Investing is one of the best ways to create passive income since you can effectively put your money to work for you. The more you have to invest, the more passive income you might be able to generate. If you have at least $200,000 to invest for passive income, here are some of the smartest ways to do it.
1. Dividend stocks
Dividend stocks pay out a portion of profits to their shareholders. Depending on how the stock pays out its dividends, you might be able to receive them as income or reinvest them in additional shares through a dividend reinvestment plan (DRIP).
Investing in dividend stocks could be a good long-term play if you’re a buy-and-hold investor. If you’re looking for the best dividend stocks, you might consider the dividend aristocrats. These are stocks that have consistently increased their dividend payout over a period of 25 consecutive years or longer.
2. Index Funds
Index funds are mutual funds that attempt to mimic the performance of an underlying stock market index. For instance, you might invest in an index fund that uses the S&P 500 as its benchmark.
Investing in index funds can help you create a steady stream of dividend income, while also enjoying some long-term capital appreciation. Cost is another advantage of index funds, as they tend to carry lower expense ratios than other mutual funds.
3. Rental Properties
Owning a rental property could be one of the most profitable ideas for how to invest $200,000 for monthly income over the long term. You could invest your $200,000 towards the purchase of a rental property, then collect rental income for as long as you hold it.
Rental properties can be a great way to hedge against inflation since housing prices tend to rise in tandem with increases in other consumer prices. There is some risk, however, as you’ll need to be able to keep the property occupied in order to create passive rental income each month.
4. Real Estate Investment Trusts (REITs)
Don’t want to own a rental property outright? You could still earn passive income from real estate with a real estate investment trust. REITs are legal entities that own investment properties and pay dividends to their investors. You get all of the benefits of owning property without having to purchase or maintain it yourself. REITs can offer exposure to a variety of property types, including office space, retail space, warehouses or multifamily housing.
5. Real Estate Crowdfunding
Real estate crowdfunding platforms offer another avenue for property investments, without requiring any direct ownership. When you invest through a crowdfunding platform, you pool your money alongside other investors to own one or more properties.
During the investment term, the crowdfunding platform can pay dividends back to you monthly, quarterly or annually. Once the investment holding period ends, you can get your initial investment back. A typical holding period can last anywhere from five to 10 years, while the minimum investment can be as low as $500, depending on which platform you’re using.
6. Fixed-Income Securities
Fixed-income securities can pay out interest or dividends to you on a monthly basis, often with minimal risk. Examples of fixed-income securities can include bonds, money market funds and brokered certificates of deposit (CDs) that earn a fixed interest rate.
In terms of risk, fixed-income securities are usually considered to be a safer bet than stocks. However, the returns may be lower so that’s important to consider, depending on your personal risk tolerance and goals.
7. Peer-to-Peer Lending
Peer-to-peer (P2P) lending platforms connect investors with borrowers who need funding and don’t want to (or can’t) get traditional financing. Similar to real estate crowdfunding, you’re pooling your money with other investors to fund loans. You then make money on your investment by collecting interest from the borrower.
Investing $200,000 in peer-to-peer loans could generate a sizable return if you’re earning solid rates but it can be risky. The lower a borrower’s credit grade, the greater the risk that they may default on their loan obligation.
8. Art and Fine Wine Investments
If you’re seeking some alternative investment options, you might consider holding fine art or fine wines in your portfolio. You don’t need to drop your entire $200,000 investment in a single painting or bottle of Merlot either, as there are online investment platforms that allow you to invest fractionally.
For example, you might be able to own a piece of famous artwork by purchasing shares in it alongside other investors. Or you could invest in wine and spirit securities without having to take possession of any physical bottles. These types of investments can add diversity to a portfolio while also creating monthly income.
9. Annuities
An annuity is a type of insurance contract in which you pay a premium to the annuity company, in exchange for receiving monthly payments beginning at a later date. Paying $200,000 for an annuity could make sense if you’re hoping to create a supplemental stream of income for retirement.
For example, you might buy a deferred annuity at age 55 with the intention of starting payments at age 62. Annuities do have some risks and some of them can be expensive when you consider the various fees you’ll pay. However, you could create a reliable, guaranteed income for retirement using annuities
“This book contains the most important results of years of work. I hope that my observations will be examined objectively and promptly for the benefit of sufferers and that cancer research will be directed in the right direction.
Hard struggles and discussions are needed to obtain the latest insights and truths, and it means great happiness for every doctor who is looking for a doctor if he knows colleagues with whom he can discuss common areas of interest.
Slander and defamation, which always come from the mouthpiece of stupidity, arrogance, and cowardice, can disappoint a researcher, but they can never discourage him.
Truths cannot be argued away in science.
The cancer epidemic, like all epidemics known to date, is caused by living pathogens belonging to the genus Protozoa. I call them Ca plasmodia.
These protozoa were microscopically detected by me with picric acid-Giemsa and other picric acid stains in the blood of all cancer and leukemia patients and recorded in many color photos.
The fact that the Ca plasmodia, which I have described and whose cell structure has been precisely proven, can be regularly detected in the blood and other infected organ tissues of all cancer and leukemia patients say more than words.”
