For those interested.. You can get yours here
@MedbedsTechnology
https://quantumfrequencymedicine.com/products/the-9010-medbed
@MedbedsTechnology
https://quantumfrequencymedicine.com/products/the-9010-medbed
Watch "MED BED TESTIMONIAL (NANCY'S STORY) MedBeds" on YouTube
https://youtu.be/2EJztqSDLE4
@MedbedsTechnology
https://youtu.be/2EJztqSDLE4
@MedbedsTechnology
[Forwarded from ORIANA★ 2.1.3.B]
Watch "Incredible New DNA Discovery Reverses the Aging Process" on YouTube
https://youtu.be/zoYMchaXDD8 @MedbedsTechnology
Watch "Incredible New DNA Discovery Reverses the Aging Process" on YouTube
https://youtu.be/zoYMchaXDD8 @MedbedsTechnology
YouTube
Incredible New DNA Discovery Reverses the Aging Process
A new discovery made by Longevity and DNA Researchers could soon lead to an increase at targeted longevity-related medicine due to rapid improvements of our understanding of DNA and gene editing. This will soon lead to anti aging and even age reversal treatments…
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Nikola Tesla developed The Violet Ray technology — penetrating the skin & can act as a disinfectant in the cells of the body. Tesla’s high-potential currents could pass the body harmlessly — these currents could be put to electro-therapeutic uses. @MedbedsTechnology
Tesla was successfully experimenting on disease and rejuvenation with ozone in the late 1800s & early 1900s. In the 20s & 30s, Oxygen-Zone Therapy was used in hospitals, clinics and sanitariums.
When Tesla was struck down in the streets by a New York taxi, he dragged himself up to his hotel room where, in seclusion and & the help of his own electrotherapy, he recovered from his fractures & contusions.
1891 Tesla published his observations in technical journals, then gave a speech to the American Electro-Therapeutic Association in which he details with drawings the Violet Ray apparatus, which included a Tesla coil.
The Violet Ray was ultimately banned by a fake doctor commissioned by the Rockefellers & Carnegies named Abraham Flexner. In his Flexner Report of 1910, the stage was set for pharmaceuticals by removing many alternative healing modalities from the AMA certification. The USA is the only country in the world where Ozone Therapy & Electrotherapy banned. Sounds familiar with what’s going on today?!
6,500 suppressed patents is coming out. A new patent for Healight just surfaced & has the potential to cure all viral infections. Big pharma is currently walking into its death bed. ✨🙏🤍✨
Cedars-Sinai-Developed ‘Healight’ Medical Device Platform Technology Being Studied as a Potential First-in-Class COVID-19 Treatment.
https://www.sec.gov/Archives/edgar/data/1385818/000165495420004215/aytu_ex991.htm
In 1901, Tesla invented a device that produced ultraviolet light when activated by coils in a “high-frequency apparatus,” a device capable of producing bolts of lightning.
https://vitalitymagazine.com/article/the-vital-light-of-nikola-tesla-healing-power-of-ultraviolet-light/amp/
Ultraviolet Irradiation of Blood: “The Cure That Time Forgot”?
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122858/
Tesla was successfully experimenting on disease and rejuvenation with ozone in the late 1800s & early 1900s. In the 20s & 30s, Oxygen-Zone Therapy was used in hospitals, clinics and sanitariums.
When Tesla was struck down in the streets by a New York taxi, he dragged himself up to his hotel room where, in seclusion and & the help of his own electrotherapy, he recovered from his fractures & contusions.
1891 Tesla published his observations in technical journals, then gave a speech to the American Electro-Therapeutic Association in which he details with drawings the Violet Ray apparatus, which included a Tesla coil.
The Violet Ray was ultimately banned by a fake doctor commissioned by the Rockefellers & Carnegies named Abraham Flexner. In his Flexner Report of 1910, the stage was set for pharmaceuticals by removing many alternative healing modalities from the AMA certification. The USA is the only country in the world where Ozone Therapy & Electrotherapy banned. Sounds familiar with what’s going on today?!
6,500 suppressed patents is coming out. A new patent for Healight just surfaced & has the potential to cure all viral infections. Big pharma is currently walking into its death bed. ✨🙏🤍✨
Cedars-Sinai-Developed ‘Healight’ Medical Device Platform Technology Being Studied as a Potential First-in-Class COVID-19 Treatment.
https://www.sec.gov/Archives/edgar/data/1385818/000165495420004215/aytu_ex991.htm
In 1901, Tesla invented a device that produced ultraviolet light when activated by coils in a “high-frequency apparatus,” a device capable of producing bolts of lightning.
https://vitalitymagazine.com/article/the-vital-light-of-nikola-tesla-healing-power-of-ultraviolet-light/amp/
Ultraviolet Irradiation of Blood: “The Cure That Time Forgot”?
