Fenbendazole - An off label use drug to cure cancer

Over the years I’ve tracked on different types of cancer cures. There are many, some better than others and a few that really stand out.

You may have heard of Joe Tippen’s by now. He cured advanced lung cancer with the anti-parasite drug called Fenbendazole. It turns out that there has been quite a bit of research showing how Fenben negatively impacts on cancer cells. Joe states that he has received thousands of testimonials from people who did the Fenben and they are now NED (no evidence of disease)

Joe has a website where you can find out more about his protocol. I highly recommend it that you read it and watch the videos. In his blog you will find the password to enter the facebook group where the Fenben protocol is discussed. www.mycancerstory.rocks

I’ve been following the Fenben story closely now since my uterine cancer diagnosis in January. I had surgery but refused radiation. Chemo was not recommended to me. I am taking Fenben and Ivermectin which also has had studies showing that it interferes with cancer stem cell replications.

I’ve collected quite a few testimonials regarding Fenben. Some of the people did chemo and radiation as well. The testimonials here with the asterisk * in front of it are from the people who did no radiation or chemo, as well as a couple who had done it years previously but the cancer returned and they refused to repeat it.

You will notice as you read the testimonials that people are using quite a few supplements as well. All the supplements that I have looked into have strong anti-cancer properties, many with research behind them.

This is the protocol that I’m currently doing.

Enjoy the read. There is hope for us! If there is an asterisk * next to the testimonial it means that no chemo or radiation was done or that such a small amount was done or that it was done long before the NED appeared, generally after the cancer getting worse.

Fenben Testimonials 1

My husband asked his oncologist about Fenben his first visit. He was very negative about it. Husband had pancreatic cancer that was found early but growing fast. He decided he had absolutely nothing to lose and did the Fenben along with chemo and radiation. We never told another oncologist that he was doing it. He was on chemo for 16 months. He took the liver supplements. He finally had enough shrinking of the tumor to have surgery. When his pathology reports came back there was no cancer and no tumors, even the original tumor was scar tissue.

‘’’’’’’’’’’’’’’’’’’’’’’’’’’’’’’’

* No Chemo, radiation or hormone blockers, surgery or immuno.

Diagnosed NSCLC Nov 2021

Started JTP ( The Original) Dec 21

Oct 2023, NED..

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* My wife chose no chemo and no surgery against strong recommendation by the doctors for stage 4 appendix cancer. A very rare and aggressive form of appendix cancer. They never gave her any hope of a long term recovery. She’s two years removed from her initial diagnosis. She changed her diet drastically, that and the protocol have held the cancer at bay but has not cured her. She recently received SOT therapy and this seems to reversing some of the effects of the cancer. (https://imcwc.com/supportive-oligonucleotide-technique/)

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* Hi. I was diagnosed w. advanced, inoperable stage 3 pancreatic cancer in 2022. I refused chemo & radiation & was offered hospice. I only did JTP, supplements & some repurposed drugs + PRAYER. Last app't. with oncologist he said I'm stage 1B & "Keep doing what you're doing.''.

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 * I’m stage iv a colon cancer and have been Ned for 3 years no chemo no radiation just the fenben protocol. My only difference is mine was removed in emergency surgery plus 7 nodes only 3 nodes were positive. Cancer was present in my blood biopsy. They recommended traditional but I refused

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* I did 1 keytruda (cancer treatment) and walked away, did not tell dr what I was taking. fenben destroyed my tumor before it was removed.

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* I had adema carcinoma endometrial lining. Grade 2. For over 5 years by the time they found it , and the insurance co. finished challenging me in a 9 month appeal, refusing me treatment

I used The Joe Tippens Protocol. Shrunk the tumor 80% in 4 1/2 months

Then did alkaline for cancer diet ( vegetables , no sugar no bread low fat - only 3 Oz meat twice a week.

Lost 35 lbs in two months. To 110 lbs

4 tumors went to the lymph node grew three times the size to 20 mm and they died !