Watch this video where a man used an anti-parasitic drug to cure his cancer when he was given three months to live.
Here is how the Veterinarian knew to tell Joe Tippens to take the anti-parasitic drug Fenbendazole:
“He told me a story of a scientist at Merck Animal Health (the veterinary side of Merck) that had performed cancer research on mice by injecting different types of cancers into different mice body parts.
And this scientist stumbled (trial and error) across a product in their canine product line that was batting 1.000 in killing these different cancers.
He told me that the scientist in question got diagnosed with 4th stage brain cancer and was told “no hope, 3 months to live”.
This person decided “what the heck” and started taking the canine medicine. Six weeks later, she was all clear.
I had just been told I’ve got no hope and 3 months to live, so it wasn’t a hard decision for me to take the leap.”
So when my PET scan in September also turned up “all clear” (meaning I had most likely been all clear for 6 months), I decided it was time to “come clean” with my trusted oncologist (who I like and trust very much by the way).
But before disclosing everything to him, I decided I need to do a little “set up” first.
After he very excitedly told me the continued good news of being “all clear” for a second consecutive quarter, I asked him a “very loaded” question.
I asked, “Doc, what is really going on here? Can you disclose to me how I am doing versus all of the other patients on the clinical trial with the exact same condition”?
His answer was what I already suspected. He said, “Joe we can’t explain it, but you are kind of a sole data outlier right now”.
Meaning with hundreds of like kind patients, I was the only one with a cure. I knew then my other alternative regimen was largely responsible, but I decided to come clean anyway.
I said, “Doc, I’m glad you told me that about my results within the trial, because I have something to share with you”.
I proceeded to tell him all about the canine de-wormer as I watched his jaw drop.
His next words I’ll never forget (and remember for context he and I had become good friends by this time).
He said, “you little shit, I knew there was something up with you…..and….I’ve had some weird days here at MD Anderson, but this one probably tops them all”
His next sentence almost floored me.
He said, “You know, we’ve known for decades that these anthelmintic class of drugs (meaning todestroy parasites) could have possible efficacy against cancer, and in fact in the 80’s and 90’s there was a drug called Levamisole that was used on colon cancer and it is an anthelmintic drug”.
NOTE: It is MICROPARASITES (intracellular) that are the cancer
I said, “Doc, if you have known for decades why hasn’t more work been done on it?”
His answer was honest.
He said, “probably because ofMONEY…all of these drugs are far off-patent and nobody is going to spend a gazillion dollars to repurpose them for cancer…..only to have generic competition the next day.”
I knew he was right.
CLICK HERE for Joe Tippens’s Cancer Protocol that saved his life.
This theory was proposed by one of the world’s most famous physicians of all time, Nobel Prize winner Robert Koch (1843-1910).
As a microbiologist, the discoverer of anthrax and tuberculosis was perfectly clear in theory.
Dr. Wilhelm von Bremer, published the article “Krebs – eine Erregerkrankheit” [Cancer – a pathogenic disease] in the journal “Fortschritte der Medizin” back in 1932
In 1962, Dr.Alfons Weber stated that in every tumor tissue there are microparasites.
For the first time he was able to prove Robert Koch’s theory and published film recordings in which one can see the parasites in the tumor tissue.
About the Cause of the Cancer Disease
by Alfons Weber M.D. 1969
“This book contains the most important results of years of work. I hope that my observations will be examined objectively and promptly for the benefit of sufferers and that cancer research will be directed in the right direction.
Hard struggles and discussions are needed to obtain the latest insights and truths, and it means great happiness for every doctor who is looking for a doctor if he knows colleagues with whom he can discuss common areas of interest.
Slander and defamation, which always come from the mouthpiece of stupidity, arrogance, and cowardice, can disappoint a researcher, but they can never discourage him.
Truths cannot be argued away in science.
The cancer epidemic, like all epidemics known to date, is caused by living pathogens belonging to the genus Protozoa. I call them Ca plasmodia.
These protozoa were microscopically detected by me with picric acid-Giemsa and other picric acid stains in the blood of all cancer and leukemia patients and recorded in many color photos.
The fact that the Ca plasmodia, which I have described and whose cell structure has been precisely proven, can be regularly detected in the blood and other infected organ tissues of all cancer and leukemia patients say more than words.”
(The National Library of Medicine has a copy of the monograph that you can go view as they will not lend it out.Click herefor info).
Alfons Weber countered by showing images in which the microbes actually caused the cell to burst, but shortly afterward they took over a new cell – quite normal for parasitic life forms, but impossible for cell organelles.
He also demonstrated that the microparasites multiply within the cell, which organelles do not.
He also provided proof that it was a microparasite:
In an experiment, Weber burned human blood under a 160-degree flame. All human cells were completely destroyed.
Weber added a glucose solution to the dead organ material and a short time later the microparasites were moving on the glass plate.
This experiment silenced all critics, but Weber’s research was still not recognized and hushed up in the future.
Here is a link to a great article on the tribulations Alfons Weber went through (they took away his medical license and put him a mental hospital, his attorney got him out but they ruined his career)
The knowledge that cancer is caused by parasites has flared up again, thanks to the Russian chemist, epidemiologist and microbiologist Tamara Lebedewa.
