Fenbendazole and Mebendazole are chemically distinct compounds, though both belong to the class of benzimidazole anthelmintics and share a similar mechanism of action. Here's how they differ:
1. Structural Differences
Fenbendazole: Contains a thioether group (-SCH2-), which gives it slightly different chemical properties and pharmacokinetics.
Chemical formula: C15H13N3O2S
Mebendazole: Contains a carbamate group (-O-C=O-NH-), which differentiates it from Fenbendazole.
Chemical formula: C16H13N3O3
2. Solubility
Fenbendazole is slightly more lipophilic due to the thioether group, which affects its bioavailability and distribution in tissues.
Mebendazole has a lower lipid solubility compared to Fenbendazole.
3. Pharmacokinetics
Fenbendazole: Known for a broader spectrum of activity and is metabolized into sulfoxides and sulfones, which also have anthelmintic properties.
Mebendazole: Is metabolized differently, primarily in the liver, and does not produce as many active metabolites.
4. Spectrum of Use
Both drugs are effective against a range of nematodes and some tapeworms, but Fenbendazole is often used in veterinary medicine for a wider range of parasites in animals.
Mebendazole is more commonly used in human medicine for treating helminthic infections such as pinworms, roundworms, and hookworms.
5. Safety Profile
Both drugs are generally considered safe, but their pharmacokinetics and metabolism may lead to slightly different side effect profiles, with Fenbendazole being generally preferred for long-term use in veterinary applications.
Summary
While Fenbendazole and Mebendazole are structurally related, their chemical differences (thioether vs. carbamate group) lead to distinct pharmacokinetic properties and applications in medical and veterinary contexts.
What type of parasites live in the brain? Mine seems like pork tape worm. Many of them move in up back base of neck into skull. Many move in at a time. They move fast feel small . Lots of pain in head. Had seizures years ago not anymore but those were on Zoloft . Possibly a combination of both issues the drugs and brain worms .
What’s a treatment ? Many years having this mostly annoying and painful . Feel them in ears and eyes as well .
There are Flatworms, White worms, Red worms.
There are parasite worms that travel to the head, and then there are parasites that destroy brain tissue, these are completely different things.
Ex ....
There are Flatworms, White worms, Red worms.
There are parasite worms that travel to the head, and then there are parasites that destroy brain tissue, these are completely different things.
Example1: While Treating flatworms, Clearing liver: parasite dies in hippocampus and or spinal column, while on Praziquantel. Painful and risk of death if you stop breathing. Go slow when these start to die. Dangerous. Pain Meds are required. Alinia may also be helpful. Resistant Flukes require TCBZ or Bithinol.
Example2: The pork tapeworm, Taenia solium, belongs to the cyclophyllid cestode family Taeniidae. Pork Tape worms cause of 30% of epilepsy cases, although Ascaris can also cause epilepsy events. Pork Tapeworms should be MRI confirmed, or differential nerve body control, before Praziquantel, and or during Praziquantel. Pork tape worms can cause thrashing while dying, focal nerve loss in brain, but most important signal you have these in brain, is left arm jerks, or right leg jerks, something in nerve system is different on one side of the body or field of vision changes locally. This difference is something to watch for, it indicates focal deficit or activation while treating pork tape worms, and the dose of med must be controlled to prevent extra damage. It can take 4 days for a parasite worm to die when in the brain, and antiparasitic dosing levels are high enough to kill them. Once they start dying, there is no stopping the reaction. Lower doses of vitamin D can slow the kill. Half the antiparasitic med for 4 days may help as well. Once they start dying, you have to see the kill through, do this as safely as possible.
In neurocysticercosis, since the destruction of cysts may lead to an inflammatory response, specialized treatment of active disease is required and may include long courses with high doses of praziquantel and/or albendazole, as well as supporting therapy with corticosteroids and/or anti-epileptic drugs, and possibly surgery. The dosage and the duration of treatment can vary depending on the number, size, location of the sac's or cysts, fluid edema, and the severity of symptoms.
Example3: Ascaris are dosed DEC, or Oxbendazole, or Piperazine citrate. Worm travels to fluid around right hemisphere for 1-4 days where the worm burns like it ingested jalapeno peppers. While painful, this is not very damaging to the overall cure rate of Ascaris. Dull Ache and toxins can persist. Filarial infections cause brain fog, of L3 stages of hyper infections of both white worm Ascarids, and red worms. Actual vision can be effected. Toxocara is actually one of the hardest white worms to treat, especially in the brain and head. Ascaris can cause memory loss, starting at age 8, but not debilitating until Age 50 - 65+.
Round Filarial worms are both a stage and a Disease. AS L3 they can be either white or red. (2 layer worm, or 3 layer worm) DEC mostly works on 2 layer worms. Fenben, OXFen, IVM, MOXI can work on 3 layer worms, along with Flax seed oil, Eucalyptus, and other oils.
Example4: Filarial or Strongyle penetration of vascular or brain tissue. This is a serious situation. Medications may make the situation worse, bacterial infections of a systemic nature may require doxy, or oregano oil, and or other paths to keep side effects to a minimum. One may need to relearn how to walk several times, or suffer loss of balance events that last for months. Ability to walk, strokes, and other events may make these infections difficult to manage. disorientation, head spinning, bouts of dementia are usually short. Sharp pain can occur with red worms in brain. Visual disturbance. Portal blood flow impact possible. Falling to floor when strongyles mate in brain vessels. Red worms can cause loss of balance. Seizures, Strokes possible, especially with Levamisole (Powder Camphor) at greater than 3.75mg/kg. Pyrantel, Red worms may burn when dosed with meds or Flax Seed oil, or Black Cumin Seed oil, or Thyme. Conventional red worm eggs are effected by Invermectin. Barberpoles are effected by monepantel.
Thankfully most worms avoid the brain, and it's immune reactions, but as populations increase, so does the possibility of brain involvement.
Loss of brain tissue can result over years of infection. At 4 years, many infections may allow for a complete recovery.
Beyond 4 years there may be significant impact to memory.
Some functional loss will occur to vision, thinking, coordination.
At 8 years there is permanent damage.
At 12 years there may be personality changes, especially if treatment is not undertaken.
Red worms can cause:
necrotizing microfilarial
necrotizing encephalitis
Necrotizing arterial vasculitis
Disseminated necrosis Especially Infecting the Brain, Heart, and Kidneys
I have all the symptoms you mention with the right arm shaking. I’ve been taking meds for 3 years and they seem to be never ending although there has been some improvement.
Especially most rec ....
I have all the symptoms you mention with the right arm shaking. I’ve been taking meds for 3 years and they seem to be never ending although there has been some improvement.
Especially most recently I feel by adding DEC. Mattk3 would you be able to PM with what you believe the type of worm I’m dealing with.
I see very long like 2-3 foot white worms every time I do enemas with Iodine and H202. I take albenzadole, prazi, and now DEC and pulse Fenben and Moxi.
Can you offer some advice on how much DEC to take and for how long before I kill these things for good.
A more detailed history and or symptoms, more detailed treatment formulas and dosing schedule undertaken is required to offer an opinion.
Without test results that indicate a specific species, ....
A more detailed history and or symptoms, more detailed treatment formulas and dosing schedule undertaken is required to offer an opinion.
Without test results that indicate a specific species, dosing may not be warranted. What is the justification?
It is hard to say what species you have in your brain. It is more common to have some small filarial stage of a species wonder around, without a particular brain infection, but head infection, sinus, eyes, ears, skull bone, teeth, throat, mouth. Most of these symptoms, or worm appearance only occur with med dosing routines. It is also possible for small blood borne stages to release enzymes that can cause brain dysfunction during their multiplication process. Symptoms can be suppressed using a stasis formula, where symptoms become more describable and discernible.
Detailed symptoms or side effects journal is required to even venture a guess. Seldom is a brain infection diagnosed, even with MRI data.
You have listed Flatworm meds, White worm meds, and red worm meds. This could be a complicated infection, or just a list of meds you have tried.
Brain infections can be flat, white, or red worms. While there are many possible species, the most common are Ascaris, or filarial stages that fog the mind. One in the group indicated Cysticercosis. Several have toxocara. Hyper strongyloides may also show up as a side infection in brain tissues. Blood flukes have been indicated in several persons.
Most longer worms are either ropeworms or tapeworms.
I would approach brain infections with scan of flatworm meds ALB, Alinia, Prazi, D3, Calcium, TCBZ, Castor oil, peppermint oil, etc. DEC would break most white worm population infections at the filarial stage. Fenben, Moxi, Pumpkin seed oil, Flax seed oil, thymol, pine needle oil, Levamisole are red worm meds for tougher species. Fenben and IVM are also used commonly in brainfog infections. Finally scan of higher doses of Mebendazole formulas. Most scan criteria are short duration of say 3 days of nominal dose levels, searching for a reaction or change. Longer than 3 days could actually kill something, which could be dangerous in brain infection situations. Getting an idea of what meds you react to could help identify potential species of infection. Slowly work into a progression of single med tests to formulas, to be a cautious as possible. Then one goes from nominal doses to higher dose patterns, to eliminate the med from potential candidates list. I would initially avoid Piperazine, OXFen and OXBen, since attacking adults is seldom a good initial idea. Doing a challenge test to identify meds that cause a reaction can be a tricky process that required knowledge of safe dosing levels and duration's. This is also known as black box testing.
The risk of progression of tests must be offset by a poor health situation. Why do this dosing unless your health, life, or situation is at risk.
There are doctors that use Dr Clark's scan method. I perceive the resolution of this technique is low. Generally these doctors also scan common meds. In certain people this approach is insufficient.
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So slow ramp to 200mg per day of DEC is a precautionary move, in your situation. Low dose carbon and bicarbonate. In my situation I had a hyper Ascaris infection that required a higher dose of DEC, but this subject is to complex to describe here.
Most people with complicated infections start and stop meds, do not zero in on specific species, or the drain on the health or immune system become to much.
It takes a lot of focus to set the most probable dose and duration for a particular infection. Identifying infections is difficult at best.
I suspect you could test low for B12, indicating a Tapeworm infection. Coconut oil may also be helpful for keytones.
Remember, catch one worm in a family, you can catch them all. Low immune with flat worms makes you susceptible to catching more and more species in the family. The sooner you clear tapeworms, the sooner you can get to the flukes.
In my infection, I was able to identify several formulas for flat worms, white worms, and finally red worms. There were hundreds of formula attempts, but ultimately only 7 flatworm formulas, 2 or 3 white worm formulas, and a few red worm formulas. The group has made attempts at Asian flukes, and Toxocara. European Flukes seam to be a new focus.
My approach was to clear flat worms first, White worms second, and Red worms third.
It took 4 tries to get flat worms. It took 2 years to clear Ascaris. I will probably never cure the red worm strongyles.
Along the way there were many lesser species that were cleared. It can be hard to distinguish between stages and or species.
