What Did Dr. Hulda Clark Think About Ivermectin?

1 comment by Oskar Thorvaldsson

I

Ivermectin


Although Hulda Clark did not write about Ivermectin she used it in her clinic and with good results. Since Ivermectin focus is more narrow than the parasite cleanse she recommended her patients take it after the triple parasite cleanse that contains the green tincture of black walnut hull, freshly ground clove capsules and wormwood capsules.

Ivermectin is an antiparasitic medication that works by paralyzing and killing certain parasites, primarily worms and external parasites like mites and lice. It is FDA-approved for specific human uses and has off-label applications (see table below), as well as widespread veterinary applications. Note that dosing depends on body weight. 

We recommend the ivermectins sold by Peter McCullough, MD, MPH from The Wellness Company (TWC) at www.twc.health. The total investment may seem a lot but the price per mg is reasonable. Dr. McCullough has a great reputation for being both vaccine literate and generous. TWC also sells mebendazole.

The Wellness Company Brand of Ivermectin

$299.99

for

90

capsules




18

mg

90

capsules

1,620

mg

total

Price per mg


$0.19






You can find Fenbendazole marked as supplements, do not trust those sources, this is a drug and can only be purchased from a licensed pharmacy in the US. Fenbendazole is for veterinary use whereas Mebendazole is for human use. Albendazole is a great drug also. Fenbendazole, mebendazole, and albendazole are all benzimidazole anthelmintics—brilliant, Nobel-adjacent warriors in the fight against parasites and emerging stars in repurposed cancer protocols.

If you don’t think you need 90 capsules or if you need smaller dosages then you can go with a company called TelyRx, - https://telyrx.com/ivermectin-scabies-treatment - they sell a brand of Ivermectin called Edenbridge. While the total investment is lower or only $80 your price per mg is higher with them. This website sells it for scabies treatment but are not going to ask for proof. Check the below dosing based on body weight. TelyRx does not sell Fenbendazole, they however sell Albendszole


TelyRx Brand of Ivermectin

$79.99

for

20

tablets




3

mg

20

tablets

60

mg

total

Price per mg


$1.33






How to determine how much to take? You need to find an ivermectin/herbal literate health care pro. Once she has gotten to know you and your situation then you may need more than is outlined in the below information. Fortunately Ivermectin has a stellar safety record from over 4 billion human doses. It is remarkably forgiving even in excess—its therapeutic index (ratio of toxic to effective dose) exceeds 100:1, far safer than everyday meds like Tylenol.


Weight-Based Ivermectin Dosage Chart (200 mcg/kg)

Body Weight (kg)

Total Dose (mcg)

Approx. Tablet Strength

40 kg

8,000 mcg

1 tab of 6 mg + 1 tab of 3 mg

50 kg

10,000 mcg

1 tab of 12 mg

60 kg

12,000 mcg

2 tabs of 6 mg

70 kg

14,000 mcg

1 tab of 12 mg + 1 tab of 3 mg

80 kg

16,000 mcg

2 tabs of 12 mg


Strongyloidiasis (200 mcg/kg):

15–24 kg → 1 tablet (3 mg)

25–35 kg → 2 tablets (6 mg)

36–50 kg → 3 tablets (9 mg)

51–65 kg → 4 tablets (12 mg)

≥80 kg → 200 mcg/kg, as per medical advice
 

Onchocerciasis (150 mcg/kg):

45–64 kg → 3 tablets (approximately 9 mg)

65–84 kg → 4 tablets (approximately 12 mg) 

Also see dosage recommendations from Edenbridge below.

Ref 1, 2

More on Safety of Ivermectin

Ivermectin indeed boasts an impressive safety legacy that outshines many pharmaceuticals in terms of sheer scale and duration of use. Approved for human use since the 1980s, it has been administered in over 3.7 billion doses worldwide through global health programs, primarily for parasitic infections, with an extraordinarily low rate of serious adverse events—often cited in studies as fewer than 1 in 10,000 treatments leading to notable issues, and most of those being mild and transient like dizziness or nausea.

This track record stems from its targeted mechanism: it binds selectively to glutamate-gated chloride channels in invertebrates (parasites), disrupting their nervous systems without significantly affecting mammals at approved doses, thanks to the blood-brain barrier in humans providing an extra layer of protection. Decades of post-marketing surveillance, including data from the WHO and Merck's donation program (which has gifted billions of doses since 1987), underscore its tolerability. For context, meta-analyses in journals like the American Journal of Therapeutics have highlighted its safety profile as "excellent" in on-label uses, with mortality risks from overdose or misuse being rare compared to everyday medications.

When stacked against acetaminophen (Tylenol), which causes thousands of emergency visits annually in the US alone due to liver toxicity (even at recommended doses, per CDC data), ivermectin's adverse event reporting is minimal. Over-the-counter staples like ibuprofen or aspirin carry risks of gastrointestinal bleeding affecting millions yearly, while prescription opioids or statins have far higher rates of severe side effects in pharmacovigilance databases like FAERS.

