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Australian scientists work with medicine that can kill COVID-19 in 48 hours59.


“En tiempos en los que estamos teniendo una pandemia global y no hay un tratamiento aprobado, si tuviéramos un compuesto que ya estuviera disponible en todo el mundo, eso podría ayudar a la gente antes. Siendo realistas –consideró la investigadora-, pasará un tiempo antes de que una vacuna esté ampliamente disponible”.

Aunque no se conoce el mecanismo por el que la ivermectina actúa en el coronavirus, teniendo en cuenta su acción en otros virus, “es probable que funcione para detener la capacidad del virus de ‘amortiguar’ la capacidad de las células anfitrionas para eliminarlo”, dijo Wagstaff.

El uso de esta medicina para combatir la COVID-19 dependería, según la científica, de los resultados de más pruebas preclínicas y, en última instancia, de ensayos clínicos, con una financiación que se necesita urgentemente para seguir avanzando en el trabajo.

Deep Breathing alone will not create new lung cells, but combined with deep relaxation, guided visualizations, and therapeutic messages (Your stem cells are going to transform themselves into new lung cells to replace those lung cells infected by the Coronavirus. Your stem cells are going to change themselves into T-Cells, B-Cells, and Natural Killer Cells which are going to seek out, identify, attack, and destroy all the Coronavirus cells in your entire body), it will eliminate the coughing, fever, headaches, inflammation, and breathing problems.

While there is no hard evidence that lung exercises can help ease the discomfort and the progression of symptoms of COVID-19, there are techniques that will restore your lungs to optimal health.

ELON Musk shared the first photos of his newborn son with singer Grimes on Tuesday.

The Tesla CEO, 48, posted a cute snap of their sleeping baby using a face tattoo filter, as well as one of him cradling the newborn at the hospital on Twitter.

Responding to a fan who said their son is “gorgeous”, Elon joked about the tattoos: “Thanks smile Never too young for some ink haha.”

A study just released by Columbia University Mailman School of Public Health is reporting a blood-DNA-methylation measure that is sensitive to variation in the pace of biological aging among individuals born the same year. The tool—DunedinPoAm—offers a unique measurement for intervention trials and natural experiment studies investigating how the rate of aging may be changed by behavioral or drug therapy, or by changes to the environment. The study findings are published online in the journal eLife.

“The goal of our study was to distill a measurement of the rate of biological aging based on 12-years of follow-up on 18 different clinical tests into a blood test that can be administered at a single time point.” said lead author Daniel Belsky, Ph.D., assistant professor of epidemiology at Columbia Mailman School and a researcher at the Columbia Aging Center.

Midlife adults measured to be aging faster according to the new measurement showed faster declines in physical and cognitive functioning and looked older in facial photographs. Older adults measured to be aging faster by the tool were at increased risk for chronic disease and mortality. In other analyses, the researchers showed that DunedinPoAm captured new information not measured by proposed measures of biological aging known as epigenetic clocks, that 18-year-olds with histories of childhood poverty and victimization showed faster aging as measured by DunedinPoAm, and that DunedinPoAm predictions were disrupted by a caloric restriction intervention in a randomized trial.

Ketamine and Naltrexone you say? Weird.


Ideal new treatments for Novel Coronavirus-19 (COVID-19) would help halt the progression disease in patients with mild disease prior to the need for artificial respiration (ventilators), and also provide a rescue treatment for patients with severe disease, while also being affordable and available in quantities sufficient to treat large numbers of infected people. Low doses of Naltrexone, a drug approved for treating alcoholism and opiate addiction, as well as Ketamine, a drug approved as an anesthetic, may be able to interrupt the inflammation that causes the worst COVID-19 symptoms and prove an effective new treatment. This study will investigate their effectiveness in a randomized, blinded trial versus standard treatment plus placebo.

Detailed Description:

There is an urgent need to develop new treatments for Novel Coronavirus-19 (COVID-19) infection using easily available and affordable medications. We need to develop a treatment protocol which prevents progression of the disease and a treatment protocol to rescue those with advanced disease. In addition to anti-viral therapeutics currently under investigation in other trials, the addition of immunomodulators to the treatment regimen appears have to potential to act as agents which can reduce the pathogenicity of this disease by reducing the dysregulation of autoimmunity which is destructive of normal tissue and when unchecked rapidly leads to mortality.

