My uncle, a very fit 88-year old, was diagnosed with prostate cancer 3 1/2 years ago and while the hormonal treatment kept it in check for a couple of years, his PSA has now risen to 1600 and the scans show has spread to his bones. He has been tinkering with different hormonal regimes, abiraterone and enzalutamide, without benefit, and has just progressed to start taking dexamethasone and is considering trying fenbendazole. I would be interested to hear of other peoples experience of fenbendazole ?
Fenbendazole: My uncle, a very fit 8... - Advanced Prostate...
Fenbendazole
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Pluvicto will be more effective
it looks like Pluvicto is not Available in the UK prostate-cancer-research.or...
You could get it here: patientinfolibrary.royalmar...
I believe Joe Tippens and his Fenbendazole work. However, as I have posted on this web site, (1) it did not work for me and (2) when I asked him about the audits that Stanford and Oklahoma Medical Research Organization had performed with respect to fenbendazole and prostate cancer his response was, at best, vague and evasive.
Thanks cigafred. I wonder whether menbendazole is as good?
Do you have the interchange with Tippens about the audits and if so would you mind messaging that to me?Stanford researchers did three well documented case control studies on the Tippens protocol which came out favorably. It would be most interesting to see something about a follow-up audit.
It was VERY roughly four months ago that Joe had a QandA on his website. facebook.com/groups/mycance...
I do not know how to access that video. Any links to the Stanford results?
Yes, I was skeptical that Stanford or Emory were hitting a lick on fenben. Joe must have been puffing. Even if they examined three cases, it wouldn't mean much.
Still, I plug ahead. Are you sure you gave it long enough? It doesn't work like ADT does. If it does its thing, it does it over time, particularly with PCa.
I have been on the FB and Ivermectin path for 4 months. I'm waiting to discuss my recent CT results with MO shortly. PC with Mets to lymphs here. Medically I'm on Eligard and Erleda. My PSA has stayed at. .02 for 3 months now. Taking FB/Ivermectin requires a lot more, such as Tudca and melatonin. The group here is a huge brain trust on traditional meds and options. As such, I've been silent as not to bog the group down with alternative/natural paths.
Lastly, FB, etc is very costly, at least in California.
you seen any PSA drop since you started FB and Ivermectin?
It's difficult to know while on ADT meds. However, fb/iver isn't for the reduction of PSA. The fb/iver protocol assumed cancer is a parasite, and the dewormers remove them.
I do not understand FB (I assume fenbendazole) being expensive. I see Amazon now has some fancy formulations at high prices, but the basic product was cheaper than most of my supplements.
Fenben is expensive to me. There are only s handful of guaranteed FB products. There are companies that create their own pills/powders but not independently tested. At last pricing. It costs me $340 + TX per month using safe-guard. Then there is the Pectasol $110 per bottle (15g/day), add Tudca at $30 x 7-8/mo. And this is just the basic protocol of protocol.
Hi in order to cut costs you can buy fenben from the happy healing store ,recommended by many patients in fenben groups. I started to use fenben pure powder 50 grams 85$ and it's very cost effective.
I dissolve it with oil and have oily meal,you can go up to 2000 mg a day so even on this high dose is a very responsible price comparing to safe guard or panacure c.
Some patients dissolves it with dmso for better absorption.
There are few different fenben in the store including fenben bio that has better bioavailability and you can take it without oil or meal.
Melatonin powder i buy from pure bulk and make my own capsules .
I used to take mebendazol before fenben now I started to take them both and ivermectin will be next every other day.
I was quite stable last few years with orgovyx and abiraterone plus mebendazole and other off label drugs and supplements, now things have changed and psa slowly rising with 2 new mets to lungs probably became mcrpc.
Waiting for a biopsy, meanwhile I got back strongly to my alternative protocol and added penben probably will combine that with chemo soon.
Be well.
I belong to a couple FB groups, I won't bash HH, but I know Merck's Safe-Guard has been tested and is what it purports itself to be.
Dimethyl sulfoxide, DMSO, is amazing. I knew a fellow who drank the stuff every day for his prostate cancer and he claimed at that time that it had given him two additional years of life. He sure worked hard at Brown and Root. However, you could smell his breath ten feet away. I do n ot know about any other treatment he might have been taking. This was twenty-five years ago.