Because she lost her entire family to cancer and none of her family members were cured by conventional medicine, she researched the disease “cancer” for 13 years.
Since she found that there was no causal cancer therapy in conventional medicine and the theory about “degenerate human cells” was never proven, she started her research from scratch.
Obviously, in 100 years of cancer research, no progress has been made.Why do you think that is?
Lebedewa found out that so-called cancer cells are actually unicellular parasites, called Trichomonas.
The flagellates have exactly the properties of so-called “cancer cells” and will be identified as such by every oncologist.
We all have microparasites but when the immune system is weakened are when parasites proliferate and start causing illness and disease throughout the body.
How do we acquire these microparasites? Dr Alfons Weber writes in his book, “About Causes of Cancer Diseases” that we can get them from mosquito or tic bites, water, soil, eating undercooked or raw meat or fish, sex, and from the mother through the umbilical cord when she is pregnant. Basically microparasites are everywhere and we all have them.
For More Research on Parasites from a German site (Google will translate) as Cancer Triggers:Click HERE andHERE
Recently, ivermectin has been reported to inhibit the proliferation of several tumor cells by regulating multiple signaling pathways. This suggests that ivermectin may be an anti-cancer drug with great potential.
Here, we reviewed the related mechanisms by which ivermectin inhibited the development of different cancers and promoted programmed cell death and discussed the prospects for the clinical application of ivermectin as an anticancer drug for neoplasm therapy.
At least nine different peer-reviewed studies demonstrate how safe and effective ivermectin wards off the Big C, threatening the multi-billion dollar cancer industry. There are two industries, in other words, that ivermectin threatens: the covid industry and the cancer industry.
1) In 2017, research published in the journal Biochemical and Biophysical Research Communicationsfound that ivermectin preferentially treats renal cell carcinoma (RCC) while protecting normal kidney cells. RCC tumor growth is also delayed by ivermectin, which induces mitochondrial dysfunction and oxidative stress while increasing mitochondrial biogenesis.
“Ivermectin has been demonstrated to be safe, following treatment of millions of patients with onchocerciasis and other parasitic diseases, which makes it a strong candidate for further studies investigating its potential use as a repurposed drug for cancer therapy,” reported the National Cancer Institute in Mexico City.
3) Another study published that same year in the American Journal of Cancer Research, also out of Mexico, determined that ivermectin is “a strong candidate for repositioning” as an anti-tumor remedy.
4) Anearlier study published in EMBO Molecular Medicine back in 2014 similarly found that ivermectin inhibits the expression of WNT-TCF targets, which are implicated in both intestinal and lung cancers.
Ivermectin selectively inhibits TCF-dependent, but not TCF-independent, xenograft growth without causing any obvious side effects.
“In vivo, Ivermectin selectively inhibits TCF-dependent, but not TCF-independent, xenograft growth without obvious side effects. Given that Ivermectin is a safe anti-parasitic agent used by 200 million people against river blindness, our results suggest its additional use as a therapeutic WNT-TCF pathway response blocker to treat WNT-TCF-dependent diseases including multiple cancers,” researchers wrote.
Ivermectin works wonders against cancers of all types
Ivermectin also preferentially targets leukemia cells at low concentrations while leaving normal hematopoietic cells alone. The drug also targets various ovarian cancer cells lines and also inhibits the proliferation of five renal cell carcinoma cell lines without affecting normal kidney cells.
6) Also in 2020, a studypublished in the EPMA Journal found that ivermectin hits specific targets in ovarian cancer, suppressing ovarian cancer cells. The drug worked so well that researchers said it can be used to make personalized drug therapy, also known as predictive, preventive, and personalized medicine (PPPM), for ovarian cancer.
7) Researchers from the Instituto Nacional de Cancerologia in Mexico City discovered that same year that ivermectin reduces both cell viability and colony formation capacity while fighting against tumors.
As you can see, ivermectin is something of a wonder drug when it comes to cancer. This is precisely why it is off-limits, and why Americans need to speak out and start demanding access to this inexpensive, life-saving medication.
More related news coverage can be found at Cancer.news.
Ivermectin: An Effective Remedy Against Various Diseases: A Literature Review
Ivermectin was used as an antiparasitic agent upon discovery, but the present status of the drug is vague due to its huge effects on very wide range of diseases and pathogens.
To the best of our knowledge, ivermectin can be used to treat and control viruses, bacteria, parasites, and cancer. Ivermectin provides new promising opportunities to control and prevent a completely new range of diseases, thus generating global interest in evaluating and conducting researches on this wonder drug.
Further studies are needed to introduce new targets and mechanism of the disease; thus the effects of this marvelous medicine may gain more prominence
Ivermectin is a specific inhibitor of importin α/β-mediated nuclear import able to inhibit replication of HIV-1 and dengue virus; Wagstaff K.M., Sivakumaran H., Heaton S.M., Harrich D., Jans D.A. Biochem J. 2012;443(3):851–856.
