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The biological process of human life is simple, we're born, we live, and one day we die. But at the cellular level, this apparently simple course is far more complicated. Every human body is a highly complex ecosystem made up of approximately 30 trillion human cells and an equally staggering number of microbes, all functioning together in concert to maintain what we recognize as life.
As researchers discover the cryptic "third state" of life, the question is one of enormity—may near-death experiences have something to do with it? If cells are able to continue and reorganize after an organism has died, could human consciousness do the same in ways we're not yet aware of? Survivors of near-death experiences report vivid dreams, a tunnel vision of light, or a feeling of calm. But what happens to those who don't come back? May their cells be undergoing a change, a try to reorganize in some fashion we haven't yet understood? This brings into question the nature of death, of consciousness, and beyond.
However, new studies indicate that for certain cells, death is not the final act but a precursor to something surprising. This groundbreaking idea—the so-called "third state"—hypothesizes that under certain circumstances, certain cells, even after the death of an organism, may reorganize and form new functions, throwing our basic definitions of life and death into doubt.
The concept of a third state initially gained scientific momentum with the emergence of xenobots—AI-created multicellular creatures that exhibit autonomy outside their initial biological purpose. These small biological robots are constructed from frog embryo cells, which, when introduced into new environments, spontaneously reconfigure and assume new functions. For instance, instead of employing their hair-like cilia to move mucus as they would in a living frog, xenobots redirect these structures for mobility.
This phenomenon proves that cells are capable of being reassembled into new shapes and functions even after the death of an organism. Researchers opine that this postmortem cellular plasticity is not exclusive to xenobots. Human cells, or "anthrobots," also display such actions, proving the ability for posthumous cellular reorganization and transformation.
At the center of this controversy stands a challenging query: are cells conscious? Physician and evolutionary biologist William Miller takes on this theory in his work The Sentient Cell, an argument that puts forth the hypothesis that cells enjoy a type of cognitive capacity. The Cellular Basis of Consciousness (CBC) hypothesis proposes that cells do not blindly obey instructions from their genetics but rather are shown to implement decision-making activity, flexibility, and self-conserve mechanisms, all of which are akin to a primitive mode of consciousness.
While classical biological models portray genes as the ultimate controllers, Miller suggests that genes behave more as tools than controllers. Cellular intelligence is instead the driver of cooperation, mutual support, and problem-solving, underpinning multicellular life. This transforms the classical survival of the fittest paradigm to one of survival through collaboration and adaptability.
Historically, death has been defined as irreversible loss of organismal biological activity. Yet such medical procedures as organ donation illustrate that some organs, tissues, and cells maintain their functional properties even after death—sometimes for hours, days, or weeks under optimal circumstances.
A number of factors will decide whether cells survive after death. Environmental parameters, the state of metabolism, and methods of preservation are all important. Human white blood cells, for instance, can last between 60 and 86 hours from the time of death, while those of mice skeletal muscle can regenerate two weeks after death. Some fibroblast cells in sheep and goats have even been grown up to a month following the organism's death.
In addition, researchers have discovered that certain human lung cells are capable of self-assembling into small multicellular structures that can move and heal themselves. These "anthrobots" exhibit a capacity to explore their environment and repair injured neurons—abilities that contradict traditional assumptions about cellular behavior following death.
Cells' survival following the death of an organism relies on a number of biochemical processes. Some researchers believe that cell membrane specialized channels and pumps act as complex electrical circuits that coordinate cellular communication, organization, and movement. Stress- and immune-related genes also have heightened activity after death, and this implies that cells are striving to make up for lost homeostasis.
Age, health, trauma, infection, and type of species affect the duration of time cells will survive after death. For instance, islet cells in the pancreas, which secrete insulin, are notoriously hard to transplant because of their high demand for energy and susceptibility to attack by the immune system. Uncovering how certain cells resist the process of decay could transform organ transplantation and regenerative medicine.
The third state has very significant implications for biotechnology and medicine. Among its possible uses are in personalized medicine, where drugs might be delivered using anthrrobots made from the patient's own cells, to repair tissues or fight diseases.
For example, engineered anthrobots could be programmed to dissolve arterial plaque in atherosclerosis patients or clear excess mucus in cystic fibrosis patients. Unlike synthetic drugs, these living cellular machines would not trigger immune rejection and could biodegrade naturally within weeks, minimizing long-term risks.
