Trust in God Episode 1 - An Interview with Dr. Judy Mikovits

Dr Judy Mikovits has a Bachelors Degree in Chemistry from University of Virginia in 1980 and a PhD in Biochemistry and Molecular Biology from George Washington University in 1992. In her forty-year quest to understand the causes, prevent and treat chronic diseases, she has co-authored seminal papers culminating at least a decade of research in each of four fields: immunology, natural products chemistry, epigenetics, and HIV/AIDs drug development. In 2009 Dr Mikovits led the team that first isolated and characterized a new family of human disease-associated retroviruses, XMRVs/HGRVS.

In this episode, we discuss the following:

- SARS-Cov-2 virus is a Pararetrovirus, it’s two part retrovirus one part coronavirus, it’s a chimera. It is one part HIV GP120, one part XMRV (that peptide called syncytin), and the third part is SARS 1 ACE receptor binding domain.
- The Moore paper of 2004 , in the Journal of Virology, showed that retroviruses were pseudotyped with the severe acute respiratory syndrome coronavirus. This was in a US Lab. The retroviruses were HIV and murine leukemia virus. See paper below.
- We discuss why would anyone do an experiment like the one in the Moore paper.
Dr Judy answers “To broaden the host range of cells, and create a deadlier , more transmissible virus”
- Luc Montagnier, who won the Nobel Prize for discovering HIV, had confirmed to Judy that the HIV GP120 was in SARS-Cov-2.
- Dr Judy knew from her thesis in 1987 that only 1 in 10 000 T cells were infected with HIV, and yet they were all dying. The thinking then was that there was only one receptor, the cd4 receptor, and that’s the only way in to the T cell. Judy hypothesised that there was another cell in the immune system that was more important in which the virus expression needed to be controlled, in order to stop the spread, prevent the virus from replicating and causing AIDS. Mary Carrington later found that it was the CCR5 receptor, and later, it was discovered that Peptide T was blocking the interaction with a different chemokine receptor called CCR5.
- We discuss the metagenomic analysis from 2011/12 of bat viruses in a Chinese cave where they took sequences from bat faeces in China, and they found many full length viruses, including the infectious synthetic molecular clone VP62 of XMRV, which they hid away from scientists in the supplemental material. See paper below.
- Dr Judy tells us that with SARS-Cov-2 they have turned down the sensors that block infection and turned up the sensors that enhanced infectivity. The type 1 interferon sensors. See the papers ‘’Syncytia formation during SARS-Cov-2 lung infection. A disastrous unity to eliminate lymphocytes. And “Syncytia formation by SARS-Cov-2 infected cells.’’
- Dr Judy talks about how our literature is literally criminal fraud, because ‘’they’’ control the literature. You don’t publish you don’t get funded. You don’t get funded, you don’t publish. That’s Fauci’s game.
- We discuss how Small Fibre Neuropathy and P