“ negative for malignancy” from 6 lymph nodes by the pathologist..

Surgeon tried to make me do intravenous chemo , before surgery. I said no. Two weeks later , biopsy said the tumors died.

The immune system is doing its job. Try to allow it first to do its job. My PH was 7.5

Very incredibly Incredible protocol.

This was November 2022. I gained from 110 lbs to 135 lbs in a year.

*I never did chemo or radiation, i only did fenben and RSO i did not take any pathways or vitamins, i didn’t have a lot of money and had to borrow, I took it for 6 months and shrunk my tumor from 3.5 to 1.9 got really sick with another disease and had the lump removed no lymph nodes taken just the lump removed, when removed the dr said it was completely dead, something about comedo nercrosis, I had tripple neg breast cancer it should have spread and been double the size in that 6 months, this was all last year, had scans done two weeks ago and still no cancer. I still do the maintenance of Joe's protocol with the fenben and RSO but that is all i have done and cancer free today.

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* I've done Budwig Protocol, artemisinin + iron bisglyconate, Laetrile, fenben, garlic and olive oil, full spectrum CBD, and within three months after my double mastectomy I was declared NED with no chemo or radiation.  Hit it with the kitchen sink and keep it up!

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* TNBC survivor never did chemo radiation pathways vitamins or anything other than Fenben and RSO went from original 3.5 cm to 2.9 in 6 weeks, took another 8 months it was 1.9 cm and completely dead when i had it removed in Nov. of last year, scans a couple months ago show NED.

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* Oh please dont do the double masectomy until your sure the protocol isnt working. I almost removed mine but the protocol shrunk it in half and killed it. No chemo or radiation nothing and still cancer free today

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May 21, 2022

Well had my scan results yesterday. Haven't had any immunotherapy treatments in 3 months, because it attacked my endocrine system. So I was worried. Well by the grace of God it still showed shrinkage and the small nodules were gone. My only treatments have been 2000mg of fenben for the last 6 months. And it's working. The oncologist was amazed. He has fenbendazole listed on my med list. But he turns the blind eye that it's that. It's working!!

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This is an update regarding a man who was stage four colon into liver. He went on 222 mg fenben twice a day. Few months later still spread by cm. However, increased the dosage to 888:mg along with milk thistle, curcumin tumeric, chaga mushroom and his last test concluded 3 mons later the white cells are dying and his liver is clear as well as colon. He has had a few rounds of chemo but everything changed when he Increased the fenben. Yes this stuff does work. Even the Drs are baffled and he was considered terminal.....no more. He's celebrating.

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Jan 12 2023

Asking for prayers on a scan result tomorrow. This was my fifth scan. When I started this journey 14 months ago they gave me 6-12 to live. The mass in my lung was 4.9cm. After eating fenben everyday for 14 months and immunotherapy it was at 1cm on last scan with no spread. Continued prayers for all warriors in this group

May 4^th  2024 ….
Praise God and all the prayer warriors! Went in for scan results and my oncologist said your in remission after 2.5 years renal cell carcinoma Mets to lungs. DONT GIVE UP!

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Update:

Stage 4 nsclc Adenocarcinoma (both lungs) with mets to many lymph nodes, liver, spine, hip, pelvic bones, malignant pleural effusion, diagnosed 2/18/19.

I saw my lung dr yesterday. He said my CT scan results were remarkable! He is amazed at results!! I went from having a huge lung mass occupying whole upper lobe & part of middle lobe on my right lung in May to... now only SCAR tissue in November, a liver tumor 2.0cm in May (.6cm in July) to 'not found' in November, bone mets unchanged from Feb CT scan/diagnosis and lymph nodes shrinking, some back to normal size. Ct scan was chest, abdomen and pelvic...no new areas found, all other organs clear!

