Vaccines
'Babies Have To Remain Alive For Organs To Be Harvested In Vaccine (plus ALL DRUG) Development Experiments.' Aaron Siri says, 'You Can't Grow Viruses Using Dead Organ Tissue, They Have To Be Born Alive ... Dr. Stanley Plotkin Admits To All Under Oath ... Unborn Babies Are Alive At Tissue Extraction' ... Dr. Plotkin gladly admits, without remorse, to Lawyer Aaron Siri, that he accepts human sacrifice as a normal, acceptable consequence in order to further science' as he is 1st & foremost a scientist & practicing Atheist. Former Vaccine Researcher & Biologist Pamela Acker has stated, "The babies are alive when the researchers start extracting the tissue. Their hearts are still beating & they're not given any anesthetic because that would contaminate the organs being harvested that need to be alive, pure & free of toxins.' According to expert Dr. Theresa Deisher, PhD, 'Babies are born alive from five to six months old, with beating hearts cut out without anesthesia for research purposes. Researchers also cut through live babies' faces to collect brain tissue.'" "Stanley Alan Plotkin is an American physician & vaccinologist renowned for his pivotal role in developing several critical vaccines. Born and raised in New York City, he attended The Bronx High School of Science, where at the age of 15, he was inspired by the books Arrowsmith by Sinclair Lewis and Microbe Hunters by Paul de Kruif to pursue a career in medicine and research. He earned his bachelor's degree from New York University in 1952 and his MD from SUNY Downstate Medical Center in 1956. Plotkin began his research career at the Wistar Institute in Philadelphia in the 1960s, where he played a key role in developing the rubella vaccine using the RA 27/3 strain of the virus, grown on the WI-38 fetal-derived human cell line ..." AI-generated answer from multiple sources. Pharma Drugs & Gain-of-function (GOF) Gene AlteringChimeric = Humanized Mice: Humanized liver mouse models are increasingly being used in preclinical trials and have allowed for groundbreaking in-vivo research to evaluate everything from human-specific drug toxicity and efficacy to gene therapies. Hera Biolabs Humanized mice, created by introducing human stem cells into mouse embryos. Human cells have been injected into the amniotic fluid of pregnant mice, where they migrated to fetal organs such as the intestines, liver, and brain, demonstrating a promising technique for creating humanized mouse models. AI generated from multiple sources. https://med.stanford.edu/news/all-news/2012/10/mice-with-humanized-livers-improve-early-drug-testing-scientist-show.html Harma: Drugs & Vaccines use Humanized Mice as a Valuable Pre-Clinical Model
Planned ParenthoodSWORN VIDEO TESTIMONY DESCRIBES INFANTICIDE IN FETAL ORGAN HARVESTING Read & Listen Planned Parenhood Procurment Managers ABR https://www.centerformedicalprogress.org/human-capital/special-report-advanced-bioscience-resources/ When did this begin?There is conflicting data on when this began - decades ago, according to AI searches: "The first documented use of humanized mice for drug testing involved the evaluation of Clemizole, a drug being developed for Hepatitis C. Scientists used chimeric mice with humanized livers to study the drug's metabolism and interactions" Clemizole was first described in the scientific literature in 1952 and was discovered in the 1950s as a first-generation ..." "The first reporting of humanized mouse models occurred in 1988, when three independent research groups successfully transplanted human hematopoietic cells into immunodeficient mice. Two of these studies utilized C.B17-SCID mice as recipients for either human peripheral blood or human fetal tissues." Humanized mice were first used in 1988 ... to model human immunodeficiency virus (HIV) infection and the human immune response to HIV. https://pmc.ncbi.nlm.nih.gov/articles/PMC7265413/ Stanford University scientists first used chimeric mice with humanized livers to predict human drug metabolism and drug-drug interactions in a landmark 2012 study. The research, led by Gary Peltz, focused on clemizole, a drug in development for hepatitis C virus (HCV) infection. The team used TK-NOG mice—a model with livers largely replaced by human cells—to test how clemizole was metabolized