That is why formulas for you are determined by getting a foot hold of basic meds, and then scanning each med for the family one at a time.
In the case of an Ascaris infection, the formula is quite complex.
The full approach uses Ph. Monitoring, Hair analysis for essential minerals and metals, and a good knowledge of metals, ions, nitrogen vs sulfur, etc.
I also discovered my stasis formula, which holds the infection under control, by taking a combination of white and red worm meds, while clearing the flat worm infection.
Taking the time to develop a stasis formula can be worth the time. This simultaneous medication, in a low dose, continuously can help break the enzyme control a species has on the body.
I failed clearing the flat worm infection a few times. Finally I won. Ultimately I used a combination of Prazi and Levamisole to clear what I believe was a final gigantic fluke infection.
Flats never returned. It was quite a battle.
Then I had an Elisa test for Ascaris. More than a battle, more like a war. I knew I had an infection with the test result, so my fighting the infection was justified.
There is a lot of education required. There is risk management. Finally there is safety issues with long term situations.
Most infections are curable. For the few management is possible. For a couple, the infections are stronger than the meds.
Thank you for such a detailed and informative summary. I can now at least reference this in the future. I’ve had all three white, tapeworm and red worms. I’ve tested different combos of meds and n ....
Thank you for such a detailed and informative summary. I can now at least reference this in the future. I've had all three white, Tapeworm and red worms. I've tested different combos of meds and naturals. I started ICU's Albenzadole & Prazi about 5 months ago and that's when I finally started to notice marked improvement.
Since I've done 4 rounds of this protocol with about 3-5 days off. I'm sure I had a massive Tapeworm and would feel very slow movement from head to toe even when the fast movement of what I'm guessing are ascarias would stop. Everything amplified around 2 and 3 am. The big Tapeworm would vibrate on the way down to my stomach and would wake me up every night. I would take benonite clay at around 5am and that's when I think I would trap some segments and felt massive pain before releasing around 30 to 50 segments with my morning garlic and h202 enemas.
Every time I would include a prazi treatment this would happen. I would feel like something in my head would tighten around the scalp and then release. Terrifying.
I've had 4 parasite tests with lab come back negative. Seem a gastrointernalist who said I was clean as a whistle. So they either hide out or I'm crazy. Yet still I feel them move around. Right now I believe I'm fighting mostly a really bad scattered roundworm and ropeworm infection. The roundworm use to come out like a garden snake almost as thick as a finger and as long as a ruler and a half. I took videos and pictures of everything. Currently, I get either one or two really long white worms every morning with enemas or clumps of tangled white worms. I also released tons of flukes on the prazi alben protocols but don't see them as much anymore.
I actually got my hands on some DEC from reading one of your articles. And that's been for about a month and what I think may have helped me turn the corner. I could feel them literally disintegrate in my head and travel down behind my ear like liquid. I might have overdosed because my head felt hot and my chest seemed to be insanely itchy maybe just a mild allergic reaction. It went away after two days.
My current treatment is alternating day of one DEC 100mg tab with one Alben 200mg and alternate day of Fenben until new DEC package arrives next week and I'll go back to 400mg for 3 days and break for 3 days till this infestation clears up.
DEC in some more regular dosing should suppress White worm birthing cycles.
Flat worms must be eliminated before attempting White worm controls.
I suspect larger migration to head is not flat wo ....
DEC in some more regular dosing should suppress White worm birthing cycles.
Flat worms must be eliminated before attempting White worm controls.
I suspect larger migration to head is not flat worm, but white worm.
Itching could be release of strongyloides, or birthing of other species. Difficult to know which med controls, or what the response to this signal is saying.
Complicated infection is a Maze.
The sequence of elimination removes the toxins parasites produce.
Flat worms must be eliminated first to save liver.
Kidneys are saved by limiting the albendazole dose.
Magnesium and potassium keeps you alive, small doses.
I concentrated on the citric cycle, so Magnesium citrate and potassium citrate.
Later on as parasites are eliminated, I focus on Orange Juice and Cranberry Juice.
I suspect you are underdosing flatworm meds, but that is fine in search for your stasis formula.
Identifying challenge meds that have effect is proper thing to be doing now.
Keep a journal.
Grow your network.
Keep your Ph up to 7
Hair analysis every 6 months to a year, to get balance in minerals and metals.
Detox MSM, Cabbage, Melon, Cucumber, distilled water.
Take some small carbon, bicarbon,
We will work on lipids, oils, etc.
l carnitine to detox cells.
bioflavonoids to activate Good Vitamins A, C, B
Black pepper as much as possible, early.
Pinches Sea Salt is better.
Limit meat dose to 4 ounces per meal.
Nuts, seeds, raisins, etc are good.
Veggies, Potatoes, white rice
I do a lot of chicken, some well done bacon.
Now that my flat worms are gone, I do tuna precooked.
Thanks Matt! I’m alternating meds and combos on different days. They all work, but nothing that I can really pinpoint that would eliminate them completely. These parasites seem to get resistant wh ....
Thanks Matt! I'm alternating meds and combos on different days. They all work, but nothing that I can really pinpoint that would eliminate them completely. These parasites seem to get resistant when I maintain the same protocol for more than a few days and when I switch things up I get a bigger kill.
Yesterday I took a dose of Moxi with yoghurt and a clove oil bath last night. This morning I took nothing other than a glass of water with MSM and had my regular h202 enema with iodine.
I had a rather large kill and included pic. Been getting these everyday for 3 years. Today more than usual. No idea. I have supplementing with magnesium at night in a glass of water and usually take an evening bath in some type of essential oil. Any idea what I'm dealing with here?
50% of the time they are cleared with naturals or white worm meds.
They indicate GI/systemic/lymph sludge/mucus
They also can exist with parasitic infections.
I suggest a pinch of Magnesium sulfate in glass of distilled water per day.
Carbon oils could be helpful. C2, C4, C8, C10, C12, C52 (Castor, Butter/Buttermilk, MCT, capric acid, lauric acid
You could be out of balance, essential minerals and metals are discovered through hair analysis.
What is your sublingual Ph. ?
Like peeling an onion, once the first layer of infections are cleared, their could be layers beneath.
I also would try castor oil 2 caps AM/PM and Peppermint oil 4 caps per day.
I would avoid anti-parasitics till ropeworms cleared, you could stir up something. Low dose at best, Single round of Pyrantel if parasite is in GI, Praziquantel if Tapeworms present in GI.
Later, when you clear ropeworms, you can try challenge tests again.
What a relief to finally have some kind of answer as to what these invaders are.
Thank you. Oddly enough I think I might have cleared up any parasitic infection I had prior and dealing with th ....
What a relief to finally have some kind of answer as to what these invaders are.
Thank you. Oddly enough I think I might have cleared up any parasitic infection I had prior and dealing with these the most as of late.
I've cut down on the anti meds and have been doing the essential oil route for about 2 months.
Alternating between Mhyrr oil, neem oil, clove baths, and eucalyptus enema. I've just received a shipment of albenzadole and DEC and will take low dose. They seem to work better with low dose anyway.
What do you suppose the length of time it will take to clear these they've been such a nuisance for so long. Thankful they aren't contagious or anything.
I haven't done a hair analysis but I take MSM, probiotic prebiotic and supplement with DE every now and then.
Thank you for your time and explanation, I'll look into the minerals and supplements you've listed here.
Some newer images.
I keep finding these sorta anxhor shaped things. And also stool, this was second time i passed something white. D2cid3d to pick ip up with ziploc.
https://ibb.co/n8F2X59
....
Fresh passed worms make for some nice pictures sometimes, but once dry, it is hard to know if it was a parasite.
All your going to see is large worms which are the minority ----most all worms a ....
Fresh passed worms make for some nice pictures sometimes, but once dry, it is hard to know if it was a parasite.
All your going to see is large worms which are the minority ----most all worms are too small to see with your eyes. The water that comes out while Liver Flushing can be loaded with worms and endless eggs.
The most common worms that can be see are liver and sheep flukes---everyone passes them when Liver Flushing properly.
What you can see, is literally the tiny tip of the iceberg.
WHAT people can not tolerate is when worms crawl out their skin from your forehead to your toes----when they see this, they go paranoid --so those types of herbs/etc., are never ever sold. Such worms have been removed with various creams that smother them--but what you can see, if not the majority, the majority you can never see with your eyes.
Removing worms and preventing worms is achieved with herbs that feed the blood and the blood does all the work.
PREVENTION and making your blood healthier is your solution....herbal use can be very simple. YOU WILL NEVER BE WORM-FREE
So I tried to kill my flukes with Triclabendazole and Praziquantel. Each time I got a bunch out, but then the effectiveness stopped. I took very high doses trying to kill them, but my flukes seemed resistant. I have a systemic issue.
I started taking Myrrh essential oil. I'm seeing new stuff that I never saw before. First of all, I'm getting tons of tiny sesame type tapeworm. But I'm also getting large hard chunks, like a shell of some sort. Perhaps it is the eggs. Perhaps it is pieces of the tegument. It is hard, like plastic. Some chunks are about 1 inch long and flat. So I assume that is the tegumentul layer. But I'm getting a ton of junk out.
I take the pure essential oil, 1 teaspoon at a time in this way. First I warm up one tablespoon of honey in the microwave for maybe 10 seconds just to reduce viscosity (make it thinner). Then I add 1 teaspoon of the oil and stir. Then I simply down it.
Myrrh doesn't taste great, but it doesn't taste awful. I could imagine it would even be pleasant in a tiny amount added to something like spiced apple cider. It has a warm earthy flavor. But naturally taking it in that concentration isn't going to be exactly pleasant, but it didn't make me want to gag.
It seems to act systemically as I feel the trematodes all over my body (even subcutaneous) moving when I take it. Though I doubt the dose I'm currently taking is strong enough to kill those in my extremities. I figure first I'll try to kill those in my liver and intestines.
I am also rubbing the oil on my arms to see if absorption through the skin will hit those in my extremities. Again, I feel them moving, but I don't know that they are dying yet. It may take a while at that reduced exposure. I'll provide an update later.
For dosage reference, I am 210 lbs. The maximum recommended that I've seen is 2 - 4 grams. I've seen other recommendations that relate to mg/kg of your body weight. I believe 1 teaspoon is around 4.5 grams. The reports I've seen say that it can speed up the heart rate and irritate the kidney over 2 - 4 grams. I've also seen reports saying it has no known toxicities. So there is a bit of conflict of information. It could be that some reports consider elevated heart rate and kidney irritation to be a side effect, not an actual toxicity. I'm not sure. So do your own research on this.
I understand that the Myrrh resin is about 6% essential oil, so obviously the dose difference between the resin and the oil would be significant. Be sure if you look this up that you know which one you want information on. I'm using the essential oil.
The only side effects I've personally noticed is that I feel kinda "wired" after taking it for a few hours, then I get really sleepy. So I avoid taking it right at bed and instead eat my main meal at around 3 in the afternoon and take a dose of this around 8 or 9.