Flavivirus: From Structure to Therapeutics Development; Rong Zhao, Meiyue Wang, Jing Cao, Jing Shen, Xin Zhou, Deping Wang, and Jimin Cao; Life (Basel)2021 Jul; 11(7): 615.
Ivermectin is a potent inhibitor of flavivirus replication specifically targeting NS3 helicase activity: new prospects for an old drug; Mastrangelo E., Pezzullo M., De Burghgraeve T., Kaptein S., Pastorino B., Dallmeier K., de Lamballerie X., Neyts J., Hanson A.M., Frick D.N., Bolognesi M., Milani M. J Antimicrob Chemother. 2012;67(8):1884–1894.
Comparative study of the interaction of ivermectin with proteins of interest associated with SARS-CoV-2: A computational and biophysical approach; Lenin González-Paz, María Laura Hurtado-León, et al; Biophys Chem; 2021 Nov; 278: 106677.
Antitumor effects of the antiparasitic agent ivermectin via inhibition of Yes-associated protein 1 expression in gastric cancer; Nambara S., Masuda T et al; Oncotarget. 2017;8(64):107666–107677.
Dysregulated YAP1/TAZ and TGF-beta signaling mediate hepatocarcinogenesis in Mob1a/1b-deficient mice; Nishio M., Sugimachi K.et al; Proc Natl Acad Sci 2016;113(1):71–80.
Breast cancer is the most diagnosed cancer in women in the world. Mebendazole (MBZ) has been demonstrated to have preclinical efficacy across multiple cancers, including glioblastoma multiforme, medulloblastoma, colon, breast, pancreatic, and thyroid cancers.
Lebedeva blames trichomonas for a number of diseases. In all cases, Ms. Lebedeva found trichomonas in the blood :
AIDS : In a series of experiments in a Moscow clinic and the Russian Oncological Center, the researcher discovered that AIDS viruses penetrate and multiply in trichomonas (chlamydia also does this).
The result is a significant increase in the aggressiveness of the trichomonad and a drastic increase in the metabolic toxins that are released into the blood.
This also explains why more malignant tumor growth is observed in the later stages of the AIDS disease.
Arteriosclerosis/thrombi/plaques : according to Tamara Lebedewa, are colonies of trichomonads.
She can prove this under the microscope. She placed thrombi in nutrient solution and the cells multiplied like tumor tissue and changed into the amoeba or flagella form.
Letters with illness histories and patient reports confirm that the symptoms have regressed after treatment for trichomonas.
Arthritis and arthrosis : In 1995, in her studies on preparations containing synovial fluid from arthritis and arthrosis patients, Tamara Lebedeva identified trichomonas, which are present in the joint in various stages, poisoning the synovial fluid and causing the cartilage to erode.
Diabetes : Trichomonads feed on insulin, which the scientist also uses to stimulate the parasites in the culture media.
She says that trichomonads colonize in the hormone-containing B cells of the islets of Langenhans, absorb the insulin and destroy the cells with their secretions.
She also concludes that this theory is correct from reports in letters in which patients have achieved significant improvement in their diabetes by treating trichomonas with metronidazole and other antiparasitic drugs.
Multiple sclerosis : Ms. Lebedewa describes how, under certain conditions, trichomonads use myelin – the substance that covers the nerve fibers – as food.
MS is usually preceded by an infectious disease, e.g. B. a middle ear infection in a child, whereby the trichomonad has gained access to the brain via the not yet closed opening in the petrous bone (the oval window), where it begins its work when the completion of the child’s development and the completion of the myelin covering comes to an end.
Adenoma/benign tumor in mucous membranes and glandular tissue : such as in the prostate. Tamara Lebedewa noticed that adenomas often grow into a point and that this point bends like a hook due to gravity.
She saw the same thing with rampant trichomonad cultures.
Here, too, she concludes from letters from patients that trichomonas treatments have a clear reversal effect on the development of adenomas.
Infertility / Impotence : Trichomonads settle in the sexual organs and feed on hormones, among other things.
In the testes they damage sperm with their metabolic toxins. They are also able to phagocytose, that is, absorb and digest up to three sperm.
The trichomonads found in the vaginal mucosa also absorb sperm. They can also damage the female gonads.
Psoriasis/psoriasis : Trichomonads were found in studies of skin preparations from sufferers and in the blood.
Tooth decay/periodontal disease : Oral trichomonads settles in the gum pockets and the area inaccessible to the toothbrush.
Especially when the immune system drops, as with chemotherapy, they become active and cause periodontitis and, through the metabolic toxins, tooth decay.
Ms. Lebedewa observed this form of parasite under the microscope. Severe periodontitis can be quickly treated by dabbing with metronidazole tincture.
Colitis : Intestinal trichomonads is said to be the trigger for various intestinal diseases. It was discovered back in 1926 and may be responsible for hemocolitis, colitis, enterocolitis and cholecystitis.
Lebedewa’s message is brief: the most important serious diseases are caused by microparasites.
Important!
Not everyone infected with trichomonads automatically gets cancer.
Lebedewa found out that certain triggers let the microparasites proliferate.
These include poisons, drugs/alcohol, chronic stress and anything that suppresses the immune system including toxins. Chronic alcohol use severely suppresses the immune system
According to the scientist, the body reacts to the malignant growth with encapsulation, which is called “tumor” in conventional medicine.
