10 Minutes of Intensive Workout Can Trigger Powerful Anti-Cancer Effects: New Study

Credit: Fitsum Admasu

Those brief, intense workouts you’ve heard about that boost fitness might also help fight certain types of cancer by releasing molecules into the bloodstream that can spur DNA repair and inhibit cancer growth signals.

When embarking on an exercise routine for the new year, take heart that new research reveals that just 10 minutes of intense exercise could help fight cancer, too.

Short bursts of energetic activity can trigger rapid molecular changes in the bloodstream, shutting down bowel cancer growth and speeding up DNA damage repair, a new study has shown.

Researchers at Newcastle University have found that exercise increases the concentration of several small molecules in the blood—many linked to reducing inflammation, improving blood vessel function, and metabolism.

When these exercise-induced molecules were applied to bowel cancer cells in the lab, the activity of more than 1,300 genes was altered, including those involved in DNA repair, energy production, and cancer cell growth.

The findings, published in the International Journal of Cancer, help explain one way exercise can protect against bowel cancer: by sending molecular signals in the bloodstream that influence the activity of genes that govern tumor growth and genome instability.

The study is another step forwards in the fight against bowel cancer and further strengthens the importance of staying active.

‘Opens door to new treatments’

“What’s remarkable is that exercise doesn’t just benefit healthy tissues, it sends powerful signals through the bloodstream that can directly influence thousands of genes in cancer cells,” said Dr. Sam Orange, Senior Lecturer in Clinical Exercise Physiology at Newcastle University, who led the study.

“It’s an exciting insight because it opens the door to find ways that mimic or augment the biological effects of exercise, potentially improving cancer treatment and, crucially, patient outcomes.

“In the future, these insights could lead to new therapies that imitate the beneficial effects of exercise on how cells repair damaged DNA and use fuel for energy.”

The Newcastle researchers found that exercise boosted the activity of genes that support mitochondrial energy metabolism, enabling cells to use oxygen more efficiently.

At the same time, genes linked to rapid cell growth were switched off, which could reduce the aggressiveness of cancer cells, and exercise-conditioned blood promoted DNA repair, activating a key repair gene called PNKP.

The study involved 30 volunteers, male and female aged 50–78, all overweight or obese (a risk factor of cancer) but otherwise healthy.

After completing a short, intense cycling test lasting approximately 10 minutes, researchers collected blood samples and analysed 249 proteins. As many as 13 proteins increased after exercise, including interleukin-6 (IL-6), which helps repair the DNA of damaged cells.

“These results suggest that exercise doesn’t just benefit healthy tissues, it may also create a more hostile environment for cancer cells to grow,” said Dr. Orange, a Clinical Exercise Physiologist at The Newcastle Hospitals NHS Foundation Trust.

“Even a single workout can make a difference. One bout of exercise, lasting just 10 minutes, sends powerful signals to the body.”

“It’s a reminder that every step, every session, counts when it comes to doing your best to protect your health.”

Bowel cancer is the 4th most common cancer in the UK, after breast, prostate and lung—and it’s estimated that physical activity reduces the risk by approximately 20%.

It can be done by going to the gym, playing sports or through active travel such as walking or biking to work, but also as part of household tasks or work like gardening or cleaning.In the future, researchers plan to test whether repeated exercise sessions produce lasting changes and explore how these effects interact with standard cancer treatments like chemotherapy and radiotherapy. 10 Minutes of Intensive Workout Can Trigger Powerful Anti-Cancer Effects: New Study
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Tiny Baby Born With Hands Smaller Than a Fingertip is Now Home After a Year–And Developing Normally

Preemie baby Gabriel Golden at Vanderbilt NICU-SWNS

A premature baby, born so tiny his hand was smaller than his dad’s fingertip, is finally home and healthy after a year in the hospital.

Gabriel Golden was born weighing one pound in September 2024 after just 22 weeks gestation.

He endured nearly a year in the Vanderbilt NICU in Nashville, Tennessee, battling chronic lung disease and multiple infections before his parents Caroline and Garreth were finally able to bring their son home three months ago.

Little Gabriel still faces respiratory challenges, but is thriving developmentally.

“It was amazing that somehow, even though his finger was so small, I could feel his grip,” said his father Garreth.

“The strength those tiny fingers held left me speechless.”

Caroline started hemorrhaging 14 weeks into the pregnancy, and for a harrowing eight weeks, doctors warned daily that she could miscarry at any moment.

She recalls bleeding constantly while on bed rest and stuck at home. When at 18 weeks, Caroline’s water broke. The preemie wasn’t considered viable, so the couple waited in limbo until 22 weeks, when Caroline was hospitalized with hopes of buying more time for their son’s development.

The medical team presented stark statistics—and the numbers were devastating: a less than five percent survival rate, with greater than 90 percent odds of neurological problems, heart defects, and vision or hearing loss.

“The biggest thing is that their lungs are barely developed,” Caroline said.

At 22 weeks and four days, Caroline went into labor during an emergency situation that put both their lives at risk. Garreth watched helplessly as medical staff rushed his wife to surgery.

“They’re having her sign paperwork that she could die from the surgery,” recalled Garreth, who spent a lot of time “not knowing what to think or what to do.”

Against all odds, Gabriel was able to use the breathing tube and survived.

Gabriel Golden is finally home -SWNS

But he still had to battle severe broncho-pulmonary dysplasia—a chronic lung disease that left his lungs scarred and rigid. The couple said goodbye to their son on three separate occasions during his first six weeks of life.

Multiple pneumonia infections also set him back, and doctors eventually determined he would need a tracheostomy to survive.

Throughout the ordeal, Garreth traveled three hours each way to his job, continuing to work so they could pay their bills and Caroline tried to maintain a bedside vigil.

Their church community provided financial support, and four primary nurses at Vanderbilt became like family during Gabriel’s extended stay. “We couldn’t have done it without them,” Caroline said.