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6122858/
Vitality Magazine
The Vital Light of Nikola Tesla: Healing Power of Ultraviolet Rays - Vitality Magazine
Nikola Tesla: UV light raises vitamin D levels, treats skin problems & cancer; ozone therapy kills germs / viruses, disinfects, treats cancer tumor cells
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A jump through time – new technique rewinds the age of skin cells by 30 years
Key points:
Research from the Babraham Institute has developed a new technique for rejuvenating skin cells. This technique has allowed researchers to rewind the cellular biological clock by around 30 years according to molecular measures, significantly longer than previous reprogramming methods.
The partially rejuvenated cells showed signs of behaving more like youthful cells in experiments simulating a skin wound.
This research, although in early stages, could eventually have implications for regenerative medicine, especially if it can be replicated in other cell types.
Research from the Babraham Institute has developed a method to ‘time jump’ human skin cells by 30 years, turning back the ageing clock for cells without losing their specialised function. Work by researchers in the Institute’s Epigenetics research programme has been able to partly restore the function of older cells, as well as rejuvenating the molecular measures of biological age. The research is published today in the journal eLife and whilst at an early stage of exploration, it could revolutionise regenerative medicine.
What is regenerative medicine?
As we age, our cells’ ability to function declines and the genome accumulates marks of ageing. Regenerative biology aims to repair or replace cells including old ones. One of the most important tools in regenerative biology is our ability to create ‘induced’ stem cells. The process is a result of several steps, each erasing some of the marks that make cells specialised. In theory, these stem cells have the potential to become any cell type, but scientists aren’t yet able to reliably recreate the conditions to re-differentiate stem cells into all cell types.
Turning back time
The new method, based on the Nobel Prize winning technique scientists use to make stem cells, overcomes the problem of entirely erasing cell identity by halting reprogramming part of the way through the process. This allowed researchers to find the precise balance between reprogramming cells, making them biologically younger, while still being able to regain their specialised cell function.
In 2007, Shinya Yamanaka was the first scientist to turn normal cells, which have a specific function, into stem cells which have the special ability to develop into any cell type. The full process of stem cell reprogramming takes around 50 days using four key molecules called the Yamanaka factors. The new method, called 'maturation phase transient reprogramming’, exposes cells to Yamanaka factors for just 13 days. At this point, age-related changes are removed and the cells have temporarily lost their identity. The partly reprogrammed cells were given time to grow under normal conditions, to observe whether their specific skin cell function returned. Genome analysis showed that cells had regained markers characteristic of skin cells (fibroblasts), and this was confirmed by observing collagen production in the reprogrammed cells.
@MedbedsTechnology
Key points:
Research from the Babraham Institute has developed a new technique for rejuvenating skin cells. This technique has allowed researchers to rewind the cellular biological clock by around 30 years according to molecular measures, significantly longer than previous reprogramming methods.
The partially rejuvenated cells showed signs of behaving more like youthful cells in experiments simulating a skin wound.
This research, although in early stages, could eventually have implications for regenerative medicine, especially if it can be replicated in other cell types.
Research from the Babraham Institute has developed a method to ‘time jump’ human skin cells by 30 years, turning back the ageing clock for cells without losing their specialised function. Work by researchers in the Institute’s Epigenetics research programme has been able to partly restore the function of older cells, as well as rejuvenating the molecular measures of biological age. The research is published today in the journal eLife and whilst at an early stage of exploration, it could revolutionise regenerative medicine.
What is regenerative medicine?
As we age, our cells’ ability to function declines and the genome accumulates marks of ageing. Regenerative biology aims to repair or replace cells including old ones. One of the most important tools in regenerative biology is our ability to create ‘induced’ stem cells. The process is a result of several steps, each erasing some of the marks that make cells specialised. In theory, these stem cells have the potential to become any cell type, but scientists aren’t yet able to reliably recreate the conditions to re-differentiate stem cells into all cell types.
Turning back time
The new method, based on the Nobel Prize winning technique scientists use to make stem cells, overcomes the problem of entirely erasing cell identity by halting reprogramming part of the way through the process. This allowed researchers to find the precise balance between reprogramming cells, making them biologically younger, while still being able to regain their specialised cell function.
In 2007, Shinya Yamanaka was the first scientist to turn normal cells, which have a specific function, into stem cells which have the special ability to develop into any cell type. The full process of stem cell reprogramming takes around 50 days using four key molecules called the Yamanaka factors. The new method, called 'maturation phase transient reprogramming’, exposes cells to Yamanaka factors for just 13 days. At this point, age-related changes are removed and the cells have temporarily lost their identity. The partly reprogrammed cells were given time to grow under normal conditions, to observe whether their specific skin cell function returned. Genome analysis showed that cells had regained markers characteristic of skin cells (fibroblasts), and this was confirmed by observing collagen production in the reprogrammed cells.