This protective measure prompts the body to stop the overgrowth.
Once the tumor is damaged and tissue leaves the tumor, it continues to spread, which is called “spread”. The body will try again to encapsulate the “spread cancer” in what is called “metastasis”.
Diseases caused by microparasites according to Dr. Weaver
These clinical pictures caused by trichomonads correspond to the findings of Dr. Alfons Weber, who, however, lists even more clinical pictures.
2.5 Reactions of the host organism to the Plasmodium infection in the blood; 2.5.1 kinetic impairment of blood circulation; 2.5.2 physiological impairment of blood circulation
2.6 damage to blood and lymph vessel walls; 2.6.1 in the capillaries; 2.6.2 in the great arteries; 2.6.3 in the lymph vessels
2.7 cancerous tumor formation and resorption; organism-specific and plasmodia-related growth substances; 2.7.2 Mitotic disorders, pathological giant cells
2.8 Manifestations on the skin and in the skin’s appendages; 2.8.1 hair loss, disturbed nail formation; increased sweat and sebum production, acne, rosacea; psoriasis, scleroderma; 2.8.4 Infection of the oral cavity and tongue
2.9 Manifestation in the bones, joints and ligaments; path and type of destruction by Plasmodium; 2.9.1 Polyarthritis, Bechterew’s disease; 2.9.2 Osteoporosis, osteomalacia
2.10 Manifestations in the brain, spinal cord and nervous tissue; 2.10.1 Multiple sclerosis, Parkinson’s disease; 2.10.2 Sciatic and trigeminal neuralgia; Psychoses: schizophrenia, etc.
2.11 Manifestations in the digestive organs : 2.11.1 in the stomach: gastric ulcer; in the small intestine: enteritis, flattening of the mucosa; 2.11.3 in the large intestine: ulcerative colitis, Crohn’s disease; 2.11.4 appendicitis; 2.11.5 in the rectum: hemorrhoids
2.12 Manifestations in the respiratory organs: 2.12.1 Bronchial asthma; 2.12.2 Pulmonary emphysema, pulmonary atrophy
2.13 Manifestations in the urinary organs: 2.13.1 glomerulonephritis, tubular nephritis, nephrosclerosis; 2.13.2 albuminuria, globulinuria; Disturbances in the evacuation of urinary substances: uremia, uricemia; 2.13.4 Lithiasis in the urinary organs: urinary stones, etc.
2.14. Manifestations in the genitals: 2.14.1 female genitals; 2.14.2 Complications in pregnancy; 2.14.3 diaplacental infection; 2.14.4 germinative infection; 2.14.5 male sex organs
2.15 Manifestations in the pancreas (diabetes)
Multiple Sclerosis
In a recent autopsy study of Multiple Sclerosis (MS) patients who died from the disease, ten out of ten (100%!!!) actually had microparasites inside the central nervous system including nematode small worms in the brain.
Alan Macdonald: Multiple Sclerosis is a parasitosis
One of our goals is to establish a firm scientific platform for some cases of Multiple Sclerosis as a brain/spinal cord chronic infection.
In 2016, using our highly specific Molecular Beacon DNA probes, we detected the specific DNA of Borrelia in the autopsy CSF of multiple sclerosis victims.
Currently, it is taught in medical schools that all cases of Multiple Sclerosis stem from a degenerative condition of unknown cause.
Borrelia spirochetes were cultured from the spinal fluid often of ten Multiple Sclerosis patients by Dr. Oystein Brorson, MD and Dr. Sverre-Henning Brorson, MD in 2001.
In addition, allwere positive for Borrelia spirochetes by Electron Microscopy.
This discovery helped make sense of what I had found in my Multiple Sclerosis study. If the MS patients had Nematodes and Borrelia burgdorferi in the central nervous system, then the proper treatment wasn’t just antibiotics but would have to be high dose antiparasitic drugs followed by antibiotics, and this combination would have to continue until all parasites in all their growth stages including eggs, had been cleared from the brain.
Why had so many missed this discovery?
In today’s fast-paced medicine, anytime MS is considered the CSF specimens are placed directly in an automated analyzer that looks for MS markers, but not for parasites. On a slide without stain, the CSF looks normal. Then if the lab looks at the slide at 40x magnification or higher, they will miss the worms. It’s like looking at an elephant’s leg an inch away and trying to figure out what the whole animal looks like.
What this means to MS patients?
Clearly this suggests that despite any other treatment, the MS patient should first be placed on an anti-parasite medicine for nematodes, followed by antibiotics for Borrelia. Treatment would have to be aggressive to get past the Blood-Brain-Barrier, and prolonged to eradicate the Borrelia.
Dr. Paul Duray MD Research Fellowship Endowment Inc
In Dr Paul Duray’s career, he single-handedly expanded the number of Borrelia illnesses to include:
Borrelia-related Parkinson’s disease; Borrelia-related intrauterine infections with fetal deaths; Borrelia muscle diseases, fasciitis and cystitis; Fatal Adult Respiratory Distress Syndrome (ARDS) due to Borreliosis; Borrelia-related necrotizing splenitis; Borrelia hepatitis
He also published many landmark manuscripts which redefined and enlarged the medical and scientific understanding of spirochetal diseases.
