24 Comments

These stories give me so much hope! Thank you for sharing it with us. 🙏❤️

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Did you know that Serviceberry/Saskatoon berry seeds contain medicinally significant amounts of Amygdalin?

For more info:

https://www.sciencedirect.com/science/article/abs/pii/S088915750700169X

Amygdalin (aka "vitamin b17") is the compound which is found in high concentrations in apricot kernels and can help to initiate apoptosis in a range of different types of cancer cells (without harming healthy cells).

For more info:

https://greenmedinfo.com/blog/do-apricot-seeds-have-health-benefits-and-anticancer-benefits

Serviceberries can grow in a wide range of climates (Cold Hardiness zones : 2 - 10) diverse soil types and high elevations and so this species is an ideal candidate for including in temperate food forest designs and medicinal gardens.

Adaptable and resilient food and medicine plants like this empower humans to cultivate health sovereignty (boycotting big pharma's scams) while also providing forage for pollinators and food for wildlife.

For more info on Serviceberries and how to grow them:

https://gavinmounsey.substack.com/p/serviceberry

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Hi. Really appreciate these stories and testimonies. I am a survivor as well but wanted to point out a great book for those who seek to understand cancer pathways first published in 2018 by Jane McLelland who has survived cancer twice. Titled How to Starve Cancer, it offers up a plan and her own research to understand how to interrupt cancer cells ability to nourish themselves and how to repurpose drugs to act on those pathways.

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Congratulations on your recovery, and thank you for sharing it as such anecdotes have a powerful effect on the many others facing a similar situation. I agree with your recommendation. McLelland’s work is transformative and has inspired several MDs (eg Marik, Hope) to investigate her approach and write their own subsequent books.

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Thank you so much for starting this series of articles and not putting it behind a paywall. It will allow me to share it with many people whose lives might be saved by this information. God bless you!

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Ivermectin for the win in many ways... Dr. Geert Vanden Bossche day ago or came out with a substack and embedded an interesting PDF that was released on 1/27/24 regarding the overwhelming proof of Ivermectin effectiveness... this quote stood out and includes the link to PDF.

GVB...

"If that’s the case, the key question is how long the virus will need to conjure up a variant that will allow it to eventually escape the life-threatening immune pressure it is currently undergoing. As nobody exactly knows, it may be prudent for all C-19 vaccinees to consider timely treatment with hydroxychloroquine and/or ivermectin (https://notesfromthesocialclinic.org/wp-content/uploads/2024/01/COVID-ANALYSIS-232g-IVERMECTIN-SUMMARY.pdf)."

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While this is a great story and I am so happy to see another cancer victim make a great recovery, the ONE THING that is seldom, if ever, addressed is the simple factor of Lifestyle and Diet in a cancer approach. Seldom do these 'doctors' EVER look at the NUTRITION profile of their patients. As an example, I was diagnosed with aggressive prostate cancer back in 2010 and after Much Research chose an alternative route to treat my cancer. Given about 2-3 years of painful debilitating life ahead, according to the several oncologists I consulted, I chose a strict Whole Food Plant Based Lifestylediet to 'treat' my body's condition. Now after almost 15 years, I remain on this DELICIOUOS Lifestylediet, take no cancer drugs (never did!) and at 77 am healthier now than ever. WHY is NUTRITON Seldom mentioned? Cash flow? See my site: https://cancersurvivor.wf4hl.com/

Oh, on the Ivermectin, we had to take the 'horse paste' during the outbreak but I do have Ivermectin tablets on hand but have not taken for cancer. We did NOT Take that Death Jab!!!

Also have written several book on this subject; links are on my web site above.

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Thank you! I looked into your cancersurvivor site.

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Great, let me know if I can clarify anything or help!

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Very kind. Mercifully, my looking-into is purely from curiosity, as neither husband nor I has the disease. And hope to keep it that way.

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I saw these yesterday. More hope for future cancer sufferers. I can only pray that tptb don’t pull IVM from the market for being a dangerous (to their pocketbook) drug of concern.

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Great article! Any info on the daily doses of Ivermectin and Fenbendazole? I believe I've seen ~24 Ivermectin, and ~450 Fenben daily...?

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We are also attending the conference and look forward to hearing from you

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So you could use mebendazole instead of fenben (as a cancer treatment)?

You can buy mebendazole (marketed as a worm treatment for humans) off the shelf here in Australia.

