Health and Me

Riya Baibhawi

Many Vegans Miss Out On Key Amino Acids Despite Getting Enough Protein, Study Reveals

YourA new study has found that while many long-term vegans consume enough total <span>protein</span> daily, a significant number still fall short of essential <span>amino acids</span>, raising concerns about protein quality in plant-based diets.

Conducted by a team of nutritionists from Massey University in New Zealand, the research analysed the diets of 193 vegans using four-day food diaries. The team used data from the U.S. Department of Agriculture and the New Zealand FoodFiles database to estimate amino acid intake from various plant-based foods. Their findings, published in the journal PLOS One, shed light on the challenges vegans face in achieving complete protein nutrition.

According to the study, around 75% of participants met their total daily protein needs. However, only about half reached the required intake for two crucial amino acids—lysine and leucine. These amino acids are classified as "indispensable" because the human body cannot produce them on its own and must obtain them through diet.

“Meeting adequate total daily protein intake in a <span>vegan diet</span> does not always guarantee a high protein quality diet,” the researchers warned. “Simply considering total protein intake without evaluating protein quality may lead to an overestimation of nutritional adequacy among vegans.”

Lead researchers Bi Xue and Patricia Soh emphasized the importance of including a diverse range of plant foods to meet the full spectrum of amino acid needs. While the body can synthesize many amino acids, nine must be sourced directly from food—making dietary balance crucial, especially in <span>vegan</span> diets.

The study pointed to legumes, nuts, seeds, and soy products as valuable sources for boosting lysine and leucine intake. These plant-based options can help vegans meet both their total protein requirements and maintain the right amino acid profile necessary for overall health.

“Achieving high protein quality on a vegan diet requires more than just consuming enough protein,” the team noted. “It also depends on the right balance and variety of plant foods to supply all the amino acids in the quantities our body needs.”

The researchers concluded by calling for further studies to explore effective strategies for improving amino acid intake in vegan populations. As more people adopt plant-based lifestyles, understanding how to maintain both protein quantity and quality is becoming increasingly important for public health.

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YourA new study has found that while many long-term vegans consume enough total protein daily, a significant number still fall short of essential amino acids, raising concerns about protein quality in plant-based diets.Conducted by a team of nutritionists from Massey University in New Zealand, the research analysed the diets of 193 vegans using four-day food diaries. The team used data from the U.S. Department of Agriculture and the New Zealand FoodFiles database to estimate amino acid intake from various plant-based foods. Their findings, published in the journal PLOS One, shed light on the challenges vegans face in achieving complete protein nutrition.According to the study, around 75% of participants met their total daily protein needs. However, only about half reached the required intake for two crucial amino acids—lysine and leucine. These amino acids are classified as "indispensable" because the human body cannot produce them on its own and must obtain them through diet.“Meeting adequate total daily protein intake in a vegan diet does not always guarantee a high protein quality diet,” the researchers warned. “Simply considering total protein intake without evaluating protein quality may lead to an overestimation of nutritional adequacy among vegans.”Lead researchers Bi Xue and Patricia Soh emphasized the importance of including a diverse range of plant foods to meet the full spectrum of amino acid needs. While the body can synthesize many amino acids, nine must be sourced directly from food—making dietary balance crucial, especially in vegan diets.The study pointed to legumes, nuts, seeds, and soy products as valuable sources for boosting lysine and leucine intake. These plant-based options can help vegans meet both their total protein requirements and maintain the right amino acid profile necessary for overall health.“Achieving high protein quality on a vegan diet requires more than just consuming enough protein,” the team noted. “It also depends on the right balance and variety of plant foods to supply all the amino acids in the quantities our body needs.”The researchers concluded by calling for further studies to explore effective strategies for improving amino acid intake in vegan populations. As more people adopt plant-based lifestyles, understanding how to maintain both protein quantity and quality is becoming increasingly important for public health.Do you want a headline suggestion or social media blurb for this article?

many vegans miss out on key amino acids despite getting enough protein, study reveals

Tanya Dutt

Eli Lilly’s Mounjaro Kwikpen Gets Indian Approval For Diabetes And Weight Loss

eli lilly’s mounjaro kwikpen gets indian approval for diabetes and weight loss

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In a significant development that highlights the increasing scrutiny over the safety of pharma products, India's Central Drugs Standard Control Organisation (CDSCO) has identified 186 drugs and formulations as Not of Standard Quality (NSQ) in its surveillance report for May 2025. These identified drugs encompass widely prescribed drugs like paracetamol as well as diabetes drugs, triggering grave concerns over the safety of drugs in one of the world's largest pharmaceutical markets.

The action, the CDSCO says, is its part of regular regulatory vigilance aimed at detecting and eliminating unsafe drugs in the market so that patients are not inadvertently left consuming substandard or spurious medicines.