Cautionary note:
Nematode infestations of the CNS require very careful treatment and monitoring by an experienced physician. Patients should not attempt to self-treat with antiparasitic drugs. Some anthelmintics can cause severe inflammatory reactions which might require concomitant steroid treatment in order to avoid fatal encephalitis.
Clearly, this suggests that despite any other treatment, the MS patient should first be placed on an anti-parasite medicine for nematodes, followed by antibiotics for Borrelia. Treatment would have to be aggressive to get past the Blood-Brain-Barrier and prolonged to eradicate the Borrelia.
Screening thousands of drugs, Stanford scientists determined that in mice, azlocillin, an antibiotic approved by the Food and Drug Administration, eliminated the bacteria that causes Lyme disease.
Dr. José Ignacio Santos Preciado (parasite researcher at the renowned University of Stanford / California and General Director at the Hospital de México) and his team found out back in 2012 that this is the main cause of all cardiovascular diseases (heart attack, heart failure/CHF, Cardiac arrhythmias, angina pectoris, etc.) is the infestation of the heart with parasites. According to Dr. Santos Preciado triggered by parasites.
Nearly one-third of the 7.25 billion people on earth, including an estimated 60 million people in the United States, are chronically infected with the protozoan Toxoplasma gondii.
A working immune system can keep the parasite in check, so only a minority of those infected has significant symptoms. But when an unsuspecting woman gets infected during pregnancy and passes the parasite on to her unborn child, the consequences can be profound.
They include devastating damage to the brain, nervous system and eyes. Now there is growing evidence that some people, maybe a lot of people, have subtler symptoms triggered by the infection.
Perhaps the immune response, while keeping the parasites in check, causes collateral damage elsewhere. Or maybe the parasites, which produce the neurotransmitter dopamine and interact with the cells it infects, modifies behavior of its host.
We asked a leading authority on Toxoplasma gondii and toxoplasmosis, Rima McLeod, MD, professor of ophthalmology & visual science and pediatrics and medical director of the toxoplasmosis center at the University of Chicago, a big question: What do we think happens when billions of people go through life with a parasitic brain infection?
Ginger extract treatment reversed T. gondii-induced pathological changes in the brain, liver, and lungs.These findings indicate that ginger extract could be a potential alternative therapeutic for treating chronic toxoplasmosis.
Click HEREfor more REFERENCE STUDIES on using Anti-parasitic drugs for cancer.
Fenbendazole, Ivermectin, Nitazoxanide, Albendazole and Mebendazole are all powerful anti-cancer drugs that have been proven to be effective in treating a variety of cancers.
The drugs that end in “azole” work by targeting cancer cells (parasites) and preventing them from growing and spreading by stopping their uptake of glucose.
With their high success rate and minimal side effects, They are an excellent choice for those looking for a safe and effective treatment for cancer. Contact your oncologist and tell him about the studies showing the efficacy of these drugs.
Nattokinase: A Promising Alternative in Prevention and Treatment of Cardiovascular Diseases
Far and away the most common question I get from those who took one of the COVID-19 vaccines is: “how do I get this out of my body.”
Nattokinase is an enzyme is produced by fermenting soybeans with bacteria Bacillus subtilis var. natto and has been available as an oral supplement. It degrades fibrinogen, factor VII, cytokines, and factor VIII and has been studied for its cardiovascular benefits.
Out of all the available therapies I have used in my practice and among all the proposed detoxification agents, I believe nattokinase and related peptides hold the greatest promise for patients at this time.
Excel Well LLC Professional Nutracueticals Fullscript dispensery is registered to accept Health Savings Account (HSA) and Flexible Spending Account (FSA) debit cards on all supplement orders
Degradative Effect of Nattokinase on Spike Protein of SARS-CoV-2
Immunofluorescence analysis showed that S protein on the cell surface was degraded when nattokinase was added to the culture medium. Thus, our findings suggest that nattokinase exhibits potential for the inhibition of SARS-CoV-2 infection via S protein degradation.
Here is an audio program on eliminating negative self talk. Negative thoughts plays a huge part in anxiety and getting stuck on them is called “rumination”. Stress increases histamine and chronic high histamine can cause OCD and rumination. Check out our page on mental health
But you should contact a medical doctor or a naturapathic doctor especially if you have cancer or Multiple Sclerosis before starting removal of the parasites.
Many common foods contain natural compounds that can help fight and kill parasites.
Give any of the below foods and herbs a try to help keep bad bugs at bay, but be sure to visit your doctor if you suspect you have a parasite infection.
They will be able to provide you with additional remedies to take care of it.
This site is not designed to and does not provide medical advice, professional diagnosis, opinion, treatment or services to you or to any other individual. Through this site and linkages to other sites, I provide general information for educational purposes only. The information provided in this site, or through linkages to other sites, is not a substitute for medical or professional care, and you should not use the information in place of a visit, call consultation or the advice of your physician or other healthcare provider. I am not liable or responsible for any advice, course of treatment, diagnosis or any other information, services or product you obtain through this site.
