão, epazote, anamu, and graviola) that was sold by Raintree and called Amazon A-P capsules. These plant ingredients deliver 14 different plant chemical which are documented to kill various parasites, protozoa, and intestinal worms.

While Raintree Nutrition is no more, these formulas still live on. Why?  Because they work!   By following the above links on the product names, you can see instructions on how to make these formulas yourself.  Most all of these formulas  are now manufactured under different herbal manufacturers’ labels in the United States, Western Europe, Eastern Europe, Ecuador, and Australia/New Zealand. You can find product search links to help you find them on the pages the formula name links to above.


I hope to find some time in the next month to create a new section of this blog called "Practitioner Insights" and share more specific details how these plants and formulas have helped so many people here in the U.S. and in my travels in the Amazon jungles. I have quite a few stories to tell!  I never trekked through the rainforest without one (or more) of each of these products/formulas in my backpack.

Abuta - Cissampelos pariera


Well, there was a lot of reading to be done to update the plant information on abuta.  There has been a significant amount of research published on abuta and/or its main active chemicals in the last ten years!  So far, research has confirmed that abuta has pain-relieving, fever-reducing, anti-inflammatory, antiviral, antibacterial, anti-allergic, bronchodilator, immunomodulatory, memory-enhancing, antidepressant, neuroprotective, anti-obesity, antimalarial, antiparasitic, anti-ulcer, anticancer, antioxidant, heart-protective, muscle-relaxant, liver protective, antidiabetic, cellular protective, antifertility, and antivenom activities.  Whew!  These documented actions do go a long way in explaining most of abuta’s traditional uses.  You can read the new information on abuta in the Tropical Plant Database and the new sitemap which will direct you to all files on abuta on the Raintree Website is accessible here.

What struck me most was all of the research done by several different unrelated research groups on abuta’s newly documented cellular protective actions (never recorded in traditional uses).  These scientists tried to damage lots of different cells in the bodies of animals with lots of different chemicals and toxins known to do damage to these cells.  Heart cells,  kidney and liver cells, gastric and stomach cells, brain cells… lots of cells!  And abuta protected them all from being damaged.  Wow, huh?  They even injected a specific type of snake venom which causes immediate cellular hemorrhaging into animals along with just a alcohol/water extract of abuta and there was no hemorrhaging at all!  None. Wow, again, huh?  I was impressed.  Of particular note, the manner and mechanism that abuta uses to protect brain cells has justified that it might be highly beneficial in the treatment of Alzheimer’s Disease.  I’m sure we’ll see more research in the future on that particular use of abuta.

Even more impressive was this specific cellular protective effect of abuta as it pertains to cancer, especially if chemotherapy is being used.  Tumors and cancers cause a big change in red and white blood cells and negatively affect other blood parameters.  Cancer’s effect also causes significant changes in the liver and liver cell counts.  When chemotherapy is used in the treatment of cancer, the toxicity of the chemo often causes toxicity to healthy cells, most especially in the blood and the liver.   One research group inoculated mice with lymphoma pre-cancerous cells and lymphoma tumors resulted.  In the animal group that got no treatment, the negative effects on blood and liver cells were evident and recorded.  In the animal group that got a chemo drug (5FU), these negative effects again, were evident and even greater.  Several groups of animals were given varying dosages of a methanol/water extract of abuta (ranging from 100-400 mg per kg of body weight of the animal) and there was absolutely no damage or changes in blood and liver cell counts and levels.  Not even at the lowest dosages used. Abuta protected these liver and blood cells from the cancer!  And, by the way, at the highest dosage of 400 mg/kg, abuta inhibited the tumor’s growth by 78%. Wow, again!