I started Fenben March 14th, missed a few weeks in April due to hospital stay & IJVT clot in my jugular vein. Started back end of April, 1pkt per day 3on/4off and I mix my powder into 2oz water, whisk it with a fork. Then eat fatty food right after. A few times a month I take Safeguard (for horses, apple paste Fenben) instead of powder. I've been doing chemo & keytruda every 3 weeks since May. This combination has brought amazing results for me!!. I was told in Feb by an Urgent Care dr to 'go home and get my affairs in order'.

DONT listen to doctors who give timeframes!!! I'm still here 9 1/2 months later and will keep up the fight as long as its needed.

I am soooooo grateful to have found Joe Tippens story. I felt I really had nothing to lose if I gave it a try. And I'm so blessed for all that I have gained If you are a new member, please dont wait! Use it alone or with chemo (always your choice), just start!

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April 2024
Hi everyone, I am officially NED. (no evidence of disease)

The diagnosis was: Invasive Pleomorphic Lobular Carcinoma Grade 3 HER+ Estrogen + Stage IIA lobular carcinoma in situ

I did 1 chemo dose of 6 of Carboplatin and Docetaxel which I quit after that one dose because it debilitated me and hospitalized me.

2 days after diagnosis I embarked in a natural healing route combining Joe Tippens and FEC0 protocols to create one for myself. 12weeks later I have just been declared NED.

Doctors still want to push 20 rounds of radiation, 1 year of PHESGO which is the combination with PERJETA (pertuzumab) & Herceptin (trastuzumab) and hormone therapy.

I strongly feel I can keep healing my body naturally with just FEC0. I pray my success story blesses you and encourages you.

Advocate for yourselves we are not all a uniform protocol

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* (no chemo for quite a while when this happened) I just wanted to give you all some good news. I joined this group for one of my friends who's not on Facebook just to get some information to her about protocols etc. My friend had melanoma 2 or 3 years ago and ended up being on chemo and went into remission and had not been into remission more than a year when they did a follow-up scan and found more nodules on her lungs and the doctor was 99% sure it was cancer but he told her they were a little bit too small to biopsy yet so he wanted them to grow more before he did the procedure. Well I believe it's only been about 10 weeks or so since she started the protocol from this group  (Fenben protocol) and we're happy to say on Friday the last week she had an updated scan and the nodules are 100% gone! Even the doctor said whatever quackery you did worked.lol We also all prayed for her so I believe God can use all sorts of things to miraculously cure people! But hang in there guys, there are still good stories at the end!

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*My hubby was Diagnosed with Pancreatic Cancer in Oct 2023. Oncologist stop his first Chemo after 3 infusions & said it's not working. You can see in the #'s below on Jan 9th his #'s were the highest. Then he started Fenben and protocol 1, 2 & 3 from Ultra Botanica...look at his #'s now!

We have appt to go over his May 3rd PET-CT.

Day by day , prayers up!

10-20-2023 155.7 U/ml

10-27-2023 174.2 U/ml

12-22-2023. 496.1 U/ml

1-9-2024. 598.0 U/ml

2-9-2024. 374.2 U/ml

3-8-2024. 280.2 U/ml

4-4-2024. 159.6 U/ml down 120.6

5-3-2024. 110.1 U/ml down 49.5

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I am writing this to encourage others. Here’s my story- I was diagnosed with Stage 4 Her-2+ breast cancer in Oct. of 2019. I had one chemo session in November, and ended up in the hospital with multiple major infections. It took months to recover from the infections, and I decided that chemo was no longer an option. My doctor did talk me into receiving Herceptin infusions, a targeted therapy. We assumed that I would die, but in May of 2020 my scan showed no signs of cancer. Life was good and we continued taking Herceptin infusions only.