On top of it i was buying Liquid Fucoidan from Japan for my father that costs $1k for 3 months supply. Also, AlgaeCal Plus is another $200 a month. I may have to stop Fucoidan now because of budget constraints and will redirect funds to other supplements. Even though i think Fucoidan helped him to maintain good QOL.
Just buy dog dewormer. Same same
I've never taken TUDCA. For liver? Haven't seen the need over four years. Everybody's different.
What is your daily Ivermectin and FB dose? Thanks
I think it's low risk and cheap. You should discuss it with your med team before taking it, but I can't see any reason not to consider it.
use Merck fenbendazole products (liquid liter size is most cost effective) 1ml has 100mg of fenbendazole so 4 ml a day. prior study on humans and fenbendazole showed that absorption into bloodstream is very poor but did increase when it is taken after large meals (so take it after a large meal)...absorption is not consistent from person to person which is not well understood. I have tried to encourage Joe Tippens to have his blood concentration tested to find out what level of absorption he personally acheives (him being a person whose cancer died taking it) It would be critical to know if he is a person that for whatever reason is able to absorb more into his blood. That really should be the basis of dosing (to actually know what blood concentration is being achieved when prior research on humans demonstrated that some people absorbed nearly nothing at all (and if that is the case then they would not achieve the benefit of fenbendazole to kill the cancer cells). To know the blood concentration one would need a pure reference sample and then analysis of blood at different intervals of time after taking a dose with HPLC (High performance Liquid Chromatography) of the samples to know what type of absorbtion (if any) is being achieved. I would highly recommend trying fenbendazole consistently for at least a couple of months to find out if it works for you since it is very inexpensive and has little to no side effects and there are numerous numbers of people with varying types of cancer that have had positive results such as Joe Tippens and the Merck lab worke who used it on her brain cancer (how joe tippens was told it may help him). 400mg (4ml of 10% suspension) should be sufficient and that is a cost of 70cents per dose
I use the liquid as well.
Which liquid? And is it 4ml x2 daily?
safe-guard dewormer (1000ml is about 170 bucks) amazon.com/Safe-Guard-Dewor...
But what is the dosage for active cancer v. Maintenance?
Joe tippens was cured with only taking I believe a packet of dog dewormer powder 4x a week (222mg). subsequently I believe he has updated via his "mycancerstoryrocks" page that the protocol can be everyday and we use 400mg some people go higher I suppose but the big issue really is that the absorption from digestion is very poor (to increase chances of absorption take it AFTER a large meal which study on it with humans showed it increased absorption for some humans from nothing to a small amount (most of it passes through and is discharged without being absorbed.) absorption is not consistent between individuals that take it and they are not sure why it varies from person to person it may have to do with disgestive ph levels or other factors in stomach so that after meals they do know it increases. there has been some study done with large animals that used DMSO as a means to get absorption but I don't know how exactly they did that, they may have had a source to get pure fenbendazole powder to mix with the DMSO but the merck products (both granule and liquid suspension are only 10% fenbendazole and 90% other ingredients (forgot now what the other inert ingredients were). Tippens does recommend using Merck as the source as there has been other people selling and with some analysis they found it didn't actually contain much if any fenbendazole.
Tippens still takes it ( I think he has now lived 6 years past the point where he had extensive metastisis of his lung cancer with a 3month to death prognosis when he started. If I remember correctly he takes it 3 or 4 times a week and I don't know the dosage it may be the same dog dewormer powder which was 222mg a packet...he would just dump packet and then wash it down with water.
try Lutetium or pluvicto and a lot of prayers.
We’re on the prayers but maybe your other recommendations are the answer to those 
Many thanks
I'm looking to start Pluvicto, either in Australia or in Europe. Until then - and because I've failed both chemos I've tried, I'm looking to add Fenben to the Ivermectin that I currently take. However, dosing seems really confusing. Should I take capsules (444mg?) or the liquid? I weigh 70kg. Amazon has it for sale - could anyone recommend a reliable source?
Stage 4 Prostate cancer. My PSA was 10.29 and Gleason over 10 with metastasis to the shoulder when I started the Tippins Protocol. 12 weeks later it was down to 0.01.I foolishly reduced the dose and in 6 weeks my PSA was 18. I went back on the full protocol and in another 6 weeks PSA was 44.
Do you have to stay on the protocol permanently? Is the healing only temporary? Did I cause my cancer to adjust to the protocol when I went off of it?
