Jim's PSA number has been steadily rising over the past year and his prostate biopsy in 2021 came back negative. From that biopsy, he ended up developing a severe testicular infection that lasted a few weeks. He went through weeks of different antibiotics and it finally went away. Needless to say, we will not be going back to this urologist. We also decided to switch his primary care physician. (Be sure to click on all the blue highlighted links for more info.)
Do Biopsies Spread Cancer?
It’s a question that many doctors quickly dismiss, but the science behind it isn’t entirely clear.
While the general medical consensus is that biopsies are safe, new research is raising concerns. Some studies suggest that certain biopsy methods, such as core-needle biopsies, could potentially increase the risk of cancer spreading (metastasis). This is because the process of obtaining a biopsy may disturb the tumor cells, allowing them to spread more easily.
Further studies have shown that biopsies can trigger changes in the body that promote metastasis, possibly accelerating the spread of cancer to other areas.
There are alternative methods, like advanced ultrasound imaging and liquid biopsies, that don’t involve puncturing the tumor. These options are less invasive and may offer safer alternatives.
Before agreeing to an invasive biopsy, it’s important to ask: Is there a safer option?
A special thanks to Dr. Adiel Tel-Oren for highlighting this important conversation.
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In 2023 we switched his primary care doctor to Dr. Paul Schmidt in Glen Rose, and also got a new urologist in Burleson. We first went to see Dr. Michael Waters (urologist) in December 2023 and discussed Jim's numbers and treatment. First thing they did was get a urine and blood sample. The blood work showed his PSA number came down (36.7 from 39.2), but not by very much. They also checked the percent of free PSA, which came in at 5.4%. (Previous years when his PSA was low, the percent was between 16% and 36%.) "Free PSA measures whatever PSA in the blood that is not bound to proteins. The higher percentage of PSA that is free, the more likely you are to be free from cancer.”
The prostate test that was done with the urine sample was called EPI, or Intelliscore, which looks for markers, or proteins, in the urine. The normal marker for this test is 15.6. If your score is above 15.6, there is a higher risk for clinically significant prostate cancer that needs further treatment, such as a prostate biopsy. Jim's number was 49.
The doctor thinks that his last biopsy did not cover the prostate 100% and could have missed any cancer. So before his next biopsy, Jim will get an MRI so the doctor can actually use that picture when he does the biopsy. The MRI is scheduled for March 1 and the biopsy is scheduled for March 14, 2024.
We won't know if he even has prostate cancer or the degree of it until we get the results back from the biopsy. What if the MRI does not show any cancer? If that's the case, there is nothing else for us to do. I will update this blog post when we find out and determine what route to take.
March 7, 2024: Jim had his MRI on March 1 and we do not know the results of that test. Since Jim does not really want to go through another biopsy, we have opted to cancel the March 14 biopsy and will meet with Dr. Waters on March 21 to discuss the results of the MRI. If the MRI does show cancer, then I want him to do one of the protocols listed below, either Ivermectin or the Fenbendazole protocol.
March 22, 2024: Had an appointment with Dr. Waters to discuss the results of the MRI. It appears that there are some lesions in Jim's prostate and we need to get a biopsy done in order for the insurance to cover any procedures. We now have to wait for his office to get back with us to schedule the biopsy, which looks like will be toward the end of April.
Jim has been taking a new liquid herbal concoction that I found called Prostadine. What this is supposed to do is clear out the toxic mineral coating that inflames the prostate, which adds pressure to the bladder. It also has a number of different types of seaweed, which help protect various organs from chronic disease and fight prostate growth. He is still working on the second bottle, and I have two more bottles.
Prostadine also has Iodine; men who lack iodine deal with ED, hair loss, and extreme fatigue. 10% of iodine is used by the thyroid (Jim's last thyroid number was 3.5, which is normal), and 90% is excreted. The best way to check to see if one needs iodine is to test yourself. Listen to Barbara O'Neill tell how to do that:
April 20, 2024: The hospital, Hugley, will not allow Jim's biopsy to take place until he is cleared by his pulmonologist. This is crazy because the pulmonologist was who we went to for Jim's c-pap. Jim did have an appointment with the pulmonologist but I canceled it because there did not seem any reason to see him as Jim has undergone numerous surgeries without that clearance. But the hospital is adamant that he has to see the guy. But since we are now in Whitney, Texas, and not Glen Rose anymore, it is a 1-1/2 hour drive to Granbury, which I am not going to do. I don't know when we will be back in Glen Rose, so we are going to have to wait for the biopsy.
In the meantime, Jim is still taking the Prostadine in the morning and in the evening is taking 1 capsule of Fenbendazole and 1 dropper of CBD. He also takes 5,000 IU of Vitamin D.
May 14, 2024. I gave in and made an appointment with Jim's pulmonologist. We arrived at Tres Rios in Glen Rose on March 9 and his appointment is this afternoon at 1pm. We will be at Tres Rios until May 26.
May 23, 2024.
This morning we went to Hugley Hospital for Jim’s prostate biopsy. We had to
leave here at 6:30 to get there for a 7:30 check in. They started on him pretty
soon upon arriving, but it he did not get taken into surgery until about 9:45.
I went out to the waiting room, where I sat until about 11:30. The surgery took
about a half hour, and then he went into recovery. Doctor said he was able to
see everything in there using the MRI which made it very easy. He took some
extra samples from around the area and they also had to go into his urethra to
make sure it was working good.
Now later in the day to pee hurts and it’s coming out red
from blood. He was prescribed two things; one for pain and one antibiotic. I
also bought him another thing called Azo which is for UTI pain relief.
Hopefully tomorrow he will feel better; and then he will
start on most of his other herbs for the prostate. We also had to stop the Prostadine and other herbal supplements a week before the biopsy so they would not interfere with the biopsy. He is back on everything, including the Fenbendazole and CBD oil.
May 31, 2024. Jim had a few miserable days when it hurt very bad to pee, but he took the UTI pills which helped with the pain.
June 5, 2024. Jim had an appointment with Dr. Waters this morning to find out the results of his prostate biopsy. He took quite a few plugs, but since Jim had that MRI, Dr. Waters was able to pinpoint where he thought the cancer would be. There were three places that showed cancer: one had a Gleason score of 3+3=6; the next had a Gleason score of 4+3=7; and the third had a Gleason score of 3+4=7.
So, what is a Gleason score? The prostate tissue that was taken is examined under a microscope to see if cancer cells are present. Only a biopsy can confirm prostate cancer. If cancer is found, the tumor is graded in the medical lab. The grade indicates the difference in appearance between normal cells and cancer cells when seen through a microscope. A Gleason grade ranges from 1 through 5 and is based on the degree of differentiation among the cells. A Gleason grade of 1 indicates that the cancer cell clusters resemble the small, regular, evenly spaced prostate tissue, while a grade of 5 indicates irregular, fused cancer cells that have spread to surrounding tissues.
Prostate cancers often have areas with different grades. Therefore, a
grade is assigned to the two areas that make up most of the cancer. These two
grades are added together to yield a Gleason score between 2 and 10. Prostate
cancers are often divided into 3 groups, based on the Gleason score: (1) Score
of 6 or less: low-grade, most likely to grow and spread slowly; (2) Score of 7:
intermediate grade; (3) Scores of 8 to 10: high-grade, most likely to grow and
spread. (Jim’s scores were 6, 7 and 7.) His grades were in the 3 and 4 group of cancer
cells.
While there Dr. Waters talked about giving men shots to help reduce the
size of the prostate, so we opted to get one of those. He was given Camcevi, which was given into his abdomen. Camcevi is a medicine used in adult men for the treatment of advanced prostate cancer that is 'hormone-dependent', meaning that it responds to treatments that lower the level of the hormone testosterone. It's an effective advanced prostate cancer therapy to lower testosterone. He got his first shot on June 5, 2024, which is good for six months. Camcevi Patient Brochure.
WHY LOWER YOUR TESTOSTERONE (T) LEVELS? Testosterone is the main hormone, or androgen, in men.
It is this hormone that “feeds” prostate cancer and allows it to grow.
Hormone-blocking therapies are designed to stop your body from making
testosterone so it can’t feed the cancer.
Patients receiving leuprolide for advanced prostate cancer:
- At first, some of your symptoms might get worse for a short time or you might have new symptoms. You might have bone pain, back pain, a tingling or numbness in the body, blood in the urine, or trouble urinating. Tell your doctor if you have any new symptoms or if your symptoms get worse.
- This medicine may affect blood sugar levels. If you notice a change in the results of your blood or urine sugar tests or if you have any questions, check with your doctor.
- This medicine may increase your risk of having a heart attack or stroke. Check with your doctor right away if you are having chest pain or discomfort, nausea or vomiting, pain or discomfort in the arms, jaw, back, or neck, confusion, slurred speech, or weakness.
- This medicine can cause changes in your heart rhythm, including a condition called QT prolongation. It may change the way your heart beats and cause fainting or serious side effects. Contact your doctor right away if you have any symptoms of heart rhythm problems, such as fast, pounding, or irregular heartbeats.
- This medicine can cause your bone mineral density to decrease, which may lead to osteoporosis or weakened bones. Talk with your doctor about how this risk will affect you.
- Using this medicine may increase your risk of having seizures. Check with your doctor right away if you start to have convulsions, muscle spasm or jerking of the arms or legs, sudden loss of consciousness, or loss of bladder control.
- Some men who use this medicine have become infertile (unable to have children). Talk with your doctor before using this medicine if you plan to have children.
Before you have any medical tests, tell the medical doctor in charge that you are using this medicine. The results of some tests may be affected by this medicine.
For males only (adults) More common side effects:
arm, back, or jaw pain
bloody or cloudy urine
blurred vision
bone pain
chest pain or discomfort
difficult, burning, or painful urination
difficulty with moving
dizziness
frequent urge to urinate
headache
increased urge to urinate during the night
muscle pain or stiffness
nausea
nervousness
pain in the arms or legs
pain in the joints
pale skin
pounding in the ears
slow or fast heartbeat
sweating
unusual bleeding or bruising
unusual tiredness or weakness
waking to urinate at night
bloody or cloudy urine
blurred vision
bone pain
chest pain or discomfort
difficult, burning, or painful urination
difficulty with moving
dizziness
frequent urge to urinate
headache
increased urge to urinate during the night
muscle pain or stiffness
nausea
nervousness
pain in the arms or legs
pain in the joints
pale skin
pounding in the ears
slow or fast heartbeat
sweating
unusual bleeding or bruising
unusual tiredness or weakness
waking to urinate at night
Potential side effects:
- Common: Hot flashes, hypertension, injection site reactions, upper respiratory tract infections, musculoskeletal pain, fatigue, and pain in extremities are common side effects occurring during a median follow-up of 336 days.
- Serious: Serious adverse reactions can occur, including subdural hematoma, cerebrovascular accident, and pulmonary embolism.
- Symptoms worsening temporarily: During the first few weeks, prostate cancer symptoms might temporarily worsen due to the initial testosterone flare.
- Potential long-term effects: Camcevi can increase the risk of hyperglycemia and diabetes, heart problems (including heart attack, sudden death, and stroke), and seizures. It can also potentially cause impotence and impair fertility in males of reproductive potential.
Jim will now get a Posluma
(imaging agent) PET imaging scan. The Posluma PET scans help develop an
informed treatment plan for prostate cancer because they provide important
information. How do PET scans work?
First an imaging agent (like Posluma) is injected into the body. Then it binds
to a target, such as cancer cells, to light it up. This can be seen on images
from a PET scan, showing the location of the disease. As an advanced diagnostic
imaging agent, Posluma is highly specific to the prostate-specific membrane
antigen (PSMA) and attaches to it, highlighting prostate cancer where it’s
located.
We have a follow-up with Dr. Waters next month, and then will be
seeing an oncologist named Matthew Cavey in Fort Worth on July 19. Luckily it will be by telehealth so we do not have to drive into Fort Worth for the initial consultation.
June 18, 2024. Jim has his PET scan today. We drove 1.25 hours into Fort Worth to Texas Health. It took about two hours for the whole procedure, with the injection of the isotope taking the longest -- one hour for it to get into his body. The scan itself only took 20 minutes.
Imaging Report
Texas Health Fort Worth
700 5th Ave
Fort Worth, TX 76104
Ph: 817-250-3568 Fax: 817-250-3544
NAME: James Kerch ACCT ID:
MRN: 2000327657ROOM/BED:
DOB: 7/27/1952E Number: E11724624
AUTHORIZING PHYSICIAN: Michael Waters
ORDERING PHYSICIAN: Needed), Thr*External Provider (Signed Paper Order
CC PHYSICIAN:
| Your Result Images |
| View Your Images Here |
Important Disclaimer: Computer aided detection markers are for radiologist use only and are not indicative of findings. Please contact your provider directly if you have questions about your results.
| Study Result |
Narrative & Impression | |
EXAM: PET/CT F-18 rhPSMA tumor imaging HISTORY: Malignant neoplasm of prostate. Elevated PSA. Acute. Initial encounter. Staging. TECHNIQUE: PET/CT images acquired from skull vertex caudad through proximal thighs. Images acquired on a PET/CT Scanner utilizing CT attenuation correction techniques, at a usual delay after intravenous administration of 8.7 mCi F-18 rhPSMA (Posluma). PET/CT images reconstructed and presented in axial, sagittal and coronal planes for review. CT images acquired for attenuation correction and anatomic localization (but not a diagnostic CT and not interpreted independently). COMPARISON: None available. FINDINGS: Focal intense abnormal increased tracer uptake from midline rightward at ventral mid prostate gland level. Maximum SUV 14.3, avidity about 2 cm AP by 1.6 cm transverse by 1.7 cm craniocaudad by PET. Compatible with PSMA avid prostate gland malignancy. Intense abnormal increased tracer uptake (much greater than background) at posteromedial left ninth rib (maximum SUV 4.8) and posteromedial left seventh rib (maximum SUV 4.7). No well-defined sclerotic or lytic bony lesional correlates at these bones by attenuation correction CT. Presumed PSMA avid bony metastatic disease at a couple of left ribs. No definitely abnormal increased tracer uptake (with respect to physiologic background) at abdominopelvic lymph nodes. Variable intensity tracer activity elsewhere appears to be within physiologic limits of normal. Additional incidental findings by attenuation correction CT include: Inflammatory paranasal sinusitis sequelae. Atherosclerotic disease including coronary artery involvement. Low-grade type patchy modestly increased density at mostly dependent lung zones (e.g. subsegmental atelectasis and/or postinflammatory sequelae). Several scattered variably sized low-density liver lesions, incompletely characterized but possibly cysts. Colonic diverticulosis. Scattered arthritic and chronic appearing other bony features. Impression: IMPRESSION: Features are most compatible with PSMA avid malignancy at the prostate gland and a couple of left ribs. -Electronically Signed By: Rodney Bowman, MD -Electronically Signed On: 6/19/2024 8:08 AM Report Ends |
| Signed |
| Electronically signed by Bowman, Rodney Russell, MD on 6/19/24 at 0808 CDT |
June 24, 2024. The results of the PET are in his Advent profile but when I looked at them, the pictures did not look anything like I expected (the above picture). They were confusing to look at and I did not understand any of it. We have an appointment with Dr. Waters on July 10 to discuss the scan.
July 10, 2024. We drove up to Hugley Hospital to see Dr. Waters this morning. What a long drive for us to see him for about 5 minutes. He verified that the PET did highlight the cancer in the prostate. He also mentioned that there were a couple of other spots in his rib cage area that were highlighted but he did not know what that meant. He said that this is Dr. Cavey’s area and he will tell us about them.