Integrating Dr. Clark's Parasite Cleanse with Ivermectin and Mebendazole

Dr. Hulda Clark's Parasite Cleanse—green black walnut hull tincture, wormwood capsules, and cloves—delivers a broad-spectrum, systemic assault on parasites (eggs to adults) via juglone, artemisinin, and eugenol, reaching hidden niches like the brain, liver, and tissues beyond ivermectin (nerve-targeting) and mebendazole (gut/microtubule-focused) drugs. This synergy mops up escapees for comprehensive eradication.

An Example of a Timing Strategy:
Take the 18-day Dr. Hulda Clark Parasite Cleanse (escalating dosage ending with 7+7 capsules and 2 tsp of tincture) After that take ivermectin/mebendazole (e.g., ivermectin 0.2-0.6 mg/kg Day 1; mebendazole 100-200 mg for 1-3 days) After the pharma phase continue the Dr. Clark once weekly dosage. Take herbs 2 hours apart from drugs to avoid interactions. Take herbs at least 13 minutes before a meal; hydrate heavily. Consult an ivermectin and herbal literate health care pro —this herbal-drug duet amplifies victory!

Sleeping During Detox and Ease Herx

To ease Herxheimer reactions and ensure restful sleep during detox (e.g., with ivermectin/mebendazole or Dr. Clark's cleanse), take Raz-Caps (1-2 capsules, 500 mg each) daily with meals—starting 3 days before and continuing throughout—to gently amplify antimicrobial action, soothe gut spasms via cramp bark, and boost circulation for smoother toxin clearance without overwhelming die-off spikes. 

For sleep, dose ornithine (2-6 capsules, 500 mg each) at bedtime nightly, ramping up as needed from detox onset; it neutralizes ammonia from dying parasites, quelling brain fog, anxiety, and insomnia for deep, restorative Z's—pair with hydration and light dinners for optimal glow!

The Jarisch-Herxheimer Reaction, often nicknamed "Herxheimer" or "Herx" in patient communities, is a transient, self-limiting inflammatory response rather than a true disease—think of it as your body's exuberant victory cheer when antimicrobial treatments like antibiotics (e.g., for syphilis or Lyme) or antiparasitics (such as ivermectin and mebendazole) rapidly slay invading pathogens. Triggered by the release of toxins, endotoxins, and debris from dying microbes (bacteria, spirochetes, parasites, or even fungi), it floods the system with cytokines, sparking a short-lived storm that signals effective therapy. First documented in the 1890s for syphilis treatment, it's now celebrated in integrative medicine as a "die-off" badge of honor, especially in chronic infections or repurposed protocols for parasites and cancer, where heavy pathogen loads amplify the effect. Take Raz-Caps and Ornithine

Ivermectin's Anticancer Arsenal: Mechanisms That Pack a Punch

At its core, ivermectin doesn't just target parasites; it unleashes a cascade of effects tailored to dismantle cancer's machinery. Drawing from extensive lab and animal studies, here's how this elegant molecule shines:

  • Proliferation Shutdown and Metastasis Blockade: Ivermectin inhibits key signaling pathways like PAK1 kinase, Wnt/β-catenin, and Akt/mTOR, starving cancer cells of growth signals and halting their spread. In breast, colon, lung, and ovarian cancers, it curbs tumor invasion and angiogenesis (new blood vessel formation), effectively choking off the fuel supply to rogue cells.

  • Programmed Cell Death Maestro: It triggers apoptosis (suicide in cancer cells), autophagy (self-devouring cleanup), and even pyroptosis (inflammatory burst that alerts the immune system). This multi-pronged death squad is particularly potent in leukemia, glioblastoma, and pancreatic cancers, where it swells and bursts malignant cells without collateral damage to healthy ones.

  • Drug Resistance Buster and Immunotherapy Booster: One of ivermectin's superpowers is resensitizing "stubborn" tumors to chemo like doxorubicin or paclitaxel, overcoming multidrug resistance via ABC transporters. It also turns "cold" tumors "hot" by flooding them with T-cells, synergizing beautifully with checkpoint inhibitors like balstilimab—early data shows enhanced efficacy in triple-negative breast cancer (TNBC).

Tested against over 28 cancer types in labs, ivermectin shines brightest in hormone-insensitive beasts like TNBC, pancreatic, and gliomas, with tumor shrinkage observed in mouse models at doses mirroring human antiparasitic levels (0.2-2 mg/kg). Its low cost (pennies per dose) and stellar safety profile—billions of human administrations with minimal side effects—make it a dream for global access, especially in resource-strapped regions.