“One nurse specifically was with us for nine and a half months. I personally couldn’t have done it without her.”

Gabriel Golden family at Vanderbilt NICU-SWNS

Caroline, who had always dreamed of being a mother, says the experience transformed the couple’s faith and perspective on life.

“I was thrust into a situation where my faith was the only thing I had to cling to. Now it’s stronger than I ever thought it could be.”

While Gabriel is home, he still requires a tracheostomy and faces respiratory challenges, but there’s good news, too.

“By the grace of God, Gabriel is completely developmentally appropriate, and has no brain issues,” Caroline told SWNS news agency.

“Other than his lungs, his body is in wonderful working condition.”

The experience gave Garreth a new perspective when he walked through the children’s hospital and saw other families facing their own battles.“As complex as Gabriel is—and as precious as his life is—you walk into Vanderbilt’s Children’s Hospital, and it hits you like a wave of gratitude when you see some of the things going on with these children.” Tiny Baby Born With Hands Smaller Than a Fingertip is Now Home After a Year–And Developing Normally
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Experts warn about risks of cosmetic face fillers


People who have cosmetic filler injections in their face should be warned of the risk of a dangerous complication involving blocked arteries that can lead to skin loss and even blindness due to damaged blood flow, say experts.

Researchers used ultrasound to study 100 cases of filler injections that had gone wrong, BBC News reported.

Clinics are now being advised to carry out ultrasounds before giving dermal fillers in the face, to avoid harming any nearby arteries.

Lead researcher Dr Rosa Sigrist says that, although uncommon, such "vascular occlusion" events - where the filler is injected into or too close to blood vessels - can be devastating because they can cause tissue death and facial deformity if not treated.

Dermal fillers are injectable substances, commonly used to target wrinkles and smooth or "rejuvenate" the skin.

Sometimes they are used to contour or shape the nose or lips.

Areas around the nose are particularly risky injection sites, says Dr Sigrist, because nasal blood vessels communicate with some very important parts of the head.

Damage to these vessels can cause severe complications including skin damage, blindness and stroke, she explains.

Dr Sigrist's team, from the University of São Paulo in Brazil, studied filler-related vascular complications in 100 patients across four radiology centers (two in Brazil, one in Colombia and one in Chile), one dermatology centre in the Netherlands and one plastic surgery centre in the US between May 2022 and April 2025.

Her work will be presented at a medical conference - the annual meeting of the Radiological Society of North America - this week.

In just under half the cases, ultrasound scans showed absent blood flow to small blood vessels that connect superficial arteries to deep ones in the face.

And in a third of cases, blood flow was absent in major blood vessels.

To avoid complications in the first place, she advises clinics to use ultrasound to plan where to inject.

If complications do arise, ultrasound can guide where to treat.

"If injectors are not guided by ultrasound, they treat based on where the clinical findings are and inject blindly," Dr. Sigrist says.

"But if we can see the ultrasound finding, we can target the exact place where the occlusion occurs."

Rather than flooding the area with a drug called hyaluronidase to dissolve the filler, clinicians can do guided injections that use less hyaluronidase and provide better treatment results, she says. Source: https://www.panorama.am/
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Fussy Girl Overcomes Vegetable Phobia and Now Loves Brussels Sprouts Thanks to Eating Disorder Specialist

Emie Williams at home -SWNS

A fussy five-year-old girl has overcome her phobia of vegetables and now loves Brussels sprouts–just in time for her mother’s Christmas dinner.

Emie Williams would scream and cry if her mom, Hayley, tried to give her anything except crackers, french fries, or other beige-colored foods.

It meant family meals were fraught with conflict—Emie wanting different food and refusing to even taste hot dinners.

“She’d just refuse to eat any vegetable or any meat. We took her for check ups and health visits for advice but they just said give her what she wants because it’s probably a phase.”

But Hayley suspected that she may have ARFID (Avoidant/Restrictive Food Intake Disorder), believing she had “all the signs”.

Emie’s energy levels dipped, and she would get really tired at the end of the day.

“I explained (to doctors) that if I don’t give her what she wanted then she wouldn’t eat.”

Last month, Emie had a routine health check-up and a blood test revealed she had erratic sugar levels, so Hayley and her husband took their daughter to the hospital where doctors warned them Emie was in danger of developing diabetes unless she changed her diet.

In desperation, Hayley decided to take drastic action and contacted David Kilmurry, who specializes in obsessive eating conditions.

“We were pretty desperate when we contacted David but the results have been amazing,” the mother-of-3 from Coventry, England, told the SWNS news agency.

After a series of two-hour sessions, Emie now counts 30 foods that she willingly eats. Her favorite is Brussel sprouts, which she even enjoys raw.

Emie Williams eating her new favorite food, Brussel sprouts – SWNS

Due to her age, Emie was not hypnotized, but David, a cognitive behavioral hypnotherapist, sat with the youngster and gradually encouraged her to try different foods.

Hayley attended all the sessions and just watched Kilmurry at work.

“He’d do magic tricks and talk to Emie to gain her trust, and then brought out different foods.

“Slowly, she tried more and more until she was really enjoying apples and oranges.

“She’s really taken with Brussel sprouts, especially eating them raw. I can’t wait to see her enjoying her first ever Christmas dinner with all the trimmings.”

David, who runs practices in Coventry and London, said: “ARFID isn’t taken seriously enough.“It doesn’t just go away.” Fussy Girl Overcomes Vegetable Phobia and Now Loves Brussels Sprouts Thanks to Eating Disorder Specialist
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Diets Rich in Tea, Coffee, Berries and Nuts Linked to Better Long-term Heart Health in New Study

Credit: Julian Hochgesang

People who regularly consume polyphenol-rich foods and drinks, such as tea, coffee, berries, cocoa, nuts, whole grains, and olive oil, may have better long-term heart health, according to a new study.