I didn't know there was a Gleason over 10?Have you had other treatments? There isn't any info in your bio about your diagnosis or treatments so it's hard to kniw what the protocol has done.
Have you done any ADT at all? I wouldn't use fenben alone to stop raging PCa in its tracks. Use it in conjunction with regular treatment.
When you say he has been 'tinkering', does that mean he's been working with an oncology team and is giving treatments time to work? It would be helpful to know what his diagnosis and treatment details are.
Thanks Pakb, thanks for your interest. in 2020 my uncle was diagnosed with prostate cancer following a PSA, reading of 60 His biopsy gave Gleason score of eight (four, four) and the MRI and other scan, showed that it had spread outside the prostate and was present in lymph, nodes, T3, N1, Mx. it was determined that only systemic treatments would be of value and additionally, that in his late 80s, chemotherapy was not a course of action for him. A multidisciplinary team of oncologists, urologists, and whatever other doctors, the UK hospital had, recommended a course of action, and he began three monthly hormonal injections (not sure which one, but it was reduced the testosterone). He initially responded well, and his PSA came down below one. Thinking he was fixed he chose to stop the hormonal treatment because he strongly disliked the feminising nature of the hormonal treatment. At the same time, he self prescribed a course of low-dose naltrexone (that’s the nature of his tinkering, in addition to the recent fenbendazole) and the LDN seemed to make him feel great but hasn’t ever seemed to impact his PSA or his cancer. Last year is PSA rose to over 100 in June and further scans showed spread to his ribs and a large 15 cm tumour beside his abdominal aortic lymph node. He reinitiated the three-monthly LHRH injections and was put on daily Bicalutamide maximum androgen blocker. By September his PSA was on 600 and a further Oncologist added abiraterone, but his PSA continued to rise , by about 100 a month, and more recently 300 a month, and is now sitting at 1600. The Oncologist has taken him off Bicalutamide and introduced dexamethasone. He is a strong-willed man who is asymptomatic.
Hi. UK here. Pluvicto is available in the UK but is self pay. £13,000 a shot plus extra for scans. See the Royal Marsden website to make enquiries.
I'm on the Care Oncology Clinic protocol alongside ADT (Prostap) and Enzalutamide (Xtandi). There is no way of telling what works but the protocol includes Mebendazole, which you take one month on, alternating with one month on Doxycycline. You also have daily Atorvastatin and Metformin. Cost is approx £300 every 3 months plus an initial consultation fee. Good luck and well done for supporting your Uncle.
Grateful thanks, that’s really useful!
I like the look of the Care oncology clinic and Will get my uncle looking at that. Best wishes for your full and speedy recovery!
How long have you been on COC protocol? I looked into it four years ago but haven't bitten yet.
I started in late January 2021, so 3 years.
Can you tell if it's doing anything at all? I use fenben, berberine, red yeast rice, but haven't found an antibiotic substitute for the one COC uses.
In all honesty I have no idea if the Care Oncology Clinic (COC) protocol works. Neither do COC themselves but so far my results 3 years in have been excellent. Doxycycline is the only part of the protocol I struggle with, when it is hot. It has a photosensitive effect on my head and hands.
Please check my detailed comment on fenbendazole in this forum or download a detailed commentary (dropbox.com/scl/fi/jnklzc3d....
Be very careful! In short: FB is a dewormer claimed to be harmless because it resorbs poorly and should therefore kill parasites only. However, it is a potent drug blocking cell division by the same mechanisms as the well-known drug docetaxel used in chemotherapy against prostate cancer, namely by blocking little protein strings within cells (tubulin) required both for transport of nutrients and for preparing cell division. So, why not using FB instead of the expensive docetaxel?
The reason is simple: FB must enter the bloodstream across the linings of the gut to reach prostate cancer cells. This is very difficult to control because FB blocks also uptake through the cells lining the guts. Thus, it must be repeatedly ingested. By doing so, it will start attacking the stem cells that produce the tissue lining the intestines, possibly ruining the small intestine. While the uncontrollable quantities of FB reaching the bloodstream might kill cancer cells, they will also kill the stem cells of the immune system and other cells producing hair or fingernails. For this reason, chemotherapies with cell-division blockers are done by controlled and precisely scheduled infusions trying to minimize the inevitable side effects such as nausea, vomiting, and reduced immunological response.
