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Why have we lost our trust in natural medicine? In this video, we’ll discuss why natural medicine is ignored and sometimes even dismissed as folklore. Is it wise to invalidate the wisdom of the past? Discover the truth about natural medicine in this video.
Just so you know, my full line of high-quality supplements is available on Amazon — search Dr. Berg Supplements.
Uncover the hidden influences shaping modern medicine. These can help you connect the dots:
▶️ https://youtu.be/vWaeDMp4mIQ
▶️ https://youtu.be/18tnJ9wLDbk
▶️ https://youtu.be/OiU1B6VNDvQ
0:00 Introduction: Natural medicine suppression
0:19 United States Dispensatory
0:38 Pharmaceutical vs. natural medicine
3:08 The advancement of medicine
6:35 Natural remedies of the past
The “United States Dispensatory” by Wood and Lawall may provide insight into alternative medicine censorship in the United States. The 21st edition, published in 1926, was the most authoritative and comprehensive reference for American medicine. At the time of publication, 75% of medicine consisted of various natural remedies, while only 25% consisted of synthetic compounds.
Since then, there’s been a gradual transition from natural remedies to synthetic drugs. When the 22nd edition of the book was published in 1943, the ratio of natural to synthetic drugs shifted to 50:50.
Today, medicine is often prescribed without considering lifestyle, eating habits, sleep patterns, stress levels, or the microbiome. Symptoms of the underlying problems are treated without addressing the root cause.
Discover these 20 natural remedies that have stood the test of time, along with the ailment they have historically been used to address.
1. Cod liver oil—Tuberculosis, tetany, nerve pain
2. Nutmeg oil—Psychotic problems
3. Olive oil—Mild laxative, gallstones
4. Pine needle oil—Eliminates mucus from the lungs
5. Castor oil—Mild laxative
6. Sandalwood oil—Gonorrhea, bronchitis, bladder infections
7. Sassafras oil—Antiseptic
8. Betaine hydrochloride—Indigestion, gastric problems
9. Pepsin—Digestive issues
10. Lugol’s iodine—Thyroid support and protection
11. Magnesium sulfate—Sleep support, anxiety, pain killer
12. Calcium chloride—Acidifies the body
13. Liver extract—Anemia
14. Methylene blue—Shrinks tumors, meningitis, bladder infections, gonorrhea, and supports the mitochondria
15. Lithium carbonate—Relaxation, anxiety, and depression relief
16. Glauber’s salt—Laxative
17. Vitamin D—Autoimmune conditions
18. Colloidal silver
19. Activated charcoal—Food poisoning, gas
20. Niacin—Lowers triglycerides, increases HDL, increases lifespan, supports cardiovascular health, acts as a NAD precursor
👉 Get Dr.Berg’s Daily Routine as a free download: https://drbrg.co/4qdDOT7
Dr. Eric Berg DC Bio:
Dr. Berg, age 60, is a chiropractor who specializes in Healthy Ketosis & Intermittent Fasting. He is the Director of Dr. Berg Nutritionals and author of the best-selling book The Healthy Keto Plan. He no longer practices, but focuses on health education through social media.
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Disclaimer:
Dr. Eric Berg received his Doctor of Chiropractic degree from Palmer College of Chiropractic in 1988. His use of “doctor” or “Dr.” in relation to himself solely refers to that degree. Dr. Berg is a licensed chiropractor in Virginia, California, and Louisiana, but he no longer practices chiropractic in any state and does not see patients, so he can focus on educating people as a full-time activity, yet he maintains an active license. This video is for general informational purposes only. It should not be used to self-diagnose, and it is not a substitute for a medical exam, cure, treatment, diagnosis, prescription, or recommendation. It does not create a doctor-patient relationship between Dr. Berg and you. You should not make any change in your health regimen or diet before first consulting a physician and obtaining a medical exam, diagnosis, and recommendation. Always seek the advice of a physician or other qualified health provider with any questions you may have regarding a medical condition.
#health #keto #ketodiet #weightloss #ketolifestyle #intermittentfasting #lowcarb
Thanks for watching! I hope this raises your awareness about natural medicine suppression. I’ll see you in the next video.