In addition, the third state of matter idea might lead to next-generation regenerative therapies, potentially enabling researchers to revive lost functions in injured organs or even extend transplantable organ preservation times. The discovery of the mechanisms behind how some cells are able to survive and adapt following death might also yield essential knowledge on aging, neurodegeneration, and immunity.
As study of the third state increases, it threatens our traditional notions of biology, consciousness, and the very nature of death. If cells are in some sense intelligent, as scientists argue, then life itself must be redefined. What we might view as the "end" is merely a stage of biological change, in which cells rearrange themselves and accommodate different functions in a manner previously unknown.
The applications of this study go far beyond the realm of medicine; they border on philosophical and ethical considerations regarding consciousness, identity, and the very nature of what it means to be alive. As science continues to peel away layers of cell behavior, one thing remains for sure—life, as we have always known it, is much more complex and mysterious than we have ever conceived.
This study also opens up an interesting possibility: might near-death experiences have something to do with the third state? Researchers have long reported instances of people having vivid, life-changing experiences at the time of clinical death—seeing light, meeting dead relatives, or feeling themselves float above their bodies. If cells are still able to function and reorganize after death, might this activity be responsible for these experiences, rather than just hallucinations?
Some scientists now question whether such experiences are a cellular-level phenomenon even in individuals who cannot be resuscitated. If cells preserve some sort of consciousness or decision-making capacity after biological death, it would change our concept of both consciousness and the line between life and death.
The third stage between life and death is no longer an outlying theory—it is a phenomenon witnessed by scientists with far-reaching medical, ethical, and philosophical consequences. While scientists continue to study how cells survive and change following the death of an organism, our perception of life itself may be poised on the verge of a paradigm shift.
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As measles continues to spread across the United States, with recent case numbers climbing to their highest level in 33 years, growing numbers of Americans are becoming concerned about how at risk they may be.
Health officials in Philadelphia confirmed a potential measles exposure at Philadelphia International Airport and several public transport locations across the city in early January. The Centers for Disease Control and Prevention has also flagged earlier measles outbreaks across Pennsylvania, New Jersey, and New York City.
Adding to the concern, infectious disease tracker BMJGroup reported that measles cases recorded in 2025 are the highest seen since at least 1992.
Against this backdrop, it is important to understand whether measles can be fatal and to recognise the symptoms that should not be ignored.
Yes, measles can be deadly and carries a significant risk of death, according to the Centers for Disease Control and Prevention.
“Measles can lead to serious health complications, including pneumonia, inflammation of the brain known as encephalitis, and death,” the CDC states. “Between one and three out of every 1,000 people infected with measles will die. Around one in five people with measles will require hospital care, and one in every 20 children with measles develops pneumonia, which is the leading cause of measles-related deaths in young children.
“One in every 1,000 people with measles will experience brain swelling, which can result in permanent brain damage.”
According to the Mayo Clinic, measles symptoms usually appear in three distinct stages.
Stage 1: Incubation period (10 to 14 days)
During this phase, there are typically no noticeable or warning symptoms.
Stage 2: Early symptoms begin
Symptoms at this stage may include a dry cough, fever, red and inflamed eyes known as conjunctivitis, a runny nose, and a sore throat.
Stage 3: Acute illness and rash
“In the third stage, a rash begins to develop, usually starting on the face. Small white spots called Koplik spots may appear inside the mouth two to three days after symptoms first appear,” the Mayo Clinic explains. “The measles rash typically shows up three to five days after the initial symptoms.
“Over the following days, the rash spreads to the arms, torso, and legs. Alongside the rash, fever often rises rapidly and can exceed 105 degrees Fahrenheit,” the guidance continues. “Eventually, the fever subsides, and the rash fades from the body starting at the head and moving downward.”
“If individuals aged six months or older are exposed to measles and do not have immunity from prior infection or vaccination, they can receive the measles vaccine within three days of contact with the virus,” the Mayo Clinic advises. “After vaccination, quarantine at home is not required.
“For children up to 11 months old who are exposed and are not immune, a dose of antibodies known as immune globulin can be given within six days of exposure to help the body fight the infection.”
Receiving this antibody treatment requires a 21-day quarantine period.
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A notice has been issued for people who use the drug spironolactone. It is commonly prescribed for heart conditions, high blood pressure, and fluid retention. However, doctors say the medication is also used for several other health concerns.
According to the British Association of Dermatologists (BAD), spironolactone is prescribed “off licence” for women dealing with acne, female pattern hair loss, and hirsutism, a condition marked by excessive hair growth in areas such as the chin and upper lip. The NHS also states that spironolactone is a well-established and generally safe medicine that is sometimes used off licence to treat acne. Off licence means the drug is not officially approved for that specific condition under the UK prescribing licence.