The manufacturers of dewormers selling it for pets usually stress that it is harmless but if you read the instructions carefully, you will usually see that feeding FB must be stopped after 3 days and new treatments postponed for weeks. This is a telltale sign for drugs suppressing stem cell division. They just do not tell you that neglecting this schedule can have severe consequences. Interestingly, a previous hype around FB has caused the disappearance of much internet information about side-effects and modes of action of FB, presumably by a concerted action of manufacturers afraid of off-label use of FB in humans. You may also check a Korean paper about this hype:
frontiersin.org/journals/on...
PS: Do not confound FB with the dewormer Ivermectin that has also antiviral and anti-inflammatory properties.
How long did you use fenben?
I've been on it 4 years. What effects should I be seeing in my intestines? I recently had a colonoscopy and a PET scan; what should show up there, based on your research?
That’s a useful, thoughtful reply. Grateful thanks and best wishes for a full recovery.
That’s a very thorough explanation of fb’s pathway but not sure how accurate it is as Joe Tippens has been on it over 7️⃣ years along w thousands of his follower's and to my knowledge hasn’t mentioned anything about it destroying or hurting the small intestines. Furthermore, there are quite a few people here on it including dhhcca that’s been on it four years and I personally have been on ivermectin for over a year and thus far the only side effect is mild lower white blood cell count ( borderline) and I counter it with Vit b3,6, and 12 and a little more organic red meat 🥩…
I have been taking Fenben for a year along with on /off cycling of Ivermectin . Worked my FBZ up to 2000mg / daily and IVM up to 60mg / single dose in evening . FBZ ITake with vit E ( succinate form) , D3/K2, B1, along with cimetidine , Tudcu. IVM taken with Bovine Lactoferrin 600mg. I mix my FBZ powder with olive oil, Vit E succinate 400mg powder and 3grams of ultra fine Clinoptilolite Zeolite powder - mixed into a very loose almost paste and then mixed into mashed Avacado. Then for my 2nd 2pm dose I take the liquid FBZ ( 10 ml ) mixed with 1/2 TSP of DMSO and distilled water 8 oz. This totals my 2000mg pr day. Feel free to prvt message me . I do much more .
Hi, my name is Andy. I have had my prostate removed in May 22. After 6 weeks my psa was 1.6. It hoes up a point a month. The oncologist wants me to do radiation but after seeing what my Uncles and best mate went through, that is not for me. I would love to know your regimen. Any advice would be greatly appreciated.My e mail is bear.ellis0151@gmail.com
Have a top day.
I will call if you want.
I've been on it for 4+ years, Lupron for 5+. I've also done numerous other things since metastatic diagnosis in mid 2018 (plant based diet, no alcohol, supplements, THC, etc.).
I'm still stable on just Lupron, but I'm not yet ready to make any dramatic claims about fenben. It did seem to raise my PSA about 3-4 months after starting it in 2020, but then PSA dropped back and fell to new low. My liver enzymes ALT and AST rose in the early months as well, but after a two-week pause, they fell back as well to new lows. Alkaline phosphatase has been excellent for four years.
Stay tuned!
For 9 months on lupron injection quarterly and aberaterone daily…..T and PSA dropped under .O2
I thought that treatment was standard for prostate lymph node cancer till PSA and T levelsturned higher ?
I am using Fenben, along with a lot of other approaches. Can't say for sure about it's effectiveness, but I am holding steady. No bad side effects from fenben, that I can see. There is a facebook page devoted to it, and you might find more info and experiences there.
I have used Fen and it dropped the PSA like a rock. I didn't detect any side effects from it. I was also on Lupron. My Onc said she never saw such a steep/quick drop in the PSA. Dose was 225/mg, 99% Purity.
May I ask what brand of FB you’re taking ? I’m currently taking Merck paste from chewy.com
If he is willing, you might try to reduce his mets using heat, such as with heating pads. Heat over 106 degrees F can kill cancer cells of all types. It may be worth a try because at his stage of PSA he needs to kill prostate cancer cells, wherever they may be. and however or whenever possible. Also consuming lycopenes such as with tomato soup or juice may help to slow down the progression of the disease. I am only 78 but I have survived well for over ten years with APC. (I'm on Lupron quarterly.)