Aytu BioScience announced on April 20, four days before the Trump remarks, that it has signed an exclusive licensing deal with Cedars Sanai Medical Center in Los Angeles. The center has developed and is testing a UV-A “Healight” designed to be inserted via a catheter inside the trachea to kill pathogens, including the coronavirus.

Ultraviolet, or UV, light is commonly used by physicians to treat skin iseases. Cedars-Sanai says UV-A phototherapy potentially could be employed in internal organs.


President Trump has been mocked relentlessly for suggesting that ultraviolet light could be brought “inside the body” to kill the coronavirus, but there is ongoing research to do just that.

For example, the pharmaceutical firm Aytu BioScience announced on April 20, four days before the Trump remarks, that it has signed an exclusive licensing deal with Cedars-Sinai Medical Center in Los Angeles. The center has developed and is testing a UV-A “Healight” designed to be inserted via a catheter inside the trachea to kill pathogens, including the coronavirus.

Ultraviolet, or UV, light is commonly used by physicians to treat skin diseases. Cedars-Sinai says UV-A phototherapy potentially could be employed in internal organs.

Fyodor Rouge, this is the church I was telling you about.


The Bradenton-based organization falsely claims that the treatment is effective for a number of conditions, including Alzheimer’s disease, brain disease, cancer, HIV and AIDS, according to the Food and Drug Administration.

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As the world grapples with the coronavirus pandemic and historically low oil prices, the missile launch may signal a new willingness to take risks by Iran.


It said the satellite — dubbed the Nour — was deployed from the Qassed two-stage launcher from the Markazi desert, a vast expanse in Iran’s central plateau.

The satellite “orbited the Earth at 425km [264 miles]”, said the website. “This action will be a great success and a new development in the field of space for Islamic Iran.”

The IRGC called it the first military satellite ever launched by Tehran. It used a Ghased, or “Messenger”, satellite carrier to put the device into space, a previously unheard-of system.

COVID-19’s genes are encoded in RNA instead of DNA. COVID-19 uses reverse transcriptase to transform its single-stranded RNA into double-stranded DNA. It is DNA that stores the genome of human cells and cells from other higher life forms. Once transformed from RNA to DNA, the new COVID-19 DNA can be integrated into the genome of the infected cells. When the DNA versions of the retroviral genes have been incorporated into the genome, the cell then is tricked into copying those genes as part of its normal replication process and making millions of COVID-19 cells… In other words, the cell does the work of the virus for it.

That’s why it was necessary to upgrade Stem Cell Neurotherapy for COVID-19 by adding T-Cells, B-Cells, and Natural Killer Cells to the arsenal. It was not enough to just regenerate new lung cells to replace the lung cells infected by COVID-19, but the COVID-19 Virus Cells had to be attacked and destroyed, and its RNA single strand had to be unraveled, in order to prevent them from invading and infecting the newly regenerated lung cells.


A retrovirus is a virus whose genes are encoded in RNA, and, using an enzyme called reverse transcriptase, replicates itself by first reverse-coding its genes into the DNA of the cells it infects. Like other viruses, retroviruses need to use the cellular machinery of the organisms they infect to make copies of themselves. However, infection by a retrovirus requires an additional step. The retrovirus genome needs to be reverse-transcribed into DNA before it can be copied in the usual way. The enzyme that does this backward transcription is known as reverse transcriptase.

Retroviruses use reverse transcriptase to transform their single-stranded RNA into double-stranded DNA. It is DNA that stores the genome of human cells and cells from other higher life forms. Once transformed from RNA to DNA, the viral DNA can be integrated into the genome of the infected cells. When the DNA versions of the retroviral genes have been incorporated into the genome, the cell then is tricked into copying those genes as part of its normal replication process. In other words, the cell does the work of the virus for it.

Retroviruses are “retro” because they reverse the direction of the normal gene copying process. Usually, cells convert DNA into RNA so that it can be made into proteins. But with retroviruses, the process has to start by going backward. First, the viral RNA is transformed into DNA. Then the cell can copy the DNA. The cell can also transcribe the DNA back into RNA as the first step in making viral proteins.