If you want to know if your trematode infection is systemic, boy, this is a sure way to tell. It really does make them twitch all over your body.
I would say it’s toxicity from taking the meds at too high a dose, causing your body to spasm, not worms. You can’t feel worms. I’m guessing if you try to kill them the pharmaceutical cartel’s way ....
I would say it's toxicity from taking the meds at too high a dose, causing your body to spasm, not worms. You can't feel worms. I'm guessing if you try to kill them the pharmaceutical cartel's way, and take a high enough dose to actually kill them all that way, it'll kill you too. And a repost of some past advice.
"There's lots of advice here about parasite killing. Avoid any of the drug crap though, it might 'cure' them temporarily but they just reinfect you immediately.
And now you are trying to heal from the damage done by the drugs on top of trying to fight off the parasites, to say nothing of the very deliberately added toxicity..
My advice?
I'd use Dr. Clark's herbs and the zapper she recommends. It kills ANY WORM TYPE parasite, period. It isn't even the frequency, it's the shape of the electrical wave. Someone said it was like sawing them into pieces.
Not a very survivable thing, and mutating??? Hardly. It take quite a mutation to not get sawed up--think about it, what would your body need to mutate to do that?
It'd take thousand of years. But any parasites who are exposed to the current are killed, so none survive TO mutate. The ones who survive are buried deep enough the current doesn't reach them, so they aren't surviving the current, just too deep to reach.
So don't let all the doom/gloom fear mongers trick you into worrying about. The same with the herbs.
Dr. Clark's herbs (the only ones I bother with) have killed the worms for millennia--why would the worms mutate now? I of course have my theories, if so, but I think those herbs are like the zapper current. It's like ripping every kind of worm apart, not just killing them, a tough thing to survive. It's not called Wormwood for no reason.
Both are necessary because the toxicity of the world (and the drugs) today is so weakening our immune systems, the worms just eat their way out extremely easily.
And the herbs are only effective in the digestive tract, maybe a bit outside, but not much. But the zapper can't reach into the deep bowls sometimes, so herbs are necessary for those."
Actually I’ve done Hulda Clark’s protocol and it doesn’t kill ANY type of worm or I’d be cured as I doubled her rate. And I know the different between a muscle moving and a trematode moving from o ....
Actually I've done Hulda Clark 's protocol and it doesn't kill ANY type of worm or I'd be cured as I doubled her rate. And I know the different between a muscle moving and a trematode moving from one location to another. Really. (rolling eyes) Could you be more arrogant?
I’m guessing you don’t use a zapper, or aren’t doing it right. Way too many ’people’ here give this kind of false advice to drive the real folks away from using what does actually work.
It’s w ....
I'm guessing you don't use a zapper, or aren't doing it right. Way too many 'people' here give this kind of false advice to drive the real folks away from using what does actually work.
It's worked splendidly for me for 15 or so years. I've gotten rid of diabetes AND cancer and a very painful hiatal hernia. Read her book, 'cure for all diseases' and do her protocol RIGHT.
So how did you zap? And are you blaming ' parasites for the 'wiggling sensations that are in fact your body spasming from toxicity?
Neither zapping nor her protocol kill the large parasites that I have. Neither did 2 times her heavy protocol. Neither did one bottle of barefoots dewormer a day. I’ve tried it all. I have very la ....
Neither zapping nor her protocol kill the large parasites that I have. Neither did 2 times her heavy protocol. Neither did one bottle of barefoots dewormer a day. I've tried it all. I have very large trematodes that are 2 - 3 inches in length and I can clearly feel them moving under my skin as they are subcutaneous. I can feel them slowly crawling up my leg or around my leg. In fact, the habitually travel from my waist up to my shoulder. No, I'm not confusing them with muscle twitching. You must not have ever have had large parasites under your skin or you would know it isn't something you can "mistake." They have painful suckers that attach and detach.
HOW DID YOU ZAP? I’m quite sure the fault lies with you and your application, not the zapper, other than that one with pennies on it. It could very well miss places as it’s field is very localized ....
HOW DID YOU ZAP? I'm quite sure the fault lies with you and your application, not the zapper, other than that one with pennies on it. It could very well miss places as it's field is very localized. You'd have to move it probably ten times over and over again.
And nope, you don't feel worms--it's a survival mechanism to remain unfelt. They know they'll be killed, because most worms back in the day were not able to get out of the digestive tract, so could be killed by herbs. They don't mutate that far in less than a hundred years. I have never felt even the slightest movement that wasn't toxicity-based. Your body wants you to know you're poisoning yourself, so you'll stop. If you had some of those exotic parasites, ones maybe that get in thru sores, but there are none here in America.
How do you know it's parasites anyway? Other than spasming? Or are you just going along with all the other scammers claiming that? And where in heck would you have gotten them?? From travel magazine description? Good thing they described the 'symptoms.
Is this how you typically respond to a person who lists a remedy that is effective to them? By telling them that the remedy isn’t really effective and that the only effective remedy is the one tha ....
Is this how you typically respond to a person who lists a remedy that is effective to them? By telling them that the remedy isn't really effective and that the only effective remedy is the one that you found effective? So eventually, if we all listen to you, we will all be doing the exact same thing? Is that what you are hoping to achieve?
That is so funny. I bow to your greatness. You know exactly the RIGHT way to do things and anyone else who doesn't achieve success in your methods must be doing it WRONG.
I'm not even going to respond anymore. The arrogance is just overwhelming.
Right. And I know that way may help but not for the problem you say you have. If indeed your ’parasite’ is in your leg, NOTHING but a zapper kills it. So HOW DO YOU ZAP??
And there’s the freew ....
Right. And I know that way may help but not for the problem you say you have. If indeed your 'parasite' is in your leg, NOTHING but a zapper kills it. So HOW DO YOU ZAP??
And there's the freeway, or some fiddle fuddle series of back roads, that will hopefully get you there, although such roads are often closed or shut down.
I know the freeway route---you can't fathom how there might be an easiest way to heal. And my certainty of that makes me arrogant? No, just not gullible. And why are you still so 'infested' after trying all these other fiddle fuddle methods? And mine such a waste of time, but yet I'm well??
There's an easiest way to do everything, even heal, which of course cuts into the pharmaceutical cartel's profit margins severely. Gee, can't imagine why any one here on CureZone would want to encourage the fiddle-fuddle methods, can you?
Do you want to suffer for a long time?? Or want others to suffer that way (since I suspect the only suffering you have is to your ego) but travel magazines are good sources of strange health issues, eh?
Yeah---after all that work, and someone doesn't believe you. Of course you're not going to talk to me any more--it's what they all do; get 'offended' and ignore me.
That user is not worth bothering with. His paranoia knows no bounds. According to him I would be front he government because I don’t believe zapper can cure everyone. It’s really simple if peke ar ....
That user is not worth bothering with. His paranoia knows no bounds. According to him I would be front he government because I don't believe zapper can cure everyone. It's really simple if peke are passing big parasites with zappers let's see it.
It's interesting how this persons cure all doesn't have anyone coming out to agree with him besides parazapper, but he hasn't either claimed that they kill the big parasites.
Also to point out logically how stupid the pharmaceutical Conspiracy is that we can get some parasite drugs online for very little money, sometimes even cheaper than a zapper so I wonder who's the one financially interested here.
I'm all for new ideas but won't bother with people who act like asshats. Let's see the people on cure zone who have been cured by zappers if not then stop thinking everyone's cure or even type of parasites they have are the same. Hula Clark was a pioneer but she isn't from the current generation. Even some big holistic doctors like Simon Yu use real medications for parasites and I'm sure he has more medical qualifications than some random person on curezone.
This may be a strange take, but after months of reading its posts, I’m convinced it is exactly what it rants against. I believe its sole purpose on CZ is to discredit CZ and its users. It is try ....
This may be a strange take, but after months of reading its posts, I'm convinced it is exactly what it rants against. I believe its sole purpose on CZ is to discredit CZ and its users. It is trying to make a mockery of CZ. It may very well be one of those "pharma Conspiracy elites" in disguise its always rambling on about. No one else brings up the subject but it. Sort of like the pot calling the kettle black. The pot isn't just like the kettle in this case... The pot IS the kettle. It doesn't like curezone and is trying to take it down. This is the most logical conclusion I can come up with.
It has obviously never experienced parasites because it never has experienced any of the symptoms the rest of us have and is often telling people they are making a big deal out of nothing and that other posters don't really have parasites. Even when they are providing photographic proof!
To quote old Willy, 'Methinks the lady doth protest too much'... If you look at it from that perspective and then go back and read some of its posts it starts to seem all too likely that its intentions are not good at all. It is evil and devisive. It serves no purpose other than to divide and discredit. The ultimate troll. Ignore all of its posts. Stop referring to it as if its a person. It has no humanity.
Treatment of human pulmonary paragonimiasis with triclabendazole:
Triclabendazole can be recommended as an alternative drug of choice for the treatment of pulmonary paragonimiasis; it is as effective as praziquantel in clearing infections and better tolerated.
[Fascioliasis (treatment)]1—Triclabendazole is used as a primary agent in the treatment of fascioliasis caused by Fasciola hepatica (sheep liver fluke) and Fasciola gigantica (giant liver fluke)
Not commercially available in the U.S.
†Not commercially available in Canada
Paragonimiasis (treatment)]1—Triclabendazole is used as an alternative agent in the treatment of paragonimiasis caused by Paragonimus westermani (lung fluke)
Triclabendazole has shown no activity against nematodes. It differs from the other benzimidazole anthelmintics (e.g., albendazole, mebendazole) currently used in humans since these compounds have selective activity against nematodes and have no significant activity against flukes and other trematode helminths
Yes Prazi is known to not cure Fascioloasis ( F. hepatica and F. Gigantica).
”Triclabendazole, a benzimidazole, is now the drug of choice as a single 10mg/kg oral dose or two doses 12 hours apa ....
Yes Prazi is known to not cure Fascioloasis ( F. hepatica and F. Gigantica).
"Triclabendazole, a benzimidazole, is now the drug of choice as a single 10mg/kg oral dose or two doses 12 hours apart." Source "Tropical Infectious Diseases", Guerrant, Walker and Weller, second edition
I am looking for triclabendazole (most commonly under the trade name Egaten) to be most effective on liver flukes. Egypt is one of the countries where human use is approved. I want to ask, will th ....
I am looking for triclabendazole (most commonly under the trade name Egaten) to be most effective on liver flukes. Egypt is one of the countries where human use is approved. I want to ask, will they sell me Egaten in a pharmacy in Egypt without a prescription? Thank you
What Kind of Cancer Can Fenbendazole Be Used For ?
Fenbendazole (brand names Panacur C ®, Safe-Guard ®) is a veterinary medication introduced in 1974.
Worldwide, veterinarians commonly use fenbendazole, FBZ, to treat a variety of parasites in animals, such as tapeworms, hookworms, roundworms, lungworms, and whipworms.