Teaming Up with Mebendazole: A Dynamic Duo for Synergistic Slaughter

Enter mebendazole (MBZ), a benzimidazole antiparasitic cousin that's equally humble yet fierce, with a knack for microtubule disruption (think: dismantling cancer's structural skeleton) and energy pathway sabotage. Alone, MBZ starves tumors by blocking glucose uptake and induces apoptosis in brain, colon, and prostate cancers, even penetrating the blood-brain barrier for gliomas. But paired with ivermectin? It's like unleashing a tag-team takedown, leveraging complementary mechanisms for amplified impact without overlapping toxicities.

  • Synergistic Mechanisms in Action: Ivermectin's ion channel tweaks and immune ignition pair with MBZ's cytoskeletal chaos and metabolic blockade, creating a "one-two punch" that eradicates cancer stem cells (the roots of relapse), boosts immunogenic cell death, and reverses resistance. Preclinical models show this combo shrinks pancreatic, breast, and colorectal tumors faster than either alone, with enhanced ROS (oxidative stress) production that finishes off survivors.

  • Emerging Protocols and Real-World Glimpses: A groundbreaking 2024 peer-reviewed protocol in the Journal of Orthomolecular Medicine outlines ivermectin (0.5-2 mg/kg, 3x/week) + MBZ (100-200 mg/day) for advanced cancers, often with fenbendazole (a veterinary analog) for extra microtubule mayhem. Case compilations (over 200 reports from 2024-2025) highlight stage IV remissions in lung, breast, and pancreatic cases, with patients noting tumor reductions of 50%+ in months—far outpacing expectations. Integrative centers are compounding these for tailored use, blending with curcumin, CBD, and keto diets to turbocharge results.

Aspect

Ivermectin Alone

Mebendazole Alone

Ivermectin + Mebendazole

Key Targets

PAK1, ion channels, immune modulation

Microtubules, glucose metabolism

Combined: stem cells, resistance, metastasis

Cancer Types

Breast, leukemia, glioma, ovarian

Brain, colon, prostate

Pancreatic, TNBC, colorectal (enhanced)

Synergy Evidence

Resensitizes to chemo

Penetrates BBB

2-5x tumor kill rate in models

Dose Example

0.2-1 mg/kg oral

100 mg BID

As above, cycled 3-5 days/week

Safety Edge

LD50 >2,000x therapeutic

Mild GI effects

No added toxicity reported

The Road Ahead: Promise Tempered with Prudence

As of October 2025, ivermectin's anticancer star is rising with phase I/II trials underway (e.g., NCT05318469 for TNBC), but we're not at "cure-all" status yet—most data is preclinical, with human trials lagging due to funding hurdles. Critics rightly caution against hype (cancer isn't a "parasite," despite viral myths), urging evidence-based paths over self-dosing. Yet, for those facing grim prognoses, this duo's affordability and multi-billion-dose safety legacy scream "worth exploring under expert guidance."

Ivermectin and mebendazole aren't sidelined benchwarmers—they're frontline innovators, poised to humble cancer's empire. With trials accelerating, they embody science's boldest spirit: repurposing yesterday's heroes for tomorrow's victories. If you're navigating this terrain, consult an integrative oncologist; the synergy could be your secret weapon.

Effectiveness against COVID

Now, its effectiveness against COVID-19: Far from the dismissive narratives, a wealth of peer-reviewed studies and meta-analyses demonstrate ivermectin's potent antiviral prowess. In vitro, it inhibits SARS-CoV-2 replication by up to 5,000-fold at low concentrations (as shown in the Australian Monash University study, 2020), via impeding viral protein transport. Clinically, the FLCCC Alliance's protocols and reviews in journals like the Journal of Antibiotics synthesize over 100 studies involving 200,000+ patients, showing:

  • Early treatment: Reduces mortality by 60-80% and hospitalization by 50-70% when dosed at 0.2-0.6 mg/kg (e.g., Bryant et al. meta-analysis in American Journal of Therapeutics, 2021, analyzing 24 RCTs).

  • Prophylaxis: Weekly use cuts infection risk by 85% in healthcare workers (e.g., studies from India and Argentina, published in Cureus and International Journal of Infectious Diseases).

  • Late-stage: Shortens recovery time and viral clearance, with IVIEW meta-analysis (2023 update) of 93 trials confirming reduced severe outcomes, even in variants like Delta and Omicron.

Countries like Japan, India (Uttar Pradesh distributed 200 million doses), and parts of Africa integrated ivermectin into COVID strategies, correlating with plummeting case fatality rates—Uttar Pradesh saw deaths drop 95% post-rollout, per local health data, outpacing vaccine-only regions in speed and accessibility. Its anti-inflammatory bonus (modulating cytokines) adds to the cure, mirroring steroids but with fewer side effects.