“As an Amazon Associate I earn from qualifying purchases.”
Starting a Business: Moving Through Fear and Into Forward Motion
Every aspiring business owner knows the same truth: the desire to build something meaningful often arrives hand-in-hand with fear. It’s not a sign that you’re unprepared — it’s a sign that you care. Fear usually comes from uncertainty, financial risk, skill gaps, and the pressure to “get it right” from day one. What matters is not eliminating the fear, but learning how to move with it.
Quick Summary
Building confidence comes from clarifying your direction, reducing ambiguity, and taking small, momentum-building actions. Fear shrinks when your decisions become structured, your plans become visible, and your risks become manageable.
Why Fear Shows Up in the First Place
People often assume fear is a flaw — but for entrepreneurs, it’s almost always a signal. Most new founders experience some version of:
Information gaps (What if I don’t know enough?)
Financial uncertainty (What if this doesn’t work?)
Identity pressure (What will people think if I fail?)
Overwhelm (Where do I even begin?)
Fear thrives in ambiguity. As you clarify what you’re building, why it matters, and how you’ll take the next step, the emotional load shifts from dread to direction.
Common Fears and Practical Responses
Common Fear
What It Really Means
A Practical Countermove
“I don’t know enough.”
You lack a mental map of the business landscape.
Build a small, structured learning plan and validate ideas with experienced operators.
You’re unclear on budget, buffers, or business model trajectory.
Start with a lean version of the idea and stress-test your numbers.
“Others are already doing this.”
You fear your voice won’t stand out.
Narrow your niche, strengthen positioning, and emphasize differentiation.
The Power of Education and Structured Skill-Building
One of the most effective ways to replace fear with clarity is through formal learning. Earning a business management degree strengthens your understanding of finance, leadership, marketing, operations, and decision-making — all of which reduce risk because they reduce uncertainty. Online degree pathways can make it easier to build your business while continuing your studies at your own pace. Explore your options to learn more about available programs.
What to Do When Fear is Loud
Use this quick sequence whenever self-doubt spikes:
Name the fear plainly. Avoid vague anxiety. Write the exact fear in one sentence.
Identify the real risk hiding beneath it. Is it financial? Social? Knowledge-based?
Define the smallest reversible step you can take this week. Reversible steps train your brain that movement isn’t dangerous.
Reduce the unknowns. Validate the idea, interview potential customers, or test your offer in miniature.
Track momentum, not perfection. Celebrate movement — the mind trusts what it can measure.
Build a habit of micro-decisions. Big decisions feel scary; small decisions build muscles.
Momentum Drivers for New Founders
Here are a few compact practices that help founders build confidence quickly:
Start with a problem you deeply understand rather than a generic opportunity.
Create a “fear ledger” — a list of anxieties paired with the action that counters each one.
Use short planning cycles (e.g., 2-week sprints) to shrink uncertainty windows.
Talk to five customers before building anything.
Make one public commitment weekly to stay accountable.
Treat every early version of your idea as a prototype — not a verdict on your potential.
FAQs
Q: How do I know if my idea is good enough? A: Ask five to ten real people in your target audience. If they describe the problem the same way you do and show interest in a solution, the idea is worth pursuing.
Q: Should I quit my job to start the business? A: Not immediately. Many founders begin with part-time testing until the business shows traction or predictable revenue patterns.
Q: What if someone copies my idea? A: Execution, positioning, and relationship-building matter more than originality. Most markets reward differentiation, not novelty.
Q: How do I keep fear from stopping me? A: You don’t eliminate fear — you override it with small, evidence-gathering actions that shrink the unknowns and build trust in your own capability.
Closing Thoughts
Fear isn’t a stop sign — it’s a signal that you’re entering new territory. When you structure your decisions, shrink uncertainty, and build skills steadily, confidence becomes a natural byproduct. Move in small steps, validate your assumptions, and surround yourself with resources that help you think clearly. Your business starts the moment you decide to move forward, even if you feel uncertain.
How Edge Computing is Revolutionizing the Internet of Things (IoT)
You wake up, your smart thermostat adjusts the temperature, your coffee brews automatically, and your car updates its navigation—all without touching the cloud. That’s not magic, that’s edge computing. This shift isn’t just about speed. It’s about autonomy, reliability, and keeping your data close. For IoT, this means devices that think and act locally. And that changes everything. Let’s dig into how edge computing is recoding the DNA of connected systems.
Understanding Edge Computing in the IoT Landscape
In the old model, data from your smart device would take a long detour—sent to the cloud, processed, then sent back. But with edge computing, the brainpower stays local. It’s the difference between asking your neighbor for help versus mailing a letter to city hall. Devices process data right where it’s generated, which means faster reactions, lower latency, and no waiting for the cloud to catch up. This change is part of a much bigger paradigm shift in data processing within IoT infrastructures, giving machines the power to think on their feet—or wheels, or gears.