July 19, 2024. Had a telemed conference with Dr. Matthew Cavey which was good as it's a 1-1/2 hour drive to his office; this was just an introduction to him and for him to give us his plan on Jim's prostate. Since Jim got the Camcevi shot, which put his cancer to sleep and reduce the size of his prostate, Dr. Cavey will not start treatment until the end of October as he wants the Camcevi to be less in Jim's prostate.
Dr. Cavey did mention the two spots on Jim's ribs, but did not seem too concerned about them. He said that we will wait until Jim gets another PET next year and see if they are still there. That will be in September 2025. However, this is what is really means.
The following is what I copied from Jim's PET results -- June 19, 2024:
History: Malignant neoplasm of prostate; elevated PSA.
Findings: Focal intense abnormal increased tracer uptake from midline rightward at ventral mid-prostate gland level.
Intense abnormal increased tracer uptake (much greater than background) at posteromedial left 9th rib and posteromedial left 7th rib. No well-defined sclerotic or lytic bony lesional correlates at these bones by attenuation correction CT. Presumed PSMA (prostate-specific membrane antigen) avid bony metastic disease at a couple of left ribs (bone metastasis cancer condition that occurs when cancer cells spread from their original site to the bones. The term "avid" can refer to how well a PET scan can detect the extent of active malignancy in the bones.) No definitely abnormal increased tracer uptake (with respect to physiologic background) at abdominopelvic lymph nodes.
When someone has avid bony metastatic disease at a couple of left ribs, it means that cancerous cells from another part of the body have spread to the ribs on the left side, and these areas show increased metabolic activity, often indicative of active tumor growth or aggressive disease.Let's break down the terms:
- Metastatic disease: This means cancer cells have broken away from the original tumor and spread to other parts of the body.
- Bony: The cancer has spread to the bones.
- Avid: In this context, "avid" indicates that the metastatic lesions in the ribs show significant uptake of a tracer substance during imaging scans, such as a PET scan. This heightened uptake typically reflects high metabolic activity, which can signify active cancer cell proliferation.
- Couple of left ribs: Specifically points to the location of the metastatic lesions.
- What does this mean? This indicates that the primary cancer has spread to the bones, specifically affecting two ribs on the left side, and these metastatic lesions are actively growing or metabolically active
Variable intensity tracer activity elsewhere appears to be within physiologic limits of normal. Additional incidental findings by attenuation correction CT include: inflammatory paranasal sinusitis sequelae. Atherosclerotic disease includes coronary artery involvement. Low-grade type patchy modestly increased density at mostly dependent lung zones (e.g., subsegmental atelectasis and/or post inflammatory sequelae).
According to AI Overview, subsegmental atelectasis in the lung bases refers to a mild form of lung collapse affecting small portions of lung tissue, typically appearing as thin, linear opacities at the lung bases on imaging. It's often asymptomatic and usually doesn't indicate a serious underlying condition, often resolving on its own.
Several scattered variably sized low-density liver lesions, incompletely characterized but possibly cysts. Colonic diverticulosis. Scattered arthritic and chronic appearing other bony features.
Impression: Features are most compatible with PSMA avid malignancy at the prostate gland and a couple of left ribs.
July 31, 2024. Dr. Cavey's office finally called to set up the dates for Jim's treatment. We have to go to Baylor Scott White in Fort Worth on October 8 at 2pm for the pre-op and to get the gold beads inserted in his prostate. He will get a CT exam on October 15, and treatment starts on October 29. It will be every other day and I am hoping it will be M-W-F of the following week. I need to check on that as I have to make RV reservations at Benbrook COE, which is about 17 miles from the hospital.
There are four different types of prostate cancer: (1) adenocarcinoma; (2) transitional cell carcinoma; (3) squamous cell carcinoma; and small cell. Dr. Cavey said that Jim as the first kind -- adenocarcinoma (which is what all prostate cancer is).
There are four stages of prostate cancer: (1-2) early (within the prostate); (3) beyond the prostate (just around the prostate); and (4) beyond the prostate (lymph nodes, etc.) Jim is in the 2B stage.
October 27, 2024. We have been staying at our place in Whitney since Jim will be undergoing radiation therapy. It is now time to head out to the COE park nearer to Dr. Cavey's office. His treatment starts tomorrow, Monday October 28; every other day for five treatments. I have kept up with the Fenbendazole and CBD oil pretty much every night. His prostate has shrunk, from the Camcevi shot maybe, but he just had blood work and his PSA number is now 4.3. He is also taking Tamsulosin which I think also shrinks his prostate.
November 10, 2024. Jim went through the five radiation treatments, every other day beginning on October 28 and ending on November 6. He was taking .8mg of Tamsulosin during treatment, but now is taking .4mg, which is the normal dosage. He is also back on Prostadine drops to help shrink his prostate and keep is small. He is also still taking the Fenbendazole and CBD oil. I am wondering if it is working as he is having trouble peeing. Says that he feels like he has to pee, but then either nothing comes out or it takes a while before the pee comes.
His next appointment with Dr. Cavey is on February 7, 2025, with a PSA test a week prior.
After reading Mr. Bollinger's chapter on Alternatives to Conventional Cancer Screenings (highlighted in the next section), I am going to ask Dr. Cavey to add another test to check to see if Jim's cancer has been eradicated. I don't think just the PSA will be enough. What about the spot on his rib? Neither doctor wanted to check into it any further, but I think one of the tests I listed will tell us if it is anything to worry about.
After studying the various forms of screenings, I think the one to get for the prostate besides the PSA is the Oncoblot, or ENOX 2, test. This one has a particular marker for prostate cancer, so we will know for certain if it's gone.
I am also going to ask for the HRB or high-resolution blood analysis. This test detects the presence of cancer cells before they become tumors. If cancer is present, HRB analysis can pick up on the particular cellular imbalances that caused it. This will pick up whether cancer may form in the future, or if it is currently present, and hopefully will give us some direction on the ribs.
November 13, 2024. Jim had an appointment with Dr. Waters stemming from a call I made to his office to find out about the spots on his ribs. Dr. Waters had no information on that and said the same thing Dr. Cavey said -- sit and wait to see what happens. However, in the meantime he wants Jim to get another Camcevi shot next month. So we are back to Tres Rios after Thanksgiving with an appointment on December 12 for Jim to get another shot.
December 12, 2024. Drove to Dr. Waters' office this afternoon for Jim to get another Camcevi shot. I really do not like the fact that this shot kills Jim's testosterone and sexual function. We don't even know at this point if the radiation treatment he got killed the cancer. We asked both doctors this question: "If he gets another Camcevi shot that puts the cancer to sleep, reduces the size of the prostate, and lowers his PSA, how will we know if the radiation treatment killed the cancer cells?"
The answer we get is that they both work together to kill the cancer cells. It does not make sense to either of us. Dr. Cavey wants him to get another one through November 2025, which would put Jim in June 2025 to get another one. We are not sure we will do that, so I think we'll get another PSA test before deciding on the shot. I do not plan on being around this area in June -- it's time to travel again.
February 8, 2025. Jim had his bloodwork done this week. His PSA came back at 0.5 and his testosterone is 23 ng/dL (VERY LOW). Normal testosterone levels for men over 61 are 150-600 ng/dL. Needless to say, his sex drive is gone. I don't like it and neither does he. Dr. Ken Berry says that T levels should be around 700-800-900 to be optimum.
During our conference call with Dr. Cavey, he agreed that the last Camcevi shot Jim got in December will affect his PSA and testosterone levels, so getting this blood work really gave no indication of the presence of cancer. We told him that Jim was not going to get any more Camcevi shots (they cost us $300), which shot costs $5,000.
- Chemical castration, or androgen deprivation therapy (ADT), involves using medications (Camcevi) to reduce testosterone levels, which can be used to treat prostate cancer or other conditions. Chemical castration is generally reversible, meaning that once the medication is stopped, hormone production usually returns to normal.
Dr. Cavey said it will take about a year (December 2025) for Jim's testosterone to come back up, and that will also depend on whether Jim alters his eating and drinking habits to normally raise the numbers. Fast forward to today, August 31, 2025 ~~ So far, Jim has not cut down on his hard liquor and does not drink his vitamins and herbs. Unless he alters his behavior his testosterone levels will not go back up.
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How does a man get his libido/testosterone back? It can be done without drugs. The drug that helps raise testosterone destroys the body's ability to produce testosterone on its own. I don't think a man would want that. So, maybe one should follow the natural methods, which you can read about in my blog on How to Raise Testosterone Naturally.Dr. Cavey said he was going to order another PET scan for August, but that just may be held off until October if we end up traveling this summer. I don't know why he would put Jim through another PET scan when a simple blood test would tell us if the cancer was still there. That test is 75 KDa ENOX2 isoform, identifiable in their serum aka "ecto-NOX disulfide-thiol exchanger 2." The other blood test that would be helpful is an HRB (high resolution blood analysis) which detects the presence of cancer cells before they become tumors. If cancer is present, HRB analysis can pick up on the particular cellular imbalances that caused it. (These blood tests are discussed below.)
May 22, 2025. Jim is coming up on the six month end of the last Camcevi shot that he got in December. He is not going to get another one. This drug may have helped his prostate cancer, but I think the side effects of this drug are worse than having prostate cancer. Not only did it crush his sex life to zero, it also caused him to fall, lose muscle and keep him fatigued.
June 2025. I made Jim an appointment with Dr. Cavey for October 15. They will set up the PET for September, and will send in for blood work to LabCorp for PSA and Testosterone. Dr. Cavey will not do any any other blood tests, so I will send a note to Dr. Schmidt because I want Jim to get a couple other blood tests that test for cancer. (These tests are explained below.)
I am going to request an AMAS (anti-malignin antibody in serum), an HRB (high resolution blood analysis. If cancer is present; this test can pick up on the particular cellular imbalances that caused it.), and an ENOX2, prostate cancer patients pick up this specific marker.
June 29, 2025. We are still trying to figure out if the Camcevi shot is still affecting him physically. He still complains about his legs feeling very weak and his joints hurting. I have decided to give him another round of Fenbendazole. If he does have an avid malignancy on his ribs, maybe this will knock it out. I'm giving him 222mg twice a day for five days; stop for five days; then another round.
August 22, 2025. Jim is still saying he feels weak; his legs especially, and he gets tired quickly. According to WebMD, these are symptoms of advanced prostate cancer. We do not know if the cancer is gone, or if these symptoms are an after effect from the Camcevi shot, even though it's been eight months since he had the shot. How long does it stay in the body? He complains of fatigue, and still has ED (from the Camcevi shot), urinary incontinence, weak bones (he does not exercise regularly), and eating and digestive problems.
What does he need to do to regain his health; his stamina? Diet and exercise mostly. I try to get him to eat better, but he still drinks too much and does not exercise regularly. He does not drink enough water. He won't take his vitamins.
Alcohol is full of carbohydrates. When you drink a lot of it, you are adding sugar into your system. You gain weight, which puts pressure on your heart and can raise the chances that your cancer comes back. Too much alcohol can also limit your doctor's choices to treat you.
"Alcohol affects your liver," Pomerantz says. "And many of the cancer drugs that we use are metabolized by the liver. When you put undue pressure on your liver, it can affect our ability to deliver certain medicines."
Alcohol can also keep your body from processing and absorbing certain essential vitamins and nutrients.
September 12, 2025. As I mentioned before, Jim has an appointment with his oncologist on October 15 and with his regular PCP on October 28. In the meantime, he has to get blood work done. In addition to the normal CMP panel that gets done, I am going to request the following blood tests that will help diagnose any cancer that he may have, and if the prostate cancer is gone as well as his testosterone panel.
(1) Testosterone & PSA
(2) DHEA, DHT, Estradiol, Pregnenolone & Progesterone (complete T panel)
(3) AMAS (anti-malignin antibody in serum) - detects any type of cancer
(4) ENOX2 - prostate cancer patients exhibit a specific ENOX2 marker (75KDa ENOX2 Isoform)
(5) HRB (high resolution blood analysis). If cancer is present, this test can pick up on the particular cellular imbalances that caused it
October 9, 2025. Well, trying to get additional blood tests failed. These specific tests are not offered through LabCorp and I don't know where to find them. Jim did not get another PET test, but we did get the other blood tests back. His PSA is now .1, which is low, but does that mean he is cancer free? Without other blood tests or the PET, we won't know.
We also do not know about the spots on his ribs. When he has his appointment with Dr. Cavey or Schmidt, I will have to ask about another oncologist who can look at the PET test and find out what to do next.
October 11, 2025. Dr. Cavey's office called and said that he wants Jim to get a PET test before he will see him again. We re-scheduled his appointment to Oct. 30 and in the meantime are waiting to hear from Harris Methodist Hospital in Fort Worth to schedule it.
I was also reading Wide Awake Media on X about how cholesterol numbers have changed over the years and why statins do nothing to help cholesterol levels. "What was considered acceptable cholesterol in 1960 was 300, then 240, then 200. ~~ "Every time they lower that number, another 50 million Americans need drugs. For every 1,000 healthy people who take statins, they prevent exactly one heart attack. The other 999 just get side effects. When researchers studied people over the age of 60, those with higher cholesterol lived longer. Not shorter, longer."
This prompted me to research why Jim's cholesterol levels went up. I wanted to find out if ADT (androgen deprivation therapy (Camcevi)) causes an increase in cholesterol levels, and I discovered that it does. It changes the blood glucose. His glucose levels went up from 113 to 120 between Feb. 2025 to Oct. 2025. Unfortunately, his doctor never requested any of these tests in 2024.
Jim's cholesterol levels from February 2025 to December 3, 2025. (Never was checked in 2024.) Total went up from 189 to 210; LDL from 110 to 138; and triglycerides from 145 to 175.
He got two Camcevi shots -- one on June 5, 2024 and the second on December 5, 2024. But how long does it take for the Camcevi to cause the increase? Note, that he did not get any cholesterol tests in 2024, and in early 2025, his levels were normal, but then rose 7 months later. This is the article that I referenced ~~ Changes in blood glucose and cholesterol levels due to androgen deprivation therapy in men with non-metastatic prostate cancer
October 20, 2025. PET/CT exam at Texas Health Center:
Imaging Report
Texas Health Fort Worth
700 5th Ave
Fort Worth, TX 76104
Ph: 817-250-3568 Fax: 817-250-3544
NAME: James Kerch ACCT ID:
MRN: 2000327657ROOM/BED:
DOB: 7/27/1952E Number: E11724624
AUTHORIZING PHYSICIAN: Matthew Lee Cavey, MD
ORDERING PHYSICIAN: Cavey, Matthew Lee, MD
CC PHYSICIAN:
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Important Disclaimer: Computer aided detection markers are for radiologist use only and are not indicative of findings. Please contact your provider directly if you have questions about your results.