Fenbendazole has been known to have a high safety margin for animal use as it is tolerated well, has low side effects, and has a low degree of toxicity.
Following anecdotal fenbendazole cancer success stories, researchers have been experimenting with the “repurposed” use of Fenbendazole for cancer – for animals and humans.
Drug “repurposing” is a new use for a medicine that is different from the original medical indication. Though the Fenbendazole studies are limited, what researchers have found so far is promising for patients with cancer.
Fenbendazole for Pancreatic Cancer
Despite the initial effectiveness of certain chemotherapies, pancreatic tumors frequently develop resistance to these treatments. Moreover, newer methods like immunotherapy have struggled to address this challenging disease effectively. All of which has led researchers to turn their attention to Fenbendazole as a possible treatment. And while there is a great need for further studies, early evidence is showing great promise.
The cancer cells in pancreatic cancer behave in a very specific way when it comes to getting energy and nutrients for their growth. They use special ways to process glucose, amino acids, and lipids, which helps them grow and spread quickly. Scientists believe that the key to using fenbendazole effectively in treating pancreatic cancer lies in figuring out how the drug targets the behavior of these cancer cells.
Fenbendazole for Breast Cancer
One study published in March 2023 investigated Fenbendazole’s ability to treat Breast Cancer while preserving healthy breast cells. This research tested the drug on three cell types: normal, low metastatic cancer, and highly metastatic cancer cells. The findings revealed that Fenbendazole induced significant stress in the highly metastatic cancer cells compared to the others. This suggests Fenbendazole could offer a new, targeted treatment for advanced breast cancer
Fenbendazole for Colorectal Cancer
Colorectal cancer occurs when cells in the colon or rectum grow out of control. Treatment typically involves a combination of surgery, chemotherapy, and radiation therapy. There have been a few very promising studies that looked at how these cells responded to fenbendazole.
Tests showed that fenbendazole not only caused cell death in the cancer cells but also stopped them from growing by blocking a specific stage of their growth cycle.
They also found that the resistant cancer cells behaved differently compared to normal cancer cells. They didn’t respond as much to a natural process called autophagy, but they were more sensitive to another process called ferroptosis, which involves cell death due to iron overload.
This suggests that fenbendazole could be a promising treatment for cancers that are resistant to 5-fluorouracil, a type of chemotherapy medicine that is often used to treat colorectal cancer
Fenbendazole for Lung Cancer
Perhaps the most well-known case of someone treating their cancer with Fenbendazole is a man named Joe Tippens was diagnosed with lung cancer in 2017 and given only a few months to live.
Tippens developed a protocol combining Fenbendazole with CBD oil, curcumin, and Vitamin E which proved successful for his case. He remains cancer-free today and his story has sparked interest in pursuing more in-depth trials of Fenben as a repurposed drug.
In principle, a molecule can act as an antiviral drug if it “inhibits some stage of the virus replication cycle, without being too toxic to the body’s cells.” [20]
The possible modes of action of antiviral agents would include the following:
(1)
Inactivate extracellular virus particles.
(2)
Prevent viral attachment and/or entry.
(3)
Prevent replication of the viral genome.
(4)
Prevent synthesis of specific viral protein(s).
(5)
Prevent assembly or release of new infectious virions.
The role of ivermectin against the SARS-CoV-2 virus
The targets of activity of ivermectin can be divided into the following four groups:
A. Direct action on SARS-CoV-2
Level 1: Action on SARS-CoV-2 cell entry.
Level 2: Action on importin (IMP) superfamily.
Level 3: Action as an ionophore.
B. Action on host targets important for viral replication
Level 4: Action as an antiviral.
Level 5: Action on viral replication and assembly.
Level 6: Action on posttranslational processing of viral polyproteins.
Level 7: Action on karyopherin (KPNA/KPNB) receptors.
C. Action on host targets important for inflammation
Level 8: Action on interferon (INF) levels.
Level 9: Action on Toll-like receptors (TLRs).
Level 10: Action on nuclear factor-κB (NF-κB) pathway.
Level 11: Action on the JAK-STAT pathway, PAI-1, that could be involved with COVID-19 sequalae.
Level 12: Action on P21 activated kinase 1 (PAK1).
Level 13: Action on interleukin-6 (IL-6) levels.
Level 14: Action on allosteric modulation of P2X4 receptor.
Level 15: Action on high mobility group box 1 (HMGB1).
Level 16: Action as an immunomodulator on lung tissue and olfaction.
Level 17: Action as an anti-inflammatory.
D. Action on other host targets
Level 18: Action on plasmin and annexin A2.
Level 19: Action on CD 147 on the red blood cell (RBC).
Level 20: Action on mitochondrial ATP under hypoxia on cardiac function.
The direct “antiviral targets” may be useful in the early stages while the anti-inflammatory targets might be addressed in the later stages of the disease.
Abstract
Considering the urgency of the ongoing COVID-19 pandemic, detection of new mutant strains and potential re-emergence of novel coronaviruses, repurposing of drugs such as ivermectin could be worthy of attention. This review article aims to discuss the probable mechanisms of action of ivermectin against SARS-CoV-2 by summarizing the available literature over the years. A schematic of the key cellular and biomolecular interactions between ivermectin, host cell, and SARS-CoV-2 in COVID-19 pathogenesis and prevention of complications has been proposed.
Introduction
A relatively recent surge in zoonotic diseases has been noted over the past few decades. Several reasons could be responsible for this “spill-over” of disease-causing agents from animals to humans. These include an exponential rise in the global population causing man to encroach new ecological habitats in search of space, food, and resources as well as improved opportunities for rampant wildlife trade causing interspecies pathogen jumps. The 1980s was known for HIV/AIDS crisis that originated from the great apes, while the avian flu pandemic in 2004–07 came from the birds. The pigs led to the swine flu pandemic in 2009 and bats were the original hosts of Ebola, severe acute respiratory syndrome (SARS), Middle Eastern respiratory syndrome, and probably SARS coronavirus 2 (SARS-CoV-2) outbreak as well.
COVID-19 has already caused millions of deaths worldwide and has paralyzed not only the world’s healthcare system but also the political and economic relations between countries [1]. The fact that the SARS-CoV-2 virus has been thought to have originated from wildlife and may have “jumped” into humans, not only highlights future risks from animal-borne diseases but also provides an important clue to its resolution. In such a scenario, where this “jump” has been made from animal to human, it seems only logical to review a drug that has worked efficiently against a disease-causing agent and is available in a form that is safe for human consumption since the early 1980s.
Ivermectin belongs to a group of avermectins, which is a group of 16 membered macrocyclic lactone compounds discovered at the Japanese Kitasato Institute in 1967 during actinomycetes cultures with Streptomyces avermitilis [2]. This drug radically lowered the incidence of river blindness and lymphatic filariasis and was discovered and developed by William C. Campbell and Satoshi Ōmura for which they received the Nobel Prize in Physiology or Medicine in 2015 [3, 4]. Ivermectin is enlisted in the World Health Organization’s Model List of Essential Medicines [5].
Drug repurposing, drug redirecting, or drug reprofiling is defined as the identification of novel uses for existing drugs. The development risks, costs as well as safety-related failure, are reduced with this approach since these drugs have a well-established formulation development, in vitro and in vivo screening, as well as pharmacokinetic and pharmacodynamic profiles. Moreover, the first clinical trial phases of many such drugs have been completed and can be bypassed to reduce several years of development. Therefore, drug repurposing has the potential to reduce the time frame for the whole process by up to 3–12 years and carries great potential [6].
Although several drugs received emergency use authorization for COVID-19 treatment with unsatisfactory supportive data, ivermectin, on the other hand, has been sidelined. Nevertheless, many countries adopted ivermectin as one of the first-line treatment options for COVID-19.
With the ongoing vaccine roll-out programs in full swing across the globe, the longevity of the immunity offered by these vaccines or their role in offering protection against new mutant strains is still a matter of debate. Thus, the search for new, effective antivirals continues.
Several doctor-initiated clinical trial protocols that aimed to evaluate outcomes, such as reduction in mortality figures, shortened length of intensive care unit stay and/or hospital stay, and elimination of the virus with ivermectin use have been registered at the US ClinicalTrials.gov [7]. Controlled clinical trials using ivermectin are underway, including one being conducted by the National Institutes of Health (ACTIV-6) [ClinicalTrials.gov Identifier: NCT04885530] in the USA and a second in the UK (PRINCIPLE) [ISRCTN registry: ISRCTN86534580] [8, 9].
Ivermectin has rapid oral absorption, high liposolubility, is widely distributed in the body, metabolized in the liver (cytochrome P450 system), and excreted almost exclusively in feces [4]. Following a standard oral dose in healthy humans, it reaches peak plasma levels at 3.4–5 h, and plasma half-life has been reported to be 12–66 h [10]. Despite its widespread use, there are relatively few studies on the pharmacokinetics of ivermectin in humans [11]. Ivermectin binds strongly to plasma proteins in healthy subjects (93.2%) [12]. Such an “avid binding” can be beneficial when administered in countries where malnutrition and hypoalbuminemia are common, leading to increased availability of “free fraction” of ivermectin [4]. Hypoalbuminemia is a frequent finding in patients with COVID‐19 and it also appears to be linked to the severity of lung injury [13]. Therefore, ivermectin could have sufficient bioavailability when used in such a setting.
This article aims to discuss the probable mechanisms of action by summarizing the in vitro and in vivo evidence demonstrating the role of ivermectin in COVID-19 based on the available literature over the years (Table 1). A schematic of the key cellular and biomolecular interactions between ivermectin, host cell, and SARS-CoV-2 in COVID-19 pathogenesis and prevention of complications has been proposed (Fig. 1).
In this candid video, I share my personal journey exploring an unconventional cancer treatment - Joe Tippens' fenbendazole protocol. During the process of being diagnosed with stage 4 pancreatic cancer but before formal diagnosis, I uncovered Joe's remarkable story of putting his late-stage small cell lung cancer into remission using fenbendazole, a common deworming medication for animals.
Inspired by his case, I decided to try incorporating fenbendazole into my treatment plan alongside other supplements like curcumin and CBD oil, just as Joe had done according to the protocol he published in 2022. However, my results were mixed - while what were potentially lung tumors seemed to respond, I soon developed aggressive new liver metastases.
In this first video of a series, I provide all the details on Joe's original protocol components, how I implemented it personally, the positives and negatives I experienced, and my overall thoughts on fenbendazole's potential role in a comprehensive metabolic approach.
Whether you're exploring all options as a cancer patient/caregiver or just interested in Joe's viral story, this video is my transparent first-hand account. The next video will dive deeper into the Science behind fenbendazole, exploring the potential anti-cancer mechanisms and research behind this dewormer drug.
