Fenbendazole treatment

[JohanPrinsloo]

I'd like to know if anyone has had success in using Fenbendazole for advanced prostate cancer.

[Tall_Allen]

How could anyone know that? What would have happened if they hadn't used the drug?

[sm60 in reply to Tall_Allen]

That could be said of the majority of pharmaceutical concoctions, as well. Especially as they are frequently given in combination with so many other things--many of them designed to soothe the negative side effects of other things.

[Tall_Allen in reply to sm60]

Pharmaceuticals, unlike supplements, are tested in Phase 3 trials. In a Phase 3 trial, half the people are given the drug, half are given just the standard-of-care. So for pharmaceuticals, we know exactly what would have happened if the drug had not been taken. Also, drug-drug interactions are carefully assessed and all side effects are monitored.

[sm60 in reply to Tall_Allen]

You'd like to think it was all so cut-and-dried, but INDIVIDUAL BODY CHEMISTRY is rarely (if ever) considered. Medicine is not cookie cutter, one-size-fits-all, despite the wishes of big pharma. Not everyone should be treated the same, and Big Pharma (and their apologists) truly know a heckuva LOT less then they tend to admit.

[Tall_Allen in reply to sm60]

The trials only predict for the group, not for the individual, but it is the best any individual can predict. If you believe you know more about your individual body chemistry, you are certainly free to take any substance into your own body. It's your body and no one suffers from your mistakes but you.

[Shooter1]

I've been using it for over 2 years, and it hasn't killed me yet... Has it helped??? don't know.

[dhccpa]

I've used since 2/2020. PSA hit new low of 0.5 in April 2021 (started Lupron 11/2018).

I haven't drawn ant conclusions yet. I have new scans and PSA test coming up in September. I report as things happen.

[Loujaro]

I have been using it for four months. It's still a bit early and I started therapy with LU-177, but it doesn't hurt me !!! It's gentle therapy, it takes time. I combine it with CBD, curcumin and a number of other supplements ... And I feel very good!

[cigafred]

The Oklahoma Medical Research Organization, later joined by Stanford, is auditing the outcomes with respect to many types of cancer. I do not believe they have reached any conclusions. mycancerstory.rocks/single-.... In my own case, I concluded it did not work, and posted about it.

[dadzone43]

Glad you reached out. There are a lot of posts about fenbendazole. Why not use the <Search> feature?

[Burk]

I used FebBen for 8 weeks in 12/20 - 01/21 and am two weeks into another round of it right now. My PSA has been declining nicely, (33 to .1) but considering that I am on Lupron and had EBRT in January I cannot attribute the decline to any one treatment.It is a low tox therapy and there are many positive testimonials out there. We cancer patients need all the help that we can get, so why not?

I agree with a statement that I once heard from a cancer survivor, He said, "I would not be here today if it were not for the professional care given by the medical community, and, I would not be here today if I had done only what was recommended by my professional care givers".

It's you body. It's your life.

[sm60 in reply to Burk]

EXCELLENT POST.

[Dropzone]

I can't make unequivocal claims but here's my experience. After my extensive and traditional initial treatments I was prescribed ADT with Lupron which managed my PSA climb for about 3.5 years. After several months of recurring PSA increase I was declared mCRPCa and prescribed Zytiga. I had zero response to Zytiga and my PSA continued to steadily rise for the next year and a half at which point my doctor said I was "becoming a concern". It was at this point that I decided to implement a artemisinin/fenbendazole protocol that I extensively researched mainly through the help of Curt Michael Graydon. My PSA was up to 5.23 when I started the said protocol and almost immediately my PSA began to decrease. Remember this was something that traditional treatments couldn't do for over a year. I continued with the protocol (and yes I was still on Lupron and Zytiga) and had a couple of up ticks but over a seven month trend I had a three point drop in PSA to 2.27. Compare that to where I'd be if my PSA had continued it's exponential climb that it was on, speculation would put me at least double the 5.23 reading. I don't know if either element would have done the same on its own but IMHO the combination protocol had a direct PSA response.

[Niso in reply to Dropzone]

What is the dosage for daily artemisinin?

[Dropzone in reply to Niso]

I do two 500mg doses 4 hours apart on an empty stomach through the night when, as it's believed, cancer is most active.

[Niso in reply to Dropzone]

Thank you bro

[Tall_Allen]

I only report what the best evidence is. If you want to risk your life because of your conspiracy theories, that is certainly up to you.

[CAMPSOUPS]

Although I try to forget and just live life to the fullest, I am dying of cancer. There are a couple of estimated expiration dates looming over my head.

What’s your deal? You don’t seem to offer anything helpful here (unless you think recommending scorpion bites is helpful) you consistently whine about government, pharma, the FDA etc. Distrust of everyone and everything.

None of that helps the fact that I am dying of cancer. Again, what do you have to offer us here?

It seems you would rather this platform disappear or become ran under your idea of what it should be.

Actually, why do you even show up? Again, I am confused as to what you are looking for here other than an argument or a platform to fight against those here looking for help.

Why don’t you just call into a radio show or find a twitter thread to voice your anti-everything diatribes? I would think that would be more satisfying for you.

[sm60 in reply to CAMPSOUPS]

I'm looking for the platform to be open to all views so that so many do NOT KEEP DYING OF CANCER. I wish only the best to you and all those who are suffering under the tyranny and lies of big pharma and their governmental allies.

[Kevinski65 in reply to sm60]

I'm M1 stage 4 , Gleason 9, almost 9 years out. I've been 2.5 years Lupron, 6 years Lupron and Xtandi. I took many supplements, herbs, zyflamend, mushroom combinations. I don't know if they helped or not. I know much of this whistles through your kidneys and liver, so you are risking things. I took loads of aspirin for a long time , maybe 2 years. I got balled out for that so I stopped. For some men , I believe prostate cancer is like a forest fire. Once it's out you stick with allopathic medicine but if you wanna take artimenisin and CBD I don't think it will hurt you, but most likely it's a waste of money. One doctor told me I was giving myself heartburn and gas. Once I stopped the supplements I farted less and didn't need Gaviscon lol. I think it gives the patient a feeling of control that's it. It might help but it's not science. If you were getting abaraterone and Lupron and then drank mare sweat , if you got a good durable response , you'd swear it was the mare sweat.

[Dropzone]

I use two products, Dr's Best artemisinin and Pytoartemisin by Allergy Research.

[Dropzone]

Yes, I opened the capsules and mixed with 15ml DMSO and topped with fruit juice. Grapefruit juice would be ideal but it would've reacted with the Zytiga that I was still taking. DMSO is nasty on its own, so is artemisinin for that matter....both very bitter.