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EXAM: PSMA PET/CT imaging HISTORY: Prostate cancer status post radiotherapy November 2024, subsequent encounter TECHNIQUE: PET images from the top of the skull through the pelvis are acquired utilizing CT attenuation correction techniques, approximately one hour after intravenous administration of 8.7 mCi Posluma (flotufolastat F18-PSMA/ glutamate carboxypeptidase II). The simultaneously acquired CT slices are obtained for attenuation correction and anatomic localization purposes with low-dose technique, using neither oral nor intravenous contrast enhancement. COMPARISON: 06/18/2024 PET/CT FINDINGS: As a reference, standardized uptake values (SUV, normalized to body weight) of mean liver background are measured at 4.3, with mean salivary uptake measured at 4.7. In the head and neck, physiologic uptake in the salivary and lacrimal glands. No cervical lymphadenopathy or suspicious nodal uptake. Unremarkable thyroid tissue. In the chest, normal caliber of the aorta and main pulmonary artery. No pericardial effusion. No mediastinal or hilar lymphadenopathy or suspicion nodal uptake. No suspicious pulmonary nodules. No axillary/subpectoral lymphadenopathy. In the abdomen, multiple simple hepatic cysts, some hypodensities are too small to be further characterized. Hepatomegaly, measures 20.3 cm at the mid clavicle line. Increased in size of the liver and spleen compared to prior PET/CT. Otherwise physiologic distributions of isotope in the liver, spleen, bowels without suspicious lesion. The expected variable tracer activity is seen within gastrointestinal and urinary tracts. Unremarkable gallbladder. Colonic diverticulosis without inflammation. No lymphadenopathy or suspicious nodal uptake in the abdomen. In the pelvis, prostatomegaly, with fiducial markers in place. Resolution of previously seen focal uptake in the prostate gland. No new suspicious focal uptake in the prostate. No lymphadenopathy or suspicious nodal uptake in the pelvis or inguinal region. In the visualized extremities, physiological uptake in the soft tissue. In the bones, interval resolution of previously seen focal uptake at left posterior seventh and ninth rib. Otherwise physiologic uptake in the bone marrow. No suspicious focal uptake. Impression: IMPRESSION: 1. Resolution of previously seen focal uptake in the prostate gland. No new suspicious focal uptake in the prostate. 2. Interval resolution of previously seen focal uptake at left posterior seventh and ninth rib. 3. No evidence of new PSMA-avid metastatic disease. 4. Increasing size of the liver and the spleen, now with hepatomegaly, please correlate clinically. (This is what concerns me now.) -Electronically Signed By: Chenxi Wu, MD -Electronically Signed On: 10/21/2025 8:26 AM Report Ends |
| Study Signed |
| Electronically signed by Wu, Chenxi, MD on 10/21/25 at 0826 CDT October 30, 2025. We had a conference call with Jim's oncologist today and he confirmed that the prostate cancer is gone as well as the spots on his ribs. It's still hard to figure it out from the pictures as we are not experts on reading them. We could not get a complete testosterone panel because Labcorp dropped the ball and did not do them when Jim got his recent blood work. His PSA is zero, so Dr. Cavey wants Jim to get tested again in six months. He said that the Camcevi shot, which knocks out testosterone levels, should still be getting out of his system and hopefully his T will come back up. We have another telemed conference set with Dr. Cavey on October 30, 2026. Jim has T herbs to take to help his T come back up, but he also has to adopt a healthier life style (stop drinking, start exercising more). April 13, 2026. The worst thing we did for Jim's cancer was to get two Camcevi shots. It killed his testosterone and it has not come back up. |
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How do you keep your prostate healthy? It takes some work and the willingness to give up some foods, such as sugar and alcohol. What if the foods you eat every day are quietly increasing your risk of prostate problems? In this video, Dr. Rena Malik breaks down eight foods linked to higher risk of prostate cancer and enlarged prostate, including fried foods, processed meats, sugary drinks, alcohol, and high-dose calcium supplements. She explains how these foods drive insulin resistance, inflammation, and metabolic issues that impact prostate health over time.
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I am reading a book by Ty Bollinger called The Truth About Cancer: What You Need to Know. This last chapter I just finished talked about mammograms and PSA tests with an emphasis on Alternatives to Conventional Cancer Screenings. Mr. Bollinger did some extensive research on cancer and his last statement in this chapter is to share this information with people to help them avoid falling victim to the radiation- and surgery-based screening methods that harm more than they help, so that's what I am doing.
Alternatives to Conventional Cancer Screenings
1) Thermography. This method is strictly an alternative to mammograms. Thermography utilizes the power infrared heat to detect physiological abnormalities indicative of a possible breast cancer diagnosis. I am not going to go into detail here. If you want more information on thermography, please visit by Blog: Staying Healthy into Your 70s and Beyond where I have more information and videos on thermography.
2) AMAS (Anti-Malignin Antibody in Serum). Anti-malignin antibody in serum testing is a highly effective screening method that's capable of detecting any type of cancer with 95% accuracy after one test, and over 99% accuracy after two tests.
AMAS is an antibody that occurs naturally in blood serum, and it becomes elevated when any type of cancer starts to flourish and spread. It shows up first before any other anticancer antibody, which means it's technically the earliest cancer detection tool available. AMAS testing is nontoxic, exceptionally accurate, and can be used both for detection and monitoring.
All cancers make anti-malignin antibody. When our immune system identifies the presence of malignin, it starts making anti-malignin antibodies. When a treatment shrinks a cancer, the AMAS will go down. Normally, a healthy immune system (one with activated macrophages) is destroying these cancer cells as they are formed. An AMAS level that rises beyond the baseline of 135 tells us that the immune system is not getting rid of those new cancer cells in a timely way, and their numbers are therefore increasing. Cancer is afoot.
AMAS testing is a highly effective method of both detecting cancers early and tracking their progression as a patient undergoes treatment and/or makes dietary and lifestyle changes to help bring AMAS levels back down to the normal range. (The normal range of AMAs is 0.0-9.0 IU/mL.)
One of the weaknesses of the AMAS test is that it can't identify precisely where a cancer might be forming: it can only pick up that a cancer is forming somewhere, which is helpful to an extent. The Oncoblot Test, on the other hand, is capable of revealing a cancer's organ(s) of origin with about 96% accuracy.
It sounds to me that you have to know what cancer you are looking for and what the marker is. What about the spots on Jim's ribs? How will this test tell us if those are malignant? We want to know about the prostate cancer, but also what is happening with the spots on his ribs.
3) Human Chorionic Gonadotrophin (HCG) Urine Immunoassay. Similar to how a pregnancy test works, an HCG urine immunoassay identifies the presence of HCG in the urine. This hormone is normally released by human embryos upon conception, but it is also released by cancer cells as a cloak to get past the immune system. The higher the levels of HCG in one's urine, the greater the malignancy of a present or impending cancer.
HCG urine immunoassay has a remarkable success rate of about 98%. It can detect brain cancer as early as 29 months before the first symptoms appear. "Thousands of cancer survivors have used this test over the years to keep track of their treatment(s) success and check the status of their remission."
A human chorionic gonadotropin (hCG) urine immunoassay can help detect a number of cancers, including:
- Testicular cancer: In germ cell testicular tumors, cancerous cells can transform into syncytiotrophoblasts, which secrete hCG. Elevated hCG levels are usually a sign of aggressive disease and poor prognosis.
- Ovarian germ cell tumors: hCG is commonly used as a tumor marker in ovarian germ cell tumors.
- Gestational trophoblastic diseases (GTDs): hCG is used as a tumor marker in GTDs like hydatidiform mole and choriocarcinoma
- Other cancers that may be associated with elevated hCG levels include:
Hepatic cancers, Neuroendocrine cancers, Breast cancers, Pancreatic cancers, Cervical cancers, and Gastric cancers.
However, hCG levels can also be elevated in non-cancer conditions, such as cirrhosis, duodenal ulcer, and inflammatory bowel disease. HCG levels can also be elevated in the presence of marijuana use.
A urine test for hCG should only be performed by an accredited lab upon the advice of a physician.
4) Oncoblot Test. Cancer cells have certain unique identifying attributes that differentiate them from normal cells, and forward thinkers are figuring out what these are, how to identify them, and how to use this knowledge to help people avoid and/or overcome cancer. The Oncoblot test fits this M.O. perfectly, but rather than look for hormone in urine or antibodies in blood, it looks for protein that only exists on the outer surfaces of certain types of cancer cells.
Discovered by Dr. James Morre when he was spraying crops with Agent Orange during his teenage years, Agent Orange is a selective herbicide, killing the weeds but did not kill the crops. He realized that human cancer cells have their own markers that can be selectively targeted, or at least identified, and one type of marker is NOX proteins. He later honed down to a single NOX protein that he dubbed tNOX, now known as ENOX2, which only exists on the outer surfaces of malignant cancer cells.
Each type of cancer has its own distinct form of ENOX2, which makes it quite simple to pinpoint the specific type of cancer from which a person is suffering. "The protein has a different weight depending on where the cancer originated." The test not only shows whether you have cancer, it can tell you exactly where it started. (According to research, prostate cancer patients exhibit a specific ENOX2 marker, which is a 75 kDa ENOX2 isoform, identifiable in their serum, with variations in isoelectric points depending on the individual case; this is referred to as "ecto-NOX disulfide-thiol exchanger 2" (ENOX2).)
5) Thymidine Kinase Test. The previous early detection protocols identify antibodies (AMAS), hormones (hCG), and proteins (ENOX2) in conjunction with cancer. This test looks for enzymes thymidine kinase 1, or TK1, an enzyme that repairs damaged DNA inside the body. It's typically associated with the proliferation of malignant cancer cells.
This test can be used not only to detect cancer but also to track its progression, furnishing patients and their doctors with an insight into the effectiveness of a particular cancer treatment. The original version of the test looked only for TK1 in blood serum, but newer technologies can also detect it in tumor tissue.
6) Nagalase Test. Our immune systems are fully equipped to make mincemeat out of cancer, but certain conditions must be met in order for this to happen. The macrophages that scope out, attack, and eradicate cancer cells must first be activated by GcMAF, short for Group Specific Component Macrophage Activating Factor, in order for this immune response to occur and be effective. One of the reasons why this often isn't the case is because cancer cells have learned how to outsmart the immune system, producing a substance known as Nagalase that blocks the production of GcMAF and effectively turns macrophages into macrofailures. Dr. Smith describes macrophages that lack GcMAF as being "zombies" stuck in a state of suspended animation.
Nagalase is basically an enzyme secreted by cancer cells as they go about their business of forming into a tumor. It attacks the extracellular matrix of GcMAF, rendering it impotent and incapable of generating an appropriate immune response to the invading cancer. "GaMAF is a protein that activates macrophages and jump-starts the entire immune response," Dr. Smith writes. "To sabotage the immune system and put the macrophages to sleep, all cancers and viruses make Nagalase, the enzyme that blocks production of GcMAF. In the absence of GcMAF, cancers, HIV, and other viruses can grow unimpeded."
A series of Nagalase tests conducted over several weeks or months will provide clarity as to whether or not a patient is dealing with a virus or cancer. And because Nagalase shows up early, long before cancer cells are able to metastasize, it's an invaluable tool for catching cancers early and eradicating them.
The solution to Nagalase is to reintroduce GcMAF into the body via a series of simply injections. There is also newer research suggesting that special GaMAF-producing cultures in yogurt may provide similar benefits without the needle.
This treatment is also highlighted in my section on Alternative Treatments as No. 7.
7) High-Resolution Blood (HRB) Analysis. Leviticus 17:11 states that the life of the body is in the blood, and from a scientific perspective, we can now say with certainty precisely why: our blood is what keeps our bodies alive, transporting oxygen, nutrients, and immune factors to cells while pulling carbon dioxide from cell tissue.
When something goes wrong inside the body, chances are it began in the blood. Thanks to modern technology, we now have the ability to examine blood closely to measure vitamin and mineral levels, protein content, and chemical composition in order to diagnose disease.
An advanced blood analysis can also come in handy for early detection of cancer. Mr. Hilu's method of high-resolution blood analysis accurately maps the structure of blood in order to identify certain abnormalities indicative of cancer.
Though not originally developed as a cancer diagnostic tool per se, HRB analysis provides an exceptionally accurate look into the complex workings of the cellular system, allowing practitioners trained in what to look for the unique opportunity to extrapolate this data into a preliminary diagnosis. The method is highly effective at detecting the presence of cancer cells long before they have the opportunity to develop into full-blown tumors. Dr. Hilu refers to these cellular imbalances as being "precancerous," treatable early on before a cancer metastasizes.
Even if a patient is already suffering from a more advanced form of cancer, HRB analysis can pick up on the particular cellular imbalances that caused it, making a customized treatment plan that much easier to develop. Preventing and treating cancer is what HRB Analysis is all about.
>>Could not get ANY of these tests. I was told that the only test they go by is the PSA.
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DIET AND CANCER CONNECTION
"Cancer Is Not A Genetic Disease. The Evidence Is Striking...It's A Metabolic Disease."
"It's The Greatest Tragedy In The History Of Medicine."
"The Problem Is Our Modern Lifestyle & Habits, It Induces Cancer."
"Cancer Is A Very Preventable Disorder. It's Within Your Control, Your Lifestyle, Your Habits."
"We Can Prevent It & Treat It With Metabolic Therapy."
Ketogenic Metabolic Cancer Prevention/Treatment:
1: Water Fasting For Autophagy & Mitochondrial Health
2: Carbohydrate Restriction/Glucose Elimination
3: Remove Ultra Processed Foods, Seed Oils
4: Vigorous Exercise To Induce Ketosis
Dr Thomas Seyfried is a Professor of Biology, Genetics & Biochemistry at Boston College. He has over 150 peer-reviewed publications & the author of "Cancer as a Metabolic Disease: On the Origin, Management & Prevention of Cancer."
"All Major Research Centers Believe Cancer Is A Genetic Disease. But That Belief Is In Stark Contrast To The Data. The Evidence Is Massive To Support That Cancer Is A Metabolic Disorder."
"Wolves In The Wild Don't Die Of Cancer, Yet Our Pets #1 Killer Is Cancer. Their Food & Lifestyle Is Killing Them Too."
"The Greatest Tragedy In The History Of Medicine Is Knowing The Cause Of Cancer & Yet The Medical Establishment Is Not Advising Changing Lifestyle To Prevent It Or As A Treatment."
Keto Diet v. Cancer with Dr. Thomas Seyfried:
Thomas Seyfried, author of 150+ peer-reviewed publications, calls the standard of care for cancer absurd and medieval. Being poisoned, irradiated and surgically mutilated can have major consequences for survivors.
His solution is a ketogenic metabolic therapy in conjunction with glutamine suppressing drugs which shrinks the cancer and allows the removal of a greater amount of the cancer. Then the focus shifts to preventing the cancer from returning.
It just so happens that metabolic therapy is not only the cure, but also the prevention. The standard of care cannot say the same.
Doctors are in too deep to admit biopsies are what spread the infection and radiation kills the organs ability to function. Think about how many people are under the spell? I wonder -- Jim had two biopsies and then radiation for the cancer.
During PET scans, tracers are “attached” to compounds such as glucose. By detecting radioactive glucose, the PET scan can show which areas of the body [tumors] are using glucose at the highest rates
Scientists have discovered molecules that inhibit tumor growth by starving cancer cells of their favorite foods: the sugar glucose and the amino acid, glutamine: ..starving cancer cells of their favorite foods could inhibit tumor growthWell, we know that sugar causes cancer. The PET scan, used to identify cancer, is a test run by injecting a sugary liquid into your arm and waiting 30 minutes before performing the scan. The sugar molecules have radioactive dyes attached. Cancer eats the sugar, and when the scan radiates you, it can identify cancer. Cancer cells eat eight times more sugar than normal cells. Certainly not every single type of cancer, but a majority of cancers, live off of one main substance, which is sugar.
So, what constitutes "sugar"?