It's been 2 years since our first video on the science of Ivermectin and cancer. It's time for an update on the science, Rachel's current plan and usage, and considerations for how to get Ivermectin for cancer.
Original 2021 Ivermectin Video:
https://youtu.be/_15tjRXeWNk
Studies Referenced:
https://pubmed.ncbi.nlm.nih.gov/36381328/
https://aacrjournals.org/cance....rres/article/82/12_S
Interview with Dr. Peter Lee:
https://www.cancerpreventionin....itiative.org/expert-
Malaria continues to cause enormous morbidity and mortality. Could mass administration of ivermectin, a broad-spectrum antiparasitic drug that also kills mosquitoes feeding on treated persons, reduce malaria transmission?
This video in our partnership with @DGlaucomflecken summarizes results of the BOHEMIA cluster-randomized trial.
View the Original Article for free: https://nej.md/DrG31
#medicaleducation #nejm
This is crazy! Can you believe it! People actually taking Ivermectin thats intended for animals to ward off Covid. Watch to learn details and find out what you should know.
Also watch: "Ivermectin for COVID?"https://youtu.be/SeQiFoH4BOk
Hello! I’m Dr. Jen. I'm a Board-Certified Family Physician, on-air health expert, and video creator. Welcome to my YouTube Channel and thank you for watching this video! Let me know what you think and please subscribe to my channel above https://youtube.com/drjencaudle.
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#ivermectin #Livestock #covidvaccine #covid #deltavariant
#parkinson #parkinsonsawareness #parkinsonsdisease #parkinsons #Neuroscience#MedicalResearch #Ivermectin #movementdisorders
In this episode we examine recent lab and animal research suggesting ivermectin — a widely used antiparasitic — can alter striatal circuits and enhance L-DOPA responses in preclinical Parkinson’s models. We’ll explain the likely mechanisms (ion-channel modulation at P2X4 and nicotinic receptors), review safety concerns (blood-brain-barrier and neurotoxicity risks), and explain why there are no human trials yet proving efficacy in Parkinson’s. Sources and further reading are here:
1. Ivermectin increases striatal cholinergic activity to facilitate dopamine terminal function https://pubmed.ncbi.nlm.nih.gov/38632622/
2. Serious Neurological Adverse Events after Ivermectin https://pmc.ncbi.nlm.nih.gov/articles/PMC5929173/
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Medical Disclaimer
All information, content, and material of this video is for informational purposes only and not intended to serve as a substitute for the consultation, diagnosis, and/or medical treatment of a qualified physician or healthcare provider.
Affiliate disclaimer:
Keep in mind that links used for recommended products may earn me a commission when you make purchases. However, this does not impact what products I recommend. If I recommend a specific product it is because it has been vetted by myself or based on personal use
In this episode, I discuss a medication known as ivermectin (Stromectol, Sklice, Soolantra).
My book is now available! It discusses my experience with Bipolar Disorder.
The Fifth Episode - Inside The Manic Mind.
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Intro Created by Leah Leblanc - leahleblanc.com
For information purposes only!
Can ivermectin help support immune system balance and reduce chronic inflammation? This video explores the growing interest in ivermectin for autoimmune support, its possible anti-inflammatory benefits, and what current research suggests about its potential to regulate immune responses.
Originally approved as an antiparasitic, ivermectin is now being studied as a repurposed drug with possible applications in managing immune-related conditions such as rheumatoid arthritis, lupus, and other inflammatory issues. We’ll also look at the possible side effects of ivermectin, safety considerations, and what to keep in mind if you're curious about this treatment.
Whether you’re exploring alternative treatments for autoimmune conditions, looking into immune-modulating medications, or simply curious about ivermectin's potential benefits, this is an informative and balanced overview to help you stay informed.
Subscribe to my newsletter through my website [a]www.myautoimmunemd.com[/a] where I send out information on news on rheumatology, autoimmune disease, and integrative medicine!
Make appointments here: www.drlifestyle.org
Autoimmune Website: [a]www.myautoimmunemd.com[/a]
My clinic is located in Newport Beach, California. I see patients virtually throughout USA and worldwide.