A little over a year ago my oncologist had me take a Signatera test, which measures microscopic levels of cancer dna in your blood. We were hoping it would be negative, but it was not. The level was low, but it was there. Soon I started getting headaches, and a scan showed a small tumor on my pituitary gland. It grew until I had it surgically removed followed by radiation. The tumor was dense and aggressive. I had had a couple of friends mention some natural supplements including high dose melatonin and fenbendazole. I don’t take incredibly high amounts of either but started adding the supplements to my routine in December. In March we did an MRI that showed no tumor remaining. And today I got the results of my latest Signatera test, the one that measures cancer dna in your blood. It had gone up as my brain tumor grew, but today it was finally negative- no sign of cancer DNA in my blood!

I am a strong Christian and give God glory for my healings. But I do want to encourage those who are struggling- I believe that the melatonin and the fenbendazole also helped. Lastly, thought control makes a big difference in my mental and physical health. This is my story, and I hope it encourages someone.

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SUCCESS STORY!!!

July 1st 2023: Mom, 55, was diagnosed with Stage 4 Adenocarcinoma of the Lung, NSCLC. Mutation T908fs*11. She has a massive plueral effusion, can’t lay down flat without feeling like she’s drowning, no appetite, a 6cm tumor in her right lung and “innumerable nodules”. Mets to her ribs, hips, spine. She never smoked and was otherwise healthy.

The oncologist gives her a 5% chance at beating her cancer. He looks at her with pity. The average life span after this diagnosis is 1.5 years. Devastating.

Fast forward through hours of research, 5 rounds of chemo + immunotherapy, and a laundry list of at home treatments listed below.

November 6th, 2023: Repeat PET scan shows a NEAR-COMPLETE RESPONSE TO THERAPY!!! Mets to her bones - GONE!!! Broken Ribs - HEALED!! Lymph nodes - CLEAR!!! Tumor - GONE!! A small bit of activity still in her right lung lesions, noted to be ”only slightly greater than the mediastinal background, MARKEDLY decreased from the prior study.”

We are just over the moon. When a stranger told me about his success story with Joe Tippens Protocol, I felt as if God had placed this information directly into my lap for it to save my Mom - and boy has it worked. I have complete faith that she is going to be okay, because we have the answer, thanks to Joe Tippens.

There is hope. The protocol WORKS. Keep faith everyone and remember you CAN do this!!!

*update*

I just left the oncologist with my sister Luci, 38% reduction and no new growth!!!

Brain mets are dissipating.

Stage 4 NSCLC with mets to brain, adrenal, lymph, and ribs.

Started Joe's protocol early May, started Tagrisso late May.

Keep the faith!!!!

Thank you for all the prayers!!

Thanks to Joe for sharing his story!!

*update*

I just left the oncologist with my sister Luci, 38% reduction and no new growth!!!

Brain mets are dissipating.

Stage 4 NSCLC with mets to brain, adrenal, lymph, and ribs.

Started Joe's protocol early May, started Tagrisso late May.

Keep the faith!!!!

Thank you for all the prayers!!

Thanks to Joe for sharing his story!!

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2x2 cm metastatic lower left lung tumor on CT/PET scan April 2019, 7 months post chemo/then cystoprostatectomy with Ilial conduit for stage 4 bladder/prostate aggressive carcinomas.. 5 weeks on original Protocol w/Safeguard a new CT/PET scan showed NED. Latest VA scan read "several areas of concern", 1st of 14 post NED CT/PET scans showing any concerns. I had a private radiologist and oncologist review VA radiologist reading of scan.They said "No areas of concern" still NED. I'd changed my intake of full Protocols 3 days on/ 4 days OTC three products only to full Protocol once every 10- 12 days as maintenance 20 months ago. It must still be working!

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https://www.facebook.com/reel/1572590763582283

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* May 2024I have stage 4 cervical cancer. Went through chemo and rads and was NED. Three months later I was in horrible pain and found out the cancer was back again in multiple places. I started chemo and Avastin then just Avastin. The cancer was better but not gone. After just being on Avastin the cancer started to grow again so on to Keytruda. While I was on the Keytruda I started Fenbendazole. I had to stop Keytruda because of side effects. I’ve been off the Keytruda since the beginning of February this year. I just got my latest scans back and the results were great even though I’m not doing anything but Fenbendazole. I never thought I would be this good for this long. I pray for you all every night.