Awesome, go go go! diagnosed @67 a little over a year ago s4/mets/bones/lymph. triplet protocol with longer term lupron and abiraterone. psa down to .3, lymph mets gone, we'll see about the bones. Do you know people or studies on the heat treatment?
Other than myself, no. Try this:
might want to check florida sharkman on truth social. fb, ivm, doxy, berberine, etc.
FB and IVM is not effective on PCa cells which are androgen dependant and does not lower PSA. I want to meet the people that don't do any conventional ADT and put their life into this unregulated cheap cancer cures from China and get success. If only it was that easy.
Nice to meet you and now you have met someone that’s only taking ivermectin cbd and a cpl supplements with absolutely no ADT for over a year now. Psa has been as high as 19 and when I tried to get off ADT it would shoot up to 6. Discovered ivm a year ago and took it one month with ADT n psa went down to an astonishing .11 and then proceeded to use ivm solely, psa went to 1.95 and had trickled down to.95 after one year. After the year I now take half the dose of ivm n psa has dropped down to .65, I’m not saying I’m out of the woods yet but my oncologist is astonished the psa keeps dropping wo ADT and says whatever your doing is working n to keep it up…as there is always wonderful hope…😁😇😎
Can I ask what brand & dosage of IV your taking ?
Sure I started using this from Mexico
Ivm
Yes but found India was cheaper from “all day chemists”, ivermectol Austra brand.
I started at about 12-19 mg/ day, 4 times a week and after a year then dropped to two days a week n then 1️⃣ now back up to 2️⃣ days a week for maintenance. It’s pretty well tolerated at .4 mg/ kg of body weight, hence 100 kg is 220 lbs, which is what I weigh at 219lbs. Also do 100 mg of cbd oil I get from Lazarus as they’ll give you a 60% discount for low income and or cancer pts I believe and then also do 1900 mg of turmeric w pepper capsules for better absorption. Also may want to do olive oil on days taking ivermectin but it does have an accumulative effect, so if you feel a little off cut back a little on the ivm as I did.
My PSA was 12.3 back in December.Been taking IV & Fenbendazole 222mg Since mid Jan also taking CBD,Bio available Curcumin 1000mg,Berberine 1200mg (JT protocol) Apricot seeds (B17 , Soursop tea ,along with cutting out sugar/carbs kind of keto style diet & 16:8 intermittent fasting. Few other supplements as well. Can you send (or pm me a link from India? Thank you in advance
Sure don’t have link but it’s all day chemists and I get the austro or ivermectol, they’re really good about following up thru the whole process. Here’s a pic
Pic of Austra brand
Thats a promising hopeful result.
Thank you sir, I can’t speak for fenben as I haven’t used it myself but can for ivermectin and thus far it’s been very effective in killing the cancer as it targets Fox A1 and ku70/ku80 in prostate cancer cells. I have a dental background so I understand the pathway to a certain extent in the way the cells are destroyed (apoptosis) n was pretty easy choice for me to give it a try. I can only say it’s worked for me and not very much risk as the drug has been safely administered millions if not billions of times w very few side effects. Also here are my psa results after testosterone returned…
Psa table
And my last most recent psa, all w no ADT for over a year…
Most recent psa
hello I was recommended Fenbendazole for pains in my prostate area I have got say the pains dropped by a good 80% within 3 days so I took them for 5 days then waited a week & took them again for 5 days I am very impressed with the results as I had found sitting down painful before now 2 months on I only take it when I feel pain coming on the other supplement I take is Black Fermented Garlic capsules as the Acillin active chemical is 12 times higher than standard Garlic & this has raised my immune system levels significantly as my bodies oxygen level is 97 to 99% & that’s using my sports watch or the fingertip pulse Oximeter which is really good & shows I’m on the right track now
There are some (largely pre-clinical) data in support of fenbendazole and mebendazole for prostate cancer, though these are far from conclusive. A warning, however, to anyone who has Gilbert's Syndrome: do NOT take these drugs as your liver cannot adequately metabolize them and they may result in rhabdomyolysis. Among drugs with anti-parasitic and possible anti-cancer properties, one that is looking more promising to me than fenben, meben or ivermectin is nitazoxanide, but, again, the data are very preliminary.y
Wow that’s great news 📰, didn’t know about nitrazoxanide but happy to hear about it, as I’m having pretty good luck 🍀 w ivermectin..
how much ivermectin are you taking and on what dosage schedule?