Critics point to larger RCTs like TOGETHER or ACTIV-6, but these often used suboptimal dosing, late administration, or had design flaws (e.g., underpowered for subgroups), as critiqued in responses published in the BMJ. Conversely, positive outliers like the ICON study and PRINCIPLE trial subsets bolster the case. At pennies per dose, it's a democratic cure, accessible where vaccines falter in logistics or hesitancy.

In essence, ivermectin isn't just safe—it's a COVID-conquering ally, backed by Nobel roots and global evidence, proving once again why it's a healthcare hero deserving of unbridled acclaim over politicized skepticism. Lives saved in the billions for parasites; millions potentially for viruses—its story is one of suppressed splendor shining through.

Under Fauci, the U.S. medical system sidelined ivermectin to enable emergency use authorization (EUA) for the unsafe, experimental mRNA vaccines—which have killed millions and will keep causing massive pain and suffering to those who are vaccine injured. It's a criminal, murderous scheme.

Edenbridge Ivermectin Dosages

https://www.edenbridgepharma.com/Ivermectin%20PI.pdf 

I can share general, educational context on how these herbs are traditionally used, but this isn’t medical advice. For suspected infections, diagnosis and treatment should be guided by a healthcare professional and evidence-based therapies.

Overview of traditional/folk uses

  • Black walnut hull (green hull tincture)

    • Traditionally used for: intestinal worms (e.g., roundworms, pinworms), and broader “antiparasitic” cleansing.

    • Key constituents: juglone, tannins; noted for astringent and antimicrobial activity in vitro.

  • Wormwood (Artemisia absinthium or A. annua family)

    • Traditionally used for: various intestinal parasites, digestive complaints. Artemisia species (e.g., A. annua) contain artemisinin derivatives effective against malaria in drug form; however, whole-herb wormwood isn’t equivalent to artemisinin therapies.

    • Key constituents: sesquiterpene lactones (e.g., absinthin), essential oils; bitter tonics that may affect GI environment.

  • Cloves (Syzygium aromaticum)

    • Traditionally used for: antimicrobial/antifungal support and to target parasite eggs in folk protocols.

    • Key constituents: eugenol and other phenolics with antibacterial and antifungal activity in vitro.

Black walnut hull (green hull tincture), wormwood and freshly ground cloves contain juglone, absinthin and eugenol, all are compounds with known antibacterial and antifungal qualities.

Important caveats

  • Evidence gap: Robust clinical trials demonstrating efficacy of these herbs as standalone treatments for specific human parasitic infections are limited or lacking. In vitro or animal data do not automatically translate to clinical effectiveness.

  • Safety considerations:

    • Black walnut: potential GI upset, allergic reactions; avoid with nut allergies; juglone can be irritating at high doses.

    • Wormwood: certain chemotypes contain thujone; excess use may be neurotoxic; contraindicated in pregnancy, seizure disorders, and with some medications.

    • Clove oil: concentrated forms can irritate mucosa and interact with anticoagulants; high doses may affect liver enzymes.

  • Drug interactions and diagnosis: Parasitic infections vary (protozoa vs. helminths) and often require specific, prescription therapies (e.g., albendazole, praziquantel, metronidazole) with proven efficacy and dosing.




===============


Human Parasites Treated



Parasite

Condition

Notes

Onchocerca volvulus

Onchocerciasis (river blindness)

FDA-approved; kills microfilariae (immature worms) but may require repeated doses.

Strongyloides stercoralis

Strongyloidiasis (intestinal threadworm infection)

FDA-approved; single dose often sufficient.

Sarcoptes scabiei

Scabies (skin mite infestation)

Off-label oral use; topical forms also available.

Pediculus humanus capitis

Head lice

FDA-approved topical lotion.

Trichuris trichiura

Whipworm infection

Treated as part of broader worm infections.

Hookworms (Ancylostoma duodenale or Necator americanus)

Hookworm infection

Effective for intestinal stages.

Ascaris lumbricoides

Ascariasis (roundworm infection)

Off-label use.

Wuchereria bancrofti (and related)

Filariasis (lymphatic filariasis)

Off-label; often combined with other drugs.

Hookworm larvae (various species)

Cutaneous larva migrans (skin infection)

Off-label; resolves migrating larvae.

Demodex mites

Rosacea (associated with mite overgrowth)

FDA-approved topical cream targets mites contributing to inflammation.

Veterinary Uses

In animals (e.g., horses, cattle, pigs, dogs), ivermectin commonly treats gastrointestinal roundworms, heartworms (*Dirofilaria immitis*), lungworms, lice, mites, and grubs. Human use of veterinary formulations is dangerous and not recommended due to overdose risks.


For the most current or personalized advice, consult a healthcare provider, as off-label uses may vary by region and guidelines.

 


1 comment


  • Maggy

    Do you have the diabetes protocol treatment with Ivermectin and also the tumor protocol treatment with Ivermectin ? For share? Please?


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