The research, led by King’s College London, found that those with higher adherence to polyphenol-rich dietary patterns had lower predicted cardiovascular disease (CVD) risk.

Polyphenols, natural compounds found in plants, are linked to a variety of health benefits, including improved heart, brain, and gut health.

Researchers followed 3,100 adults from the TwinsUK cohort for over a decade and, for the first time, the researchers also analyzed a large number of metabolites in the urine that are produced when the body breaks down polyphenols.

They found that diets rich in specific groups of polyphenols were linked to healthier blood pressure and cholesterol profiles, contributing to lower CVD risk scores.

These biomarkers confirmed that higher levels of polyphenol metabolites—especially those derived from specific groups of polyphenols, flavonoids, and phenolic acids—had lower cardiovascular risk scores. They also had increased HDL cholesterol, also know as ‘good cholesterol’.

The study, published recently in BMC Medicine, used a newly developed polyphenol dietary score (PPS) to capture intake of 20 key polyphenol-rich foods commonly consumed, ranging from tea and coffee to berries, olive oil, nuts, and whole grains.

This score showed stronger associations with cardiovascular health than estimates of total polyphenol intake, likely because it captures overall dietary patterns rather than individual compounds.

This finding suggests that considering the whole diet provides a more accurate picture of how polyphenol-rich foods work together to support long-term heart health.

“Our findings show that long-term adherence to polyphenol-rich diets can substantially slow the rise in cardiovascular risk as people age,” said Professor Ana Rodriguez-Mateos, Professor of Human Nutrition at King’s College London.

“Even small, sustained shifts towards foods like berries, tea, coffee, nuts, and whole grains may help protect the heart over time.”

Dr. Yong Li, first author of the study, said the research provides “strong evidence that regularly including polyphenol-rich foods in your diet is a simple and effective way to support heart health.”

Additionally, while cardiovascular risk naturally increases with age, higher polyphenol intake was associated with a slower progression of risk over the 11-year follow-up period. Diets Rich in Tea, Coffee, Berries and Nuts Linked to Better Long-term Heart Health in New Study
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Amputee Thrilled With Hand Transplant is Now Left-handed: ‘Feels so incredible, as if I’ve had it my whole life’

Amputee Kim Smith pre- and post-transplant – SWNS

A woman who lost all her limbs after contracting an infection and getting sepsis while on vacation in Spain eight years ago is now thrilled after receiving a new hand.

Kim Smith and her doctors were trying for a double hand transplant during the 14-hour surgery, but the right hand had to be abandoned. Despite that, she’s ‘over the moon’ and has declared herself now to be left-handed.

“I was right-handed, but now I just do everything left-handed and it came naturally,” said the 64-year-old. “I have even written with my left hand.”

“I am absolutely over the moon about my new arm, because it feels so incredible, almost as if I’ve had it my whole life.”

The woman from Buckinghamshire, England, even joked how her husband Steve was going to buy her new wedding and engagement rings because the fingers of her new hand were slightly bigger.

“I’ve gone full-on glass-half-full now—just grateful that at least one transplant worked,” Kim told SWNS news agency.

“The hand itself is perfect—and beautiful—and looks like it’s meant to be mine.”

Kim Smith after hand transplant – SWNS

Kim described how she was overjoyed when she first saw her new hand, and has been amazed how quickly she’s been able to use it.

“I honestly didn’t expect to be able to do so much so soon, even though motor skills can take a year or so to come back—four years until I get full feeling.

“I’m already picking things up and managing to clean my teeth, do my hair, and put on my makeup.

“The day after the operation, when they finally unbandaged the arm and let me very gently move my fingertips, it felt absolutely incredible because I could feel myself moving it, and from that moment it has just gone from strength to strength.”

“I was most excited to brush my teeth and feed myself again because holding a toothbrush or a fork—and actually being able to use it—felt like the loveliest little miracle after being told for so long that ‘it might never work’.
Kim Smith – SWNS

“The first time I picked up a glass of wine with no problem and then held an ice cream without dropping it, I was in disbelief at how far I’d already come.”

Kim has pretty much given up on her dream of having two hands, but is happy with her lovely new left hand.

“While I never say never about a right-hand transplant, I’m 64, now and it would mean waiting another year even to be considered.”

“I’m honestly just happy to have this one for the rest of my life because it’s already giving me so much independence.

“I don’t know who the donor was, but I’ve written to their family to say how grateful I am, knowing they’re grieving and (they) might not reply.

“Meanwhile I’m regaining strength little by little, able to hold my phone, type on it, and wear my Pandora bracelet again.”

Kim’s transplant was carried out by Professor Simon Peter Jabir Kay OBE at Leeds Teaching Hospitals NHS Trust, who commented on the surgery.

“Hands are so much more than mechanical parts, they play an irreplaceable role in human communication and connection, and so it is always an honor to be able to carry out such a life-changing surgery.

“Kim faced unexpected and severe complications during surgery which meant we could only successfully complete one hand transplant, not the double replacement we had hoped to carry out.”

“Nonetheless her recovery has been remarkable.”

“It is heart-warming to see how much her life has changed with her new hand, thanks to the generosity of her donor and their family.”Kim’s journey of overcoming tragedy is the subject of The Gift, a powerful new Sky News documentary released a week ago. You can watch it here on YouTube, or watch the trailer below… Amputee Thrilled With Hand Transplant is Now Left-handed: ‘Feels so incredible, as if I’ve had it my whole life
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Study decodes how females and males experience depression

(Photo: AI generated image/IANS)

New Delhi, (IANS) A team of Australian researchers has decoded important genetic differences in how females and males experience depression for the first time, an advance that could pave the way for more targeted intervention and treatments.

In the study, published in Nature Communications, scientists found that genetic factors contribute more to depression risk in females than in males.