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Stage 4 NSCLC (non-small cell lung cancer) Just received my CT scan results today. 26 weeks on Joe Tippens protocol. God is good!

Thank you goes out to everyone here!

Thank you Joe Tippens for sharing your story and your protocol, God bless you.

I did add Turkey Tail, Berberine, vitamin C and Elderberry to Joe's protocol! Always praying for everyone! Couldn't of had a better birthday gift!

Type in my name to see other info. of previous post.

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Yes I was in the same boat. It’s the chemo! I had to stop after 3 rounds of Keytruda! Sick everyday! Dr changed to obtiva and yerovoy and I was 100% better. Just a little nauseous and tired. I started JTP immediately and was on it during both treatments. I was stage 4 lung metastatic to bones lymph nodes and adrenal glands, did the original protocol and in 6 months no longer in bones and lymph nodes. In 9 months shrunk 1/2 in lung and 7 mm in adrenal glands. Kept doing protocol every day and here I sit cancer free! Dr amazed knowing that I was in the protocol said he could lose license if he recommended it! I did 10 radiation treatments in the beginning on bones in leg, neck and spine because I mess in a lot of pain. I’m thankful for the radiation because my pain was gone and I could use my leg and walk. After 18 months I no longer am on immunotherapy and keep doing the original protocol, just had another PEt scan Monday and NED, no evidence found of cancer! I give Gid the glory and JTP. Here’s what I did every day. It has to be the exact brand Joe used and that’s what I do.

1. Panacur C by Merck 222 mg in yogurt

2. Theracurmin by Integrative Therapeutics 2 pills

3. Gamma E by Life Extension 1 pill

4. CBD by Lazarus 25 mg chased with honey

That’s it every day!

I lost my appetite to but I ate something every 2-3 hours and I would chase it down with milk or water I had lost 30 pds, but I had my mom making me all kinds of casserole and I just had to eat and chase down with milk to get it down. I denied any pharmaceutical drugs, and stuck with Aleve or Tylenol for pain. I did anti nausea medicine and vitamin b12. I didn’t cut out sugar or watch what I ate because my mom was doing the cooking. I put all my weight back on in 3 months. I am thriving now and cancer free because I believe that God has healed me and gave me the protocol to help. I ordered everything on Amazon. If you have any questions or would like to talk I am available anytime. Feel free to reach out. I had no side effects from this protocol that I know of! Keep doing it just like I said in my text and make sure it is exactly what Joe used because it worked for me it will work for him. Blessings to your son and you! I’ll be praying for you both! 