Let's take a look at what sugar is and what sugar isn't. You do realize that companies hide it from you? They give sugar code names so you don't even know you are eating it. Here are 61 code names for sugar:
Barbados sugar Glucose solids
Barley malt Golden sugar
Barley malt syrup Golden syrup
Beet sugar Grape sugar
Brown sugar HFCS
Buttered syrup Honey
Cane juice Icing sugar
Cane juice crystal Invert sugar
Cane sugar Malt syrup
Caramel Maltodextrin
Carob syrup Maltol
Castor sugar Maltose
Coconut palm sugar Mannose
Coconut sugar Maple syrup
Confectioner's sugar Molasses
Corn sweetener Muscovado
Corn syrup Palm sugar
Corn syrup solids Panocha
Date sugar Powdered sugar
Dehydrated cane juice Raw sugar
Demerara sugar Refiner's syrup
Dextrin Rice syrup
Dextrose Saccharose
Evaporated cane juice Sorghum syrup
Free-flowing brown sugars Sucrose
Fructose Sugar (granulated)
Fruit juice Sweet sorghum
Fruit juice concentrate Syrup
Glucose Treacle
Turbinado sugar
Yellow sugar
And don't think you can go to "sugar-free" products. Those sugars are more deadly than the above sugars. Take aspartame: it is toxic and causes the brain to be hypoglycemic, which can lead to brain damage, increase the risk of dementia, and cause headaches. Artificial sweeteners weaken the immune system, which increases viral infections. They have also been linked to seizures, episodic incidents of violence, learning disorders, and degenerative brain disorders.
New data in Nature reveal how Fructose can Fuel Cancer. The mechanism is shocking, and sneaky. Basically, cancer can hijack your liver to turn fructose into building blocks for its construction project. In this video, we break down the data, provide insights on high fructose corn syrup and fruit, and offer several solutions to the Fructose Problem.
Dr. Lee Merritt : “Doctors around the world are showing that cancer is intracellular parasites”
“If you look at cancer under a light microscope, its essentially indistinguishable from parasite egg sacs”
Is that why they tried so hard to shut down Ivermectin and other anti-parasitics during #Covid?
Should we be looking at cancer in a different way? Is cancer related to parasites, worms or fungus?
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Prostate cancer occurs when abnormal cells
undergo uncontrolled growth in the prostate gland, resulting in the formation
of a malignant tumor. The prostate is a walnut-sized organ situated deep within
the pelvis, and it plays a vital role in the production of semen, which serves
to nourish and facilitate the transport of sperm. Prostate
cancer ranks as the most prevalent cancer and the second-highest cause of
cancer-related mortality among men in the United States. Around 1 in 8 men will
develop prostate cancer within their lifetime. The number of new prostate
cancer cases in 2024 is estimated to be nearly 300,000, and the cancer
accounted for about
15 percent of all new cancer cases in 2023. An estimated 34,700
men died of prostate cancer in 2023, representing 5.7 percent of all
cancer-related deaths. Fortunately, the five-year relative survival rate from
2013 to 2019 was 97.1 percent.
What Are the Types of Prostate Cancer?
Prostate
cancer types are determined by the specific cells in which the cancer
originates. Doctors may also categorize prostate cancer according to its
location. Localized prostate cancer remains confined within the prostate,
whereas metastatic prostate cancer extends beyond the prostate, spreading to
other areas of the body.
The following are the main types of prostate cancer:
- Adenocarcinoma: Adenocarcinomas, the most prevalent form of
prostate cancer, originate in the gland cells lining both the prostate
gland and its tubes. These gland cells play a role in the production of
prostate fluid. The subtype acinar adenocarcinoma makes up 90 percent of
all prostate cancers and originates in the gland cells lining the
prostate. The second subtype, ductal adenocarcinoma, originates
in cells lining the tubes of the prostate and tends to grow more
aggressively.
- Transitional cell carcinoma: Also known
as urothelial carcinoma of the prostate, transitional cell carcinoma of
the prostate represents 2 percent to 4 percent of prostate cancers. It
originates in the cells lining the urethra, the final tube that empties
the bladder during urination. Typically beginning in the bladder
and spreading to the prostate, it can infrequently initiate in the prostate
and extend to the bladder entrance and adjacent tissues.
- Squamous cell carcinoma: This type arises from flat cells
covering the prostate and typically grows and spreads very aggressively. It makes up less than 1
percent of prostate cancers.
- Small cell: The rarest of these types, small cell prostate
cancer represents less than 2 percent of all prostate cancers, and it
falls under the category of neuroendocrine prostate cancer. Distinguished
by rapid growth, small cell prostate cancers often present
in an advanced stage at the time of diagnosis, with the cancer
having spread to distant parts of the body.
What Are the Stages of Prostate Cancer?
Prostate
cancer staging can be complex, involving tumor size, lymph node involvement,
presence of metastasis, prostate-specific antigen (PSA) blood level, and the
appearance of the biopsy cells under a microscope. In general, it is
categorized into four
stages:
- Stages 1 and 2: In the early stages, the tumor remains localized
within the prostate. (Dr. Cavey said that Jim's cancer is a 2B.)
- Stage 3: The cancer has extended beyond the prostate but is confined to
nearby tissues. This is a locally advanced stage.
- Stage 4: The cancer has progressed beyond the prostate, spreading to
distant parts of the body, such as lymph nodes, bones, or vital organs.
What Are the Symptoms and Early Signs of
Prostate Cancer?
During
its initial phases, prostate cancer typically has no apparent symptoms.
Approximately 85 percent of prostate cancers are identified through early or
routine PSA screenings prior to the onset of any noticeable symptoms.
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In a recent study, researchers found men who had drunk heavily from their mid-teens to almost age 50 – at least seven drinks per week – were three times more likely to get high-grade prostate cancer than those who didn’t drink alcohol. “High-grade” refers to a scoring system of how cancer tissue appears under a microscope. Less healthy and more aggressive cells get higher numbers and indicate more intensive treatment is needed. Though researchers in this study didn’t find a link between current drinking patterns and high-grade prostate cancer, others have.
Current Drinking Habits Factor Big, Too. A long-range Canadian study on people who had been diagnosed with prostate cancer found men who drank more than eight alcoholic drinks a week had a higher mortality rate than non-drinkers.
And a recent, in-depth study found alcohol ramped up the growth of prostate tumors and speeded the tissues’ progression to metastatic prostate cancer. This means the disease has spread to other areas of the body. The researchers in this case advised men diagnosed with prostate cancer to promptly cut out all alcohol. (It’s key to do it gradually, under your doctor’s care, especially if you drink often or heavily.)
Jim has been a heavy drinker most of his life and I think that has affected his health a lot; it causes fatty liver, fat around the belly, low testosterone levels (which you know what that affects!) and inflammation in the body.
What I read about alcohol, it's a contributing factor to a lot of health issues, one being inflammation and arthritis. Does Alcohol Cause Inflammation? Drinking and the Risk of Chronic Illness
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From The Truth About Prostate Cancer, the levels of testosterone in men affects them, including reduced libido, low energy/fatigue, reducing muscle mass, reduced bone density, and erectile dysfunction.
Other symptoms of hypogonadism are:
- Decreased sex drive
- Infertility
- Decreased muscle mass
- Hot flashes
- Slowed growth
- Sparse body hair
- Delayed or absent puberty
- Sleep disturbance
- Poor concentration and memory
Interesting. "In 1896, Dr. Charles F. Craig (a respected MD who later became a key figure in tropical medicine) published 'The Parasitic Origin of Carcinoma' in Connecticut Medical Society proceedings.
He observed parasite-like bodies (psorozoa/coccidia) in cancer cells, noted similar findings by others (e.g., Plimmer, Ruffer claiming them in hundreds of cases), and suspected they might contribute to causation—though he wasn't fully convinced.
This reflected 1890s debates on whether carcinoma had a parasitic cause, like bacteria for other diseases. The theory faded as evidence shifted to other factors. Full public-domain PDF
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MRNA Cancer AI vaccine? let's break it down to 1799
Natural solutions: Apricot seeds, Soursop, Turkey Tail mushroom, Fasting, Mistletoe, and Baking Soda ***************************
ALTERNATIVE CANCER TREATMENTS
In the meantime, I have been doing research on alternative methods of treating cancer. I have looked at Ivermectin, Fenbendazole, Chlorine Dioxide, Essiac Tea, Baking Soda, the Burzynski Clinic protocol, the GcMAF treatment, Vitamin B-17 (found in Bitter Apricot Kernels), Soursop or guanabana fruit, along with other methods of curing cancer. I will put information on all those there. These methods are for all types of cancer, not just prostate.
An article in the Journal of Orthomolecular Medicine entitled Targeting the Mitochondrial-Stem Cell Connection in Cancer Treatment talks about some of the alternative methods discussed below, i.e., Ivermectin, Fenbendazole, and the use of vitamins and minerals in cancer treatment.
(1) Ivermectin and hydroxychloroquine
Eprinomectin: a derivative of ivermectin suppresses growth and metastatic phenotypes of prostate cancer cells by targeting the β-catenin signaling pathway Prostate cancer (PCa) is the second leading cause of cancer death among men in the USA. The emergence of resistance to androgen deprivation therapy gives rise to metastatic castration-resistant prostate cancer. Eprinomectin (EP) is a member of a family of drugs called avermectins with parasiticide and anticancer properties. The purpose of this study was to evaluate the anticancer effects of EP against metastatic PCa using cellular models.
Abstract: Ivermectin is a widely used antiparasitic drug and shows promising anticancer activity in various cancer types. Although multiple signaling pathways modulated by ivermectin have been identified in tumor cells, few studies have focused on the exact target of ivermectin. Herein, we report the pharmacological effects and targets of ivermectin in prostate cancer. Ivermectin caused G0/G1 cell cycle arrest, induced cell apoptosis and DNA damage, and decreased androgen receptor (AR) signaling in prostate cancer cells. Further in vivo analysis showed ivermectin could suppress 22RV1 xenograft progression. Using integrated omics profiling, including RNA-seq and thermal proteome profiling, the forkhead box protein A1 (FOXA1) and non-homologous end joining (NHEJ) repair executer Ku70/Ku80 were strongly suggested as direct targets of ivermectin in prostate cancer. The interaction of ivermectin and FOXA1 reduced the chromatin accessibility of AR signaling and the G0/G1 cell cycle regulator E2F1, leading to cell proliferation inhibition. The interaction of ivermectin and Ku70/Ku80 impaired the NHEJ repair ability. Cooperating with the downregulation of homologous recombination repair ability after AR signaling inhibition, ivermectin increased intracellular DNA double-strand breaks and finally triggered cell death. Our findings demonstrate the anticancer effect of ivermectin in prostate cancer, indicating that its use may be a new therapeutic approach for prostate cancer.
Discussion: In this study, we reported that ivermectin, an antiparasitic drug, showed promising anticancer activity against prostate cancer progression. Ivermectin was primarily developed for the treatment of onchocerciasis caused by the parasite Onchocerca volvulus in poor populations around the tropics [10]. Recently, research has shed light on the potential of ivermectin as an antibacterial [40, 41], antiviral [42, 43], and anticancer agent [9, 11]. In particular, owing to its wide margin of clinical safety [44], ivermectin is an ideal candidate for drug repurposing and has been listed in the drug repurposing hub established by the Broad Institute [45]. Our results indicate that ivermectin inhibited dramatically prostate cancer in cell lines representing the hormone-sensitive stage (LNCaP), castration resistance stage (C4-2), and AR variant positive stage (22RV1). In addition, there is controversy regarding the cellular targets of ivermectin, and several alternative action mechanisms have been proposed. To address this issue, we performed an integrated analysis including RNA-seq and TPP-TR to identify the targets of ivermectin in prostate cancer. Our data strongly suggested that ivermectin could bind to FOXA1 and Ku70/Ku80 and inhibit AR signaling, E2F1 expression, and DNA damage repair activity, thereby leading to G0/G1 cell cycle arrest, DNA damage, and triggering synthetic lethality (Fig. 8).
In another case, a 70-year-old man with a PSA of 26.35 had an enlarged prostate suspicious of cancer [01:42:37]. Following two vaccine doses, his PSA rose to 51.29. Dr. Makis said to use 1 mg for 1 kg of weight; so for a 60kg person the dose would be 60mg. Jim weights 190lbs (86kg) so he would get 86mg of Ivermectin.
“Immediately, his PSA shoots up to 51 after those first two doses [01:42:59]. He takes a booster on January 6, and his PSA shoots up to 61.75.”
Another PSA showed him to be at 89.11.
“[01:44:12] We immediately brought him up (Ivermectin) to 45 mg per day.” Five weeks after the Ivermectin, he stopped having nocturnal urinary frequency. “On October 5, he sees his Urologist – and the results are spectacular [01:44:31]. What do we see? From the 89.11 PSA he had on August 30 was reduced to 10.94. This 10.94 is less than one-half of his PSA in 2019. This is an indication of how effective Lactoferrin and Ivermectin are together.”
Dr. Chetty admits that at this point, the combination of Ivermectin and Lactoferrin may not be a cancer cure, but it is “really, really effective.”
“Immediately, his PSA shoots up to 51 after those first two doses [01:42:59]. He takes a booster on January 6, and his PSA shoots up to 61.75.”
Another PSA showed him to be at 89.11.
“[01:44:12] We immediately brought him up (Ivermectin) to 45 mg per day.” Five weeks after the Ivermectin, he stopped having nocturnal urinary frequency. “On October 5, he sees his Urologist – and the results are spectacular [01:44:31]. What do we see? From the 89.11 PSA he had on August 30 was reduced to 10.94. This 10.94 is less than one-half of his PSA in 2019. This is an indication of how effective Lactoferrin and Ivermectin are together.”
Dr. Chetty admits that at this point, the combination of Ivermectin and Lactoferrin may not be a cancer cure, but it is “really, really effective.”
Can Ivermectin Treat Cancer? – 9 Papers Reviewed Oncologist and cancer researcher Dr. William Makis uncovers what Big Pharma doesn’t want you to know about ivermectin’s anti-cancer mechanisms.
Is Ivermectin a Cancer Solution? By Dr. Joseph Mercola. Ivermectin has notable antitumor effects, which include inhibiting proliferation metastasis angiogenic activity, ...in cancer cells. It appears to inhibit tumor cells by regulating multiple signaling pathways, which researchers explained in the Pharmacological Research journal, "suggests that Ivermectin may be an anticancer drug with great potential." Their graphic, below, shows the multiple ways that Ivermectin may target cancer, including inducing apoptosis and autophagy while also inhibiting tumor stem cells and reversing multidrug resistance. They stated that Ivermectin, "exerts the optimal effect when used in combination with other chemotherapy drugs."
Prostate cancer is a malignant tumor derived from prostate epithelial cells, and its morbidity is second only to that of lung cancer among men in Western countries [49]. In Nappi's experiment, it was found that IVM could enhance the drug activity of the anti-androgen drug
enzalutamide in the prostate cancer cell line LNCaP and reverse the resistance of the prostate cancer cell line PC3 to docetaxel [50]. Interestingly, IVM also restored the sensitivity of the triple-negative breast cancer to the anti-estrogen drug tamoxifen [36], which also implies the potential for IVM to be used in endocrine therapy. Moreover, IVM was also found to have a good inhibitory effect on the prostate cancer cell line DU145 [51].
Dr. Kathleen Ruddy, a cancer surgeon, observed a resounding improvement in three patients under her consultation after they started using ivermectin with additional therapies. One patient, facing terminal stage 4 prostate cancer and given only three weeks to live after all treatments failed, began using ivermectin. Remarkably, within two months, his indicators of prostate cancer plummeted, and by six months, his cancer had significantly receded. Less than a year later, he was energetically dancing for four hours, three nights a week. This miraculous recovery was not isolated, as two more patients experienced similar outcomes. Dr. Ruddy, with over 30 years in cancer surgery, reflected on these cases, saying, “I’ve been a cancer surgeon for over 30 years. I’ve never seen anything like this in one patient—let alone three in a row.”