The list, published by the country's national drug regulator on 27 June, 2025, contains common drugs like paracetamol and insulin used to treat diabetes, prompting critical questions on drug safety, regulatory scrutiny, and public health in one of the biggest pharma markets in the world.

The CDSCO's recent warning follows central and state drug testing laboratories in India reporting scores of samples from pharmacies and distribution centers across the country. Of the total 186 failed quality test samples, 128 were detected by state drug testing laboratories, and 58 by central labs. All this aggressive monitoring forms part of CDSCO's constant vigilance to ensure the quality of drugs being sold to Indian consumers.

Of the 186 substandard drug samples, 128 were identified by state drug testing labs and 58 by central labs, as per the official notification. All these drugs failed one or more of the quality parameters such as potency, dissolution rate, microbial load, or content uniformity, and hence were not fit for use by patients.

In a statement that released with the move, CDSCO sought to point out that one failed batch of drug is unique to that batch and does not always mean all batches of the same brand or product are unsafe. Still, the detection of even a single poor batch can have implications for public health, particularly in the case of life-saving and chronic disease drugs.

The CDSCO also established that two of the Bihar drug samples were spurious, i.e., produced by unauthorized parties with the brand name of a different licensed company. These results suggest counterfeit operations in India's huge and intricate drug distribution system.

The regulator has assured that the incidents are being investigated and action would be taken under the Drugs and Cosmetics Act and the accompanying rules.

This is not a one-off case. CDSCO reported 900 samples as substandard and 20 as spurious in the year 2024 alone, all of them selected from pharmacies, hospitals, and distribution outlets throughout the nation.

<h2>What Are "Not of Standard Quality" (NSQ) and Spurious Drugs?</h2>

CDSCO defines NSQ as an occurrence of failure to satisfy one or more of the stipulated quality parameters during laboratory testing. The parameters would involve potency, purity, dissolution, and contaminants or impurities. Significantly, the regulator points out that a failed batch does not necessarily incriminate all the products of the same brand or company.

Aside from NSQ medicines, the CDSCO also marked two samples from the state of Bihar as "spurious." These were discovered to have been produced by illegal manufacturers with the use of the brand name of another firm—a grave offense which is being investigated. Adulterated and spurious medicines are especially threatening since they can have the wrong or harmful ingredients and therefore directly threaten patient safety. 

<h2>How India Monitors Drug Quality?</h2>

India's pharma industry is one of the biggest in the world, serving not just the domestic market but also exports to more than 200 nations. With such a huge market, maintaining drug safety is no small effort. The CDSCO, along with state regulators, regularly takes drug samples from sales and distribution points. The samples are tested thoroughly in the laboratory, and the findings are made available on the CDSCO portal on a monthly basis.

This openness achieves several functions: it warns medical professionals and the general public to possible danger, raises responsibility on manufacturers, and preserves the level of trust for the healthcare system. In the words of Dr. Rajeev Singh Raghuvanshi, India's Drugs Controller General, only roughly 1.5% of drugs tested in recent surveys turned out to be less effective, indicating that the overwhelming majority of medicines available are safe. Still, a small proportion can add up to potentially great public health threats in view of India's population and the magnitude of drug use.

<h2>Threats to Public Health and World Drug Supply</h2>

India has been commonly referred to as the "pharmacy of the world," exporting generic drugs to more than 200 nations. Any quality lapse not only impacts Indian consumers but also tarnishes world confidence in Indian pharmaceuticals. Paracetamol and anti-diabetics are consumed by millions — any compromise on their effectiveness or safety can be devastating health-wise.

Substandard or counterfeit drugs are one of the greatest dangers to contemporary medicine," an independent pharmacovigilance expert in New Delhi said. "They may not treat the disease, may worsen patient outcomes, or lead to antimicrobial resistance."

The public, clinicians, and policymakers need to address CDSCO notifications not as run-of-the-mill bureaucracy but as canary-in-the-coal-mines warnings of broader systemic problems in manufacturing regulation, supply chain integrity, and quality control procedures.

<h2>What Can Healthcare Providers and Patients Do?</h2>

Awareness is the best defense for patients. The CDSCO's medicine alert system seeks to inform consumers and healthcare providers about possible dangers of certain drugs. Patients must go see their doctors or pharmacists if they have issues with their medication and avoid buying drugs from unofficial sources.

Healthcare professionals, on their part, must remain up to date on the current CDSCO reports and advisories, particularly when dispensing or prescribing high-risk drugs. Keeping an eye on the CDSCO portal regularly and being subscribed to alerts can help ensure that patients receive only safe and effective medicines. Patients must:

<ul><li>Inquire about the batch number and manufacturer prior to taking prescribed drugs.</li><li>Immediately report any side effects.</li><li>Do not buy drugs from illegal online pharmacies.</li></ul>

In addition, hospitals and states should institutionalize pharmacovigilance programs in order to identify adverse trends early.