I want to share an update to my Boyfriends Cancer experience. In May of 2023 he was diagnosed with Bladder Cancer. His surgery was scheduled for August 24th for them to remove a 5 cm × 6 cm tumor and if his bladder was strong enough he would put Chemo in his bladder after removing tumor. So during the 3 month wait he went on a Plant Based Diet, eliminated Red Meat, Pork, Dairy, and Sugar from his diet. He drank PH Water and Green Tea, We went to Mothers Market daily for him to get fresh Wheat Grass Shots and their Juiced Vege drinks. He then began the Panacur dog dewormer at first 1 gram daily then after 2 weeks 2 grams daily. He did 1 Frequency Therapy Treatment, Additionally he started taking 2 drops of Frankencense Oil, 2 Drops Oregano Oil, Black Walnut Oil, and Turkey Tail Oil, Magnesseum, Selenium, Turmeric/Curcumin, Dandilion Root, Vitamins D & K², Super B Complex, Vitamins C & Calcium/Mag/Zinc, CoQ10, Super Fish Oil, & CBD Oil. So finally he has his surgery knowing that if that huge tumor had gone through the first layer of his bladder wall then it would be considered Metasticized. The Dr promised him he would wake up with his bladder but they would access the cancer to see what their next course of action will be. Normally Bladder Cancer is diagnosed when its tje size of an eraser head and his was far bigger. He was told that their would be a 90% chance of recurrence as well. The location of the tumor made things possibly worse as well as it was located between the incoming and outgoing tubes so they wouldnt be able to cut that part of his bladder out. The Doctor spent 2½ hours removing the tumor but never put Chemo in his bladder,not because his bladder was to weak instead the Doctor didnt feel he needed it. So on his first follow up Appointment the Doctor informs him that as of that Day he is Cancer Free but still needs to do a round of immunotherapy. He was then informed that it was the worst most aggressive form of bladder cancer that he had and still would have a 40-60 % chance of reoccurance. He was told to return in 3 months for a Cytoscopy of his bladder to screen him again for more cancer. He was late going in for that procedure and just did it last week and the Doctor and Nurses were blown away to find No Cancer again and as the Doctor stated, " You Dodged a Huge Bullet". Recently we also started him taking Lions Mane, Turkey Tail, Reishi, Chaga, & Cordyceps as well as Bitter Apricot Seeds. His Outcome through Medical Science and Medicine, He should be having major problems and reoccurrance but he does not! The Doctor doesn’t know all the things he did prior to surgery so its left them scratching their head in shock! I wanted to share our Journey with You all hoping it may help someone else.

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Positive progress!!!

My husband was Diagnosed with esophageal cancer on Dec 4th 2023…. Stage 2 no lymph involvement. Stent placed ( kept falling out due to rapid shrinking of tumor due to JTP and Gods Grace) within 10 days the first stent fell out ( only 1 chemo and 1 radiation treatment) they placed another stent added surgical clamps and 3 days later it FELL out again!!!

We did JTP FULL PROTOCOL within 7 days of diagnosis! MERCK PANACUR C 1/4 teaspoon morning and night… onco adjunct 1-4 ordered through Ultra Botanica

• Tagamet/cimetidine morning and night

• turkey tail

• rapid immune recovery

• baking soda bi carb morning and night

• sea buckthorn oil

• ivermectin in the weekends

•vit D3 k2

• high dose melatonin 300 mg

• 1 81 mg aspirin

• AG1 smoothie x1 for extra vitamins

• with the help of nutritionist and naturopath went to a keto biome diet… no red meat, no pasta, bread or dairy… very very low levels of sugar( almost impossible to avoid altogether) and are taking a deep dive into where my husbands body broke down allowing cancer to grow!

• 6 weeks of chemo

• 22 radiation treatments

Yesterday 3/18/24 scope revealed the tumor is GONE!

After the second stent fell out about two weeks into treatment, tumor had shrunk to less than half of its original size of 5 cm to 2 cm !

There is SOOO MUCH HOPE! I devoured Jane McClellands book ( read 3 times), spoke to other esophageal survivors here…. Huge shout out to AL DREWETT AND JOE WALLACE… mighty warriors, winning against this disease! I know we aren’t out of the woods yet….We are still waiting on biopsies to confirm scope and PET SCAN but this community has meant everything! I have quietly read all the posts, prayed for the hopeless, the brokenhearted and celebrated the victories. We will continue to fight, and I’m encouraging all of you to research, reach out and ask questions! Listen to your gut, which is so hard during this terrifying journey, and most importantly…lean on God

I will update again once are PET scan and biopsies come in!

Thank you JTP… another life saved because you spoke out! We SERVE an awesome GOD! Praying for every cancer patient here…keep fighting

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Don't feel alone I also take the pills at 444 mg. It stopped my lung tumor.

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This is going to be lengthy. The pictures posted are of the actual review of treatments and findings from the beginning of my mother’s journey. Pages 3-4 are not included as they go over oral medications and her overall feeling that day.