Enhancing Real-Time Decision-Making in Industrial Settings
In places like smart factories or oil rigs, hesitation can be expensive—or dangerous. You need systems that don’t blink. That’s where local computing becomes more than a convenience. Sensors detect a pressure change, and the response kicks in instantly. No lag, no relay race to the cloud. Edge computing enhances real-time data analysis in industrial settings, enabling decisions to be made where the action is. It’s not about predicting the future—it’s about reacting faster than it arrives.
Rugged Mini PCs at the Edge
Let’s talk hardware. You can’t drop a full data center into a delivery drone or mount it to a tractor plowing a remote hillside. But rugged, palm-sized computers? Those workhorses thrive in dust, heat, vibration—anywhere the cloud can’t reach. These compact units deliver real compute power in unforgiving conditions. From autonomous vehicles to remote weather stations, the advantages of using mini industrial computers are undeniable: they think fast, survive anything, and don’t need a stable Wi-Fi handshake to do their job.
Synergy Between Edge and Cloud Computing
This isn’t a breakup with the cloud—it’s a rebalancing. Think of edge and cloud like two arms of the same brain. The edge handles reflexes; the cloud stores memory. You process time-sensitive data locally, then sync the big-picture insights when it’s safe to reconnect. This synergy between edge and cloud computing balances autonomy with oversight, letting systems be both nimble and smart. It’s not about choosing one—it’s about using both, together, better.
Security and Privacy Benefits of Edge Computing
Every time data moves, it risks exposure. So what if it didn’t have to move at all? That’s the edge advantage: by processing data on-site, you slash the number of hands it passes through. Sensitive info—think patient vitals or industrial controls—never leaves the premises. And fewer transfers mean fewer attack surfaces. That’s why this model enhances data security and privacy not just as a feature, but as a built-in habit. You protect by staying put.
Scalability and Network Efficiency in Edge Computing
Every new device adds pressure to already crowded networks. When ten thousand sensors flood the cloud, systems choke. But shift that load to the edge? You get breathing room. For systems to grow without collapsing under their own weight, you need strategies like building scalable edge computing architectures that trim the fat and cut the noise. Data is processed locally, trimmed to essentials, and only what matters is sent upstream. That’s how you scale without breaking the pipes.
Future Outlook: Edge Computing’s Expanding Role in IoT
The devices are getting smarter. The edges are getting closer. And tomorrow’s networks? They won’t wait around for approval from the cloud. AI, machine learning, adaptive routing—these tools aren’t just coming, they’re arriving pre-installed. What started as a speed hack is fast becoming the default architecture. As demand for autonomy rises, understanding the future of real-time data processing becomes essential—not just for engineers, but for every system that runs on insight.
Edge computing isn’t a buzzword—it’s a structural shift. A push toward smarter, faster, closer systems. IoT isn’t just expanding; it’s evolving. Devices no longer wait for orders from afar. They decide. They act. They survive on the edge. And in doing so, they redraw the map for what’s possible in real-time, decentralized intelligence. As the world connects more deeply, the edge becomes not a boundary—but a beginning.
Discover the path to a healthier, stress-free life with Excel Well LLC and explore their expert insights on managing stress and enhancing your well-being today!
The Great Seal of The Unites States with a pyramid, eagle, Latin phrases, etc. has been reproduced on the reverse side of every American dollar bill, but few in America know what these symbols mean.
The key to understanding the meaning behind all of these symbols is found in the translation of the Latin phrase “NOVUS ORDO SECLORUM,” (“The New World Order”) found underneath the pyramid on what is known as the Reverse Side of the Great Seal.
Ralph Epperson has spent 27 years in researching the history of the two sides of the Great Seal, and has discovered that those who designed them committed America to what has been called “A Secret Destiny.”
This future “destiny,” called THE NEW WORLD ORDER, is so unpleasant that those who wanted the changes it entails had to conceal that truth in symbols.
This book, THE NEW WORLD ORDER, is the amply documented explanation of what those symbols mean and how they connect to this nation’s future. Mr. Epperson is making his research available to the American people so that they may know just what these planners wanted for our future. And so that they can take corrective action.
I managed a false flag operation for the Central Intelligence Agency (CIA). No
one died. False flags are very real, as is mind-control.
I am quite certain that 9/11 was managed by Dick Cheney and that every major shooting in the USA has
been a false flag operation designed to frighten the public and justify the further
militarization of the police and increased government surveillance and control
over the public on behalf of the Deep State that is owned and operated by the
Vatican and the Rothschilds using Freemasons (the 34th, 35th, and 36th levels not
known to most Freemasons) and the Knights of Malta as their “consigliere.”
It is important to note that the European Black Nobility is responsible for the insidious entanglements of numerous secret societies, lodges, and organizations, which are backed by high finance and powerful
political connections.
Such organizations include: the Trilateral Commission, Bilderberg Group, Council on
Foreign Relations (CFR), United Nations (founded by CFR), Illuminati order Skull & Bones (inner circle of the CFR), International Monetary Fund (IMF), World Bank, Bank of International Settlement, Club of Rome, Chatham House (formally the Royal Institute of International Affairs – RIIA), Round Table, Tavistock Institute for Human Studies (England’s psychological warfare think tank), Associated Press, Reuters (Rothschild owned news monopoly), and many others, all of which, work in favor of their one world government agenda.