and how it interacted with ritonavir, a known CYP3A4 inhibitor. US Government WITH Pharma Companies & UniversitiesFDA, NIH Buying Aborted Human Fetal Parts for Experiments link to read Judicial Watch reveals that the U.S. Food and Drug Administration (FDA) has paid tens of thousands of taxpayer dollars to obtain human fetal tissue from the California-based “procurement” firm Advanced Bioscience Resources (ABR), undoubtedly supplied by abortion providers such as Planned Parenthood. According to the report, the fetal tissue was used in a sort of Frankenstein project to create “humanized mice” to test “biologic drug products.” To this day, research continues unimpeded. E-mail dated September 27, 2012, Howard submitted an application to Larton for “tissue purchases” in the amount of $12,000. The contract reportedly requested tissue from an aborted fetus with a gestational age of 16 to 24 weeks and “One set of tissue (thymus/liver) approx. twice monthly.” Instructions stated that the tissues were to be shipped “fresh; on wet ice." Judicial Watch - Freedom of Information Act (FOIA) documents Link to readNIH Fetal Tissue Use "The National Institutes of Health (NIH) has specific requirements for research involving human fetal tissue obtained from elective abortions, including the procurement and use of fresh fetal organs for pharmaceutical and medical research purposes. As of September 25, 2019, NIH implemented updated requirements for grant applications and research and development (R&D) contracts proposing the use of human fetal tissue (HFT) ..." Multiple sources Covid Bioweapon "vaccines" created with aborted cells/tissue/organs Many people only view the HEK 293 cell line (derived from human embryonic kidney cells from an aborted baby in the 1970s: There is no statute of limitations on the issue), while ignoring the fresh tissue and organs being obtained for research of drugs: "vaccines", bioweapons, cancer drugs, "particularly the progagation of adenoviral-based ad retroviral-based vectors." "Independent testing and expert testimony have confirmed the presence of residual DNA fragments in vials of mRNA Covid-19 shots, levels exceeding safety guidelines. Molecular biologist and cancer geneticist Phillip Buckhaults presented to a South Carolina Senate committee on September 12, 2023, stating that DNA pieces were present in leftover Pfizer/BioNTech vaccine vials and expressing concern about the potential for genome integration and cancer risks. Similarly, genomic expert Kevin McKernan reported finding DNA contamination in Pfizer and Moderna bivalent vaccine vials." "J&J uses a modified adenovirus, Adenovirus 26, as the vector to deliver the genetic material encoding the SARS-CoV-2 spike protein to cells. The mRNA is packaged within a modified virus, known as a viral vector. The double viral vector approach involves using two viruses: the adenovirus vector and the SARS-CoV-2 virus. The adenovirus vector carries the genetic material encoding the SARS-CoV-2 spike protein, which is then expressed by the cells." From J&J website "... it was developed using a cell line originally derived from fetal tissue obtained from an elective abortion in the 1970s, known as the PER.C6 cell line." An exhaustive list of every drug tested on humanized mice - aka dissected/sacrificed child organs or tissue put into animals aka abomination to God - is impossible to create because drug companies often keep preclinical data private. However, published scientific literature details numerous examples and classes of medicines tested in these models, particularly for research on immuno-oncology, infectious diseases, and drug metabolism.
Humanized mice are immunocompromised mice that have been engrafted with human genes, cells, or tissues, allowing researchers to study human-specific biological responses and disease processes. Immuno-oncology. Cancer immunotherapies (Chemo) are tested in humanized mouse models, which can be engineered with human immune cells and cancer cell lines (CDX) or patient-derived tumor tissue (PDX).
Humanized mice are essential for studying human-specific infectious agents and testing antiviral therapies.
Humanized mice can be engineered with human liver or metabolic enzymes to predict how the human body will process and break down a drug.