The CDSCO's forward-looking attitude—constant vigilance, open reporting, and rapid enforcement against violators—is reflective of India's seriousness in protecting public health. Nevertheless, the challenge persists. As the pharmaceutical sector continues its expansion, so must regulatory capability, laboratory facilities, and public awareness.

banned medicines in india

cdsco drug alert 2025

substandard medicines india

paracetamol quality issue

diabetes drug recall

spurious drugs india

nsq drug list cdsco

india drug safety news

In a significant development that highlights the increasing scrutiny over the safety of pharma products, India's Central Drugs Standard Control Organisation (CDSCO) has identified 186 drugs and formulations as Not of Standard Quality (NSQ) in its surveillance report for May 2025. These identified drugs encompass widely prescribed drugs like paracetamol as well as diabetes drugs, triggering grave concerns over the safety of drugs in one of the world's largest pharmaceutical markets.The action, the CDSCO says, is its part of regular regulatory vigilance aimed at detecting and eliminating unsafe drugs in the market so that patients are not inadvertently left consuming substandard or spurious medicines.The list, published by the country's national drug regulator on 27 June, 2025, contains common drugs like paracetamol and insulin used to treat diabetes, prompting critical questions on drug safety, regulatory scrutiny, and public health in one of the biggest pharma markets in the world.The CDSCO's recent warning follows central and state drug testing laboratories in India reporting scores of samples from pharmacies and distribution centers across the country. Of the total 186 failed quality test samples, 128 were detected by state drug testing laboratories, and 58 by central labs. All this aggressive monitoring forms part of CDSCO's constant vigilance to ensure the quality of drugs being sold to Indian consumers.Of the 186 substandard drug samples, 128 were identified by state drug testing labs and 58 by central labs, as per the official notification. All these drugs failed one or more of the quality parameters such as potency, dissolution rate, microbial load, or content uniformity, and hence were not fit for use by patients.In a statement that released with the move, CDSCO sought to point out that one failed batch of drug is unique to that batch and does not always mean all batches of the same brand or product are unsafe. Still, the detection of even a single poor batch can have implications for public health, particularly in the case of life-saving and chronic disease drugs.The CDSCO also established that two of the Bihar drug samples were spurious, i.e., produced by unauthorized parties with the brand name of a different licensed company. These results suggest counterfeit operations in India's huge and intricate drug distribution system.The regulator has assured that the incidents are being investigated and action would be taken under the Drugs and Cosmetics Act and the accompanying rules.This is not a one-off case. CDSCO reported 900 samples as substandard and 20 as spurious in the year 2024 alone, all of them selected from pharmacies, hospitals, and distribution outlets throughout the nation.What Are "Not of Standard Quality" (NSQ) and Spurious Drugs?CDSCO defines NSQ as an occurrence of failure to satisfy one or more of the stipulated quality parameters during laboratory testing. The parameters would involve potency, purity, dissolution, and contaminants or impurities. Significantly, the regulator points out that a failed batch does not necessarily incriminate all the products of the same brand or company.Aside from NSQ medicines, the CDSCO also marked two samples from the state of Bihar as "spurious." These were discovered to have been produced by illegal manufacturers with the use of the brand name of another firm—a grave offense which is being investigated. Adulterated and spurious medicines are especially threatening since they can have the wrong or harmful ingredients and therefore directly threaten patient safety. How India Monitors Drug Quality?India's pharma industry is one of the biggest in the world, serving not just the domestic market but also exports to more than 200 nations. With such a huge market, maintaining drug safety is no small effort. The CDSCO, along with state regulators, regularly takes drug samples from sales and distribution points. The samples are tested thoroughly in the laboratory, and the findings are made available on the CDSCO portal on a monthly basis.This openness achieves several functions: it warns medical professionals and the general public to possible danger, raises responsibility on manufacturers, and preserves the level of trust for the healthcare system. In the words of Dr. Rajeev Singh Raghuvanshi, India's Drugs Controller General, only roughly 1.5% of drugs tested in recent surveys turned out to be less effective, indicating that the overwhelming majority of medicines available are safe. Still, a small proportion can add up to potentially great public health threats in view of India's population and the magnitude of drug use.Threats to Public Health and World Drug SupplyIndia has been commonly referred to as the "pharmacy of the world," exporting generic drugs to more than 200 nations. Any quality lapse not only impacts Indian consumers but also tarnishes world confidence in Indian pharmaceuticals. Paracetamol and anti-diabetics are consumed by millions — any compromise on their effectiveness or safety can be devastating health-wise.Substandard or counterfeit drugs are one of the greatest dangers to contemporary medicine," an independent pharmacovigilance expert in New Delhi said. "They may not treat the disease, may worsen patient outcomes, or lead to antimicrobial resistance."The public, clinicians, and policymakers need to address CDSCO notifications not as run-of-the-mill bureaucracy but as canary-in-the-coal-mines warnings of broader systemic problems in manufacturing regulation, supply chain integrity, and quality control procedures.What Can Healthcare Providers and Patients Do?Awareness is the best defense for patients. The CDSCO's medicine alert system seeks to inform consumers and healthcare providers about possible dangers of certain drugs. Patients must go see their doctors or pharmacists if they have issues with their medication and avoid buying drugs from unofficial sources.Healthcare professionals, on their part, must remain up to date on the current CDSCO reports and advisories, particularly when dispensing or prescribing high-risk drugs. Keeping an eye on the CDSCO portal regularly and being subscribed to alerts can help ensure that patients receive only safe and effective medicines. Patients must:Inquire about the batch number and manufacturer prior to taking prescribed drugs.Immediately report any side effects.Do not buy drugs from illegal online pharmacies.In addition, hospitals and states should institutionalize pharmacovigilance programs in order to identify adverse trends early.The CDSCO's forward-looking attitude—constant vigilance, open reporting, and rapid enforcement against violators—is reflective of India's seriousness in protecting public health. Nevertheless, the challenge persists. As the pharmaceutical sector continues its expansion, so must regulatory capability, laboratory facilities, and public awareness.