The beginning of my mom’s story is a cough in November of 2022 that was misdiagnosed 3 times as bronchitis. She had difficulty breathing and lost her voice. This turned out to be because of a tumor in her lymph node that was sitting on top of her aorta and her left vocal cord, keeping the cord in the open position. Thank God for an ENT that took the time to listen to her. He sent her immediately for CT scans.

The short version is stage 4, high grade metastatic satcomatoid carcinoma, likely of pulmonary origin. Only .1-.4% of people have this. Gene testing showed genetic mutations, although I am not sure of the gene. ( I can dig through her paperwork to find out). Incurable and inoperable. She was given 3 months if she went untreated. Cancer markers were at 58.

The chemo nearly got the best of her and did not work. It did however cause her body a lot of problems, including blood clots and swelling to the point of needing wound care and home health for months. We thought she would lose both feet. She couldn’t eat. My mother has never been sick, other than common cold, never taken pain meds that weren’t OTC, and never taken anti-nausea meds. What we discovered is that none of those meds really do her any good. They just don’t act the way they should to do the job as prescribed.She barely made it through to complete radiation on the one gluteal mass. It was bad. Chemo was stopped. I didn’t expect her to make it through the summer. Cancer markers 52.

On to immunotherapy. This was working, as you can read in the paperwork posted here. She went in to remission, cancer markers .03. BUT… her body reacted terribly to it. The rash was from head to toe and itched her 24/7. As you can imagine, being on the blood thinners made this even more horrific. Dermatologists couldn’t stop it, steroids couldn’t stop it, wound care couldn’t stop it…now cue up the terrible yeast infection that set in on her upper rear/lower back in addition to the other rash. Immuno was stopped in June of 23, with the intention of starting back at a lower dose once the rash cleared. The rash raged on until about March of this year. The medication listed below that was given in January of this year is what finally began to give her relief.

Now let’s back up to October of 23. She began taking PanacureC, the original dosage in the blog, once a day. Mind you, she has had no treatment since June of 23.

Fast forward now to the 2/28/24 PET scan. We were scheduled to see her oncologist for results, but had an appointment with her radiologist on 3/1/24. This is a day that I will NEVER forget. Dr. E came in and asked how she felt and she said she felt pretty good. Dr E. said, “your PET scans are remarkable. There are no tumors. I had your results checked to be sure they were yours. I can see the swelling that remains from the tumor I radiated. They are your scans. Would you like to see them?” It’s one of the most beautiful things I have ever seen. She showed us side by side comparisons. The first looked like a Jackson Pollock and the second was dark. NED

At the follow up appointment with the oncologist, Dr. N, the week after the PET scan, he wanted to try targeted therapy. One pill, twice a day. It made her hurt all over within 2 days. She couldn’t take it. She couldn’t walk, sit or lie down without pain. She took a break for a few weeks to let the pain subside. Dr N urged her to try one pill once a day, reminding her that there is no cure and that her cancer could come back at any time. She will only ever be in remission. She tried for a few days and it hurt her just as bad, so she stopped. Still on the Panacure.

Last Friday, I took her for a new abdominal and pelvic CT. Today was her follow up with Dr N. Still NED! Her bloodwork all looks great and she has been at 0.0 on her cancer markers for months. He told her that for now, he is withholding treatment. She said that’s what she had hoped to hear. He told her that short of a miracle, it would come back. She told him that she believed in miracles, and he said he did too, and that we may be seeing one, but come back in a month with new labs and we will see if she needs treatment.

I can’t say that this works, but I sure can’t say that it doesn’t. My mother has been through it. The hospital stays, the 9 procedures for blood clots( which she was awake for because the meds don’t work), the weight loss, crying, pain, vomiting and the trips 3/4 days a week to appointments, not sleeping, not being able to wake up, horrible cough, no voice ( I literally HAD to be her voice) , loss of hair , bleeding and weeping skin, inability to walk ….she’s one tough lady.