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#ivermectin #autoimmunedisease #autoimmunehealing
A Pilot, Randomised, Placebo-Controlled, Double-Blind Trial of a Single Oral Dose of Ivermectin for Post-Exposure Prophylaxis of SARS-CoV-2
https://www.mdpi.com/1999-4923/17/9/1205
People who took one small oral dose of ivermectin after exposure,
took longer to test positive and had more time alive and free of symptoms.
Multiple reports from in vitro infectious models document Ivermectin’s antiviral properties
https://pmc.ncbi.nlm.nih.gov/a....rticles/PMC7564151/p
Ivermectin has broad-spectrum antiviral activity.
Randomised, double-blind, placebo-controlled
Single oral dose of Ivermectin as prophylaxis for SARS-CoV-2
Trial to evaluate the effectiveness of a single oral low dose of Ivermectin
Ability to prevent SARS-CoV-2 infection?
Ability to reduce symptoms if infection did occur?
Methods
Asymptomatic community-dwelling adults
Enrolled within 72 h of close contact with a case of SARS-CoV-2.
Single oral 200 µg/kg dose of Ivermectin or placebo.
65Kg woman given 13mg
80Kg man given 16mg
The primary outcome
Conversion to a positive PCR or RAT test within 14 days of close contact.
Secondary outcomes
(for those who tested positive)
Days alive free of symptoms in the 14 and 28 days following ivermectin
Days from close contact until a positive PCR or RAT
Results
N = 536 (86 met inclusion criteria and were randomised)
68 adhered and were included in the analysis.
Ivermectin arm
11/36 tested positive
Placebo arm
11/32 tested positive
So, ivermectin did not prevent people testing positive
Days from close contact until a positive PCR or RAT
Increased by 2.3 days in ivermectin group.
P = 0.033
So, ivermectin lengthened the incubation period
Viral load needed to precipitate clinical disease took longer to develop – indicating an antiviral effect.
Infection may have been prevented from primary contact, - indicating an antiviral effect.
Days alive free of symptoms
Increased by 2.5 days in ivermectin group.
P = 0.036
So ivermectin delayed onset of symptoms in people who tested positive
(Longer asymptomatic period)
Controlling included
Age, prior SARS-CoV-2 infection, body mass index, hypertension, lung disease
Conclusions
We did not demonstrate that a single oral low dose of Ivermectin administered to asymptomatic adults within 72 h of close contact with a case of
SARS-CoV-2 prevents conversion to a positive PCR or RAT.
(may have done with a larger sample size)
Amongst those who did convert to a positive PCR or RAT
Ivermectin significantly lengthened the time from close contact to conversion
Ivermectin increased the number of days alive free of symptoms
More details
Initiation of this trial in late 2021
Discovery in 1975
Massively used around the world
Nobel Prize in 2015
Very low incidence of serious adverse side effects
No instance of resistance reported in over 25 years.
Ivermectin can bind to and inhibit the nuclear transport roles of the host importin α (IMPα) protein,
which is known to mediate the nuclear import of various viral proteins and key host factors.
Other quite distinct antiviral actions of Ivermectin have been proposed
High (therapeutic) concentrations collect in the lungs, stable for more than 30 days in cattle
Trial was based on the strong clinical retrospective association of statistically significantly lower mortality in patients who received oral Ivermectin (200 μg/kg) compared with usual care
https://www.sciencedirect.com/....science/article/pii/
Ivermectin patients 15% mortality
Controls, 25.2% mortality
In subjects with severe pulmonary disease
Ivermectin patients, mortality 38.8%
Controls, 80.7% mortality
The War on Ivermectin by Dr. Pierre Kory, https://www.amazon.com/War-Ivermectin-Medicine-Millions-Pandemic/dp/151077386X/ref=sr_1_1?dib=eyJ2IjoiMSJ9.EVlbDojnY-TDtm3BgepTIg.q5qDUxkwO3stZL9DZRUFMVYBLM5ix5BlzBT_LKusDLA&dib_tag=se&keywords=kory+the+war+on+ivermectin&qid=1762207712&sr=8-1
COVID-19 treatment: real-time analysis of 6,252 studies, https://c19early.org/
Ivermectin and Mebendazole in Cancer Patients
https://zenodo.org/records/19455636
The Clinical Benefit Ratio
Complete Response + Partial Response + Stable Disease / Total Patients
(CBR) was 84.4%
Overall, it is estimated that annual costs of standard chemotherapies average $111,000 per year.