Despite this, the NHS says spironolactone is available through the health service and is considered a useful alternative to long-term antibiotics. A study published in 2022 found that the drug is effective and safe for women who have persistent acne.
Spironolactone, sold under the brand name Aldactone, is also used to help manage polycystic ovary syndrome, commonly known as PCOS. However, it is not usually prescribed to men for skin-related conditions.
While the medication can be helpful for many women, experts warn that it does come with side effects and certain dietary restrictions. Here is what patients should know before starting treatment.
The NHS explains that spironolactone does not permanently cure acne, but it can help control breakouts and gradually clear the skin. The drug works slowly, meaning results are not immediate.
Most women begin to see improvement after about three months of use, but treatment usually needs to continue for at least six months. In some cases, it may take the full six months to experience the maximum benefit.
For acne, spironolactone is usually prescribed at doses ranging from 50mg to 150mg per day. Many patients start with 50mg daily for the first month, depending on how well they tolerate the medication and whether any side effects appear.
If there are no concerning side effects and blood test results remain normal, a doctor may increase the dose to 100mg per day. NHS guidance says the tablets should be swallowed whole with water and taken after food.
High potassium levels in the blood, especially in people over 45 or those with heart or kidney disease
Changes in kidney or liver blood tests, which usually return to normal if the dose is reduced or stopped
Cancer, which has been linked to very high doses in animal studies, but not seen in people taking standard doses.
The NHS advises that spironolactone should not be taken during pregnancy or while trying to conceive. It should also be avoided by people with Addison’s disease or serious kidney problems.
Alcohol can worsen certain side effects, such as dizziness, so cutting back on drinking is recommended. Reliable contraception should be used while taking spironolactone, and the combined contraceptive pill may help reduce side effects while also improving acne.
Doctors advise that it is usually safe to try for a baby one month after stopping the medication. The NHS stresses the importance of informing your doctor about any other medicines you are taking before starting spironolactone. This includes ACE inhibitors, anti-inflammatory painkillers such as aspirin or ibuprofen, certain antibiotics, other diuretics, heart medications like digoxin, drugs for high blood pressure, and potassium supplements.
As per Mirror, people taking spironolactone are advised not to use low-sodium salt or salt substitutes such as Lo-Salt, as these products contain high levels of potassium. Using them alongside spironolactone can raise potassium levels to a dangerous range.
The NHS also recommends limiting foods and drinks high in potassium, including bananas, avocados, pulses, nuts, and salmon. A doctor or dietitian can help plan a low-potassium diet if needed.
Disclaimer:
This article is for general information only and is not a substitute for medical advice. Always consult a qualified healthcare professional before starting, stopping, or changing any medication, including spironolactone.
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The NHS has issued advice for anyone taking a widely prescribed medication, warning of possible “serious” side effects. If you are currently on atorvastatin, it’s important to be cautious about what other medicines or supplements you take alongside it.
Atorvastatin belongs to a class of drugs called statins, which help lower cholesterol levels. It is usually prescribed for people with high cholesterol to reduce the risk of heart disease, including heart attacks and strokes.
Your GP may also recommend atorvastatin if you have a family history of heart disease or a long-term condition such as type 1 or type 2 diabetes or rheumatoid arthritis. As with any medicine, it’s vital to follow official guidance on how to take it safely.
On its website, the NHS lists certain “cautions with other medicines.” This means you should check that atorvastatin is safe to take alongside any other drugs or supplements.
The NHS explained: “Some medicines can affect the way atorvastatin works and can increase the chances of you having serious side effects, such as muscle damage.” You should tell your doctor or pharmacist if you are taking any of the following:
If you need to take one of these medicines while on atorvastatin, your doctor may:
These are not all the drugs that can interact with atorvastatin. “For a full list, see the leaflet in your medicine packet or speak to your pharmacist,” the NHS said.
The health service also advised checking with your doctor or pharmacist before taking supplements like St John’s wort or CoQ10 while on atorvastatin.
The NHS lists these common side effects, which affect more than one in 100 people:
“Drinking large amounts of alcohol regularly increases the risk of side effects and liver problems while taking atorvastatin,” the NHS added. “If side effects make you want to stop taking the medicine, speak to your doctor first. They may be due to another cause, and your doctor can suggest lowering the dose or switching medicines.”
Stop taking atorvastatin and contact a doctor or call 111 immediately if you experience:
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