Read the full report in the comment below:
"His doctor said, 'there's really nothing else we can do.'…The poor guy was suffering, had cancer in 11 bones in his body."
A few months later, this patient was told he was in remission. So what happened? He had started taking ivermectin.
Cancer Surgeon: “Ivermectin Is SAFER Than a Sugar Pill”
“You’d have to take a lot to make yourself sick.”
Dr. Kathleen Ruddy has also observed multiple late-stage cancer patients make dramatic recoveries after taking ivermectin.
Ivermectin is also:
• A Nobel Prize-winning discovery (2015)
• Recognized, 2nd to penicillin, for having the greatest impact on human health
• Credited for bringing river blindness to the brink of elimination
• used globally in HUMANS, with over 3.7 billion doses administered.
Dr. Paul Marik, an American physician and former professor of medicine, made the bombshell announcement during a new interview.
Marik, a former critical care doctor at Sentara Norfolk General Hospital who also served as chair of the Division of Pulmonary and Critical Care Medicine at Eastern Virginia Medical School in Norfolk, Virginia, revealed that “the cancer disappeared” when patients were given ivermectin.
Dr. William Makis: NEW ARTICLE: IVERMECTIN - Articles and Protocols for CANCER, Research studies and access to Ivermectin pills
Recently, I have seen tremendous demand for some sort of initial guidance “WHERE TO START” with High Dose Ivermectin for CANCER.
So I'm reposting my Ivermectin Cancer Protocol. It's very simple to use.
Did you know that Ivermectin is annually taken by close to 250 million people?
Ivermectin has a dozen anti-cancer mechanisms but they can be summarized into two main ones:
1. Inhibits cancer proliferation signaling pathways (Akt, mTOR, Wnt)
2. Inhibits Cancer Stem Cells
IVERMECTIN will act against regular CANCER as well as Pfizer and Moderna COVID-19 mRNA Vaccine Induced TURBO CANCER (which is highly resistant to chemo)
Here are recent studies on IVERMECTIN use in certain types of cancer:
BLADDER CANCER - (2024 Fan et al) - Ivermectin Inhibits Bladder Cancer Cell Growth and Induces Oxidative Stress and DNA Damage
LUNG CANCER - (2024 Man-Yuan Li et al) - Ivermectin induces nonprotective autophagy by downregulating PAK1 and apoptosis in lung adenocarcinoma cells
GLIOMA - (2024 Xing Hu et al) - Ivermectin as a potential therapeutic strategy for glioma
MULTIPLE MYELOMA - (2024 Yang Song et al) - Gene signatures to therapeutics: Assessing the potential of ivermectin against t(4;14) multiple myeloma
OVARIAN CANCER - (2023 Jawad et al) - Ivermectin augments the anti-cancer activity of pitavastatin in ovarian cancer cells
PROSTATE CANCER - (2022 Lu et al) - Integrated analysis reveals FOXA1 and Ku70/Ku80 as targets of ivermectin in prostate cancer
COLON CANCER - (2022, Alghamdi et al) - Efficacy of ivermectin against colon cancer induced by dimethylhydrazine in male wistar rats
PANCREATIC CANCER - (2022 Lee et al) - Ivermectin and gemcitabine combination treatment induces apoptosis of pancreatic cancer cells via mitochondrial dysfunction
MELANOMA - (2022 Zhang et al) - Drug repurposing of ivermectin abrogates neutrophil extracellular traps and prevents melanoma metastasis
IVERMECTIN has proven anti-cancer activity against some 20 cancer types, although these are pre-clinical studies. We will never see clinical studies because Ivermectin is off patent and cheap.
Merck, which used to have a patent on Ivermectin, has partnered with Moderna on mRNA Cancer Vaccines.
IVERMECTIN is so safe, that in much of the civilized world, it is available over the counter, no prescription needed. That’s how it should be.
I recently wrote about how a doctor in Saskatchewan, Canada was just given a $44,800 penalty by the College of Physicians and Surgeons for prescribing Ivermectin to a few patients during 2020-2022.
The Ontario College of Physicians even had an Investigator go undercover and dress up as a Canadian Trucker to ensnare a young doctor prescribing Ivermectin in Ottawa in 2022 during the Trucker Convoy.
Canadians must realize that the Colleges of Physicians and Surgeons are private corporations, fully bought off by big pharma and run by mafia lawyers who are putting pressure on doctors to comply or else
No healthcare bureaucrat or lawyer has the right to deny anyone access to life saving medication. And if they do, they are committing a very serious crime.
It's time for Canadians to bring the Colleges of Physicians and Surgeons to Justice for their many COVID-19 crimes, take them over, dissolve them, and start over.
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Dr. William Makis: PODCAST Episode 018: High Dose IVERMECTIN and CANCER
Your Oncologist is not allowed to suggest High Dose Ivermectin to you, despite the fact that Ivermectin kills Cancer Stem Cells that standard chemotherapy doesn't.
Ivermectin has been shown to act on Turbo Cancer (caused by COVID-19 Vaccines), including Stage 4, even after all other treatments failed.
This was my most popular podcast episode.I found two sources for Ivermectin:
Patient with stage four prostate cancer gets his PSA score down to remission levels after regularly taking ivermectin.
The media once mocked this drug as nothing more than “horse dewormer.”
The doctors were surprised by “how quickly” he got better with “no problem/side effects at all.”
In a letter, the patient wrote to Dr. William Makis:
“I combined your protocol for ivermectin along with the chemo treatments. We reached our goal of bringing my PSA score down to 0.02 quite quickly. Doctors were surprised at how quickly this happened. They do not know that I was taking ivermectin.”
Dr. Makis responded: “It's often better that way. 
”
”
“Within a couple of weeks, he sounded stronger. He could swallow. He had gained six pounds. His voice was better,” reported Dr. Ruddy.
Several weeks later, Dr. Ruddy said to Eddie, “You need to get a scan.”
Guess what happened?
“We got the scan. No tumors. Gone. Gone,” Dr. Ruddy said with astonishment. “The problem was that he had sold his fishing boat. That was the biggest problem. He was getting better. His tumor was gone. Now he’s got to buy another fishing boat … I was like, ‘Well, now, that’s interesting.’”
Renowned oncologist, radiologist, and immunologist Dr. William Makis has revealed that one patient made an amazing recovery from stage 4 prostate cancer.
The patient said they have been secretly taking ivermectin along with other treatments and left their doctors stunned by recovering “quite quickly.”
They told Makik that they followed his protocol for ivermectin without telling their own doctor.
As a result, the patient saw his PSA scores fall to remission levels “quite quickly” after taking ivermectin.
Doctors were shocked to see “how quickly” the patient recovered with “no problem/side effects at all.”
The patient told Makis they have been “battling a very aggressive stage 4 prostate cancer.”
“I combined your protocol for ivermectin along with the chemo treatments,” the patient told Makis.
“We reached our goal of bringing my PSA score down to 0.02 quite quickly.
Ivermectin is the future of cancer treatment. This drug was once labeled "horse de-wormer." Today, extensive research reveals it has 15 powerful ANTI-CANCER mechanisms of action. Let’s look at the science behind how it works:
First off, IVM had earned Merck’s scientists a Nobel Prize in 2015 for saving millions from parasitic diseases. WHO even listed it as an “essential medicine.” During COVID, it was a target of ridicule. Today, we look at it as a potential anti-cancer drug.
Ivermectin has at least 15 anti-cancer mechanisms of action (apoptosis, autophagy, pyroptosis, etc.)
Apoptosis > Apoptosis is a programmed cell death—a natural process where cells are instructed to self-destruct in an organised way. Cancer cells evade this mechanism, but treatments like Ivermectin may help restore this cellular cleanup system.
Autophagy > It forces cancer cells to "eat themselves" through their internal recycling system. Studies on breast cancer cells showed IVM increases LC3, Bclin1, Atg5 (autophagy proteins) forming "self-eating" structures. Scientists proved this by blocking the process. Cancer-killing stopped.
Pyroptosis > Think of it as your body's controlled explosion system. Cells detect threats via inflammasomes, activate caspase-1, and trigger Gasdermin D, causing them to swell and explode. This inflammatory death releases signals alerting the immune system, potentially key in fighting cancer and infection.
Other IVM’s anti-cancer mechanisms of action:
• Inhibits tumor growth/proliferation
• Inhibits tumor initiation/progression
• Regulates tumor micro-environment
• Causes cancer cell mitochondrial dysfunction
• Stops cancer cell migration, invasion & metastasis
According to Dr. William Makis: “They [researchers] have found that if you give higher doses of Ivermectin than what’s been used for COVID-19, that it actually can stop the growth of these cancer cells, it can stop their metastases, and it can actually engage apoptosis and autophagy and kill these cancer cells.”
A new book, "IVERMECTIN - Testimonials by Clinicians Worldwide" (English version) is now on sale.
Dr. William Makis: “I had patients suffering from Parkinson’s…that are now out golfing…after taking Ivermectin…”
If you thought the war on ivermectin ended when they stopped mocking it on late-night TV, buckle up, buttercup. That was just Act One. Act Two? Slip chemical landmines into the new formulations and pray nobody reads the fine print.
Spoiler: we read it. And now we’re torching the narrative down to its carbon credit ashes.
Meet the new tag-along chemicals hitchhiking inside modern ivermectin products:
Polysorbate 80 — An emulsifier that also happens to open the blood-brain barrier like a drunk guy kicking down a saloon door. Fantastic if you’re trying to smuggle molecules into places they don’t belong.
Titanium Dioxide — You know, the same industrial pigment used in house paint and sunscreen. Recently classified as a “possible human carcinogen” in the EU if inhaled. And hey, if it’s bad for your lungs, why wouldn’t you want it in your bloodstream?
The original ivermectin didn’t need polysorbate 80.
The original ivermectin didn’t need titanium dioxide.
The original ivermectin didn’t send your immune system scrambling like a drunken rooster.
The Pharmaceutical Industrial Complex is going to MELT DOWN HARD…
Children’s Health Defense just EXPOSED THE SCAM…Ivermectin is CRUSHING cancer like chemotherapy NEVER could.
Nearly 200 patients.
Multiple cancer types.
84% POSITIVE OUTCOME.
BREAKING NEWS: The EXACT Ivermectin dosage that's helping Cancer patients is being HIDDEN from you!
12mg daily for 5 days, then 12mg twice weekly maintenance.
Big Pharma doesn't want you to know this costs $2 per pill instead of $10,000 chemo treatments.
They're TERRIFIED of losing profits while Cancer patients get better for pennies! 
This is what they're desperate to keep under wraps.I've seen it work over and over. Don't let them keep you in the dark.
This is what they're desperate to keep under wraps.I've seen it work over and over. Don't let them keep you in the dark..jpg)
Effects of fenbendazole and vitamin E succinate on the growth and survival of prostate cancer cells
Here is where I buy Fenbendazole. I gave him this along with CBD oil and he also ate the bitter apricot kernels.
Fenbendazole and Mebendazole are similar in that they both eliminate parasitic worms, but there is a difference. Mebendazole is approved for human consumption by the FDA, while fenbendazole is only approved for veterinary use and has not been approved for human use.
Fenbendazole for Humans Vs. Mebendazole. Recently, researchers have been experimenting with fenbendazole for humans cancer. Though the studies are limited, what researchers have found so far is promising for cancer patients.
Many cancer patients have been following the Fenbendazole for cancer Protocol:
Fenbendazole 222mg 1x per day
Curcumin 600 mg 1 x per day
CBD oil 25 mg 1 x per day sublingual
Berberine 500 mg 2-3 x per day
Quercetin 250 mg 1-2 x per day
Vitamin E 1,000 IU 1 x per day
However, fenbendazole isn’t the only worming medication that has the potential to fight cancer. Researchers have also been studying how Mebendazole, a drug that can treat worms in humans, could be just as, or even more, effective at shrinking tumors and killing cancer cells.
There are two people who have used Fenbendazole as a cancer treatment. One is Joe Tippens who used Fenbendazole at 222mg, Vitamin E at 800 IU, Curcumin at 600 mg and CBD oil at 25mg. This is called the "Joe Tippens Protocol."
I also listened to the following video done between Patel Patriot and Gregg Phillips where Gregg talks about how he cured himself with the Joe Tippens Protocol.
Another successful healing from cancer using Fenbendazole:
A man diagnosed with terminal cancer and given only six months to live refused to accept his fate. Instead, he went home, did some research and discovered the 'Joe Tippens Protocol.' This alternative treatment approach involved the use of FENBENDAZOLE, a medication typically used to treat parasitic infections in animals.
According to the man, Fenbendazole was the key to saving his life.
“They told me that I only had 6 months to live and to go home and DIE”
“I’m totally CANCER FREE today, because of Fenbendazole”
Listen to this
Study on Fenbendazole for Cancer by Internal Healing & Wellness. For active malignancies, www.fenbendazole.com suggests 444mg of fenbendazole capsules daily, with one day per week off. Tolerance is unlikely, but periodic rest periods may be beneficial. To enhance effects, adding 25mg CBD oil before bed is recommended. Strengthening the regimen with 600mg of curcumin and 250mg of milk thistle (take both twice daily with food) is also advised. Absorption improves when fenbendazole is ingested during or after meals.
The Overlooked Miracle Drug for Cancer? Why Big Pharma Fears Fenbendazole. "Fenbendazole has at least 12 proven anti-cancer mechanisms in vitro and in vivo," wrote cancer researcher Dr. William Makis.
"So why are there no Fenbendazole clinical trials for cancer? The answer seems rather obvious: it’s very cheap, it’s safe, and it seems to be very effective. Fenbendazole is not going to make anyone rich, and in cancer treatments, that is a non-starter."
"What an enemy of the people," Joe Rogan responded. "They're preventing information and preventing people from using things that save them."
Podcast by Dr. Tom Rogers on the use of Fenbendazole for the treatment of cancer.
He also mentioned another treatment called Artemisinin, which is actually Sweet Wormwood, a Chinese medicine that they have used for centuries for inflammation. It is cheap, nontoxic, you do not develop a resistance, it's well tolerated and no side effects.
Cancer cells rely on iron to spread. When iron and Artemisinin enter a cancer cell together, they form free radicals that kill the cancer cell without harming the normal cell.
The one thing wrong with this treatment is the affect Fenbendazole has on the liver. If one has high liver enzyme -- AST, ALT, and ALP, you should not take this without the advice from your doctor.
Can using fenbendazole for extended periods be toxic to the human liver? Although fenbendazole is generally well tolerated, there have been reports of elevated liver enzymes from the use of Fenbendazole, as well as the similar human medications mebendazole and albendazole. Elevated liver enzymes indicate a liver that is stressed and inflamed, and adding to its burden with Fenbendazole would not be recommended. Jim has high liver enzymes because of his long term drinking, which has harmed his liver. His liver enzymes have been high for a very long time.
Dr. William Makis: NEW ARTICLE: FENBENDAZOLE for Cancer - for best absorption, take it with fatty meal, Olive Oil, or butter.
How is Fenbendazole Best Administered?
Enhancing the Bioavailability of Fenbendazole with Oleic Acid. Oleic acid is a fatty acid that occurs naturally in various animal and vegetable fats and oils.