Transcript:
0:02
two years ago I was diagnosed with stage
0:05
four inoperable pancreatic cancer
0:07
against the odds I'm still here in those
0:09
dark days I searched for Survivor
0:11
stories and came across Joe tippens a
0:14
stage four lung cancer patient who
0:16
incredibly sent his disease into
0:17
remission using an unconventional
0:19
protocol involving a dog dewormer drug as
0:22
many comments suggest I try Fenbendasol
0:24
over three videos I'll share why
0:27
Joe inspires me my reasons for trying
0:30
and my reasons for stopping
0:32
Fenbendasol after being diagnosed with stage
0:35
three small cell lung cancer which had
0:37
widely metastases to 40 or 50 locations
0:40
following standard treatments Joe
0:42
tippens was given just months to live in
0:44
January
0:45
2017 the hedge fund private Equity CEO
0:48
did the same thing I did he started
0:50
relentlessly researching how he could
0:53
turn this around the 59-year-old who
0:56
strongly believes in the power of
0:57
positive thinking and prayer had already
1:00
gone chemotherapy fasting and radiation
1:02
but the cancer had only spread further
1:04
to multiple
1:06
organs then Joe came across an
1:08
incredible post on an Oklahoma State
1:10
message board from a veterinarian
1:12
alumnist call me if you've got cancer
1:15
the vet told Joe how his research
1:18
scientist friend at MK had inadvertently
1:21
cured mice of cancer after worming them
1:23
with fendol a common deworming compound
1:26
the scientist herself then used fendol
1:29
and was cleared of her stage four G gleo
1:32
blastoma within weeks Joe was included
1:35
in the 1,100 person key truda
1:37
immunotherapy trial aimed at extending
1:40
Life by just 3 to 6 months but he also
1:43
decided to take the inexpensive pet
1:45
Dormer Fen bendol himself combining it
1:48
with supplements like CBD and circumin
1:51
the results were astonishing within 6
1:54
weeks Joe's widespread tumors had
1:56
disappeared on scans $1.2 million of
2:00
conventional treatments had failed but
2:02
this $5 dog medication seemed to have
2:04
worked a miracle Joe was the only
2:07
participant who finished the trial in
2:09
complete remission Joe soon took to
2:11
social media to share his protocol
2:14
inspiring many other late stage cancer
2:16
patients around the world to explore Fen
2:18
bendol as an unconventional last hope
2:21
this was my kind of story like Joe I'd
2:24
scoured to find anything that could help
2:26
with my stage 4 pancreatic cancer my
2:29
Research into antiparasitic drugs agreed
2:32
Fen bendol showed potential for
2:34
pancreatic cancer though par bendol
2:37
actually seem more effective for
2:38
pancreatic cancer specifically I tried
2:41
unsuccessfully to obtain parb benzol
2:44
before settling on the more accessible
2:46
fend Bend resol combined with other
2:48
supplements and off labels that I was
2:49
taking at that time Joe's protocol was
2:52
originally fenben every 3 days on four
2:55
off with thumin vitamin E and CBD oil
2:59
later adding fermented wheat germ and
3:01
berberine he credited positive thinking
3:04
as key I took fendol with avocados for
3:08
absorption using a high absorption
3:10
curcumin and lowd dose CBD alongside
3:13
other off labels this was when doctors
3:15
suspected stage 4 pancreatic cancer
3:18
before confirming with a biopsy so no
3:20
standard treatments yet I regret not
3:23
taking milk thistle then strongly
3:26
advised in Joe's group over time Joe
3:29
find tuned advising continuous Fen Bol
3:32
after a 2018 scare from reducing it he
3:35
now combines it with ultra botanicas
3:37
enco junct Botanicals specifically
3:40
formulated as a complimentary protocol I
3:43
started Fen bendol at the 220 milligram
3:47
dose in June 2022 though research showed
3:51
potential benefits really required 500
3:53
milligrams I only took the 222 milligram
3:56
dose 3 to 7 days per week until August
4:00
when low blood pressure after chemo
4:02
forced me to stop all off labels and
4:04
reset my mixed feelings stem from my
4:06
cancer aggressively metastasizing to my
4:09
liver soon after starting F bendil in
4:13
hindsight I didn't have all metabolic
4:15
pathways blocked nor was I protecting my
4:18
liver with milk thistle so when the lung
4:21
tumors may have initially responded I
4:23
think Fen Bend resol potentially allowed
4:26
the cancer to spread to my unprotected
4:28
liver however overhauling my protocol
4:31
which still included Fen Bend resol led
4:34
to significant tumor reductions on my
4:36
next scan overall I've stepped away from
4:38
most off labels for now and I've had my
4:40
best results without them but I'm open
4:42
to revisiting fenol as part of a
4:44
comprehensive metabolic approach down
4:46
the line not as a standalone therapy I
4:49
note the success others like Noel Watson
4:51
with stage four pancreatic have had with
4:53
Fen bendol in the next video I'll dive
4:56
deeper into the Science exploring the
4:58
mechanisms of how this worming drug
5:00
works against cancer cells and the
5:02
research investigating its anti-cancer
5:05
properties thanks for all your wonderful
5:07
comments on my last video I deeply
5:09
appreciate the messages of support
I came across your video--was not looking but it ”stands” out and have seen the affects of pancreatic cancer, parasites etc.
1. The average pancreatic duct is a ”protected” hotel for Liver Fluk ....
I came across your video--was not looking but it "stands" out and have seen the affects of pancreatic cancer, parasites etc.
1. The average pancreatic duct is a "protected" hotel for Liver Flukes, where they lay thousands of eggs, endlessly your entire lifetime....protected because of no blood flow in the duct and the duct is almost always "blocked" with mineral "stones" that act like a door protecting the Liver Flukes.
When Russia was building the first zappers so humans could stay in space with out "swelling-up", one of the first side affects was curing diabetes. I discovered that when taking the internal zappers properly 3x, on the second pass, often people expel a fist size amount of Liver Flukes following a flow of rock hard stones that flushed out of the pancreatic duct and pictured the stones and worms for Dr. Hulda Clark long ago...
2. Clark proved gold fillings affect the pancreas health badly leading to cancer---she was 100% correct.
3. A full mouth full of crowns and metal fillings is certainly asking for cancers.
4.If you have cancer anywhere, you had it first in the liver...when they tell you liver cancer "after" years of treating cancers elsewhere, they often say your hopeless once they do tell you your liver is full of it.
5. PARASITES---you surely have 3# of Lyme and never know it, all the endless other parasites will die easily in comparison to Lyme; Lyme has been the last great plague for the past 300 years and entered into just about everything with blood above and below the water.
6. Animal / Drug / Heavy Metals to kill worms----does not cure cancers and diseases, they are just "toxic" substances....professional / gimmick websites can not change cancers--- WHEN they are n ot addressing the endless reasons for cancers and "IF" parasites cause cancers and poisons that kill parasites is the cure for 1 of the deadliest cancers known---WOW, the cancer industry would crumble and all the hospitals would empty as everyone went on chemicals--- no one can take a poison and expect better health, what they can expect is that the poisoned blood cells defend themself and they kill/dissolve/expel parasites.
7. Not that long ago, every house had a very toxic parasite killer--- farmers used it to treat their horses, dogs, cats, kids.....vets still today use it for dog heart worm---injecting it in the front legs for 3 days-----it is always used by drops going up daily and then coming back down--because it is extremely toxic, but not long ago, every house had it in their bathroom---but after bad people used it to kill people they did not like---it became outlawed and only the vets use it....
8. Back in the days every family had the most powerful parasite killer known--- they also were plagued with cancers.
9. Cancers and Parasites: The parasites feast on the rot. They thrive on slow / low oxygen death.
10. 4th stage pancreatic cancer is no small deal and for anyone to survive after they did chemo-----is rare. Great M.D. always said no one do chemo after age 50, just for the fact it is too toxic for old people. Poisons can never cure anything, they just "force" a response.
11. The best cancer M.D. 15 years ago, said if you want to survive pancreatic cancer in America, you must leave America and got to China. Others will say Russia--both use a completely different approach. He said "if" your in america and want to try--1 M.D. in Texas doing extreme Pancreatic Hormone therapy has some success, but ignoring all the foundational problems and supplying hormones is insuring the pancreas will close down and become dependent on the synthetics..
12. Pancreatic Cancer ends up with orange colored eyes, degradation of the face and body and requires "STINTS" in the pancreas to allow the worms and fluids to flow out and down into the intestines and instantly their eyes lighten up as it drains down and out...and during that time period, is when people discover thy may need to pull every toxic tooth in their mouth. Stop all the toxic foods/drinks/drugs...stop everything bad....
13. the idea a person can continue what caused their cancer and just take some de-wormer----would be in the "Miracle" Class and YES, that happens;
"IF" a person believes--------their subconscious will CURE any disease, all cancers......you will become what your truly believed in..... long ago called POW WOW or just faith healing. The brain can make you or break you; we are what we believe.
SO YES, some scary cat, dog, horse de-wormer powders can indeed aid you to cure yourself; medical proved that over 100 years ago; Jesus proved it over 2,000 years ago, Elijah, Enoch etc. long long ago understood The Miracle Cure.
BEWARE animal products, the commercial types often ad poisons as a method to stop human consumption. EXAMPLE, Lugol'sIodine often used for animals, but they ad chemicals so no human can use it and actually, Lugol'sIodine since Dr. Lugol Synthetically made it in the 1800's was/is toxic and no human should ever touch it.
BE GLAD your miraculously self-cured; but something seems very fishy when you have the ability to make fancy websites.....
The Curezone foundation was all about Dr. Hulda Clark , I knew her well (enough) and her dental info surely saved allot of lives......I do not care how much magic powders a human consumes---if their dental disaster is the root cause for their cancers..that cancer is never staying away until all that rot is out and even then---the accumulated dental poisons in the cells takes years to cleanse...
Dental Disaster takes 100% of your immunity 100% of your day, every day until you die---by design. YOUR BLOOD will never stop dissolving your dental poisoned teeth and that fact, allows cancers to develop....it takes a professional dentist/dr that can cut all your rotted teeth out in 1 day...and those rotted teeth will be so dissolved they will break into pieces and take a full day for just 1 person...as cancerous puss oozes out of the jaw..
Then BEWARE! When the surgeons discover you learned how to cure pancreatic cancer and they replace your pancreatic stint with a permanent stint and say your next check up with be 1 year....do not be surprised that you never ever eat again--due to an aggressive Thrush that resulted from "dirty" instruments and they say--whoops, our bad. Go to your local hospital and get a thrush shot and if you make it past 3 days after your last ever stint--that would be a true miracle... "they" don't those that learn how to beat their system.
If your lucky enough to stop a cancer with a simple poison--use that time to CLEAN UP the dirty body....
The Hormones must be helped with true hormones---not synthetic /animal hormones...true hormones make old people act like they are young.