I wonder if abuta was administered to these animals along with the chemo drug, could it still protect the cells from damage?  I bet it could, and I bet we’ll be seeing new studies in the future reporting this.  It’s not too far-fetched – another rainforest plant, copaiba, has been studied recently and reported to reduce side effects of chemo drugs through a cellular protective effect, and it helped to make the chemo drugs work better against cancer.  You can read more about abuta and cancer in the new text in the Tropical Plant Database and in my book. You can also read the full research paper on abuta and lymphoma I am referring to here (warning: it might be too technical for the average reader).

The other BIG news on abuta is that it may well be a new cure for Dengue Fever.  Dengue is a viral infection carried and spread by a mosquito (much like malaria) and it’s all over the world in the tropics. Almost 400,000 people in the world get infected with dengue fever annually. Typically, where ever dengue can be found in the world, abuta can be found growing naturally (How cool is that?), including in India.  Starting in 2012, several studies were published by scientists in India that abuta can kill the dengue virus, prevent dengue infections and it lowers the high fever associated with the virus.  This group of Indian researchers have formed a partnership with a pharmaceutical company to produce a new abuta drug to treat dengue.  I don’t know if this new drug will ever reach the Amazon, but they just used a simple water/alcohol extract of abuta in their studies and these can certainly be prepared by local inhabitants in the rainforest to treat dengue fever themselves with it.  Abuta is found all over the Amazon rainforest.

With such a remarkable effect on this wide-spread virus, one has to wonder if abuta is capable of treating other disease-causing viruses.  I hope more research on abuta’s antiviral actions will be conducted and reported on in the future. I’ll be keeping an eye out for it!

In the meantime, it is still a wonderful remedy for menstrual pain, cramping and excessive bleeding and is being used to relieve the symptoms of fibroid tumors and endometriosis.  I created a Raintree formula for this purpose called Amazon Menstrual Support.  It’s also helpful for PMS (abuta is a documented diuretic and reduces water retention, and it has shown anti-anxiety and antidepressant effects to help with that PMS-related moodiness some women experience).  I also used abuta in a formula called Amazon Menopause Support and another called Amazon F-Tonic (a balancing female tonic formula) because of its studied actions in balancing female hormones.  Abuta has shown in animal studies to lower blood pressure and to have a protective and tonic effect on the heart.  I used it in the Amazon Heart Support formula I created for that purpose.  Abuta also has a long history of traditional use for kidney problems, including kidney stones and it has clinically demonstrated pain-relieving, smooth muscle relaxant (like the smooth muscles found in the kidney and urinary tract), and antispasmodic actions. I used abuta in the Amazon Kidney Support for those documented actions.  The Amazon Kidney Support formula was widely used and worked quite well for kidney stones; while a different formula called Amazon Urinary Support (which didn't contain abuta) which was used for kidney and urinary tract infections.

Abuta is a really good example of why herbal medicine drives conventional doctors crazy.   Conventionally trained MDs are used to prescribing one drug for one thing.  They just can’t wrap their head around the concept that one plant can be used for so many completely different things.  What they fail to understand is that drugs are just a single chemical, that mostly works in a single way (mechanism of action), and medicinal plants are the exact opposite of that!  A highly active medicinal plant like abuta can have well over 100 plant chemicals in it.  Abuta has 38 verified alkaloid chemicals alone! (Alkaloids are commonly found in plants and usually have demonstrable biological activities.) IF they can understand that concept, then the next question/worry is always… “Well, how do I really know how it will work if I don’t know the affects of all of these active chemicals by themselves, much less in combination with one another?”  When I tell them that he/she can’t quantify that, and that herbal medicine is based on the empirical knowledge of 100’s of years of knowledge of how these plants work (which results in the quantifiable traditional uses of the plants) that’s typically when I lose them and their eyes roll back in their head.   “Hocus-pocus, hee-bee-gee-bee stuff” they say.  I say, to each their own.  Especially when I oftentimes achieve better results with less side effects than they do.

Welcome to Leslie Taylor's New Blog

Hello! My name is Leslie Taylor and I am the founder of Raintree Nutrition, Inc ., a company that was a leader in creating a world-wid...