The most readily available, oleic acid-rich, practical substance is olive oil. Most likely due to its role as an emulsifying agent, Liu et al (2018) found that pairing mebendazole with oleic acid (olive oil) greatly enhances the bioavailability of mebendazole.
(Liu, C. S., Zhang, H. B., Jiang, B., Yao, J. M., Tao, Y., Xue, J., & Wen, A. D. (2012). Enhanced bioavailability and cysticidal effect of three mebendazole-oil preparations in mice infected with secondary cysts of Echinococcus granulosus. Parasitology research, 111(3), 1205–)
The magnitude of the effect was substantial, 1.6 to 2.8 times greater serum levels of mebendazole were obtained when co-administering mebendazole with various oils compared to controls.
Fenbendazole is a versatile medication frequently prescribed to treat parasitic infections in both animals and humans. It’s categorized under the benzimidazole group of drugs. Its primary function is to disrupt the energy-producing processes of the parasites, causing them to perish.
Fenbendazole is commonly employed as an antiparasitic treatment. The usual recommended dosage is 222-444 milligrams, administered daily for five consecutive days. The treatment may need to be repeated after three weeks. A regimen that some adopt (which may be geared more towards cancer, but is possibly addressing parasitic infections) is to take 222 mg daily for three days, pause for 4-5 days, and then recommence the cycle.
Olive oil was the most effective mebendazole booster. As should be expected, the increased serum levels of mebendazole translated into more effective parasite killing effects in the animals models used as well.
"A chemist recently wrote in suggesting that fenbendazole taken with a teaspoon or so of butter would have optimal absorption characteristics…”take it with a small amount of saturated or monounsaturated fat — something with a carbon chain above 14, to optimize absorption. Butter is an ideal choice.” She estimated that approximately 85% of the ingested fenbendazole would survive first-pass metabolism* en route to the target cells."
Taking fenbendazole is one thing, making sure it is actually absorbed can be a matter of life or death. Source: Dr. Frank Yap MD
Both Mebendazole and Fenbendazole are in international spotlight as some of the most promising repurposed drugs for treatment of Cancers, including Turbo Cancers caused by Pfizer and Moderna COVID-19 mRNA Vaccines.
Cancer Patients Experience Complete Remission After Taking Fenbendazole. Cheap & Readily Available Anti-Parasitic Drug Typically Used In Veterinary Medicine. Fenbendazole disrupts microtubules & kills cancer without negative side effects.
The website Fenbendazole Help gives a lot of information on the drug along with articles on its use in cancer therapy.
Craig Brockie on X: Fenbendazole is the future of cancer treatment.
It's helped terminal cancer patients achieve complete remission when chemo failed. Big Pharma can't patent it, so they ignore it. Here's everything you need to know:
Fenben is a cheap veterinary medication you can buy at any pet store.
has documented complete cancer remissions in advanced patients using this drug. We're talking about kidney, breast, and prostate cancers disappearing. The mechanism?
Fenben attacks cancer in three ways:
• Breaks its ability to divide
• Starves it of glucose
• Forces cell death
Healthy cells stay mostly unaffected.
Think of cancer cells like a factory that needs fuel and transportation.
Fenbendazole cuts the power lines and breaks the conveyor belts.
The factory shuts down while the buildings next door keep running normally. That's why it's so much safer than chemo.
The evidence is getting hard to ignore. Three patients with advanced kidney/bladder cancer took 1000mg fenbendazole 3x weekly. All 3 achieved complete remission after chemo failed them. No side effects. No cancer recurrence.
Lab studies show fenben works against multiple cancer types:
• Colorectal
• Breast cancer
• Lung cancer
• Melanoma
• Prostate cancer
It starves tumors by shutting down their glucose transporters.
I used to be able to purchase it through Amazon, but no more. When I went to reorder, it was no where to be found. However, I was able to purchase Fenbendazole from a company called BPLife.
(3) Chlorine Dioxide.
I learned about the use of Chlorine Dioxide about 15 years ago when I discovered Jim Humble when he worked on a gold mining expedition in South America, I discovered that chlorine dioxide quickly eradicates malaria. Since 1996, it has proven to restore partial or full health to hundreds of thousands of people suffering from a wide range of disease, including cancer, diabetes, hepatitis A, B, C, Lyme disease, MRSA, multiple sclerosis, Parkinson’s, Alzheimer’s, HIV/AIDS, malaria, autism, infections of all kinds, arthritis, high cholesterol, acid reflux, kidney or liver diseases, aches and pains, allergies, urinary tract infections, digestive problems, high blood pressure, obesity, parasites, tumors and cysts, depression, sinus problems, eye disease, ear infections, dengue fever, skin problems, dental issues, problems with prostate (high PSA), erectile dysfunction and the list goes on.
The Universal Antidote Documentary. The science and story of Chlorine Dioxide. NASA proclaimed it a universal antidote in 1987. Since then, thousands have recovered from illness using this substance, and now many physicians and scientists are saying it is powerfully effective for many applications. The documentary explores the history, safety, and efficacy of the universal antidote and provides interviews with physicians and people who have used it. The Universal Antidote Documentary was released free to the public on February 1, 2021.
Chlorine Dioxide by Dr. Mark Sircus. Most doctors and the vast majority of health officials have forgotten how to reason about medicine. Of course, there are many reasons that rational thought was beaten to a pulp in medicine, but the real point is to start rational discussions starting with cancer.
Where to buy Chlorine Dioxide? Here at Waterpureworld.com
According to Dr. Liu, the principal pioneer in this treatment, chlorine dioxide therapy has caused tumors shrink by more than 30% in just one hour.
- directly destroys tumors,
- shows immediate visual response,
- improves daily life, and
- does not weaken the body.
“This is not just a new technique; it represents a new philosophy for treating Cancer. The upcoming clinical trial in China will be the first large, systematic validation of this approach. If the data confirms what we already observe, it could pave the way for a new global standard in tumor therapy,” says Dr. Liu.
Chlorine Dioxide is truly amazing! 
It not only kills parasites…but yeast & Candida too — the hidden culprits behind SO MANY issues in the body: chronic fatigue, bloating, brain fog, skin problems, inflammation, and more.
This selective oxidizer is a precision SNIPER: Attacks yeast cell walls — especially chitin — inhibiting synthesis so new cells can’t form.
Targets parasites at EVERY life stage: eggs, cysts, larvae, and even resilient adults.
It goes where other agents can’t reach, works across a wide pH range, and makes resistance extremely difficult. If parasites and yeast are silently draining your vitality… this could be the breakthrough you’ve been looking for.
It not only kills parasites…but yeast & Candida too — the hidden culprits behind SO MANY issues in the body: chronic fatigue, bloating, brain fog, skin problems, inflammation, and more.
It not only kills parasites…but yeast & Candida too — the hidden culprits behind SO MANY issues in the body: chronic fatigue, bloating, brain fog, skin problems, inflammation, and more.
This selective oxidizer is a precision SNIPER: Attacks yeast cell walls — especially chitin — inhibiting synthesis so new cells can’t form.
Targets parasites at EVERY life stage: eggs, cysts, larvae, and even resilient adults.
It goes where other agents can’t reach, works across a wide pH range, and makes resistance extremely difficult. If parasites and yeast are silently draining your vitality… this could be the breakthrough you’ve been looking for.
It not only kills parasites…but yeast & Candida too — the hidden culprits behind SO MANY issues in the body: chronic fatigue, bloating, brain fog, skin problems, inflammation, and more.This selective oxidizer is a precision SNIPER: Attacks yeast cell walls — especially chitin — inhibiting synthesis so new cells can’t form.
Targets parasites at EVERY life stage: eggs, cysts, larvae, and even resilient adults.
It goes where other agents can’t reach, works across a wide pH range, and makes resistance extremely difficult. If parasites and yeast are silently draining your vitality… this could be the breakthrough you’ve been looking for.
Watch the full mechanism breakdown here:
(4) Essiac Tea.
The history of Essiac tea is actually quite interesting. It was discovered by Nurse Rene Caisse in 1922 who learned of an herbal remedy used by the Ojibwa nation while working as a nurse at a clinic in Haileybury, Canada. Caisse prepared the original herbal formula as a tea for her patients, which she called Essiac® In the 1940s as news of Essiac® herbal tea gains widespread recognition, Nurse Caisse continues to use Essiac® with much success. The town of Bracebridge, Ontario provides her with a hotel to use as a clinic to treat her patients. Administering the formula at no charge, she only accepted donations to support her operations. To honor her legacy, a statue of Nurse Caisse is erected in the town of Bracebridge, Ontario.
In 1977, Rene Caisse provided her formula and historical records to a firm which promised to do research on her formula. In August 1978, Rene Caisse received an award from Frank Miller, the Minister of Health for Ontario from 1974 to 1977. Nurse Caisse passed away in December 1978, at the age of 90. Her legacy continues. There are over 70 research papers on Essiac® or the components of our high-quality formulation. In 51 countries around the world, Essiac®, with the green label bearing her photo and signature, is the only Essiac® allowed to be sold. Accept only the real Essiac®.
AFTER 100 YEARS, THE TRIED AND TRUE (ESSIAC) MEETS THE NEW (AHCC). Essiac Gold takes Essiac® time honored formula and adds AHCC®, an immune system supplement with over 30 human clinical studies supporting its efficacy. Studies on AHCC® have been conducted at some of the finest research institutions worldwide, including ivy league universities and major health centers. These two formulas together form a hard to beat combination! This information came from Essiacproducts.com
(5) Baking Soda.
Dr. Tullio Simoncini on baking soda and cancer:
I saw this on Twitter:
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This made me to do some more research on baking soda. This is what I found on the Crunchy Betty website:
So, now that we know there’s no aluminum in baking soda (but that there often is in baking powder), what’s the difference between, say, Bob’s Red Mill and Arm & Hammer baking soda?
Why on earth would you want to pay dollars more per pound for something like Bob’s Red Mill when you can get Arm & Hammer for a stick of gum?
It has to do with the way the two things are procured. A brand like Bob’s Red Mill (or Frontier or various other natural brands of baking soda) are mined directly from the ground in their natural sodium bicarbonate state (also known as nahcolite). In fact, Bob’s Red Mill is mined right here in Colorado, so for me it’s kind of like buying local. Which is nice.
There are no chemical reactions, nothing added or fiddled with. It’s just pure sodium bicarbonate, the way the earth made it.
On the other hand, Arm & Hammer baking soda uses a chemical reaction process through which trona ore is mined, then heated until it turns into soda ash. Then the soda ash is treated with carbon dioxide, and baking soda pours forth through the glorious brilliance of science.
It’s just a lot of effort to go through to procure something that’s abundantly available at this point.
However, I do not look down on the use of Arm & Hammer (or similar brands). In fact, it’s the only baking soda I use for cleaning. It’s okay enough, for me, to use on counter tops and bathtubs and more.
I choose, though, to only use naturally mined sodium bicarbonate (like Bob’s or Frontier) when I cook, make my own skincare items (like deodorant or exfoliant), or take it internally when I have the occasional heartburn.
Sodium Bicarbonate Treatments. There are many studies in this link with some of them in other languages. I am putting the whole website here so we can search through it for what you want to read.
Some Troublesome Facts About Cancer. The 5 facts about cancer below are indeed disturbing, but what's even more disturbing is the fact hat nobody even talks about them. If we want to get to the root of this disease, ignorance is not the answer.
Vernon Johnston was diagnosed with stage IV aggressive prostate cancer which metastasized to his bones. He initially turned to Cesium, but ended up using a baking soda molasses protocol as a natural cure which eliminated his cancer and has worked for hundreds of others.
Johnston says, "it is
very important for those of us who have done or are doing this [baking soda
cancer cure] that we focus on an Alkaline Diet. At the very least, for
those of us who are recovering I suggest a diet of at least 80% Alkaline and
20% Acidic..."
Protocol ~~ Buy Arm & Hammer Baking
Soda OR Bob's Red Baking Soda. (Arm & Hammer was used in this
protocol.)
Buy Black Strap molasses OR
Organic Maple syrup, Grade B.
Buy pH test strips; strips
don't run and are easy to use. Litmus paper may also be used along with the
strips.
Buy a good brand of
potassium.
Days 1 to 5: Mix 1 teaspoon baking soda
& 1 teaspoon molasses/syrup in 1 cup water. (May be warmed in a pan for dissolving, but this isn't required; room
temperature is fine. If you heat it, heat on low. Heat the water and baking
soda together, turn off heat, and then add the molasses or syrup. Don't use
a microwave!) Always drink the solution 2 hours before or after a meal.)
Test your pH often; both your
saliva and your urine. (The pH must be brought to the normal/alkaline level which is 7.2 - 7.5. This
level should cause cancer cells to go dormant; and a level of 8.0 - 8.5 should
kill them; and so it is advisable to bring your pH level to 8.0 - 8.5 for 4 to
5 days ONLY, and then lower again to normal.)
On days 6 and 7, mix 2 teaspoons
baking soda & 2 teaspoons molasses/syrup in 1 cup water; drink twice a day.
Continue this formula through day 7. (You may begin to feel a little nauseous
or queasy, and your stool may become yellowish. This is expected. Something
good is happening in your body - something bad to the cancer. Also, your lips
may tingle and you may get Oxygen Euphoria and even a slight headache. This is
expected and may eventually lessen.)
On days 8 to 11, drink the mixture 3
times a day. (You may get some diarrhea and feel a little weak.
This is expected. But taking potassium daily while on this BAKING SODA CURE
should lessen your loss of energy. You should take a high dosage of potassium
daily with this cure. On day 9 or 10 of this dosage, you may get night sweats.
This is expected.
What you are doing right now
is getting your pH to 8.0 - 8.5 and (more or less) holding that for a few days.
If you feel the side effects are too strong, you may always go back to taking
the mixture twice a day, and when the symptoms lessen, go back to 3 times a
day. Experimentation is fine - listen to your body; it will tell you when to
back off.)
On day 12, if you believe
you're cured, you can stop taking the BAKING SODA CURE. But if you think you
ever need a "tune-up" for cancer at any time, repeat all the above
steps.
If you're cancer free, it is
advisable to use 2 teaspoons baking soda and only one teaspoon molasses/syrup
in 1 cup of water once or twice daily for 7 days: i.e., if you're only trying
to raise your pH to the alkaline range of 7.2 - 7.5.
Can an Alkaline Diet Successfully Treat Cancer? It never ceases to amaze me how often conventional doctors fail to address the correlation between food and cancer prevention and treatment. Your diet can not only cause cancer, but it could also prevent or cure you from cancer. Meat, dairy, refined sugar, and processed foods are all known to increase one's risk of cancer, and all of these are considered acid-forming foods.
Cancer is a systemic, metabolic disease that forms as a result of nutrient deficiencies, high amounts of toxins, and usually a pH level that's too low, meaning the body is too acidic. In order to neutralize the constant acid generation, we need to supply the body with more alkaline foods. An alkaline diet may be your best defense against cancer.
Baking Soda and Cancer. University of Arizona Cancer Center member Dr. Mark Pagel will receive a $2 million grant from the National Institutes of Health to study the effectiveness of personalized baking soda therapy to treat breast cancer.
Treating Cancer with Sodium Bicarbonate. Bicarbonate is an essential nutrient and our stomachs, pancreas and kidneys often have to struggle to produce enough - especially as we get older. Good question would be, is it a good idea for cancer patients to help these essential organs? Older people do have bicarbonate deficiencies and the perfect thing medically speaking to do is to alleviate these deficiencies. For cancer patients it could make the difference between life and death because cancer patients are universally very acid so the alkalinity provided by bicarbonate is crucial.