india’s drug regulator flags 186 medicines for failing quality test, paracetamol and diabetes meds included

This New Blood Test Could Spot Leukemia Risk Without The Painful Bone Marrow Sampling

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Just days after their laboratories were devastated by an Iranian missile attack, Profs. Liran Shlush and Amos Tanay of the Weizmann Institute of Science have published a landmark study that could transform how we detect and predict leukemia and other blood disorders. Their research, released in Nature Medicine, introduces a revolutionary blood test that may one day replace the painful, invasive bone marrow biopsy—a procedure dreaded by patients and clinicians alike.

Developed by Professors Liran Shlush and Amos Tanay, this innovation replaces the traditionally painful and invasive bone marrow biopsy with a cutting-edge, non-invasive blood test.

This development is poised to revolutionize diagnostics in hematology and could dramatically reduce global dependence on bone marrow sampling — a procedure that over a million people endure each year globally.

<h2>Why Bone Marrow Biopsies Have Been the Gold Standard?</h2>

For decades, diagnosing blood cancers such as leukemia has relied on extracting bone marrow—a process that involves drilling into the bone, typically under local anesthesia or sedation. The procedure is not only uncomfortable and anxiety-inducing but also costly, technically demanding, and sometimes inconclusive. Even when a sample is obtained, pathologists may disagree on whether the cells are healthy or diseased, leaving patients and their families in limbo.

The study found a way to detect and analyze rare blood-forming stem cells that occasionally escape the bone marrow and enter the bloodstream. These elusive cells, though few — often just one in a million — carry a wealth of diagnostic information.

“As we age, our blood stem cells accumulate mutations,” explains Prof. Shlush. “These mutated cells eventually dominate the blood system, failing to produce healthy blood cells and laying the groundwork for conditions like myelodysplastic syndrome (MDS) and leukemia.”

Traditionally, these defective cells are hidden within the bone marrow, undetectable by standard blood tests. Bone marrow biopsies, while effective, are painful, costly, and often inconclusive. But this new method captures and analyzes the rare migratory stem cells through a simple blood draw, combined with advanced single-cell genetic sequencing.

<h2>How a Simple Blood Test Changes <span rel="noindex">Cancer</span> Diagnosis?</h2>

The breakthrough came when Dr. Nili Furer, Nimrod Rappoport, and Oren Milman, collaborating with researchers in Israel and the U.S., discovered that rare blood stem cells occasionally escape the bone marrow and circulate in the bloodstream. These migrating cells, though extremely scarce—sometimes just a handful in a milliliter of blood—carry crucial diagnostic information.

By applying advanced single-cell genetic sequencing, the researchers were able to isolate and analyze these rare cells, identifying early signs of MDS and assessing an individual’s risk of developing blood cancer. This approach allows for the detection of disease processes long before symptoms arise, offering a window of opportunity for early intervention.

<h2>Focus on Myelodysplastic Syndrome</h2>

The study centers on myelodysplastic syndrome (MDS) — an age-related condition where stem cells fail to mature properly, leading to ineffective blood production and a heightened risk of progressing to acute myeloid leukemia (AML), a particularly aggressive form of cancer.

Previously, diagnosing MDS required extracting marrow with a needle — an uncomfortable procedure that many patients dreaded. Now, thanks to this innovation, the same diagnosis can be made using peripheral blood samples. Dr. Nili Furer, along with collaborators Nimrod Rappoport and Oren Milman, played a critical role in demonstrating that these rare stem cells in blood are sufficient for detecting MDS and its progression risk.

<h2>Why Men Age Faster — At Least in Their Blood?</h2>

One of the study’s more striking revelations involves gender differences in blood aging. The researchers observed that stem cell aging occurs faster in men than in women, which may explain why blood cancers are more prevalent in males.