The team from QIMR Berghofer Medical Research Institute discovered about twice as many genetic "flags" for depression in the DNA of females as they did in that of males.

"We already know that females are twice as likely to suffer from depression in their lifetime than males," said Dr. Brittany Mitchell, Senior Researcher at QIMR Berghofer's Genetic Epidemiology Lab.

"And we also know that depression looks very different from one person to another. Until now, there hasn't been much consistent research to explain why depression affects females and males differently, including the possible role of genetics," Mitchell added.

The team identified about 7,000 changes in the DNA that could cause depression in both sexes, and about a further 6,000 DNA changes (a total of 13,000) that could cause depression in females only.

Researcher Dr. Jodi Thomas said the study also pinpointed how depression could show up differently for females and males.

The team found that the genetic factors linked to depression overlap more with those associated with metabolic traits in females.

"We found some genetic differences that may help explain why females with depression more often experience metabolic symptoms, such as weight changes or altered energy levels."

For the largest global study of its kind, the scientists analysed DNA from hundreds of thousands of people with and without depression, including around 130,000 females and 65,000 males with depression.

The changes in DNA that the scientists have identified are genetic differences people are born with, not changes that happen because of life experiences.

Traditionally, most drug trials and therapies are tested on males, but Drs Mitchell and Thomas hope their work will also translate to a greater clinical understanding of female depression.

"Unpacking the shared and unique genetic factors in males and females gives us a clearer picture of what causes depression -- and opens the door to more personalized treatments," Dr. Thomas said.The findings highlight the importance of considering sex-specific genetic influences in studying depression and other health conditions. Study decodes how females and males experience depression | MorungExpress | morungexpress.com
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RSV infections in babies may raise asthma risk later, vaccine offers hope: Study


(Photo: AI generated image/IANS)

New Delhi, (IANS) An international team of scientists has found compelling evidence that early-infancy infection with respiratory syncytial virus (RSV) significantly increases the risk of developing childhood asthma.

The risk is especially higher in children with a family history of allergy or asthma.

The study, published in the Science Immunology journal, suggests that protecting newborns against RSV could substantially reduce asthma cases later in life.

"Childhood asthma is a complex disease with many contributing factors," said Prof. Bart Lambrecht from VIB (the Flanders Institute for Biotechnology) and Ghent University in Belgium.

"We found that early-life RSV infection and genetic allergy risk interact in a very specific way that pushes the immune system toward asthma. The encouraging news is that this process can be prevented," Lambrecht added.

The team, including researchers from Denmark, combined population-wide health registry data from all Danish children and their parents with controlled laboratory experiments. They found that early viral infection and inherited allergy risk amplify one another.

Infants who experience severe RSV infections in the first months of life show an increased likelihood of immune cells overreacting to common allergens, such as house dust mites.

This effect is dramatically intensified when asthma or allergy runs in the family, as allergen-specific antibodies passed from parents to the newborn further heighten sensitivity.

Importantly, the team found that when newborns were protected from RSV in experimental models, these harmful immune shifts did not occur -- and asthma development was prevented.

"With RSV prevention now becoming widely accessible, we have an opportunity to improve long-term respiratory health, not just prevent RSV hospitalisations," said Prof. Hamida Hammad (VIB-UGent).

"This is not just a laboratory insight. It's a message that should help parents choose RSV prevention with confidence," Hammad added.

Maternal vaccination during the third trimester of pregnancy and passive immunisation of newborns with long-acting antibodies are being introduced in many countries. Yet despite their strong ability to prevent RSV hospitalisations, uptake remains inconsistent."This is a moment where policy, science, and paediatricians can come together," Lambrecht said. “If preventing RSV infection also reduces asthma risk, the benefits for families and health systems could be enormous.” RSV infections in babies may raise asthma risk later, vaccine offers hope: Study | MorungExpress | morungexpress.com
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Worried after sunscreen recalls? Here’s how to choose a safe one

Katie Lee, The University of Queensland

Most of us know sunscreen is a key way to protect areas of our skin not easily covered by clothes from excessive ultraviolet (UV) radiation.

But it’s been a rough year for sunscreens.

In June, testing by Choice identified 16 products on Australian shelves that don’t provide the SPF protection they claimed.

In July, the Therapeutic Goods Administration (TGA) released a review recommending the amount of certain chemical ingredients allowed in sunscreens should be lowered.

Since then, several other sunscreens have been recalled or are under review, either due to manufacturing defects or concerns about poor SPF cover.

All this has left many of us feeling confused about which sunscreens are safe, effective and do what they say on the label.

Here’s what you need to know so you can stay safe this summer.

The good news first

There’s very little evidence sunscreens cause cancer and plenty of evidence they prevent skin cancer.

This is vital in Australia, where two in three people will get skin cancer at some point in their lives.

One randomised controlled trial in Queensland, run over four and a half years between 1992 and 1996, asked 1,621 people to either use sunscreen every day or continue their usual use (usually one or two days a week or not at all).

It found using sunscreen every day reduced the numbers of squamous cell carcinomas by 40%, compared to the group that didn’t change their habits. Ten years after the study, the number of invasive melanomas was reduced by 73% in the daily sunscreen group.

Significantly, this study was conducted in the 90s using SPF 16 sunscreen. Modern sunscreens are expected to routinely provide SPF 30+ or 50+ protection.

Companies should provide the SPF levels they’re advertising. But this research shows even sub-par sunscreen (by modern standards) provides significant protection with daily use.

Making sure SPF claims stack up

In Australia, the TGA regulates how SPF is assessed in sunscreens, but doesn’t do the testing itself. Instead, companies perform or outsource the testing, which must be done on human skin, and provide the TGA with their results.

But when Choice independently tested 20 Australian sunscreens, it found 16 did not meet the SPF factor on the label.