OUR APPROACH TO CANCER:
Our goal is to provide sophisticated cancer care utilizing a personalized and precision targeted immunotherapy approach.
Our personalized cancer therapy utilizes an understanding of each patient’s cancer genetic and immunotherapy make-up to unravel the biology of their cancer and to identify effective treatment strategies using targeted therapies and immunotherapies that are aimed at specific genes or proteins that are found only in cancer cells or their environment.
TREATING CANCER SINCE 1977
Established in 1977, the Burzynski Clinic has grown to be a nationally and internationally recognized cancer center that provides cutting-edge cancer treatments.
For over 40 years, Dr. Burzynski’s cancer research and patient care has been inspired by the philosophy of the physician Hippocrates: ‘First, do no harm’. Therefore, our approach to treatment is ‘personalized’ in an attempt to maximize effectiveness and minimize side effects for each cancer patient.
Treating Cancer with Sodium Bicarbonate. Bicarbonate is an essential nutrient and our stomachs, pancreas and kidneys often have to struggle to produce enough - especially as we get older. Good question would be, is it a good idea for cancer patients to help these essential organs? Older people do have bicarbonate deficiencies and the perfect thing medically speaking to do is to alleviate these deficiencies. For cancer patients it could make the difference between life and death because cancer patients are universally very acid so the alkalinity provided by bicarbonate is crucial.
(6) The Burzynski Clinic, Houston, Texas
I also added some contact information on Dr. Burzynski who has a clinic in Houston, Texas. This video has some history about Dr. Burzynski:
Our goal is to provide sophisticated cancer care utilizing a personalized and precision targeted immunotherapy approach.
Our personalized cancer therapy utilizes an understanding of each patient’s cancer genetic and immunotherapy make-up to unravel the biology of their cancer and to identify effective treatment strategies using targeted therapies and immunotherapies that are aimed at specific genes or proteins that are found only in cancer cells or their environment.
TREATING CANCER SINCE 1977
Established in 1977, the Burzynski Clinic has grown to be a nationally and internationally recognized cancer center that provides cutting-edge cancer treatments.
For over 40 years, Dr. Burzynski’s cancer research and patient care has been inspired by the philosophy of the physician Hippocrates: ‘First, do no harm’. Therefore, our approach to treatment is ‘personalized’ in an attempt to maximize effectiveness and minimize side effects for each cancer patient.
(7) GcMAF ~~ type of immunotherapy; treatment that revs up the immune system. In 2008, a group of published studies claimed that a treatment called Gc protein-derived macrophage-activating factor (GcMAF) had wiped out breast, colorectal, and prostate cancers. The studies were led by a researcher named Nobuto Yamamoto.
GcMAF is a type of immunotherapy, a treatment that revs up the immune system. It activates macrophages, which are white blood cells the immune system sends out to gobble up foreign cells like bacteria and cancer. Our bodies make the protein GcMAF to activate macrophages. But scientists think cancer cells release an enzyme called Nagalase that blocks the making of GcMAF to protect themselves against attack. Some scientists think that adding GcMAF to our bodies will combat the power of Nagalase and can destroy cancer cells.
Dr. Leigh Erin Connealy, Irving, California. Check nagalase in blood; sensitive test for monitoring the efficacy of therapy in cancer and certain viral infections. When we make bad cells, they make an enzyme called Nagalase which poison the macrophages, inhibiting them attacking the bad cells. The macrophages are the pac men of your immune system. In tests, people with cancer tend to have high Nagalase numbers.
For various types of tumors, various levels of Nagalase activity were found. It appears that the secretory capacity of individual tumor tissue varies among tumor types depending upon tumor size, staging, and the degree of malignancy or invasiveness. Increased Nagalase activity has not been detected in the blood of healthy humans.
(8) Vitamin B-17, or Laetrile. What is it? It's actually a form of cyanide which is found in the seeds of different fruits, and it just so happens that it is most potent in bitter apricot kernels. When I read that they can be used to treat cancer, I bought some for Jim. The serving size is 3 kernels. Any more than 5 can be harmful. This is a good article by G. Edward Griffin called World Without Cancer: The Story of Vitamin B-17.
I bought these bitter Apricot kernels from Amazon. Jim is eating 6 every night. I does say that 3 kernels is the serving size, but when you are battling cancer, there is nothing wrong with taking more. He is also taking Fenbendazole, Vitamin D, turmeric, curcumin.
McQueen was feeling great and decided to have the bulge removed for cosmetic reasons. It was a complication of that surgery, not cancer, which caused his death. Not a word of his prior recovery was to be found in the major press. Consequently, millions of Americans who followed the story came away with the conviction that Laetrile is just another hoax.
Apricots: The Hunza’s Golden Secret to Longevity and Vitality
Doctrine of Signatures: Liver, Skin, & De-Plaques Cancer Sites
Benefits of Apricots
Cancer Crusader: Packed with beta-carotene and lycopene, apricots are formidable in the fight against prostate, breast, and other cancers.
Blood Pressure Balancer: With their high potassium and magnesium content, apricots are natural regulators of blood pressure.
Vision Guardian: The beta-carotene in apricots converts to vitamin A, essential for eagle-eyed vision.
Age-Defying Antioxidants: Loaded with antioxidants, apricots keep you youthful and vibrant.
Brain Booster: The B vitamins in apricots may shield against Alzheimer’s and cognitive decline.
Legendary History
Alexander the Great’s Treasure: This conqueror discovered apricots in Asia and brought them back to Europe, forever changing the fruit landscape.
Roman Precocity: Named from the Latin word for "precocious," apricots were cherished for being the first fruit of the season.
Nutritional Goldmine
Vitamin and Mineral Explosion: Apricots are a treasure trove of vitamin C, iron, fiber, and B vitamins.
Lycopene and Beta-Carotene: These potent antioxidants are your body’s best defense against free radicals.
Iron Infusion: Snacking on dried apricots can skyrocket your iron levels, making them a natural remedy for anemia.
Health Powerhouse
Cancer Fighter: Bursting with lycopene and beta-carotene.
Six fresh apricots daily can significantly reduce cancer risk.
Heart Hero: Essential nutrients like iron, potassium, and copper keep your heart ticking healthily. Fiber in dried apricots helps banish bad cholesterol.
Vision Virtuoso: Rich in vitamin A and beta-carotene.
Essential for keeping cataracts at bay and maintaining crystal-clear vision.
Longevity Legend: The Hunza tribe’s apricot-rich diet is linked to their remarkable health and longevity.
Fresh apricots in season and dried apricots in winter are their secret weapons.
Mind Marvel: B vitamins in dried apricots protect against Alzheimer’s and mental decline.
Traditional and Medicinal Magic
Constipation Crusher: The cellulose and pectin in apricots act as gentle, natural laxatives.
Digestive Dynamo: Apricots eaten before meals can aid digestion and prevent nervous indigestion.
Anemia Annihilator: High copper content makes iron more available, boosting hemoglobin production.
Fever Fighter: Fresh apricot juice mixed with honey or glucose cools and detoxifies the body.
Skin Savior: Fresh apricot juice can treat scabies, eczema, sunburn, and other skin ailments.
Apricot Gold
Chinese Medicinal Gem: Apricot kernels, or "Apricot Gold," are famed in traditional Chinese medicine for their life-prolonging properties and benefits for women’s health.
Cosmetic Charm: Apricot flowers are a staple in Chinese beauty treatments.
Apricots: The Golden Fruit of Longevity and Health
Unleash the power of apricots in your daily diet to harness their incredible health benefits. From warding off cancer to promoting longevity, this golden fruit is your ticket to vibrant health and vitality. Embrace the Hunza’s secret and make apricots your go-to superfruit!
I also found the following, which I found quite interesting. I was wondering if I should give Jim Fenbendazole and CBD along with the apricot kernels. Rupert's wife gave him quite a large protocol for his cancer. I won't go into this detail, but if you have a lot of cancer in your body, it may be a good idea to attack it this way.
(9) Soursop or guanabana. This fruit is called soursop or guanabana and has been proven to be 10,000 times more effective than chemotherapy at reversing the affects of cancer. However it does this very differently to chemo though, instead of killing all the cells surrounding the cancer cells often resulting in hair loss, fatigue, nausea, vomiting, anemia, infection, easy bruising/bleeding plus many more! On the contrary "the compound extracted from the Graviola tree selectivelyhunts down and kills only cancer cells. It does not harm healthy cells!"
Why haven't you heard of this amazing fruit?! Well long story short a large company years ago spent millions to find a cure for cancer. However in order for them to have made their money back and further profit from their finding they needed to create a synthetic duplicate of the compound found in the soursop as they could not pattern something natural. Unfortunately for them they were unable to do this so they left it all and didn't publish their findings. Luckily there was one scientist who was unable to let this amazing finding slip under the rug, so he contacted a company that is dedicated to harvesting medical plants in the Amazon rain forest.
Hopefully this post gives you a better understanding at how powerful plants are and why more and more people are becoming plant-powered/vegan to be as healthy as possible and to reverse and avoid chronic disease like coronary heart disease.
(10) Hoxsey Bio Medical Center. I read about Harry Hoxsey in the book The Truth About Cancer: What You Need to Know by Ty M. Bollinger. The book starts out explaining how the AMA came into existence and why doctors prescribe toxic chemical-derived drugs to patients for their ailments. Harry Hoxsey learned about certain herbs that cured people of cancer from this great-grandfather. He opened up clinics around the country and cured thousands of people of cancer, but by the 1960s, was forced to shut down all of his clinics. Hoxsey then opened up new clinics in Mexico that still operate to this day. His clinic is located in Tijuana, just across the border from San Diego beyond the reach of U.S. regulators.
(11) Hold on now. I just found another natural cure for cancer; called EBC-46. While going through my X feed, look at what I found:
EBC-46, also known as tigilanol tiglate, is a naturally occurring compound derived from the seeds of the Blushwood tree (Fontainea picrosperma), which is native to the rainforests of Queensland, Australia. It is an experimental anticancer drug primarily being studied for its ability to treat certain types of solid tumors.
How EBC-46 Works:
•Tumor Destruction: EBC-46 works by triggering a local immune response that destroys the tumor’s blood supply. This leads to rapid necrosis (death) of the tumor cells.
•Selective Action: It is injected directly into the tumor (intratumoral injection), making its effects highly localized and minimizing systemic side effects.
•Rapid Results: In preclinical and clinical studies, tumors treated with EBC-46 have been observed to shrink significantly or completely disappear within days.
Current Applications:
•Veterinary Use: EBC-46 has been approved for use in veterinary medicine under the name “Stelfonta.” It is used to treat certain types of skin cancers in dogs, such as mast cell tumors.
•Human Clinical Trials: The drug is undergoing clinical trials for its potential use in treating solid tumors in humans, including melanomas, head and neck cancers, and soft tissue sarcomas.
Advantages and Limitations:
•Advantages:
•Rapid and localized action with minimal systemic toxicity.
•Non-surgical treatment option for accessible tumors.
•Limitations:
•Currently limited to tumors that can be directly injected.
•Still under investigation for broader applications in human oncology.
EBC-46 represents a promising step in cancer treatment, particularly for tumors that are challenging to remove surgically or treat with systemic therapies.
EBC-46 – The Truth About The Australian Anti-Cancerous ‘Miracle’ Berry Extract
Ivermectin, Fenbendazole, Vit C and Sodium Bicarb. But don't worry your cancer is safe because the FDA would never allow it.
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I found this video on Cancer, the Forbidden Cures:
Before BIG pHARMa, CA patients were given 2 large bottles of peroxide, and a bag of cotton balls and told to use it daily and return in 2 weeks to find 100% of it was cured.
(12) DMSO (Dimethyl sulfoxide). How DMSO Naturally Eliminates Cancers. This article was written by A Midwestern Doctor, April 2025.
Because of the controversy surrounding DMSO, once its pioneers realized it also treated cancer, a decision was made to downplay this facet of DMSO as "unproven" cancer cures are always attacked by the medical system. As a result, DMSO's anticancer properties still remain relatively unknown.
In the first part of this series, I presented dozens of studies that show DMSO effectively treats cancer pain (which is often very challenging to address) and dramatically reduces many of the complications experienced from radiation therapy and chemotherapy (as it selectively protects healthy cells from those agents).
Given how debilitating each of those can be for a cancer patient, it is remarkable DMSO has not been adopted for any of those applications, particularly since addressing those does not take business from the cancer industry (and if anything would make more patients want to undergo conventional cancer care).
Note: 65% of oncologists' revenue comes from chemotherapy drugs3 (which coincidentally are by far the most profitable drug market4).
In the first part of this series, I presented dozens of studies that show DMSO effectively treats cancer pain (which is often very challenging to address) and dramatically reduces many of the complications experienced from radiation therapy and chemotherapy (as it selectively protects healthy cells from those agents).
Given how debilitating each of those can be for a cancer patient, it is remarkable DMSO has not been adopted for any of those applications, particularly since addressing those does not take business from the cancer industry (and if anything would make more patients want to undergo conventional cancer care).
Note: 65% of oncologists' revenue comes from chemotherapy drugs3 (which coincidentally are by far the most profitable drug market4).
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This post is not meant to be an exhaustive treatise on the prevention and treatment of cancer, but only to explain as simply as possible the scientific theory behind Adam Gaertner’s anti-cancer protocol, which combines 4 simple and cheap therapies that have been separately used and studied for a wide variety of human cancers with mixed results, but together have powerful synergistic effects that may, it is hoped, effectively eliminate any cancer.
Doctors told him: “You have Stage 4 colon cancer that has spread to your liver and lungs.
You have 6 months to live.” He had 7 tumors in his lungs, 7 in his liver, and one in his colon.
A year and a half later… He’s still alive and doing better than ever.
His wife says she built a regimen after months of research that included:
• Fenbendazole
• Ivermectin
• Quercetin
• Curcumin (turmeric)
• Vitamins C, D, E, and B-complex
• Grape seed extract
• Chlorella
• Essiac tea
• Soursop (graviola)
• Propolis
• Beetroot powder
She documented changes along the way:
• Coughing stopped
• Skin color returned to normal
• Hemoglobin levels improved
• Tumor markers dropped
Today, he’s still here.
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Scientists just discovered a way to smash cancer cells apart using light — no drugs, no chemo. And they had a 99% kill rate in lab tests.
In a striking leap forward for cancer treatment, scientists have developed a new technique that uses light to physically destroy cancer cells without harming healthy tissue.
Researchers at Rice University, working with Texas A&M and the University of Texas, discovered that when dye molecules called aminocyanines—commonly used in imaging—are attached to cancer cells and hit with near-infrared light, they vibrate intensely. This synchronized movement, dubbed “molecular jackhammering,” generates mechanical force that ruptures the cancer cells' membranes.
The approach has shown dramatic results in early experiments, obliterating 99% of melanoma cells in petri dishes and triggering full remission in about half of tested mice. Because it relies on physical force rather than chemicals or genetic modification, it sidesteps the issue of resistance that plagues many existing therapies. Moreover, the use of near-infrared light means the treatment can penetrate deeply into tissue with minimal damage to surrounding cells—raising hopes for non-invasive therapy options. Researchers are now optimizing the method and preparing for human trials, eyeing a future where light becomes a powerful weapon against cancer.
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Pablo Kelly begins his 10th year of survival with terminal stage 4 brain cancer without ever receiving radiation or chemotherapy. Please visit his website for information on his non-toxic metabolic therapy.