“Men’s stem cells begin to exhibit cancer-prone mutations earlier than women’s,” notes Prof. Shlush. “This gender-based variance in blood aging is an eye-opener and may inform future prevention strategies.”

The test not only identifies disease but also acts as a biological clock, providing new insights into how blood ages — revealing patterns that even bone marrow biopsies have failed to detect.

Capturing and characterizing these rare cells required a blend of cutting-edge laboratory techniques and sophisticated data analysis. Each cell yielded tens of thousands of data points, and the team analyzed millions of cells from participants ranging in age from young adults to 95-year-olds. Prof. Tanay’s expertise in computational biology was instrumental in making sense of this vast dataset, enabling the team to distinguish healthy cells from those showing early signs of disease.

<h2>Implications of The New Blood Test On Treatment</h2>

The implications of this discovery are profound. Clinical trials based on the new blood test are already underway at multiple medical centers worldwide. The researchers believe that, in time, this test could be used not only for MDS and leukemia but also for a broad spectrum of blood-related disorders. By providing a non-invasive, highly sensitive diagnostic tool, the test has the potential to spare millions of patients from the ordeal of bone marrow biopsies each year.

“As part of the aging process, stem cells—the ones capable of generating all blood cells—undergo genetic changes and mutations,” explains Prof. Shlush. “With time, these cells accumulate mutations and begin to dominate the blood system. They stop differentiating properly, produce only themselves, and suppress the production of healthy cells. Eventually, this can lead to deadly diseases like blood cancers.”

The research itself is as resilient as its scientists. Just days before the study’s release, the labs of Profs. Shlush and Tanay at the Weizmann Institute were severely damaged in an Iranian missile attack. Despite the destruction, the team pushed forward, ensuring the findings reached the scientific community on time.

The study reflects the combined efforts of a global team of physicians, biologists, and data scientists across Israel and the United States, proving that science endures even in the face of adversity.

The prospect of replacing an invasive, expensive, and often ambiguous diagnostic procedure with a quick, precise, and painless blood test is a major leap forward. For millions worldwide, this means earlier detection, better prognosis, and more effective treatment strategies — all from a single vial of blood.