An ABC investigation pinpointed two potential sources of the problems: a poor quality base ingredient manufactured by Wild Child Laboratories, and suspicious SPF testing data from Princeton Consumer Research, which many of the brands relied on.

The TGA has since recommended that people stop using 21 products that contain the Wild Child base, listed here.

What about the chemical ingredients?

The TGA regularly reviews scientific research to make sure Australian sunscreens keep up with advances in safety and effectiveness. To be sold in Australia, sunscreens must use active ingredients from a specific list, limited at maximum concentrations.

July’s safety review found evidence that two permitted ingredients – homosalate and oxybenzone – can cause hormone disruptions in some animals exposed to high doses for a long time. These doses were far higher than someone would be exposed to from sunscreen – even at the maximum usage – thanks to the TGA’s ingredient limits.

Still, chemical risks are managed strictly. The amount absorbed during consistent, high-dose sunscreen use, year-round, must be less than 1% of the dose known to cause problems in animals.

The new results suggest that absorption could go over this “margin of safety”. So the TGA has recommended the amount allowed be reduced.

Homosalate and oxybenzone are not being banned, and you don’t need to throw out sunscreens containing these ingredients.

But if the idea of using them makes you nervous, you can check ingredient lists and buy sunscreens without them.

What should I look for in a sunscreen?

When buying a sunscreen there are four non-negotiables. It must have:

  • 30+ or 50+ SPF
  • broad spectrum UV protection (filters both UVB and UVA rays)
  • water-resistant (for staying power in Australia’s sweaty climate)
  • TGA approval mark on the packaging (“AUST L” followed by a number).

Sunscreen only works if you use it, so choose a sunscreen you like enough to actually wear.

There are milks, gels and creams, unscented, matte, tinted and many other varieties. Since faces are often the most sensitive, many people use a specialty sunscreen for the face and a cheaper, general one for the rest of the body.

Spray-on sunscreen is not recommended, however, because it’s too hard to apply enough.

You need to apply more than you think

Sunscreen works best when you apply it 20 minutes before you go into the sun, and reapply every two hours and after swimming, sport or towel drying.

How you apply it affects how well it works. You need about one teaspoon each for:

  • your face and neck
  • back
  • chest and abdomen
  • each arm and leg.

It’s also common to miss your ears, hands, feet and back of the neck – don’t forget these either.

Sunscreen usually lasts two to three years stored below 30°C, so keep an eye on the use-by date and follow any instructions about shaking before use.

If the sunscreen seems to have separated into thinner and thicker layers even after shaking, the ingredients providing SPF may not be mixed evenly throughout and might not work properly.

But remember – sunscreen isn’t a suit of armour

If you’re planning to be out in the sun for more than a few minutes at a time, slip on sun-protective clothing and slap on a hat. Use sunscreen to protect the areas you can’t easily cover.

Slide on sunnies and seek shade where possible to complete your sun-protection practice for a burn-free summer.

The Conversation

Katie Lee, Postdoctoral Researcher, Dermatology Research Centre, The University of Queensland

This article is republished from The Conversation under a Creative Commons license. Read the original article.

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Normal Thyroid Function in Pregnancy Linked to Lower Autism Risk in Large Study

Getty Images for Unsplash+

Persistent hormone disruption during pregnancy trimesters appears to increase the likelihood of autism in children, shows a new large cohort study.

Women who experience continuing thyroid hormone irregularities throughout pregnancy may face a higher chance of having a child diagnosed with autism, according to a study released in The Journal of Clinical Endocrinology & Metabolism.

Thyroid hormones supplied by the mother play an important role in fetal neurodevelopment. When these hormones become disrupted during pregnancy, previous work has linked the imbalance to atypical brain development and a higher likelihood of autism spectrum disorder (ASD).

Autism is a multifaceted condition that shapes how an individual communicates, interacts socially, and interprets the world.

Untreated Multi-Trimester Imbalance Carries Higher Risk

“We found that while adequately treated chronic thyroid dysfunction was not associated with increased autism risk in offspring, ongoing imbalance across multiple trimesters was,” said Idan Menashe, Ph.D., of the Ben-Gurion University of the Negev in Israel.

“These findings underscore the need for routine monitoring and timely adjustment of therapy to maintain normal thyroid hormone levels throughout pregnancy.”
A Clear Pattern

The research tracked more than 51,000 births between January 2011 and December 2017
and reported that mothers with persistent thyroid hormone imbalance across their pregnancy had an increased likelihood of having children with autism.

A total of 4409 (8.6%) of the mothers showed abnormal thyroid function.

The authors also documented a dose-response pattern, meaning the risk rose as the number of affected trimesters increased.No funding was received for this study.Normal Thyroid Function in Pregnancy Linked to Lower Autism Risk in Large Study
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Exercising in mid and later life can reduce dementia risk – new study

For years, scientists have known that moving our bodies can sharpen our minds. Physical activity boosts blood flow to the brain, enhances neuroplasticity and reduces chronic inflammation. These processes are believed to protect against cognitive decline, including dementia.

Yet despite decades of research, major questions have remained unresolved.

Does exercising at any age help reduce your risk of dementia? Or only when you’re young? And what if you have a higher genetic risk – can exercising still make a difference?

New research from the long-running Framingham Heart Study in the United States, published today, offers some of the clearest answers to date. Their findings support what many clinicians already tell patients: exercise helps.

But the study also offers new insight into the potentially protective effect of staying active at the age of 45 and over – even for those with a certain genetic predisposition to dementia.

What did the study examine?

The new research draws on data from 4,290 participants enrolled in the Framingham Heart Study Offspring cohort. This study began in 1948, when researchers recruited more than 5,000 adults aged 30 and over from the town of Framingham, Massachusetts, to investigate long-term risk factors for cardiovascular disease.

In 1971, a second generation (more than 5,000 adult children of the original cohort, and their spouses) were enrolled, forming the Offspring cohort. This generation then had regular health and medical assessments every four to eight years.