Humanized models are also used for research into a variety of other conditions:
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by Rose RohloffThis blog is not medical advice - below is a compilation from experts; we are all individuals and need to ascertain what is needed on an individual basis. What are in the shots? |
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| Gain of function (GOF) gene therapy Creating something that attaches (attacks) ACE2 in the human body with a foreign protein Leaving furin cleavage site - bioweapon Sars-Co-V-2 rejected by DARPA - funded under NIH & private $Baires & intelligence agencies (deposition link) |
CARE OPTIONS
Nattokinase, Bromelain, NAC | Vitamin D3 C NAC Honey&Black Cumin Zinc + (Elderberry GreenTea Quercetin Hydroxychloroquine Ivermectin), |
4Gs - Garlic, Ginger, Ginseng, Ginko
Garlic & Onions
Ginger
Ginseng
NIH Link and "A clinical study reported that KRG slowed down the depletion of CD4 T-cells and diminished the antigen level of serum soluble CD8 in patients infected with HIV type-1" NIH Pharm potentional link
Zinc (+ Copper) and Ionophore (Quercetin, EGCG, HCQ) link
Natural defense known in 2010 Increasing the intracellular Zn2+ concentration with zinc-ionophores like pyrithione (PT) can efficiently impair the replication of a variety of RNA viruses, including poliovirus and influenza virus. For some viruses this effect has been attributed to interference with viral polyprotein processing. In this study we demonstrate that the combination of Zn2+ and PT at low concentrations (2 µM Zn2+ and 2 µM PT) inhibits the replication of SARS-coronavirus (SARS-CoV) and equine arteritis virus (EAV) https://pmc.ncbi.nlm.nih.gov/articles/PMC2973827/
Zinc ionophores pyrithione inhibits herpes simplex virus July 15, 2013 - Pyrithione (PT) known as zince ionosphore, is effective against several pathogens from the Streptococcus and Staphylococcus genera ... link
Intravenous (IV) Vitamin C
Trauma DNP CV-ICU Early treatment Now in Functional Medicine private practice, Clinical Research Whistleblower medical murder http://FLCCC.net US Army wife
"The pioneers of intravenous vitamin C cancer treatment, Cameron and Pauling, observed improved survival times for many cancers (lung, stomach, colon, breast, kidney, rectum, and bladder). They observed survival times multiplied by 55 after 1 year, in terminal cancer patients treated with intravenous injections of ascorbate: 22% in the treated group and 0.4% in the control group in patients considered to be incurable following standard treatment. Their intervention consisted of:
an IV of 10 g/day for approximately 10 days, and orally thereafter (Cameron & Pauling, 1978).
Why aren’t oncologists using high dose IV Vitamin C? Because it’s cheap."
"Multiple reports providing higher doses of IV vitamin C in a range from 30 to 150 g showed beneficial effects in cancer patients [14]. Moreover, in addition to all the benefits that high-dose IV vitamin C exerts, it is important to point out that it is very safe and non-toxic. Recently, there was a study published using high-dose IV vitamin C on COVID-19 patients [15], and results showed multiple improvements but, most importantly, no adverse effects."
- anti-viral mechanisms
- suppresses oxidative stress
- inhibits cytokine storm due to antioxidant capacity
- suppresses thrombosis & prevents vascular tissue damage
- protects RBCs & averts hemoglobinopathy & iron metabolism dysregulation
World Council of Health Detox options
https://www.worldcouncilforhealth.org/wchresources/spike-protein-detox-guide/
- The spike protein
- ACE2 receptors
- Interleukin 6 (IL-6)
- Furin**
- Serine protease
SoursopBy Barbara O'NeillFrom Telegram channel, edited by Rose Rohloff for punctuation & spacing. | This fruit is called soursop/guanabana, and has been proven to be 10,000x more effective than chemotherapy at reversing the affects of cancer, but doing 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 etc. Contrarily, "the compound extracted from the Graviola tree selectively hunts down and kills only cancer cells. It does not harm healthy cells! |
Anthelmintics (kills helminths/worm-like parasites: flukes, roundworms & tapeworms)
Previously suppressed studies - peer reviewed
BREAKING NEWS: First-in-the-World Ivermectin, Mebendazole and Fenbendazole Protocol in Cancer has been peer-reviewed and published on Sep.19, 2024! 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.
LAB OPTIONS
Rose Rohloff
First ever Informed Refusal Document
Informed Consent - Refusal
Informed Consent
1- All alternatives, including naturopathic, diet, lifestyle, and underlying conditions, to be addressed versus symptoms, such as Covid shot massive side effects, heavy metal toxicity, etc.
2- Time for information:
- Emergent: something must be done within an hour to prevent severe morbidity or mortality, very little time to make a decision, so information must be processed quickly.
- Urgent: something must be done within 24 hours to prevent severe morbidity or mortality. Clinicians must give time to evaluate, research, and question for decisions.
- Elective/nonemergent: Clinicians must stop pushing patients when not life-threatening to work with them with ALL information presented, discussed, and thought through.
Informed Refusal
| You may download the word format for free to add/edit/change at will. |
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