cancer

leukemia blood test

non invasive cancer detection

bone marrow biopsy alternative

blood stem cell aging

myelodysplastic syndrome diagnosis

early cancer screening

weizmann institute research

Just days after their laboratories were devastated by an Iranian missile attack, Profs. Liran Shlush and Amos Tanay of the Weizmann Institute of Science have published a landmark study that could transform how we detect and predict leukemia and other blood disorders. Their research, released in Nature Medicine, introduces a revolutionary blood test that may one day replace the painful, invasive bone marrow biopsy—a procedure dreaded by patients and clinicians alike.Developed by Professors Liran Shlush and Amos Tanay, this innovation replaces the traditionally painful and invasive bone marrow biopsy with a cutting-edge, non-invasive blood test.This development is poised to revolutionize diagnostics in hematology and could dramatically reduce global dependence on bone marrow sampling — a procedure that over a million people endure each year globally.Why Bone Marrow Biopsies Have Been the Gold Standard?For decades, diagnosing blood cancers such as leukemia has relied on extracting bone marrow—a process that involves drilling into the bone, typically under local anesthesia or sedation. The procedure is not only uncomfortable and anxiety-inducing but also costly, technically demanding, and sometimes inconclusive. Even when a sample is obtained, pathologists may disagree on whether the cells are healthy or diseased, leaving patients and their families in limbo.The study found a way to detect and analyze rare blood-forming stem cells that occasionally escape the bone marrow and enter the bloodstream. These elusive cells, though few — often just one in a million — carry a wealth of diagnostic information.“As we age, our blood stem cells accumulate mutations,” explains Prof. Shlush. “These mutated cells eventually dominate the blood system, failing to produce healthy blood cells and laying the groundwork for conditions like myelodysplastic syndrome (MDS) and leukemia.”Traditionally, these defective cells are hidden within the bone marrow, undetectable by standard blood tests. Bone marrow biopsies, while effective, are painful, costly, and often inconclusive. But this new method captures and analyzes the rare migratory stem cells through a simple blood draw, combined with advanced single-cell genetic sequencing.How a Simple Blood Test Changes Cancer Diagnosis?The breakthrough came when Dr. Nili Furer, Nimrod Rappoport, and Oren Milman, collaborating with researchers in Israel and the U.S., discovered that rare blood stem cells occasionally escape the bone marrow and circulate in the bloodstream. These migrating cells, though extremely scarce—sometimes just a handful in a milliliter of blood—carry crucial diagnostic information.By applying advanced single-cell genetic sequencing, the researchers were able to isolate and analyze these rare cells, identifying early signs of MDS and assessing an individual’s risk of developing blood cancer. This approach allows for the detection of disease processes long before symptoms arise, offering a window of opportunity for early intervention.Focus on Myelodysplastic SyndromeThe study centers on myelodysplastic syndrome (MDS) — an age-related condition where stem cells fail to mature properly, leading to ineffective blood production and a heightened risk of progressing to acute myeloid leukemia (AML), a particularly aggressive form of cancer.Previously, diagnosing MDS required extracting marrow with a needle — an uncomfortable procedure that many patients dreaded. Now, thanks to this innovation, the same diagnosis can be made using peripheral blood samples. Dr. Nili Furer, along with collaborators Nimrod Rappoport and Oren Milman, played a critical role in demonstrating that these rare stem cells in blood are sufficient for detecting MDS and its progression risk.Why Men Age Faster — At Least in Their Blood?One of the study’s more striking revelations involves gender differences in blood aging. The researchers observed that stem cell aging occurs faster in men than in women, which may explain why blood cancers are more prevalent in males.“Men’s stem cells begin to exhibit cancer-prone mutations earlier than women’s,” notes Prof. Shlush. “This gender-based variance in blood aging is an eye-opener and may inform future prevention strategies.”The test not only identifies disease but also acts as a biological clock, providing new insights into how blood ages — revealing patterns that even bone marrow biopsies have failed to detect.Capturing and characterizing these rare cells required a blend of cutting-edge laboratory techniques and sophisticated data analysis. Each cell yielded tens of thousands of data points, and the team analyzed millions of cells from participants ranging in age from young adults to 95-year-olds. Prof. Tanay’s expertise in computational biology was instrumental in making sense of this vast dataset, enabling the team to distinguish healthy cells from those showing early signs of disease.Implications of The New Blood Test On TreatmentThe implications of this discovery are profound. Clinical trials based on the new blood test are already underway at multiple medical centers worldwide. The researchers believe that, in time, this test could be used not only for MDS and leukemia but also for a broad spectrum of blood-related disorders. By providing a non-invasive, highly sensitive diagnostic tool, the test has the potential to spare millions of patients from the ordeal of bone marrow biopsies each year.“As part of the aging process, stem cells—the ones capable of generating all blood cells—undergo genetic changes and mutations,” explains Prof. Shlush. “With time, these cells accumulate mutations and begin to dominate the blood system. They stop differentiating properly, produce only themselves, and suppress the production of healthy cells. Eventually, this can lead to deadly diseases like blood cancers.”The research itself is as resilient as its scientists. Just days before the study’s release, the labs of Profs. Shlush and Tanay at the Weizmann Institute were severely damaged in an Iranian missile attack. Despite the destruction, the team pushed forward, ensuring the findings reached the scientific community on time.The study reflects the combined efforts of a global team of physicians, biologists, and data scientists across Israel and the United States, proving that science endures even in the face of adversity.The prospect of replacing an invasive, expensive, and often ambiguous diagnostic procedure with a quick, precise, and painless blood test is a major leap forward. For millions worldwide, this means earlier detection, better prognosis, and more effective treatment strategies — all from a single vial of blood.

this new blood test could spot leukemia risk without the painful bone marrow sampling

Why Whooping Cough, Measles And Rubella Still Haunt U.S. Families, Here's What Vaccine Hesitancy Overlooks

Why Whooping Cough, Measles, and Rubella Still Haunt U.S. Families, Here's What Vaccine Hesitancy Overlooks

Hepatitis A Outbreak In Europe: ECDC Confirms Over 2,000 Cases In Austria, Hungary, Czechia, Slovakia

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RFK Jr.’s Vaccine Panel Votes Against Flu Shot Preservative: All About The Controversial Thimerosal Ingredient

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Oxford Researchers Develop 'One-Dose' Malaria Vaccine; Could It Transform Global Prevention Efforts?

oxford researchers develop 'one-dose' malaria vaccine; could it transform global prevention efforts?

Before the era of widespread vaccination, infectious diseases cast a long and deadly shadow over American childhood. In 1900, nearly one in five children in the United States never reached their fifth birthday, with diseases like whooping cough, measles, rubella, and polio claiming millions of young lives or leaving survivors with lifelong disabilities. Over the next century, vaccines would transform this grim reality, virtually eradicating once-dreaded scourges and drastically reducing the toll of others. Yet, as immunization rates decline and vaccine hesitancy rises—even among public officials—these diseases are making a troubling comeback.

The very success of vaccines has, paradoxically, bred complacency and skepticism. “This concern, this hesitancy, these questions about vaccines are a consequence of the great success of the vaccines – because they eliminated the diseases. 

In a time before vaccines, childhood illness often meant death. Infectious diseases like polio, measles, rubella, and whooping cough once swept across communities unchecked, claiming young lives and leaving others permanently disabled. In 1900, nearly one in five American children didn’t live to see their fifth birthday, and infectious disease was the primary cause but with the advent of vaccines, these illnesses were nearly eradicated.