@MedbedsTechnology
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Dr Diljeet Gill
Age isn’t just a number
To show that the cells had been rejuvenated, the researchers looked for changes in the hallmarks of ageing. As explained by Dr Diljeet Gill, a postdoc in Wolf Reik’s lab at the Institute who conducted the work as a PhD student: “Our understanding of ageing on a molecular level has progressed over the last decade, giving rise to techniques that allow researchers to measure age-related biological changes in human cells. We were able to apply this to our experiment to determine the extent of reprogramming our new method achieved.”
Researchers looked at multiple measures of cellular age. The first is the epigenetic clock, where chemical tags present throughout the genome indicate age. The second is the trannoscriptome, all the gene readouts produced by the cell. By these two measures, the reprogrammed cells matched the profile of cells that were 30 years younger compared to reference data sets.
The potential applications of this technique are dependent on the cells not only appearing younger, but functioning like young cells too. Fibroblasts produce collagen, a molecule found in bones, skin tendons and ligaments, helping provide structure to tissues and heal wounds. The rejuvenated fibroblasts produced more collagen proteins compared to control cells that did not undergo the reprogramming process. Fibroblasts also move into areas that need repairing. Researchers tested the partially rejuvenated cells by creating an artificial cut in a layer of cells in a dish. They found that their treated fibroblasts moved into the gap faster than older cells. This is a promising sign that one day this research could eventually be used to create cells that are better at healing wounds.
In the future, this research may also open up other therapeutic possibilities; the researchers observed that their method also had an effect on other genes linked to age-related diseases and symptoms. The APBA2 gene, associated with Alzheimer’s disease, and the MAF gene with a role in the development of cataracts, both showed changes towards youthful levels of trannoscription.
The mechanism behind the successful transient reprogramming is not yet fully understood, and is the next piece of the puzzle to explore. The researchers speculate that key areas of the genome involved in shaping cell identity might escape the reprogramming process.
Diljeet concluded: “Our results represent a big step forward in our understanding of cell reprogramming. We have proved that cells can be rejuvenated without losing their function and that rejuvenation looks to restore some function to old cells. The fact that we also saw a reverse of ageing indicators in genes associated with diseases is particularly promising for the future of this work.”
Professor Wolf Reik, who lead the research, said: “This work has very exciting implications. Eventually, we may be able to identify genes that rejuvenate without reprogramming, and specifically target those to reduce the effects of ageing. This approach holds promise for valuable discoveries that could open up an amazing therapeutic horizon.”
@MedbedsTechnology
Age isn’t just a number
To show that the cells had been rejuvenated, the researchers looked for changes in the hallmarks of ageing. As explained by Dr Diljeet Gill, a postdoc in Wolf Reik’s lab at the Institute who conducted the work as a PhD student: “Our understanding of ageing on a molecular level has progressed over the last decade, giving rise to techniques that allow researchers to measure age-related biological changes in human cells. We were able to apply this to our experiment to determine the extent of reprogramming our new method achieved.”
Researchers looked at multiple measures of cellular age. The first is the epigenetic clock, where chemical tags present throughout the genome indicate age. The second is the trannoscriptome, all the gene readouts produced by the cell. By these two measures, the reprogrammed cells matched the profile of cells that were 30 years younger compared to reference data sets.
The potential applications of this technique are dependent on the cells not only appearing younger, but functioning like young cells too. Fibroblasts produce collagen, a molecule found in bones, skin tendons and ligaments, helping provide structure to tissues and heal wounds. The rejuvenated fibroblasts produced more collagen proteins compared to control cells that did not undergo the reprogramming process. Fibroblasts also move into areas that need repairing. Researchers tested the partially rejuvenated cells by creating an artificial cut in a layer of cells in a dish. They found that their treated fibroblasts moved into the gap faster than older cells. This is a promising sign that one day this research could eventually be used to create cells that are better at healing wounds.
In the future, this research may also open up other therapeutic possibilities; the researchers observed that their method also had an effect on other genes linked to age-related diseases and symptoms. The APBA2 gene, associated with Alzheimer’s disease, and the MAF gene with a role in the development of cataracts, both showed changes towards youthful levels of trannoscription.
The mechanism behind the successful transient reprogramming is not yet fully understood, and is the next piece of the puzzle to explore. The researchers speculate that key areas of the genome involved in shaping cell identity might escape the reprogramming process.
Diljeet concluded: “Our results represent a big step forward in our understanding of cell reprogramming. We have proved that cells can be rejuvenated without losing their function and that rejuvenation looks to restore some function to old cells. The fact that we also saw a reverse of ageing indicators in genes associated with diseases is particularly promising for the future of this work.”
Professor Wolf Reik, who lead the research, said: “This work has very exciting implications. Eventually, we may be able to identify genes that rejuvenate without reprogramming, and specifically target those to reduce the effects of ageing. This approach holds promise for valuable discoveries that could open up an amazing therapeutic horizon.”
@MedbedsTechnology