In the new study, participants self-reported their physical activity. This included incidental activity such as climbing stairs as well as vigorous exercise.

Participants first reported these activities in 1971, and then again over several decades. Based on the age at which each participant was first evaluated, they were grouped into three categories:

  • young adulthood (26–44 years): assessed in the late 1970s

  • midlife (45–64 years): assessed during the late 1980s and 1990s

  • older adulthood (65 years and over): assessed in the late 1990s and early 2000s.

To examine how physical activity influences dementia risk, the researchers looked at how many people developed dementia in each age group and at what age they were diagnosed.

Then they considered physical activity patterns within age groups (low, moderate, high) to see if there was any link between how much exercise people did and whether they developed dementia.

They also looked at who had a known genetic risk factor for Alzheimer’s disease, the APOE ε4 allele.

Research has long shown moving our bodies can sharpen our minds. Jonathan Borba/Unsplash

What did they find?

Over the follow-up period, 13.2% (567) of the 4,290 participants developed dementia, mostly in the older age group.

This is quite high compared with other long-term longitudinal dementia studies and with Australian rates (one in 12 or 8.3% Australians over 65 currently have dementia).

When researchers examined physical activity levels, the pattern was striking. Those with the highest levels of activity in midlife and later life were 41–45% less likely to develop dementia than those who had the lowest levels of activity.

This was the case even after adjusting for demographic factors that increase dementia risk (such as age and education) and other chronic health factors (such as high blood pressure and diabetes).

Interestingly, being physically active during early adulthood did not influence dementia risk.

A key innovation of this study was its examination of the genetic risk factor, the APOE ε4 allele. This analysis suggests something new:

  • in midlife, higher physical activity lowered dementia risk only in people who didn’t carry this genetic predisposition

  • but in later life, higher physical activity lowered dementia risk in both carriers and non-carriers.

This means for people genetically predisposed to dementia, staying active later in life may still offer meaningful protection.

How significant are these results?

The findings largely reinforce what scientists already know: exercise is good for the brain.

What sets this study apart is its large sample, multi-decade follow-up, and its genetic analysis across different life periods.

The suggestion that midlife activity benefits some individuals differently depending on their genetic risk, while late-life activity benefits nearly everyone, may also add a new layer to public health messaging.

But there were some limitations

Physical activity was largely self-reported in this study, so there is a possibility of recall bias. We also do not know what type of exercise brings the best benefits.

Dementia cases in the youngest age group were rather rare too, so the small sample limits how definitively we can make conclusions about early adulthood.

The cohort is also predominantly of European ancestry and share environmental factors as they come from the same town, so this limits how much we can generalise the findings to more diverse populations.

This is particularly important given global inequities in dementia risk and diagnosis. Knowledge about dementia and risk factors also remains low in ethnically diverse groups, where it is often still seen as a “normal” part of ageing.

What does this mean for us?

The takeaway is refreshingly simple though: move more, at any age. At this stage we know there are more benefits than harm.

The Conversation

Joyce Siette, Associate Professor | Deputy Director, The MARCS Institute for Brain, Behaviour and Development, Western Sydney University

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November 19 is World COPD Day



World Chronic Obstructive Pulmonary Disease Day is observed on November 19.

Chronic obstructive pulmonary disease (COPD) is the third leading cause of death globally, yet the condition is relatively unknown and often underprioritized and underfunded. This is despite the fact that over 3.5 million people die from COPD each year - equivalent to the cumulative death toll from a plane crashing with 400 passengers every hour, WHO reports.

The theme for this year’s World COPD Day is “Short of breath, think COPD”, aligned with the common symptoms of cough, difficulty breathing, wheezing and tiredness which have a major impact on those who live with the condition. The day aims to raise awareness about COPD and promote early diagnosis and effective management. Earlier diagnosis and treatment results in better clinical outcomes, including improvement in symptoms, lung function, and quality of life.

Armenia recorded a COPD mortality rate of 21 per 100,000 people in 2021, with men disproportionately affected. Male mortality reached 32.6 per 100,000, the sixth-leading cause of death, while the rate for women was 14.2, ranking tenth. Overall disease prevalence stands at 6.2%.

Smoking remains the country’s dominant risk factor. A 2022 survey found that 22.2% of Armenians smoked, including nearly half of all men but just 1.7% of women. An estimated 60.9% of COPD-related deaths were attributed to smoking alone.

As in many countries, early-stage COPD in Armenia often presents with few or atypical symptoms, leading to delayed diagnosis and treatment. custom title
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Stem cell therapy may help reduce heart failure after a heart attack

(Photo: AI generated image/IANS)

New Delhi, (IANS) Patients with weak heart function who receive stem cell therapy shortly after a heart attack are less likely to suffer heart failure, according to a study.

Heart failure can occur after a heart attack when the heart muscle is extensively damaged, weakening its ability to pump blood effectively.

This can be a sudden complication (acute heart failure) or a long-term one. Symptoms include trouble breathing, fatigue, swelling in the legs, and an irregular heartbeat.

The clinical trial, published by the BMJ, suggests stem cell therapy may be a valuable add-on procedure for this particular group of patients after a heart attack to prevent subsequent heart failure and reduce the risk of future adverse events.

An international team of researchers, including those from Queen Mary University of London in the UK, set out to assess the impact of delivering stem cells directly into coronary arteries (known as intracoronary infusion) after a heart attack on the development of heart failure over three years.

“The results suggest that this technique may serve as a valuable adjunctive procedure after myocardial infarction to prevent the development of heart failure and reduce the risk of future adverse events," the team said.

The trial included 396 patients (average age 57-59 years) with no previous heart conditions at three teaching hospitals in Iran. They had all experienced a first heart attack (myocardial infarction).