I started at about 12-19 mg/ day, 4 times a week and after a year then dropped to two days a week n then 1️⃣ now back up to 2️⃣ days a week for maintenance. It’s pretty well tolerated at .4 mg/ kg of body weight, hence 100 kg is 220 lbs, which is what I weigh at 219lbs. I do 100 mg of cbd oil I get from Lazarus as they’ll give you a 60% discount for low income and or cancer pts I believe and then do 1900 mg of turmeric w pepper capsules for better absorption. Also may want to do olive oil on days taking ivermectin but it does have an accumulative effect, so if you feel a little off cut back on the ivm as I did.
I have Gilberts Syndrome and take fenbendazole. I would appreciate any links you can give me regarding the liver being unable to metabolize fenbendazole. Thank you.
I've seen a couple case histories and am myself intolerant to it; have Gilbert's. I am happy it has not affected you; so the adverse effect may be highly variable. I cannot tolerate statins either and they have been reported to affect those with Gilbert's adversely. How long have you been taking fenben and at what dosage? The link to this case history is for mebendazole which is biochemically very closely related to fenben.
This notwithstanding, the anti-parasitic drugs are very deserving of further research for their pleiotropic therapeutic effects. Look into nitazoxanide which demonstrated remarkable benefits in an animal model of metastatic PC, where very little has been demonstrated to work, either in preclinical or clinical trials. Also want to note that there seems to be net benefit to having Gilbert's despite some downsides. You may be familiar with that literature.
If appreciate any info about Gilbert's net benefit. I've not heard about that I always just pictured old red blood cells circulating past their prime.
Here's one of the earlier reports on the signifiant benefits of Gilbert's. There are many others. doi.org/10.1111/jgh.12279 here's one more recent:
My 84 year old husband has been on it for over a year. He was diagnosed with stage 4 PCa with a psa of 96 and his last scan, a couple of months ago, was clean. NO SIGN of cancer. He's also been taking a lot more than fenben, Search "Jane McClelland cancer". She's in the UK and has written a book . Also has a list of docs all over the world who have integrated her findings into their protocols. Check her Facebook page for those names. My husband was also on Lupron, which gave him a headstart but dangerous side effects for the long haul. Good luck to you!
how much fenben is he taking and on what schedule, cycling on and off, or continuous?
He takes Panacur for small dogs, 1 gram packet, 3 days on, 4 days off. In addition, he's on a vegan diet, and takes supplements designed to block cancer feeding pathways recommended by Jane McClelland. Like I said, he took Lupron for about a year which also gave him a headstart but isn't viable indefinitely because of serious side effects and the fact that cancer will eventually become insensitive to it, which is a very big problem.
get him on Paw Paw 100 mg and Fenben --1000 mg 4 days on 3 days off , nitazoxanide, 1000 mg daily 30 days then recheck scans,
ultrabotanica.com/product-c...
no side effects on that dosage of nitazoxanide?
Take with a healthy fat and meals
Two for one sale, fenbendazole and a free bag of cat litter..............at your local health-food shoppe.
Good Luck, Good Health and Good Humor.
j-o-h-n
this is JWP & I’m telling you Fenbendezol saved me, I was diagnosed 2 years & 3 months ago & stage 4 Gleason 9 Metastasis bones- lymph nodes- & both lungs extremely weak within a month of Fenbendezol I was running stairs
I've been looking into Fenbendazole for almost a year now, mining threads like these for experiences. Also scouring Facebook Fenbendazole groups, group chats and forums, etc. There are lots of anecdotes but I haven't found any convincing evidence that Fenbendazole does anything for advanced prostate cancer. Universally I'll read about a "success story", but then keep reading or press the poster for more info and find they went on ADT drugs at the same time and/or a kitchen sink's worth of other off-label meds or concentrated supplements. So it's impossible to nail down that it's the Fenbendazole doing the heavy lifting. This thread is chock full of similar examples.
The only interesting "case study" of isolated effect I've come across, assuming the guy was telling the truth, was of an older gentleman with aPCa who reduced his PSA from 79 to 51 and has kept it around there for years using only a gram of Fenbendazole a day (5 packs of Panacur). He mixes it with DMSO to help absorption. This shows it's possible (again assuming he wasn't lying about being only on the Fen), but let's be honest, ~50 PSA is still indicative of extensive metastasis and activity and is hardly a cure by any measure. Still, the guy is apparently alive and kicking and lives a very active and healthy lifestyle with no symptoms (but then again, could this be what's keeping the cancer in check, and not the dog meds?)