Background: Drug repurposing offers a pathway to identify accessible, low-toxicity cancer therapies.
Ivermectin and mebendazole have demonstrated multi-target anti-cancer activity.
This paper evaluates real-world patient-reported outcomes, safety, and adherence in a cohort of cancer patients utilizing this combination protocol.
Methods:
Prospective observational cohort of 197 cancer patients,
who were prescribed ivermectin and mebendazole off-label through telemedicine (platform by licensed U.S. healthcare providers)
Participants received compounded oral capsules containing 25 mg ivermectin and 250 mg mebendazole.
Data were collected via voluntary, standardized digital surveys at baseline and at approximately 6-month follow-up.
Of the initial cohort (N = 197), baseline characteristics, including cancer type and disease status, were assessed.
A total of 122 participants completed the follow-up survey (61.9% response rate)
Results:
Mean age of 67 years, (52.3% male, 47.7% female).
Cancer types included
Prostate 27.9%
Breast 18.3%
Lung 8.6%
Colon 5.1%
Urologic 4.6%
Pancreatic 3.0%
Liver 2.5%
Gynaecologic 2.5%
Hematologic 2.5%
Median duration since initial diagnosis, 1.2 years
37.1% experiencing active disease progression.
6-month follow-up
Medication adherence, 86.9%
Full initial 90-capsule ivermectin-mebendazole prescription.
The Clinical Benefit Ratio
Complete Response + Partial Response + Stable Disease / Total Patients
(CBR) was 84.4%
Notably, 48.4% of cohort, strongest positive outcomes:
Regression, 15.6%
No current evidence of disease (NED), 32.8%
Disease stability, 36.1%
Disease progression, 15.6%
No significant dose-response association was observed for cancer outcomes (p = 0.91),
without a clear dose-response gradient for efficacy.
Side effects
Mild side effects (primarily gastrointestinal), 25.4%
(93.6% of those affected continued treatment through minor dose adjustments)
Concurrent conventional therapies
Chemotherapy, 27.9%
Radiation therapy, 21.3%
Surgery, 19.7%
Adjunctive interventions such as supplement use, 49.2%
Dietary modification, 37.7%
Conclusions: In this prospective real-world cohort, the combination of ivermectin and mebendazole was associated with high rates of self-reported clinical benefit, with nearly half of participants reporting tumours regression or no current evidence of disease across a heterogeneous population of cancer patients.
These findings provide a compelling clinical signal that these well-tolerated, repurposed agents may offer therapeutic benefit.
However, observational design, reliance on self-reported outcomes, and potential for selection bias and uncontrolled confounding, these findings should be interpreted as hypothesis-generating.
Urgent prospective, randomized, placebo-controlled clinical trials
Validate these observations and further define optimal dosing strategies.
Mechanism (pharmacodynamics)
Ivermectin and mebendazole are antiparasitic agents,
demonstrated highly promising anti-cancer activity.
Ivermectin
Shown to exert over 14 distinct anti-cancer mechanisms across more than 12 cancer types,
inhibiting cancer cell proliferation, metastasis, angiogenesis, mitochondrial function.
Has demonstrated excellent safety in cancer patients (including those actively undergoing chemotherapy)
Ivermectin and mebendazole selectively target cancer stem cells
Mebendazole
Microtubule disruption, leading to effective cell cycle arrest
Potent induction of apoptosis
Significant inhibition of tumour growth
Inhibition of angiogenesis
Disruption of glucose uptake
When used together
Target non-overlapping pathways, resulting in synergistic tumour regression,
cancer stem cell depletion, and reversal of multidrug resistance in multiple in vitro and in vivo models
Biodistribution, ivermectin and mebendazole document excellent tissue penetration
Pierre Kory is most famous for being a piece of shit fraud who got up in front of a Senate Committee and proclaimed that if you take ivermectin you can't get COVID, only to then promptly get COVID. He also made a fortune prescribing and selling it online, at the cost of many human lives who wasted precious time taking snake oil instead of getting actual treatment. Watch me expose this script of lies right to his dumb face.
Watch my other debunks/debates/discussions: http://bit.ly/ProfDaveDebunk
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