It's been a long time since we heard about the toxicity of different vaccine batches. Here's a clip on that. It would have been good to keep track of this over the years to see how people are doing who got the different batches.
For those who want to follow the interview:"Three biopsies were taken—two before death and one after. The person died of this diagnosis within 30 days."
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"Those samples were analyzed using a tool called PCR to look for the Pfizer vaccine sequence. We then resorted to a process known as Illumina sequencing to sequence the tissue to determine if any Pfizer sequence was present. Shockingly, there was a significant amount, which was unexpected."
View the entire manuscript:Research findings demonstrating high levels of plasmid DNA in the Pfizer and Moderna vaccines, as well as SV40 promoter enhancer sequences in Pfizer above the permissible limit, have now been peer-reviewed, published, and will appear on PubMed.
This manuscript describes several mechanisms by which these vaccines may pose significant and unquantified risks to human health.
(…)Using fluorometry, total DNA in all vials tested exceeded the regulatory limit for residual DNA set by the US Food & Drug Administration (FDA) and the World Health Authorization (WHO) by 36–153-fold for Pfizer and 112–627-fold for Moderna after accounting for nonspecific binding to modRNA. When tested by qPCR, all Moderna vials were within the regulatory limit, but 2/6 Pfizer lots (3 vials) exceeded the regulatory limit for the SV40 promoter-enhancer-ori by 2-fold. The presence of the SV40 promoter-enhancer element in Pfizer vials raises significant safety concerns. This study emphasizes the importance of methodological considerations when quantifying residual plasmid DNA in modRNA products, considering increased LNP transfection efficiency, and cumulative dosing presents significant and unquantified risks to human health.
Had a meeting with the super the other day regarding my return to work almost two years ago. Had a conversation about the whole vax debacle and he largely agreed. Got on the subject of flu shots, he and at least 3 other colleagues got shingles after their flu shots. He also had the shingles shot too. That's quite the cluster, talking to my colleague at drill last night, he's asking the doctor for an exemption, fingers crossed!Colleague took 4 covid shots back in the day, no obvious reactions but had the bug 4 times in one year, thought the first infection was going to kill him. Took the flu shot in June, few days later he was floored by covid again, according to the RAT anyway. Few days after gets smashed by shingles, internal shingles and developed an angry purple weal on his right hip about the size and shape of a sourdough loaf. However, it wasn't finished with him yet and an angry patch developed internally on his right temple, threatening his eyesight. I told him it was probably the flu shot but I'm an anti-vaxxer! Thoroughly juiced up on anti-virals his doc told him it was probably the flu jab that caused the problem! Strike her off! He went and had his heart checked and told me everything was in order, then goes out and buys a defibrillator! I hope he's OK, he's a nice bloke but he'll probably get the flu shot next year. Been multiple shingles cases in town this year and it's likely they're all jabbed.
Friend's husband, 80 had 2 pfizzers back in the day, had an eye problem so off to the scanner. Large chunk of dead brain, lower left occipital, happened some time ago with no obvious signs. Wife told me there was a slight personality change a couple of years ago. Another 80ish 2 pfizzer, had a scan, multiple micro-strokes throughout the brain. We're toast, there's likely 100s of 1000s of people with this and if it's not in their brains. It's in their lungs, heart and other regions.

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Over the past few years, millions have reported lingering health problems after COVID-19 infection or vaccination — from neurological issues and heart irregularities to vision changes that conventional medicine has struggled to explain. Today I’m speaking with Jen Dhillon, a researcher and electronic homeopath, who helped develop what’s called the Homeopathic Spike Detox protocol, or HSD — a therapy designed to help the body clear residual spike protein and restore normal immune and cellular function.
Case 1 An 83-year-old female. October 2021. Stage 4 breast cancer. Initially diagnosed in 2009.Treated 2009, bilateral mastectomy.
Recurrence was diagnosed in 2021. Liver biopsy, confirmed metastatic breast. Ascitic fluid confirmed metastatic breast carcinoma. Magnetic resonance imaging of the spine, October 2021 metastatic breast cancer, T10, T12, L1, L2, L3, L4, L5, S1, S2, and the iliac bones. A PET/CT scan on December 29, 2021, showed six hypermetabolic lung lesions. Largest was 2.8 × 1.5 cm. Hypermetabolic liver lesions, 2.9 × 1.7 cm. Hypermetabolic bone lesions, notably a 5.0 × 2.9 cm lytic lesion in L4, extending into the spinal canal, etc. The patient declined further conventional chemotherapy or radiation therapy and was placed under hospice care.
November 22, 2021. Self-administering FBZ daily at a dose of 222 mg. In December 2021, she received fulvestrant injection, (an estrogen receptor blocker) intended to inhibit cancer growth. January 2022- Targeted radiation for two painful spinal metastases. These tumors disappeared rapidly, relieving her pain within a few days. Continued taking 222 mg/day of FBZ for 8 months. During this time, her liver enzymes normalized. CA 27.29 tumor marker dropped from 316 (November 2021) to 36.6 (July 2022). April 20, 2022, PET scan confirmed the absence of any abnormal metabolic activity indicative of cancer. June 2022- Patient was confirmed to have no evidence of active disease. All treatments were discontinued, and she was considered to be in complete remission. Follow-up monitoring was scheduled every 3–6 months. Throughout her FBZ treatment, she continued her regular supplementation of vitamin D (5,000 IU) and a multivitamin. Subsequent PET scans showed no abnormal metabolic activity. The FBZ treatment period revealed no adverse effects at this dosage. The patient remains recurrence-free and continues to take FBZ daily nearly 3 years after being declared to be in remission.
Joe Tipp’s Protocol - Fenbendazole Dosage Guide Calculator
Case 2, Prostate cancer, 75 year old man
Bone scans and CT scans, metastases in the spine, pelvic bones, and right humeral head. Conventional treatments. Complementary treatments. The use of FBZ coincided with continued regression of metastatic lesions and sustained undetectable PSA levels. After 26 months of sustained regression and no new progression, the patient remains in near-complete response and continues FBZ with conventional therapy.
Case 3, 63-year-old man
Hip growth, melanoma. PET-CT showed multiple hypermetabolic foci – peritoneal and retroperitoneal nodules, focal uptake in the stomach and small bowel, lesions in the right gluteus medius, quadratus femoris, and L5 vertebra. Conventional and complementary treatments. The patient remains melanoma recurrence-free over 11 months after being declared to be in remission.
Case Presentations. All three patients, no reported adverse effects. Conclusion- FBZ demonstrates potential as a novel promising therapeutic option for repurposing in oncology. Its ability to contribute to tumor regression and achieve disease remission warrants further clinical research to establish its efficacy and optimize its use.