Of these, 136 patients in the intervention group received an intracoronary infusion of allogenic Wharton's jelly-derived mesenchymal stem cells within 3-7 days of their heart attack in addition to standard care.

The remaining 260 control group patients received standard care alone.

Compared with the control group, intracoronary infusion of stem cells was associated with reduced rates of heart failure (2.77 vs. 6.48 per 100 person years), readmission to hospital for heart failure (0.92 vs. 4.20 per 100 person years), and a combined measure of cardiovascular death and readmission for heart attack or heart failure (2.8 vs. 7.16 per 100 person years).

The intervention did not have a statistically significant effect on readmission to the hospital for heart attack or death from cardiovascular disease.However, by six months, heart function in the intervention group showed a significantly greater improvement compared with the control group, said the researcher, while also urging the need for additional trials confirming the finding. Stem cell therapy may help reduce heart failure after a heart attack | MorungExpress | morungexpress.com
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Should I take a magnesium supplement? Will it help me sleep or prevent muscle cramps?

Nial Wheate, Macquarie University and Wai-Jo Jocelin Chan, UNSW Sydney; University of Sydney

Magnesium supplements are everywhere – lined up on pharmacy shelves and promoted on wellness blogs and social media.

Maybe you have a friend or family member who swears a daily tablet will help everything, from better sleep to alleviating muscle cramps.

But do you really need one? Or it is just marketing hype?

What is magnesium and why do we need it?

Magnesium is an essential metal the body needs to make and operate more than 300 different enzymes.

These enzymes build protein, and regulate muscle and nerve function, help in the release of energy from our food, and help to maintain blood function. The body doesn’t produce magnesium so we need to get it from external sources.

The government recommends a daily magnesium dose of 310–420 mg a day for adults and 30–410 mg for children, depending on age and sex.

This is easily met through a good diet. Foods rich in magnesium include nuts and seeds, whole grains, seafood, meat, legumes and green leafy vegetables.

You can even get some of your magnesium needs met through dark chocolate. It has 146 mg per 100 g of chocolate.

How do I know if I’m deficient?

People at risk of experiencing magnesium deficiency include people with restricted diets, gastrointestinal problems such as Crohn’s and coeliac diseases, type 2 diabetes, and alcohol dependence. Older adults are also more likely to be deficient.

You will only need a magnesium supplement if you show signs of low magnesium. One of the most common signs is muscle spasms and twitches. Other symptoms to look out for include low appetite, nausea and vomiting, or your heart beating abnormally.

Magnesium deficiency can be properly diagnosed by a blood test ordered by your doctor. If you need this test, it’s covered by Medicare.

What conditions can it help?

Commercially available magnesium supplements have been promoted to prevent muscle cramps, manage insomnia and help with migraines.

While magnesium deficiency is linked to muscle cramps, the cause of most muscle cramps is unknown.

And the current evidence does not demonstrate that magnesium supplements can prevent muscle cramps in older adults.

There is conflicting data as to whether the use of magnesium helps with sleep. One study reported magnesium was able to reduce the time for a person to fall asleep by 17.4 minutes while others didn’t show an effect.

For migraines, the most recent research suggests taking 122-600 mg of magnesium supplements daily for 4–24 weeks may decrease their frequency and severity.

Are magnesium supplements safe?

Magnesium supplements are generally well tolerated.

However, they can cause gastrointestinal discomfort such as nausea, abdominal cramping and diarrhoea. Magnesium causes diarrhoea by drawing water into the intestine and stimulating movement in the gut.

It is possible to take too much magnesium and you can overdose on it. Very large doses, around 5,000 mg per day, can lead to magnesium toxicity.

Most of the research investigating the clinical use of magnesium focuses on magnesium in oral formulations.

What other formulations are available?

As magnesium is a small metal ion, it can pass through skin – but not easily.

Magnesium bath salts, patches and topical cream-based formulations may be able to raise your blood magnesium levels to some extent.

But due to the amount needed each day, tablets and foods are a better source.

Things to watch out for when taking magnesium

Commercially available magnesium products can vary widely in dose, formulation and cost. Magnesium supplements have between 150 to 350 mg of the metal per tablet. Your required dose will depend on your age and sex, and whether you have any underlying health problems.

Magnesium supplements sometimes contain other vitamins and minerals, such as vitamins C and D, and the metals calcium, chromium and manganese. So it’s important to consider the total quantities if you’re taking other vitamins and supplements.

Many magnesium supplements also include vitamin B6. While this vitamin is important for supporting the immune system, high intakes can it can cause serious health issues. If you’re already taking a B6 supplement, a magnesium supplement that also includes it can put you at risk.

What if you’re considering supplements?

If you think you might be deficient in magnesium, speak to your doctor who can order a blood test.

If you suffer from migraines, cramps, or poor sleep, talk to your doctor or pharmacist who can advise on and monitor the underlying cause. It may be that a change in lifestyle or an alternative treatment may be more appropriate for you.

If you do decide to take a magnesium supplement, check you won’t be taking too much of any other vitamin or mineral. A pharmacist can help select a supplement that suits you best.The Conversation

Nial Wheate, Professor, School of Natural Sciences, Macquarie University and Wai-Jo Jocelin Chan, Pharmacist and Lecturer, UNSW Sydney; University of Sydney

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Never Too Late to Start Eating the MIND Diet That May Prevent Dementia: New Study of 90,000 People

Monika Grabkowska for Unsplash+

It’s never too late to start eating better to prevent dementia, according a new analysis of research involving 90,000 adults.

People over the age of 45 who followed a dietary pattern known as the MIND diet were “significantly” less likely to develop Alzheimer’s disease or related forms of dementia, said the University of Hawaii scientists.

The MIND diet stands for Mediterranean Intervention for Neurodegenerative Delay, and was developed by the late Martha Clare Morris, ScD, a Rush University nutritional epidemiologist. It combines the traditional Mediterranean diet with the blood pressure-lowering DASH diet (Dietary Approaches to Stop Hypertension).