Case Studies of Fenbendazole and its Effects on Cancers
Case Report: Squamous Cell Carcinoma, age 80, Female
Surgical biopsy, oral fenbendazole then topical fenbendazole eradicates squamous cell carcinoma
'Fen Ben' - a substack publication Sep 28
Fenbendazole Can Cure Cancer presents Case Reports of people who have treated their own cancers along with other articles to help understand how fenbendazole works to treat cancer.
Previous articles covering other cancers are in the Archives link.
According to the Mayo Clinic, squamous cell carcinoma of the skin is a type of cancer that starts as a growth of cells on the skin, originating in cells called squamous cells. Squamous cell carcinoma is a common type of skin cancer. Squamous cell carcinoma of the skin is usually not life-threatening. But if it's not treated, squamous cell carcinoma of the skin can grow large or spread to other parts of the body.
Squamous cell carcinomas can appear anywhere on the skin. In people who sunburn easily, the cancer is usually found on areas of skin that have had a lot of sun. In people with black and brown skin, squamous cell carcinomas are more likely to be on skin that isn't exposed to sun, such as the genitals - which conflicts with the notion that topical UV radiation is the primary cause.
The following Case Report is submitted by the daughter of an 80-year-old woman who had a persistent lesion on one of her fingers. Initially diagnosed as a basal cell skin cancer that diagnosis was revised to squamous cell skin cancer after biopsy results. After about a 3 month course of systemic (oral) fenbendazole treatment, with a topical component added about one month into the treatment, the lesion is completely healed.
Hi Ben,I've followed the Substack for a while and was curious enough to buy FenBen powder from the LITHUANIAN supplier. No one had cancer but I thought it would be good to at least use it as a dewormer and do a 3 day clean out of any parasites every few months. Hopefully, this would also provide some protective benefits from any cancers. As "luck" would have it, my 80 year old mom was diagnosed with a basal cell carcinoma (later revised to squamous cell) of the finger. For several years (she says about 4) the finger has bothered her.
(my comment- could this Lithuanian supplier be the Fe Ben Lab product that has been so brutally discredited by Happy Healing?)
She thought it was an injury that wasn't healing well because it was in her knuckle. Combine that with thin ageing skin and she would regularly knock the sore open just as it seemed to be healing. Over the past year it had been getting infected on a regular basis. It would scab over, heal slightly but still be stiff and painful. A slight bump and it would burst open oozing yellow pus. She saw her GP as no amount of bandaging and antiseptic lotion seemed to effect any healing. Travacort and an oral fungicide were prescribed. No improvement.
They then dipped a swab and off the back of finding bacterial growth she was given a course of Antibiotics . It almost seemed to worsen with a nasty open wound causing her tremendous pain in the finger joint. She saw a nurse at the local hospital wound clinic who scraped it all clean, bandaged it up and strongly suggested she request her GP do a biopsy as “sores which don't heal over several years are suspicious”. This was duly done and it proved to be a basal cell carcinoma (later revised to squamous cell).
The problem now was how to excise it. On a joint. No skin left to suture and she's 80 years old. He said to leave it a couple of weeks as he was going to be away and he would give it some thought as to how to proceed but it would likely require in hospital treatment and anaesthesia to be able to do a skin graft. This worried me greatly as mum is 80.So I went over to her with the FenBen powder and told her she was going to be the family Guinea pig. At worse she'd be thoroughly dewormed and there might be some benefit. I have attached 3 photos. The first is the sore on the day the biopsy was done. Call it Day 1 and you'll see the pus and raw nature of the sore.
Day 7. Looking vastly improved and she had no pain for the first time in over a year.
Day 21. The last photo is taken 3 weeks after the initial oral dose of powder. 222mg as dosed by the little spoon in the tub. Taken daily with cheese or something fatty.
As you can see, the skin has healed over. She has free use of the finger and there is no pain.
She's had no obvious side effects from taking the Fenben.
She's seeing her GP on Tuesday next week and I'm keen to hear what he says. Hopefully he won't mess with it and we can go back in a few months once the new skin has matured and do a follow up biopsy.
Hope this is interesting to you! She's not the best of photographers but there's clearly been a massive improvement. We are so grateful to you for posting these self studies!
Follow-up 5 weeks later
My mother saw her GP not long after I last emailed you and he seemed quite surprised to see how well the finger was doing and ascribed it to the fact that when he'd previously seen her, that he had cut some of it out when he sampled for the biopsy and put the stitches in. She mentioned the FenBen and said he was reluctant to believe that it had anything to do with it but he had to concede that it was looking very good and all plans to surgically remove the carcinoma and do a skin graft under general anaesthesia could be shelved. For now.... I suspect he thinks it will be back.
Since the wound had closed completely she has been applying FenBen paste topically every day (Panacur “horse dewormer”). She leaves her finger exposed to the sun and fresh air as much as possible, putting a plaster over when she goes out as she’s worried about knocking the new skin open after years of pain.
It continues to look good with no external signs of infection, no pain in the affected area or joint and the skin has healed beautifully. Really quite astonishing given how many years this carcinoma has had to eat away at the skin and being 80 it’s quite thin without any extra stresses on it.
Mom says she sometimes imagines there might be a small amount of the cancer left as she sometimes “feels” like there's “something” moving around under the skin but this is as likely to be residual deep tissue damage resolving itself as it is any cancer. She says it tingles sometimes but this really does seem more likely to be healing than cancer. The sutures she had a few months ago have also left a bit of lumpy skin. There’s no way she will biopsy the area to confirm if the cancer has gone, as there's just no obvious reason to traumatise healthy looking skin.
I've attached photos of the finger as of today. I'm not sure of where you are in the world but it's midwinter here so her skin does look a bit dry but that's the weather.
As far as we can see, there's no cancer left. She has had no obvious side effects from taking the FenBen and will continue with it both orally and with the topical cream. I bought her a milk thistle supplement but only because I read there could be effects on her liver and if she's been clearing the cancer it might be a good thing. Just me fussing there was no obvious reason to do so!
June 19, 2024
Mom went to see her GP today. He says he's not convinced the cancer is gone and wants to carry on with an excision off the back of the pathology report, which I have attached. Since he excised some of the carcinoma when he took the biopsy sample, he feels this is the reason for the improved appearance. I'm not so sure .... cancer sores don't get better as far as I'm aware!!
In any event, the full diagnosis is attached. Seems it’s a squamous cell carcinoma and there's also some signs of Bowen’s disease and solar elastosis.
We're about 2 months down the road treating a 4 year old tumour. At the age of 80, I honestly believe my mom should leave it alone and continue with the Fenben and just see where it goes. I find it hard to believe there's a festering tumor underneath all that healthy new skin as she has full use of the finger and has no pain at all. At any other point in time she would not be seeing a GP......
August 10, 2024
It's been 3 months now and my mom's finger seems to have healed completely since we last corresponded. In her words "If you didn’t know history you’d never guess".
NEW ARTICLE: MEBENDAZOLE and Thyroid Cancer - Inhibits tumor growth and prevents lung metastasis - shocking new Johns Hopkins research on Fenbendazole's sister drug
In a 2020 paper by Johns Hopkins researchers led by Tara Williamson, Mebendazole halted Anaplastic Thyroid Cancer and shrunk Papillary thyroid tumors.
For those of you who know, Anaplastic Thyroid Cancer is one of the most aggressive cancers that exist.
"The purpose of this study was to determine if mebendazole could be repurposed to effectively treat thyroid cancer, in particular before metastasis."
"In vitro, mebendazole potently inhibited the growth of a panel of human papillary and anaplastic thyroid cancer cells"
"In aggressive anaplastic thyroid cancer cells, mebendazole significantly repressed migratory and invasive potential"
"In vivo, mebendazole treatment resulted in significant papillary thyroid tumor regression and growth arrest of anaplastic tumors, with treated tumors displaying reduced expression of the proliferation marker Ki67 and less vascular epithelium"
"Most importantly, daily oral mebendazole prevented established thyroid tumors from metastasizing to the lung"
"Given the low toxicity, this novel preclinical study of mebendazole has promising therapeutic implications for patients with treatment refractory papillary or anaplastic thyroid cancer."
As I continue to do Cancer Consultations, I've been approached by a number of Thyroid Cancer patients who have run out of options.
Seeing the tumors shrink in mice like this is something you don't see everyday and is shocking and impressive.
While Fenbendazole and Ivermectin get all the glory for being the top repurposed drugs for Cancer today (including COVID-19 mRNA Vaccine Induced Turbo Cancers)
it's important to remember that Fenbendazole's sister drug Mebendazole also has a vast body of preclinical research that is, in many cases (including this one), absolutely stunning.
I have been taking Ivermectin horse paste for a few weeks now and am getting some results.As I'm sure many of you know the doses are divided into 25kg's.I weigh 8 stone 6 pounds(118 pounds),just under 55kg.I have been taking a 50kg dose each time.
What has been bothering me is what about the 5kg of my weight which is not being accounted for in this dose.I want to attack them 100%,not 90%.Also what if you weigh 65kg and only take a dose for 50kg because the doses are measured in 25kgs?That would mean that 15kg of your weight would not be accounted for in your dose.
So last night I measured out my 50kg dose.Then I measured out a seperate 25kg dose onto a teaspoon.I then divided this,as best I could by 5.I took my 50kg dose and also my tiny 5kg dose.About half an hour later I felt it going to work.I had small random painful like contractions from my stomach right down to the bottom of my intestines,and from extreme left to extreme right hand side.I don't normaly react so strongly to the 50kg dose.
What does everyone else do?Have I missed something on the posts advising on measuring,dosing that accounts for this?Or is it the case that the extra amount needed to be exact would not make that much difference anyway?What do you all think?
I assume you are using the same Bimectin stuff as you said you were using before? If it is the same as mine then it is labeled as 18.7 mg/g Ivermectin and each tube has a total mass of 6.42g of pa ....
I assume you are using the same Bimectin stuff as you said you were using before? If it is the same as mine then it is labeled as 18.7 mg/g Ivermectin and each tube has a total mass of 6.42g of paste and is marked as being for a total of 600kg of (horse!) bodyweight. If you follow the bodyweight markings exactly on the horse paste syringe for your own exact bodyweight (as you have been doing) then you get the correct 0.2 mg/kg bodyweight dose that you need in the ICU protocol!
Don't believe me? Well, here is the maths:
Total mass of Ivermectin in tube = 18.7 × 6.42 = 120 mg
Entire tube is for 600 kg bodyweight, therefore Ivermectin dose per marked kg of bodyweight on scale = 120 ÷ 600 = 0.2 mg
Here is the recommended Ivermectin dosage as stated on drugs.com for strongyloidiasis:
"
Usual Adult Dose for Strongyloidiasis:
0.2 mg/kg orally once
In immunocompromised (including HIV) patients, the treatment of strongyloidiasis may be refractory requiring repeated treatment (i.e., every 2 weeks) and suppressive therapy (i.e., once a month), although well-controlled studies are not available. Cure may not be achievable in these patients.