If a patient has the type of personality where they'll try dog meds to fight their cancer, chances are they're on 20 other unconventional things purported to fight cancer too. And because this type also likes to go "all-in" when they fight, they'll start taking everything within a very short period too. So what's working, and how would they ever know? If their PSA goes down, was it the Fenbendazole? The artimisinin? The ivermectin? High-dose Turkey Tail or Reishi mushroom extract? Multivitamin????
Half full or half empty. I can honestly tell you that I use ivermectin, cbd oil, turmeric n multi vitamins and absolutely no other natural substances and or heavy exercise worked until I tried the regiment I’m on now. So you can try n convince yourself otherwise but read my posts as the ivermectin definitely seems to be killing the cancer. I follow Joe Tippens protocol except for ivm instead of fenben, so I tend to go w the proof is in the pudding. It’s up to you whether you want to try it or not but I’m a firm believer along w thousands of others that have taken it. Also you refer to it as a dog med but it’s actually a human med that won a Nobel prize for its efficacy and most important safety after being used not millions but billions of times on humans. Hope this helps and yes we have to do anything possible to kill the disease 🦠 not just suppress it. Good luck n feel free to ask me any questions if you have any…😁😇😎
NFLer the OP's question was about Fenbendazole, not your success with Ivermectin. That's amazing that IVM smoked your cancer, but my point remains - almost all of the *Fenbendazole* success stories with advanced PCa are muddled with the inclusion of powerful ADT drugs and/or a boatload of other supplements. And in the one anecdote I saw where the FB was the only thing used with PCa, the results were less than stellar.
"So you can try n convince yourself otherwise" isn't the issue. You don't start with the belief that a dewormer drug cures or controls prostate cancer, then look at evidence to convince yourself it doesn't. You investigate the evidence to determine if there's effectiveness, and if there's enough evidence THEN you're convinced. This is what I've been doing with Fenbendazole, and it's actually the starting point of the entire scientific method.
With this said though I should also say I've seen lots of testimonials about people controlling or outright eliminating SCLC, PanCan, glioblastoma, etc with Fenbendazole alone when conventional medicine fell short. But for prostate cancer it appears to be weak, IF it has any effect at all. In fact for treating CRPC I've found interesting evidence for other off-label meds that control prolactin like cabergoline, bromocriptine, and Levo-dopa (search my posts on this), so I'm not against using an off-label med as long as there's evidence it works.
Last thing, calling Fenbendazole a "dog med" seems to upset its proponents, but despite the past accolades in human use its primary use today IS literally for dogs and livestock (the Panacur packaging in every market has a dog face on it). You can see I literally just got back from the vet because my dog has the runs, and they gave me Fenbendazole for him. If you or I go see the doc for a case of the sh**ts, they don't prescribe us Fenbendazole. Casually calling it a dog med isn't talking down on it, it's calling it what it's primarily used for nowadays.
Dog prescription
Haha I guess they won’t prescribe fenben to us if we have the Shiites but it did seem like you were discounting as only a dog med so my bad, and I thought u were throwing ivm under the bus as well, thanks for clarifying it. I didn’t realize fb was not as effective killing pcA as it is other cancers. Joe Tippens n his Drs claim it’s effective in just about all cancers but I haven’t verified that. I’m not out of the woods yet by no means but thus far the ivm seems to b really working…😁
Last LAST thing, I actually stumbled into taking "75%" of the original Joe Tippens protocol too pretty much by accident.
Since around the time of my diagnosis I've been taking 1000mg of turmeric with piperine daily, after I saw some research showing it can slow or block the formation of bone mets. I started taking 30mg or more CBD nightly too to sleep, with only a couple days off every few weeks since. And a multivitamin with K2 has been part of my daily nutrition since forever. By the time I came across mycancerstory.rocks, the Fenbendazole was the only novelty. I may add an anti-parasitic one day if the beast becomes castrate-resistant, but for the reasons I've already stated I'd go with Ivermectin over Fenbendazole.
OK that’s great info and ironically I also stumbled into following 75% of jt protocol as I read up on pub meds recommendation of repurposing IVM as an anti cancer drug especially pcA only to later find out he was doing the same except w fenben
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