Cancer Cells shattered through resonant frequencies- Anthony Holland at TEDx Skidmore College is being shared with sole intention to spread awareness about how Frequencies can benefit everyone to precious life of their near and dear ones. Cancer Cells can be shattered with a painless Non-Invasive Micro Current Frequencies treatment.
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I found this video on Cancer, the Forbidden Cures:
For anyone dealing with cancer(s)...Here are a few helpful tips:
1st, don't have them "test" the tumor. Tumors are the body's way of protecting us from allowing the CA cells to traverse the body and mutate healthy cells. Once it's punctured for "testing", the cells travel and the beasties cause more issues. (Why not right? It's a $ making racquet.)
1A. CANCER IS A PARASITE. Start the Ivermectin (dosage 1am1 pm by bodyweight) & Fenbendazole (dosage one 222mg pill/day for 6 days, skip the 7th to let the renal system rest).
2nd, STOP ALL SUGARS. CA loves sugar in ALL FORMS.
3rd, HYDROGEN PEROXIDE: H202 has the extra Oxygen molecule that CA can't stand. Put it on a cotton ball, or wash cloth for larger areas and rub all over skin. 3x/day, more-so when you're out of the bath & shower, as your pores are open and more apt to getting it into the bloodstream. The skin absorbs the HP, and kills the CA cells almost immediately.
4th, ALKALINE WATER: CA can't survive in an alkaline body. Start drinking alkaline water w/ lemon consistently thru the day. Lemon is an acid outside of the body, but the hydrochloric acid in your stomach converts it to an alkaline base. This travels through your blood stream and will help to eradicate the crud.
5th, DETOX BATHS: 1 cup Baking Soda, 1 Cup Borax, 1 Cup Epsom Salt, & Bentonite Clay. Draw the hottest bath you can muster... Soak as long as you can, as hot as you can, and it will help to detox the CA and the nano-particulates (gr@phine oxide), out of the body. Do this at least 2-3x a week.
6th, The BIG BOMBER: VITAMIN B17 which NO ONE wants ANYONE to know about!
Apple seeds, Apricot, Peach, & Plum Pits, - ALL of it! You can get them on Amazon, or any other place online. The B17 vitamin has been removed from our knowledge, because: BIG pHARMa. 1/4 teaspoon a day of the powder, or just eating a couple apricot pits thru the day, (like 3 or 4), will also eradicate the Cancer. (I bought apricot seeds (bitter) from Amazon.)
A World Without Cancer The Story of Vitamin B17 by G. Edward Griffin - 1974 Presenting evidence that cancer is a deficiency disease. It is not caused by the presence of a virus or X- factor, but by the lack of essential food, which increasingly is deleted from the modern menus.
I really hate the fact that non-suspecting people are dealing w/ all the bioweapon B.S. The turbo cancers are all a part of it. ..
We have LEGIT CURES now. There's no longer a need for Chemo and Radiation which do nothing more than kill the good tissue. 9/10, the patient passes from chemo & radiation poisoning than the actual cancer.
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The two drugs are Ivermectin and Fenbendazole, both initially discovered and used as gastrointestinal anti-parasite drugs. They kill parasites, mainly in the gut. They are basically animal dewormers. Ivermectin is used on many animals, but most famously on horses, and Fenbendazole on dogs. But Ivermectin has also been used as an antiparasitic for humans for many decades.
So there is plenty of data on that. But over recent years, in part thanks to the COVID pandemic, research has shown them to also kill cancer, in the lab, in mice, and even in humans. And all with no serious side effects.
Approved for human use in 1987, [Ivermectin] has been instrumental in tackling some of the world’s most harmful tropical diseases, such as Onchocerciasis, lymphatic filariasis (also known as Elephantiasis), strongyloidiasis and scabies. It also effectively fights parasitic infestations in animals, which can be economically devastating to the livestock industry… Ivermectin is one of the safest drugs known. It is on the World Health Organization’s list of essential medicines, has been given over 4 billion times around the globe, and won the Nobel Prize for its global and historic impacts in eradicating endemic parasitic infections in many parts of the world.”
WHO Guidelines for Scabies: “the majority of side effects are minor and transient” Prof. Jacques Descotes, Toxicologist and Expert on Safety of Ivermectin: “severe adverse events are unequivocally and exceedingly rare” LiverTox Database: Not considered toxic to the liver Nephrotox Database: Not considered toxic to the kidney PneumoTox: Not considered toxic to the lungs
The standard dose of Ivermectin as an antiparasitic in humans is 0.2mg/kg per day. That’s 17.2 mg for a 190 lb. man. But it’s extremely safe even at much higher doses, as much as 10X higher:
The key thing to understand about Ivermectin is how safe it is, which means there really isn’t a downside to taking it, even as a prophylactic. And as you can see from the footnotes so far, there’s a lot of information out there in the medical literature about Ivermectin. But more importantly, there are at least nine (9) research papers on the anti-cancer properties of Ivermectin published in medical and pharmacological journals over the past five years.
To summarize the findings as briefly as possible, Ivermectin has at least 15 anti-cancer mechanisms of action.
There is evidence that Ivermectin can treat almost every type of cancer, most-importantly including colon cancer, even Stage 4 colon cancer. Ivermectin has been shown to kill cancer cells, both in vitro (in petri dishes) and in vivo (in living organisms, primarily mice):
In Vitro Studies:
breast cancer, ovarian, prostate, colon, pancreas, head and neck, melanoma – inhibits cell proliferation, induction of apoptosis, autophagy, reversion of tamoxifen resistance, inhibits metastases
glioblastoma – growth inhibition, apoptosis, and anti-angiogenesis
In Vivo Studies (done on immune deficient mice):
acute myeloblastic leukemia – reduce tumor volume up to 70%
glioblastoma – reduce tumor volume up to 50%
breast cancer – reduce tumor volume up to 60%
glioma – reduce tumor volume up to 50% (at 0.24mg/kg), however at human dose equivalent to 0.8mg/kg tumors were not detectable!
colon cancer – reduce tumor volume up to 85%
median dose employed was equivalent to 0.4 mg/kg in humans from 10 to 42 days (oral, intraperitoneal or intra-tumoral)
the in vitro and in vivo antitumor activities of Ivermectin are achieved at concentrations that can be clinically reachable based on the human pharmacokinetic studies done in healthy and parasited patients.
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According to a study available from the European Medicine Agency, doses up to 500 mg per person did not result in serious adverse effects. This suggests that Fenbendazole may be safe for use in humans at this dose level. Additionally, single doses of up to 2,000 mg per person were reported to cause no serious adverse effects over ten days.
Oncologists in North America are not allowed to talk about repurposing drugs with extensive proven anti-cancer activity (proven in pre-clinical studies). All they do since 2021 is push failed Pfizer or Moderna COVID-19 mRNA Vaccines on their Cancer patients, which either accelerate their existing cancer or cause cancer recurrence if they were in remission.
Thousands of COVID-19 mRNA Vaccinated individuals are coming down with extremely aggressive cancers called "Turbo Cancer". Thousands are dying from these cancers every day as Oncologists are "baffled" and don't know what to do beyond what big pharma orders them to sell - which doesn't work for these cancers.
My fellow Oncologists - you won't save lives if you're scared of the corrupt Medical Boards or Colleges of Physicians and Surgeons. They won't let you save lives. They don't get bought by big pharma to save lives. Well you know what, all these useless medical bureaucrats can go to hell... There are lives that can be saved and no paper pusher is going to stop me. Not in Alberta. Not anywhere.
Dr. William Makis: "You can use high dose Ivermectin for majority of cancers...Merck is in a 50:50 partnership with Moderna for the new mRNA cancer vaccine...it's all about money...that's why you don't have any clinical trials for high dose ivermectin, that's why you don't have any clinical trials for mebendazole or fenbendazole...
Dr. William Makis: NEW ARTICLE: FENBENDAZOLE and MEBENDAZOLE in the treatment of Multiple Myeloma “Multiple myeloma is the second most prevalent hematologic malignancy and is uniformly fatal, very often as a result of development of drug resistance." "we showed that benzimidazoles (Fenbendazole and Mebendazole) significantly reduce the secretion of cytokines essential for multiple myeloma survival” “In the present study, we show that benzimidazoles (Fenbendazole and Mebendazole) induce cell death in multiple myeloma cell lines and in primary CD138+ myeloma cells and overcome drug resistance.” Anti-parasitic drugs Fenbendazole and Mebendazole are extremely popular right now, due to their ability to kill cancer cells & shrink tumors, by increasing p53 tumor suppressor levels (people who took COVID-19 Vaccines may have low p53 levels) and inhibiting glucose utilization by cancer cells. For Multiple Myeloma, Mebendazole shows advantage over Fenbendazole at every dose. At lower doses, Mebendazole is significantly superior to Fenbendazole, but as you go higher in dose, that advantage almost disappears. At the highest dose, the difference between the two is maybe 5% and Mebendazole is still the winner, but Fenbendazole is “almost as good”. Most people can get Fenbendazole, Mebendazole is more difficult to get and more expensive (even generic versions) Pfizer and Moderna COVID-19 mRNA Vaccines cause aggressive cancers called "Turbo Cancer" - one proposed mechanism is p53 tumor suppressor impairment. Fenbendazole and Mebendazole address the p53 problem in ways chemotherapy can't. Most Oncologists are not mentally equipped to treat Turbo Cancer patients with any kind of success. They use conventional chemotherapy which doesn't work in most cases of Turbo Cancer. In the COVID-19 Vaccine era, if you rely on your mRNA Vaccinated Oncologist, you are not going to make it. Article Link in photo to avoid shadowban, just re-type the URL in the 1st photo at the top, into your browser to access...
BREAKING NEWS: First-in-the-World Ivermectin, Mebendazole and Fenbendazole Protocol in Cancer has been peer-reviewed and published on Sep.19, 2024! The future of Cancer Treatment starts NOW. My thanks to lead authors Ilyes Baghli and Pierrick Martinez for their incredible inspired work, FLCCC’s Dr.Paul Marik for his extensive work on repurposed drugs and every co-author who worked hard to bring this paper to life. I hope that this peer-reviewed paper lays the groundwork for a brand new future for Cancer Treatment. Many of you know that I have been helping thousands of Cancer patients with high dose Ivermectin, Mebendazole, and Fenbendazole. We are already starting to see incredible successes with these repurposed drugs. Mainstream Oncology collapsed after the rollout of contaminated COVID-19 mRNA Vaccines. Most Oncologists abandoned their Hippocratic Oath, gave contaminated mRNA Vaccines to all their cancer patients and took the mRNA jabs themselves. Some Oncologists have now developed mRNA Induced Cardiac arrests, blood clots and Turbo Cancer. Others have already died suddenly. These Oncologists buried their heads in the sand and abandoned everything that it takes to be a good competent doctor. However, there are doctors who are blazing a new path into the future. See you there!
Fenbendazole and Ivermectin for Prostate Cancer? A Case Series of 56 Patients (January 2026 Edition)
A recent study documented COMPLETE REMISSION of Stage 4 cancers using fenbendazole. Patients with advanced melanoma, breast, and prostate cancer saw their tumors disappear.
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In this article Dr. Thomas Seyfried talks about the effects of diet on prostate cancer.
Dr. Thomas Seyfried uses the Ketogenic diet along with drugs to fight cancer. In the following video, Dr. Thomas Seyfried discusses metabolic approaches to cancer. Learn how depriving cancer cells of fermentable fuels like glucose and glutamine can starve and kill them. Challenge the genetic disease model and discover the impact of ketosis on mitochondrial health. The truth about cancer is that it is a metabolic, not genetic, disease. Empower yourself with the knowledge to combat cancer through metabolic strategies and learn about the dangers surrounding us: processed foods.
I also have a video with Dr. Ken Berry and Dr. Thomas Seyfried where they discuss the Proper Human Diet in connection with cancer. This is a great video -- a must listen.
The Ketogenic Diet in Colorectal Cancer: A Means to an EndI have read that doctors like to use the drug Avastin for colorectal cancer. According to Dr. Seyfried, it is the worst drug you can take and should be outlawed.
The Truth About Cancer ~~ This is just one excerpt from a series done by numerous doctors. Here is the rest of the series.
17 hours of fasting kills cancer cells? When fasting... ~Cancer cells are wired to guzzle glucose and when we fast, insulin levels drop. Cancer needs insulin for growth. ~Autophagy is enabled. It's spring cleaning on a cellular level. Our body seeks out anything that is damaged and tries to recycle it or get rid of it. ~Our immune system produces "natural killer" cells that are more effective when cancer cells are not being nourished. ~Stem cells migrate and seek out things to repair, including the damage caused by cancer. This makes cancer’s environment less hospitable.
DR. LEE MERRITT - CANCER IS REALLY PARASITES! MULTIPLE SCLEROSIS is PARASITES in SPINAL CORD & BRAIN. IT'S ALL PARASITES - ALMOST ALL DISEASES - CANCER - LYME - LEUKEMIA ETC. This is extremely safe to take every day, no days off. No elevated liver enzymes with this protocol. TAKE FENBENDAZOLE 3 DAYS ON, 4 DAYS OFF, 1gr pkg. 1 GRAM = 1,000mg. Save your life and don’t let your doctors frighten you that this will harm your liver. It’s just not true! God bless, and good luck.” ~~ Joe Clark JOE TIPPENS PROTOCOL - FENBENDAZOLE - BROAD SPECTRUM PARASITES TREATMENT: FENBENDAZOLE CBD OIL BERBERINE QUERCETIN TURMERIC NATURAL BERBERINE: BARBERRY (small red berry) GOLDENSEAL OREGON GRAPE PHELLODENDRON CHINESE GOLDTHREAD TREE TURMERIC (INDIAN BARBERRY) PRICKLY POPPY YELLOWROOT Berberine regulates blood sugar, improves insulin sensitivity, and supports fat metabolism. Consume berberine-rich plants such as barberry, goldenseal, Oregon grape, and Chinese goldthread. Best Natural Sources of QUERCETIN: 1. Onion 2. Nettle 3. Oak 4. Pomegranate 5. Sea Buckthorn 6. Chamomile 7. Black Grapes 8. Blackberries 9. Oregano Turmeric = curcumin? Turmeric is the spice that gives curry its yellow color. It has been used in India for thousands of years as both a spice and medicinal herb. Turmeric contains compounds with medicinal properties. These compounds are called curcuminoids. The most important one is CURCUMIN, which is the main active ingredient in turmeric.
A recent paper that introduced a new cancer theory based on faulty mitochondria function in cancer stem cells. We go through this introductory paper to see why the authors propose renewed attention to cancer development and treatment based on mitochondria function, especially for metastatic cancers.
Originally published on Patreon on December 21, 2024
What we cover: *Different cancer origins theories *Why the predominant somatic mutation theory does not work *Why the mitochondria function theory makes sense *Review of the mitochondria stem cell connection theory.
What causes cancer? It's all still theoretical. "The mitochondria respiration theory, was proposed in 1920. Imagine if this turns out to be true and we could have been treating according to this theory for over 100 years. And we act as if this theory doesn't even exist when it comes to cancer treatment." And then there is the Cancer Stem Cell theory. The prevalent theory is the somatic mutation theory. But what if the mutations are not the cause of cancer, and they are bystanders? Why does it matter? Because if the mitochondrial-stem cell connection is the cause of cancer, then a treatment that addresses that issue would be the better approach. Mainstream cancer treatments are based on the somatic mutation theory and cannot target cancer stem cells.
Mitochondrial–Stem Cell Connection: Providing Additional Explanations for Understanding Cancer
How can we cure Cancer - The Cure has been known since the 1930’s.
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