The widespread success of vaccines may ironically be their undoing. "This concern, this hesitancy, these questions about vaccines are a consequence of the great success of the vaccines – because they eliminated the diseases. The decline in visible cases has led to a loss of fear, and in many cases, respect for the devastating consequences of these illnesses.

The current climate has given space for anti-vaccine activists to amplify rare side effects while ignoring the profound benefits of immunization. Suspicion around well-established vaccines has even reached political figures like Robert F. Kennedy Jr., a longtime anti-vaccine advocate.

However for some families, the horrors of these once-common diseases remain a vivid reality. For them, every news report of a measles outbreak or rising whooping cough cases is a painful reminder of lives forever changed—and a plea to spare others from similar suffering.

Janith Farnham, 80, from Sioux Falls, recalls with clarity the moment she realized her newborn daughter Jacque wasn’t developing normally. Jacque was born with congenital rubella syndrome after Janith contracted the virus early in pregnancy, a time when the rubella vaccine wasn’t available.

"Things weren’t right," Janith said. Jacque was unresponsive to sound, resisted touch, and had a purring heart murmur that required early surgery. Today, Jacque is 60, living with numerous complications including deafness, diabetes, glaucoma, and arthritis. Despite these challenges, she maintains a close and affectionate bond with her mother, who still sees her nearly every day.

Janith, who once taught special education, knows firsthand the consequences of a disease now preventable with a routine shot. "It’s more than frustrating. I mean, I get angry inside," she said. "I know what can happen, and I just don’t want anybody else to go through this."

Patricia Tobin still remembers the scream of her mother the day her younger sister Karen collapsed in their home. It was 1970 in Miami, and Karen, only six, had contracted measles during an outbreak. The vaccine was available but not yet mandatory.

Tobin, then 19, had rushed Karen to the hospital, where she immediately fell into a coma and died of encephalitis. "We never did get to speak to her again," she said.

Today, vaccination is required for school entry in all U.S. states, but increasing exemptions are threatening herd immunity. The legacy of fraudulent studies falsely linking the MMR vaccine to autism has left a long shadow. Most states now fall below the 95% threshold needed to prevent measles outbreaks.

"I’m very upset by how cavalier people are being about the measles," Tobin said. "I don’t think that they realize how destructive this is."

Lora Duguay, 68, of Clearwater, Florida, has lived through polio not once, but twice. Her first encounter was at age three, when she was hospitalized and packed in ice. Doctors told her parents she would never walk again.

After extensive therapy, she regained mobility and led a full life until her 40s, when post-polio syndrome struck. Her condition worsened over time, but she found purpose through art. "Art gives me a sense of purpose," Duguay said.

Today’s polio vaccine is far more effective, and widespread use has all but eradicated the disease in the U.S. Thanks to herd immunity, even imported cases don’t spread. But Duguay’s story is a stark reminder of what could happen if vaccination rates drop.

Katie Van Tornhout, from Lakeville, Indiana, lost her daughter Callie Grace to whooping cough in 2010, just 37 days after her birth. Born premature but healthy, Callie started coughing a month in. Within days, she was gone.

Callie was too young for her own Tdap vaccine and was likely infected by someone who hadn’t had their booster. Her ashes rest in a small urn beside mementos and a plaster cast of her tiny foot.

Van Tornhout now shares her story widely and advocates for childhood immunizations through Vaccinate Your Family. "It’s up to us as adults to protect our children – that’s what a parent’s job is," she said. “I watched my daughter die from something that was preventable … You don’t want to walk in my shoes."

The resurgence of diseases like measles and whooping cough is a stark warning. Falling vaccination rates, fueled by misinformation and complacency, threaten to undo decades of public health progress. The consequences are not abstract—they are deeply personal for families who have lived through the suffering these diseases cause.

Experts note that if you’re not familiar with the disease, you don’t respect or even fear it. And therefore you don’t value the vaccine. The stories of Janith, Patricia, Lora, and Katie are a powerful reminder of what’s at stake.

Vaccines are among the greatest achievements of modern medicine, saving countless lives and sparing families untold grief. Yet, as memories fade, so does vigilance. The experiences of those who have suffered—and those who have lost—should serve as a call to action.