And now, she eats, sleeps, drives, puts on makeup and fixes her hair, HAS HER VOICE, and looks forward to each new day with vigor! There are no words to express how bad it was. None. But there are also no words to describe how good it is now.

Never give up hope! Never give up praying! Never give up on yourself!

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I have estrogen positive as well. I take fenbenzadole and I also take tudca for my liver. I just recently had a CT scan and my cancer is going away! I also take soursop and turkey tail and other supplements as well!

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As this somewhat depressing post from the day when my cancer metasisised to my liver seems to have randomly popped up again, just making sure everyone knows, I am still alive and documented my entire journey on YouTube on a channel called She Dares Live. The cancer was misdiagnosed as stage 4 pancreatic sarcoma and then diagnosed as stage 4 pancreatic adenocarcinoma.

Hello, so although I have been feeling a lot better since my last scan on 6 June, my cancer in my pancreas today appears to have spread to my liver 5 or 6 spots. They unfortunately still haven't managed to work out exactly what type of cancer it is, and it may be sarcoma. Are there any types of cancer that fenbendrazole affects negatively and makes worse? I have seen some sarcoma patients on here stopping because it seems to them to have made their cancer bigger... would really appreciate some views here.

Today was a bit of a surprise as I was genuinely feeling a lot better over the past 2 weeks of starting everything. I was expecting them to tell me it was already smaller.

(This woman still alive in March 2024… seeing and update on her story)

So I talked with Lucy and she told me that she hasn’t written an extensive report but she did offer this video testimonial dated 8 months ago at this time. I made a copy of it because eventually youtube removes althernative therapy cancer testimonials.

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Praise post. Scans on Monday, just left oncology. No signs of any cancer. Diagnosed stage 4 out of the box in late October. 2cm tumor on lung with lesions to plural cavity. They did a small wedge resection then, and since then 2 scans have shown the same…..no signs. NSCLC with egfr mutation and the Exxon 19 deletion. Been on protocol and other things since day 1. I believe God is helping me with more time.

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Well, I had my 3 month check up yesterday. Not long ago I reported the results of my scans done 1 year and then 2nd year after stage 4 with wide spread mets prostate cancer diagnoses. I began a repurposed drug cocktail about the same time as I began the testosterone blocking prescription drugs. My PSA dropped from 6 to undetectable ( < 0.05 ng/ml ) in just 30 days, which I suspect is exceptionally fast. Then, since PSA remained undetectable, no more scans until 1 year, which were MUCH improved. Then again at 2 years, much improved yet again, very close to NED, now only 1 small spot vs wide spread mets. Yesterdays 3 month PSA was: still undetectable. Praise the Lord! ............................................. Also, I had been wondering about a comment on my last CT scan: "Unchanged osseous sclerotic lesions likely representing prior metastatic disease. 2. No significant change from prior studies.” ...................... I wanted to know what they meant by "likely representing prior metastatic disease"? Someone here commented it meant what I hoped: no longer metastatic. Probably looking at something dead. My NP yesterday confirmed(volunteered to me) that is indeed what that meant. "Sclerotic lesions" and "Prior" together meant "no longer metastatic". No longer living, growing cells, just something left over. I hope she is right.......................... So, was it all the doctors drugs? Seems unlikely to me. Was it the drugs being helped by my repurposed drug cocktail(added FenBen to that cocktail a couple of months before the last scan)? That seems very likely to me. Was it mostly the repurposed drug cocktail, especially the continuing regression over 2 years? Possibly. I don't know............................................. I did get the NP to admit that the drugs often stop working after 1 year, but sometimes keep on for 2 years or even a bit longer. I am now at 2.5 years since starting the drugs( and repurposed drug cocktail), and 1 month shy of 2.5 years with an undetectable PSA. Unless PSA starts rising, there won't be any more scans until about 9 months pass. Praise the Lord!