Dosage guidelines based on body weight:
15 to 24 kg: 3 mg orally one time
25 to 35 kg: 6 mg orally one time
36 to 50 kg: 9 mg orally one time
51 to 65 kg: 12 mg orally one time
66 to 79 kg: 15 mg orally one time
80 kg or more: 0.2 mg/kg orally one time
"
Therefore you are doing it right, but if you actually weigh 55kg but take the Ivermectin at the 50kg mark (10 mg total Ivermectin) then you are getting a dose of 0.18 mg/kg bodyweight which is still within normal dosage recommendations and probably about right for you. If you up that to the 75kg mark (15 mg total Ivermectin) then you'd get a dose of 0.27 mg/kg bodyweight, which is a bit much but will probably do you no harm and be more potent.
You are probably going fine as you are but roughly splitting the difference between 50 and 75 kg (which will give you 12.5 mg Ivermectin total) will prob be easier than trying to get exactly 5 kg. If it were me though and I wanted that little bit of extra potency then I'd probably be too lazy and save myself the hassle and take it at the 75 kg marker (if it doesn't kill you!!!) now and then, while mainly using the 50 kg.
Paul,thank you for the fantastic,informaive post!I have no reason to disbelieve you.You have helped me with many questions in my quest to educate myself in my parasite battles,for which I will be ....
Paul,thank you for the fantastic,informaive post!I have no reason to disbelieve you.You have helped me with many questions in my quest to educate myself in my parasite battles,for which I will be forever grateful.
I am a stickler for detail especially in things which are important to me.You explained it all so well and I now understand it completely.I think I will divide a 25kg dose by 4 as best I can and add that to my 50kg dose.I really did feel the benefit of the extra in my last dose.
I don't think I will go for the full 75kg dose,I don't want to risk killing myself!That would be no fun at all and I wouldn't be around to celebrate my triumphs.Seriously though, thank you.
Was exaggerating a little with the ”killing” thing. (I weigh 85kg and first took it at the 75 kg mark at first, but then later took it at the 100kg (0.23 mg/kg) mark no trouble.
There was a g ....
Was exaggerating a little with the "killing" thing. (I weigh 85kg and first took it at the 75 kg mark at first, but then later took it at the 100kg (0.23 mg/kg) mark no trouble.
There was a guy who posted here a few weeks ago who took a whole 600kg tube at once -- said he recovered, but really scared himself with it and had difficulties with eyesight and went to A&E. As long as you don't go overboard nuts like that guy did it'll prob be OK if you're not being exactly as precise as you are trying to be.
Not sure though that IVM was right for me and at the minute back again with the horrible taste of PZQ!
I knew you were exaggerating,i was just going along with it.
I remember reading that post about the chap who took all of that Ivermectin.At the time I didn’t realise how much it was.Poor thing ....
I knew you were exaggerating,i was just going along with it.
I remember reading that post about the chap who took all of that Ivermectin.At the time I didn't realise how much it was.Poor thing he must have been very ill after taking it.
You have mentioned before how you hate the taste of prazi,have you thought of getting the powder and putting it into veg gel caps?I do this and can't taste anything.I also remember you saying you can't be bothered with the hassle,which I understand.Maybe you could persuade someone to do them for you.I do 3 days worth at a time,only takes about 10 mins,plus added bonus,works out a lot cheaper.Do you mind if I ask what you are treating for?I remember a while back you mentioned schistosomiasis.Are you getting any further with the help of the infectious disease doctor?
I did make an app with a private gastro,who I was referred to by my GP.I cancelled it for a few reasons.At the time I didn't want to have to cope with the stress of it.I was also debating whether or not to take Ivermectin,I also needed to buy lots of other meds and suppps,so money was another factor.To be honest I have a fear,probably an irrational fear of an endoscope.Not the actual procedure,but I have read here of a member who had severe scattering after having one done.As I don't know for sure what I have,this puts me off.Stupid I know.At least I still have it as an option for the future.
Why are you even taking ivermectin? You need the Safeguard fenbendazole 10% paste, two turns on the dial each day. Equimax also and it has a bit of iver inside it along with the praziquantel. Pamo ....
Why are you even taking ivermectin? You need the Safeguard fenbendazole 10% paste, two turns on the dial each day. Equimax also and it has a bit of iver inside it along with the praziquantel. Pamoate pyrantel paste goes with the equimax, two turns each, one in the morn and the other in the afternoon. reatments can be pulsed, as in one week on, one week or month off. Ivermectin is the least effective and the most side effects of all the anthelmintics.
Prazi in the mouth is very important to experience, you need to see my pics of what lives under our gums. Whenever they mature and move about, you will experience great pain and swelling.The prazi ....
Prazi in the mouth is very important to experience, you need to see my pics of what lives under our gums. Whenever they mature and move about, you will experience great pain and swelling.The prazi stops them but you must eat it in the paste form.
Thanks for the suggestions.Do you mind me asking,are you medically trained or are these suggestions from your own personal experiences?If they are from your own personal experiences what research ....
Thanks for the suggestions.Do you mind me asking,are you medically trained or are these suggestions from your own personal experiences?If they are from your own personal experiences what research did you use for your protocol and what did you treat yourself for?Did you get tests done?
Hi Hope, Most of us that suffer from Morgellon’s disease have had horrible experiences with DR visits, mine were demeanoring, embarrassing, confusing and then I was called paranoid and delusional, ....
Hi Hope, Most of us that suffer from Morgellon's disease have had horrible experiences with DR visits, mine were demeanoring, embarrassing, confusing and then I was called paranoid and delusional, then I was told that I was doing this to myself. Most have had the same experiences, as for the tests, O&P along with skin biopsy showed nothing, confirmation that I was delusional.
I have not had any formal medical training. As for personal experiences with others using the same treatments as those used by myself, there have been a few.
You asked what research,...Entomology, Mycology, Ethnobotany, molecular Biology and Chemistry. Morgellon's disease requires that anyone researching it's cause and symptoms will need to have a general understanding of all these areas of study.
Initially I found clear threadworms in a stool that was so full of them that it was alarming, the next day the same mess exited from my genitals, an amount equal to 1/2 cup. So far none of the clear larva have been found to be in any research articles nor in any Peer Reviewed journals.
The many different things inside us require anthelmintic therapy from more than one type of dewormer. Safeguard fenbendazole 10% Equine paste has proven to be the most successful anthelmintic and the one with least side effects. It would require 60X the dose that I use before a possible overdose could occur and even then, it can't be said that a problem would occur. Each individual is a bit different, so anyone using any drug needs to listen to their own body and what it is telling them.
The Equimax dewormer is Praziquantel 14% & Ivermectin 1.78%, this set of drugs is a bit harsher than the Fenbendazole but is necessary to use for those with M. I've seen women eat a whole tube of Equimax at one time. One lady had the worms in her brain and we had seen the nodule as it moved to her brain. Here face was swollen and she was in bad shape. The heavy dose of Equimax took care of her brain invaders but she scared when the mess moved out of her head. She had a mini stroke or a light seizure and passed out in the yard. It was over quickly and she made a wonderful recovery. In hindsight, she need to have stayed at home with a monitor such as myself. It's a fine balance when working with someone as sick as many are and with the responsibility that one assumes when advising them as to treatments. Pamoate pyrantel paste can be added to the equimax paste each day as it makes the Prazi and iver mix much more effective. Do not drive, make sure someone is close by that knows your plan and remember to keep the stool loose with something like ice cream, which has fat in it and that may be necessary for the dewormers to attach to. Olive oil, grapefruit sections and other things also help. Morgies have a large mass inside their small intestines and things attached to the intestinal wall, inside the large intestine. All organs are usually infested with black fibers, short and pointed on each end, other insect life forms, fungi and arboviruses. M sufferers do not have bacteria issues unless they have a secondary issue such as a tick bite.
Most sufferers that do the anthelmintic therapy will need to pulse the treatments, such as five days on and 10 days off, or more but some don't stop until all internal issues have cleared. I've seen some of the latter discharge as many as 16 lbs of unwanted things from all orifices and some that weren't exits, such as the tongue and eyes, saliva glands, belly buttons, skin, ears, nose, and anywhere the things decide to leave from. You can place a lettuce strainer, the old aluminum type or a self made screen over the toilet so that you can see exactly what you were holding inside you. I use coffee filters and an old filter holder for urine samples. Gross but after 3,000 of these traps are checked, one gets a good idea of what needs to leave his or her body.
I clean strain and place in alcohol all my artifacts unless I am intent on growing the sample, which I can and have done. That's another story.
I hope that I have properly answered your concerns about any knowledge that I might possess. Perhaps I know nothing. morgellon's research and treatment certainly is humbling, for the numbers are astounding and the level of suffering is often unfathomable.
Many never make it back home, I suspect they didn't ever find any help. I hope to prevent this outcome from happening to anyone else and there are others here that are simply doing all they can in order for the suffering and death to be stopped.There are also too many sufferers being locked up and forgotten about. mental institutions are no place for treatment of this disease.
The critical path through a parasitic infection appears to be gated by several key systemic parasites.
Several of these can be quite small.
This post summarizes the findings of the last three months, and identifies the role and the informed use of some critical essential oils.
Background:
I cleared many species of flat worms, Ascaris twice, hook worms, Strongyloides, Strongyles, and Prehistoric.
October:
Work in essential oils continued.
Prehistoric research and parasites came as a surprise.
Early work showed prehistoric hair worms, thin migrans, in several people.
Eventually the formula took shape, and I had some 10 pounds of granulomas sand came out with doses of peppermint, castor oil, and ginger.
Prehistorics:
It was such a shock, that its importance, or need to be removed early in parasitic treatment cannot be underestimated, and challenge test for prehistorics needs to be moved earlier in the deworming process.
Then came thyme:
I knew I had several small species of red worms.
I knew eventually, that no antiparasitic med had any clearing effect, irrespective of dose and time.
Eventually in back tracking antiparasitic essential oils, I rediscovered thyme.
From my notes it was tested early, some 4 years ago, apparently with no success.
Eventually through events, and correspondence with others to sick to make the journey, a shortcut needed to be found.
I believe thyme is that shortcut.
It has had miraculous killing capability on critically infected correspondents, and my self.
Let me explain.
In the last few months, experimenting exclusively with essential oils, we have made a few new discoveries.
Prehistoric worms are killed using peppermint oil.
Long hair worms, like Anisakis, are killed using peppermint.
Prehistoric worms evolved many millions of years ago, and still exist in seafood.
The current antiparasitics do not have any effect on them, they may recede for a short time, but the infections remain.
The DNA never evolved to a point where current antiparasitic meds will cure an infection, and continued dosing will only end in death.
We had some topical success with neem, castor, ginger, thymol, Rose constituents, terpines, Invermectin, Pyrantel, and alike.
Continued testing made us kind of knowledgeable in how these worked.
Bearing less fruit were Phenols, and other molecules.
Early reactions to peppermint showed higher doses had an increasing effect.