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If you mean combantrin, it is very expensive for 2 tablets

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Two things. Thing one; truly integrative cancer treatment which includes many of the therapies mentioned in this article is being practiced at The Oasis Of Hope Hospital (https://www.oasisofhope.com ) in Tijuana, Mexico. I suspect that they will be if that have not already, make both Ivermectin and Mebendazole part of the regimen. I have a very close, personal relationship with the first person at Oasis to be treated with Ivermectin.

Thing two; there is a clinical trial that is in the recruitment phase being conducted in Los Angels in which Ivermectin and a monoclonal antibody will be used together to treat Triple Negative Breast Cancer.

The main question that needs to be answered for both Ivermectin and Mebendazole is this: What is the most effective dosing regimen.

Our federal "public health" agencies owe the American People an apology.

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Thank you for this! My vrother in Green Valley is suffering it will be a challenge to convince ... this article helps! As a CDN visitor I'm wondering where to locate what I'll need if he's open to trying something outside the box.

Trump kinda killed the ivy league med options - the way he presented it way back in 2020 sounded like malaria drugs and made himself look more disrespected - if that's possible - obvious media dishing!

* https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685699/

* https://www.theguardian.com/us-news/2021/aug/30/rand-paul-ivermectin-covid-donald-trump

I'm hoping you would please share the outcomes of this presentation also: Shedding is Real: Dr. Pierre Kory and Scott Marsland

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Doesn't one of the B vitamins help with neuropathy? Maybe B3, I forget which one.

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Try methylated B-complex.

My 62yo husband has had idiopathic neuropathy in his feet for years. He doesn’t have diabetes and his circulation has been tested and is fine, but he had unexplained nerve damage in his feet, and it was starting to appear in his hands. He could step barefoot in a puddle of cold water and not even feel it. He once stumped his foot against something while walking, only noticed because it made him stumble, but it didn’t cause pain. By that night, his big toe was black, and the nail eventually fell off.

Over the last year+, he has spent thousands of dollars on specialists trying to get a sore on his toe to heal, because since he couldn’t feel the toe, he couldn’t tell which shoes were making it worse or when the bandage had fallen off letting the sore keep rubbing and being torn open. (Gross!)

His wound care doctor recently recommended that he take a genetic test (available on Amazon) to check for a variant in the MTHFR gene, and he does have the variant that means his body is unable to properly methylate B vitamins, causing nerve damage. So he recently started taking a methylated B-complex supplement, and has had noticeable improvement in his neuropathy. (The supplement is all the B’s, not just B3, in methylated form.)

He complained just this morning about the cold tile floor in the bathroom - yay!!

My dad also has neuropathy, and recently started taking a prescription methylated vitamin supplement prescribed by his doctor, and he’s also noticing improvement.

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Thank you so much for this information. I’ve been suffering from neuropathy for 9 years and unfortunately all treatments have failed. My doctor called it idiopathic too, but I’ve recently diagnosed diabetic and I know how badly the body responds to it.

Can you tell me where you ordered what he’s taking? Is it only prescribed?

Gah! It’s such a nasty pain that totally affects one’s life.

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I ordered it from Amazon. My husband’s doctor didn’t recommend any particular brand so I just searched for methylated B-complex and decided on one from Igennus described as “Super B-Complex – Methylated Sustained Release Clean Label B Complex with Methylfolate, Boosted B12 Methylcobalamin…”

The one my dad takes is a prescription called “Elfolate Plu 3-35-2MG

Generic.’L-Methylfolate w/ Vit B6-Vi…” I think it’s pricey at some pharmacies but reasonable at others.

The gene test was from Amazon. It was “empowerDX at Home MTHFR gene test.” It wasn’t covered by insurance, but it was eligible for FSA (flex-spending) or HSA funds.

Best wishes to you for healing! I’ve seen firsthand how frustrating and debilitating neuropathy is, especially when highly-regarded specialists run all kinds of expensive tests, then just shrug their shoulders and say “Beats me.”

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Thanks again for your help. I will definitely order the brand he used and hope for the best.

I ordered other vitamins, but I react weirdly to lots of drugs and they flared the neuropathy up.

Mine is probably coming from my back which has lots of weird pathology and the only tests were an mri and nerve conduction which I will never have again. I see no reason why people need to be awake for a…shudder at the memory.

Wouldn’t it be something if just the vitamin takes it away and I can have my life back?

Cheers.

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Thank you 🙏

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Total 100% bs.

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