Disclaimer: This article includes story inputs and reporting from the Associated Press (AP) agency.

measles vaccine

whooping cough death

rubella pregnancy risk

polio survivor story

vaccine preventable diseases

vaccine hesitancy risks

childhood immunization stories

Before the era of widespread vaccination, infectious diseases cast a long and deadly shadow over American childhood. In 1900, nearly one in five children in the United States never reached their fifth birthday, with diseases like whooping cough, measles, rubella, and polio claiming millions of young lives or leaving survivors with lifelong disabilities. Over the next century, vaccines would transform this grim reality, virtually eradicating once-dreaded scourges and drastically reducing the toll of others. Yet, as immunization rates decline and vaccine hesitancy rises—even among public officials—these diseases are making a troubling comeback.The very success of vaccines has, paradoxically, bred complacency and skepticism. “This concern, this hesitancy, these questions about vaccines are a consequence of the great success of the vaccines – because they eliminated the diseases. In a time before vaccines, childhood illness often meant death. Infectious diseases like polio, measles, rubella, and whooping cough once swept across communities unchecked, claiming young lives and leaving others permanently disabled. In 1900, nearly one in five American children didn’t live to see their fifth birthday, and infectious disease was the primary cause but with the advent of vaccines, these illnesses were nearly eradicated.The widespread success of vaccines may ironically be their undoing. "This concern, this hesitancy, these questions about vaccines are a consequence of the great success of the vaccines – because they eliminated the diseases. The decline in visible cases has led to a loss of fear, and in many cases, respect for the devastating consequences of these illnesses.The current climate has given space for anti-vaccine activists to amplify rare side effects while ignoring the profound benefits of immunization. Suspicion around well-established vaccines has even reached political figures like Robert F. Kennedy Jr., a longtime anti-vaccine advocate.However for some families, the horrors of these once-common diseases remain a vivid reality. For them, every news report of a measles outbreak or rising whooping cough cases is a painful reminder of lives forever changed—and a plea to spare others from similar suffering.Janith Farnham, 80, from Sioux Falls, recalls with clarity the moment she realized her newborn daughter Jacque wasn’t developing normally. Jacque was born with congenital rubella syndrome after Janith contracted the virus early in pregnancy, a time when the rubella vaccine wasn’t available."Things weren’t right," Janith said. Jacque was unresponsive to sound, resisted touch, and had a purring heart murmur that required early surgery. Today, Jacque is 60, living with numerous complications including deafness, diabetes, glaucoma, and arthritis. Despite these challenges, she maintains a close and affectionate bond with her mother, who still sees her nearly every day.Janith, who once taught special education, knows firsthand the consequences of a disease now preventable with a routine shot. "It’s more than frustrating. I mean, I get angry inside," she said. "I know what can happen, and I just don’t want anybody else to go through this."Patricia Tobin still remembers the scream of her mother the day her younger sister Karen collapsed in their home. It was 1970 in Miami, and Karen, only six, had contracted measles during an outbreak. The vaccine was available but not yet mandatory.Tobin, then 19, had rushed Karen to the hospital, where she immediately fell into a coma and died of encephalitis. "We never did get to speak to her again," she said.Today, vaccination is required for school entry in all U.S. states, but increasing exemptions are threatening herd immunity. The legacy of fraudulent studies falsely linking the MMR vaccine to autism has left a long shadow. Most states now fall below the 95% threshold needed to prevent measles outbreaks."I’m very upset by how cavalier people are being about the measles," Tobin said. "I don’t think that they realize how destructive this is."Lora Duguay, 68, of Clearwater, Florida, has lived through polio not once, but twice. Her first encounter was at age three, when she was hospitalized and packed in ice. Doctors told her parents she would never walk again.After extensive therapy, she regained mobility and led a full life until her 40s, when post-polio syndrome struck. Her condition worsened over time, but she found purpose through art. "Art gives me a sense of purpose," Duguay said.Today’s polio vaccine is far more effective, and widespread use has all but eradicated the disease in the U.S. Thanks to herd immunity, even imported cases don’t spread. But Duguay’s story is a stark reminder of what could happen if vaccination rates drop.Katie Van Tornhout, from Lakeville, Indiana, lost her daughter Callie Grace to whooping cough in 2010, just 37 days after her birth. Born premature but healthy, Callie started coughing a month in. Within days, she was gone.Callie was too young for her own Tdap vaccine and was likely infected by someone who hadn’t had their booster. Her ashes rest in a small urn beside mementos and a plaster cast of her tiny foot.Van Tornhout now shares her story widely and advocates for childhood immunizations through Vaccinate Your Family. "It’s up to us as adults to protect our children – that’s what a parent’s job is," she said. “I watched my daughter die from something that was preventable … You don’t want to walk in my shoes."The resurgence of diseases like measles and whooping cough is a stark warning. Falling vaccination rates, fueled by misinformation and complacency, threaten to undo decades of public health progress. The consequences are not abstract—they are deeply personal for families who have lived through the suffering these diseases cause.Experts note that if you’re not familiar with the disease, you don’t respect or even fear it. And therefore you don’t value the vaccine. The stories of Janith, Patricia, Lora, and Katie are a powerful reminder of what’s at stake.Vaccines are among the greatest achievements of modern medicine, saving countless lives and sparing families untold grief. Yet, as memories fade, so does vigilance. The experiences of those who have suffered—and those who have lost—should serve as a call to action.Disclaimer: This article includes story inputs and reporting from the Associated Press (AP) agency.

why whooping cough, measles and rubella still haunt u.s. families, here's what vaccine hesitancy overlooks

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