We determined the maximum dose per weight.
Many had beneficial results.
Castor oil showed many again, showed an improvement, several others dropped granulomas sand like myself(30%).
We verified the dosing of various ginger root, leaf, oil.
This process became known as the prehistoric parasite formula, I forget the number but 25.5 comes to mind.
Following this formula, several in our group were loosing the battle.
A new approach was needed, and fast.
We simply had run out of things to test.
What remained was all there was.
A quick scan of dosing of Thyme showed activity.
It was at a high dose.
Little time existed for the usual safety, research, gentle ramp.
The REDS formula 31 started in January with an initial dose of some 2 grams of leaf four times a day 100kgs.
The stir of many species and their nitric acid was attenuated using pipperazine.
The GI was kept clear using Pyrantel.
In formula 31 Revisions 6 - various co-factors were tested and several additional elements were identified, including castor oil, Miralax, potassium citrate, etc.
The thyme dose was increased to 4 grams some 8 times per day (100kgs).
Eventually the formula entered a form, and those early adopters improved with increasing doses of leaf.
The reactions were severe.
One now on an electrode oscillator, the other critical infection soon to be.
The formula clears Promastigotes, red hair worms, red migrans.
The formula seams to aid in the removal of Ascaris, Strongyloides.
Pictures I have seen show worms larger than any pictures before it.
After prolonged agony, eventually the last early adopter went into remission.
Co-infections of Ascaris and large Strongyloides presented in them.
In myself, a large Ascaris eventually was pushed out of a hidden missed nest.
The value and importance of thyme leaf, and essential oil has been proven by this effort.
Critical infections can be walked back by using thyme, and a support mixture of antiparasitics and co-factors.
After years of searching, the importance of early thyme use has been discovered, the underlying infections it addresses (systemic Promastigotes, red Nanos, systemic red hair worms, systemic red bone migrans worms, systemic Strongyloides, systemic Ascaris, and probably many other parasites, has been demonstrated.
Thyme is broad spectrum.
I did not discover thyme, the Egyptians did.
I am simply reporting on its use, position and importance in the de-worming process, and inferences.
This is good information. you know what else works well?
don’t be a liar (10 pounds of granuloma)
dont be a weird cult guy and just post like regular people do on the forums
all parasites ....
Thanks Sir Matt! You know I’m gonna try some of these oils. Does it matter if the Thyme is Red or White?
I saw this about prehistoric worms from the pleistocene... great ... neanderthal nemato ....
Thanks Sir Matt! You know I'm gonna try some of these oils. Does it matter if the Thyme is Red or White?
I saw this about prehistoric worms from the pleistocene... great ... neanderthal nematodes!
"Scientists have brought the "dead" back to life in a groundbreaking study that saw Siberian roundworms survive 42,000 years of being frozen.
Cryogenics have long been the subject of Science fiction, but new research proves that it could be part of the future. A pair of nematodes withstood thousands and thousands of years in the permafrost, waking up to an entirely new world in 2018."
The Thyme we use is Swanson Thyme leaf Vulgaris - White.
The dose is 32 grams per day, 8 doses of 4 grams. (100kgs)
Reports of promastigotes, Nano burning on skin, death of red hair worms, ....
The Thyme we use is Swanson Thyme leaf Vulgaris - White.
The dose is 32 grams per day, 8 doses of 4 grams. (100kgs)
Reports of promastigotes, Nano burning on skin, death of red hair worms, exodus.
Massive exit of strongyloides, Large scale Ascaris kills reported.
REDS Formula 31:
Formula 31 has several balance agents, cofactors, etc.
Promastigotes, red hair worms, red bone worms. Symbiotic infections and systemic.
REV 6
>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>>for 100kgs
Ramp up slowly. The sudden onset of thyme may result in a near death experience if several systemic infections are present.
Zapping may be required to protect eyes, ovaries, testes, throat, mouth, etc.
The rapid rise in activity is possible. The exodus of parasites described so far is nothing short of amazing.
Thyme leaf ()
DEC 200mg (104mg yield from citrate tablet) 4X/D with 2 ounces orange juice.
(tested with staggered dosing time of pyrantel, (tested DEC simultaneously taken with pyrantel... for those who follow that issue.. )
All at once works, staggered time may need lighter doses of PPZ/Pyrantel. This dose is a bit tough, 75 kgs person doing 133mg citrate.
Banana helps tolerate DEC. Clear urine may indicate the need for a lower Dose of DEC. This wipes larval stages most nematodes.
5cc PPZ liquid 4X/D (50mg/ml)taken with ginger ale - Drink fluids with this med!
10cc (50mg/ml) Pyrantel liquid taken with Greek gods yogurt and teaspoon of jam.
Potassium citrate 99mg (startup may require 3-4 per day, thereafter 1 per day at noon.
Noon Miralax 5CC
Noon Castor oil cap 650
Noon 2 Black Ginger caps
External skin applied thymus vulgaris, limit drops at a time.
7 days to full effect to assist to Ascaris (OxBen single 5mg/kg "lower" when on thyme..., MBZ 600 total in day, Papain 10cc in cranberry sipped for lung or throat burning mucus).
21 days to full effect to assist in Strongyloides removal (FenBen 5mg/kg..."lower" when on thyme, IVM 2X/D)
Quite a few Saltines for nausea.
Liquid diet/egg during nausea, fruit juices, less than 2 ounces OJ per dose, will weaken formula.
Substitute Oils cap for Pyrantel dose - Thyme/Clove/Oregano cap Alpine Clinic 4X/D
Rev 7 a bit milder, less stress.
__________________________________________
The white paper is still being written.
Everything is dosed per weight, person of 57kgs doses a bit less than half the dose of a 100kgs person.
MBZ may be required to quite red bone worms, use same dose as Ascaris if Ascaris not present, omit if bone worms not present, they chew joints, feet, hips, back. Pain and movement is obvious.
2- Mucuna Pruriens Extract DOPA 1000mg for sleep at bedtime 100kgs
I recall getting a toxic reaction after sprinkling thyme herb on my food. I wasn’t sure if it was the thyme. Since I’ve been using quite a lot of antiparasitic at different intervals I didn’t st ....
I recall getting a toxic reaction after sprinkling thyme herb on my food. I wasn’t sure if it was the thyme. Since I’ve been using quite a lot of antiparasitic at different intervals I didn’t stop to think it was the thyme. I’ll give it a try.
Do you recommend ingesting thyme essential oil as well as peppermint oil?
For some reason Thyme EO excites parasites. Clove all forms excites parasites. The mixture of Thyme/Clove/Oregano causes less energy, which is essential for bone worms. In addition, the mixture ....
For some reason Thyme EO excites parasites. Clove all forms excites parasites. The mixture of Thyme/Clove/Oregano causes less energy, which is essential for bone worms. In addition, the mixture prolongs suppression of bone (red) worms. So I kind of poo poo internal oil ingestion, unless it is in the mixture described in Reds Formula 31. EO oils ingested are to strong unless measured and diluted. To much fuss for such a critical ingredient.
We have used oregano caps 150mg 10:1 swanson in other formulas. It appears safe. Clove had disastrous results with exciting nanos, but when tempered with thyme and oregano at the same time, it appears to work. Reason unknown.
External thyme EO, and Rose constituents, Neem, Castor, etc are safe with measured amounts.
In reply to your inquiry regarding the need to possibly double the dose of Ivermectin for a Strongyloides infection - I know of several doctors who are using double to quadruple the dose of oral ivermectin for several reasons.
For many, they are seeing that more patients are not absorbing therapeutic doses for various reasons. The main reason involves a parasitic and/or pathogenic infection(s) in the stomach and/or intestinal tract which impedes absorption of nutrients and drugs.
This topic has even been discussed at several veterinarian conferences when many of the vets noticed ivermectin was not working in many animals. At first, they thought the drugs were not working. Though, upon testing, they discovered after oral ivermectin administration therapeutic drug levels were not appearing in the blood in about half of the tested groups.
I have read i several medical journals where they have administered ivermectin parenterally because the patients were not showing therapeutic levels in their blood after oral administration. They believed it was due to the fact that strongyloides burrows into the stomach and lining of the intestines which significantly impedes absorption, especially if the infection has been present for quite a while. Other co-infections ( parasite or pathogen) can also do this.
In these cases they gave ivermectin IM, subcutaneously or by IV.
Parenteral administration routes include: subcutaneous (SC, SQ), transdermally, IV, or intramuscularly (IM).
In a couple cases the patients were diagnosed with severe strongyloides infection and they cleared up after receiving ivermectin intravenously or IM, taking daily doses for 1 week and then repeating this regimen 1-2 weeks later.
Another reason involves the fact that many people are showing severe acidosis due to multiple parasitic and pathogenic infections all of which create a lot of acid byproduct. In addition, the drugs create an acidic byproduct. So, it is important to ensure the urine pH is 7.0 - 7.2, 7.4 if possible. Most drugs are absorbed better and are more effective in the human body at this pH range. Many enzyme systems in the body operate in a very narrow pH range.
My physician gave me a regimen in which I was taking 12 mg of ivermectin, four times a day, on an empty stomach, for 14 days. I had to repeat my entire regimen a week or two later.
Also, they are using Ivermectin for other medical conditions and have found higher doses are needed.
Re: Thyme importance and the critical pathway to curing parasitic infections
Thank you! Now I've got to rummage and find the White because I can only find the red. ~sigh~ and I can only seem to find stuff when I'm not really looking....
I have been brought up to speed on Dr Klinghardt’s efforts by a correspondent, in this area for Lyme and parasites.
I was informed he (Dr K) has a store of bulk bottles of EO.
I was told he has ....
I have been brought up to speed on Dr Klinghardt's efforts by a correspondent, in this area for Lyme and parasites.
I was informed he (Dr K) has a store of bulk bottles of EO.
I was told he has some type of store which sells EO.
I am uncertain what the website contains.
Google - Dr Klinghardt essential oils
The Overlap with Lyme infections causes EBay prices and internet prices to fluctuate wildly.
This overlap indicates that any use of oils may conflict with the high demand of the Lyme community.
Promastigotes are the parasite family that underlie many diseases.
There are many species, I recall 8.
I currently believe it is this co-infection that makes parasite removal difficult.
I blew white urine a lot while dosing formula 31.
Is this an underlying Bb or other bacteria?
EO efforts have moved fast and apparently has gone from early snippets of information to full blown mob consumption.
Research also has gone into high gear.
Guess it is time to do some reading to get up to speed.
Mattk is the thyme in capsules? Is it liquid? I converted th 100kg to pounds so I follow you there. I have been using zero Rx meds and have been killing tons of parasites with natural stuff. Some days I get depressed , but I think that is the parasites talking. My body is much strongerand that is the main reason I know I am getting rid of them.
Interested in using herbs/traditional remedies against parasites? Go to Parasites Support Forum. Interested in debating? Go to Parasites Debate Forum
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