It includes proven ‘brain-healthy’ foods such as leafy green vegetables, berries, nuts, fish, and olive oil.

The study found that the MIND diet had a stronger and more consistent risk reduction relationship with dementia than other ‘healthy’ diets for the majority of racial groups in the study.

Participants who improved their adherence to the diet the most over time showed the greatest pattern of risk reduction.

Overall, participants who scored higher for MIND adherence at the start of the study had a 9% lower risk of dementia, with an even greater reduction, of around 13%, among those who identified as African American, Latino or White.

The beneficial relationship was seen similarly among younger and older groups, which suggests that there are benefits to adopting the diet at any age.

“Our study findings confirm that healthy dietary patterns in mid to late life, and their improvement over time. may prevent Alzheimer’s and related dementias,” said Dr. Song-Yi Park, Associate Professor at the University of Hawaii at Manoa.

“This suggests that it is never too late to adopt a healthy diet to prevent dementia.”

Dr. Park and her colleagues analyzed data from more than 90,000 American adults who provided information about their diet, starting in the 1990s.

The participants were between 45- and 75-years-old at the outset, and more than 21,000 developed Alzheimer’s or related dementias in the years that followed.

The results also showed that people who improved their adherence to MIND over 10 years—including those who didn’t follow the diet closely at first—had a 25% lower risk of dementia compared to those whose adherence declined.

Dr. Park said that trend was consistent across different ages and racial groups.

However, the protective relationship between a healthy diet and dementia was not as apparent among Asian Americans and even less so for Native Hawaiians.

“A tailored approach may be needed when evaluating different subpopulations’ diet quality,” said Park, who added that further studies could help clarify those patterns.Dr. Park presented the findings at the annual meeting of the American Society for Nutrition in Orlando, Florida, on June 2. Never Too Late to Start Eating the MIND Diet That May Prevent Dementia: New Study of 90,000 People
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Is it healthier to only eat until you’re 80% full? The Japanese philosophy of hara hachi bu

Aisling Pigott, Cardiff Metropolitan University

Some of the world’s healthiest and longest-living people follow the practice of hara hachi bu — an eating philosophy rooted in moderation. This practice comes from a Japanese Confucian teaching which instructs people to only eat until they’re around 80% full.

More recently, it’s been gaining attention as a strategy for weight loss. But while hara hachi bu might emphasise eating in moderation and stopping before you’re full, it shouldn’t really be as seen as a method of dietary restriction. Rather, it represents a way of eating that can help us learn to have awareness and gratitude while slowing down at mealtimes.

Research on hara hachi bu is limited. Previous studies have evaluated the overall dietary patterns of those living in regions where this eating philosophy is more commonplace, not the “80% rule” in isolation.

However, the available evidence does suggest hara hachi bu can reduce total daily calorie intake. It’s also associated with lower long-term weight gain and lower average body mass index (BMI). The practice also aligns with healthier meal-pattern choices in men, with participants choosing to eat more vegetables at mealtimes and fewer grains when following hara hachi bu.

Hara hachi bu also shares many similar principles with the concepts of mindful eating or intuitive eating. These non-diet, awareness-based approaches encourage a stronger connection with internal hunger and satiety cues. Research shows both approaches can also help reduce emotional eating and enhance overall diet quality.

Hara hachi bu may also have many advantages that go beyond losing weight.

For instance, hara hachi bu‘s focus on awareness and eating intuitively may offer a gentle and sustainable way of supporting long-term health changes. Sustainable health changes are far easier to maintain in the long-term. This may improve health and prevent weight regain, which can be a risk for those who lose weight through traditional diet approaches.

The ethos of hara hachi bu also makes perfect sense in the context of modern life and may help us develop a better relationship with the food we eat.

Evidence suggests that around 70% of adults and children use digital devices while eating. This behaviour has been linked to higher calorie intake, lower fruit and vegetable intake and a greater incidence of disordered eating behaviours including restriction, binge eating and overeating.

As a dietitian, I see it all the time. We put food on a pedestal, obsess over it, talk about it, post about it – but so often, we don’t actually enjoy it. We’ve lost that sense of connection and appreciation.

Being more aware of the food we eat and taking time to taste, enjoy and truly experience it as hara hachi bu emphasises, can allow us to reconnect with our bodies, support digestion and make more nourishing food choices.

Trying hara hachi bu

For those who might want to give hara hachi bu or taking a more mindful and intuitive approach to improve their relationship with food, here are a few tips to try:

1. Check in with your body before eating

Ask yourself: Am I truly hungry? And if so, what kind of hunger is it — physical, emotional, or just habitual? If you’re physically hungry, denying yourself may only lead to stronger cravings or overeating later. But if you’re feeling bored, tired, or stressed, take a moment to pause. Giving yourself space to reflect can help prevent food from becoming a default coping mechanism.

2. Eat without distractions

Step away from screens and give your meal your full attention. Screens often serve as a distraction from our fullness cues, which can contribute to overeating.

3. Slow down and savour each bite

Eating should be a sensory and satisfying experience. Slowing down allows us to know when we’re satiated and should stop eating.

4. Aim to feel comfortably full, not stuffed

If we think of being hungry as a one and being so full you need to lie down as a ten, then eating until you’re around “80% full” means you should feel comfortably satisfied rather than stuffed. Eating slowly and being attuned to your body’s signals will help you achieve this.

5. Share meals when you can

Connection and conversation are part of what makes food meaningful. Connection at meal times is uniquely human and a key to longevity.

6. Aim for nourishment

Ensure your meals are rich in vitamins, minerals, fibre and energy.

7. Practice self-compassion

There’s no need to eat “perfectly”. The point of hara hachi bu is about being aware of your body – not about feeling guilty over what you’re eating.

Importantly, hara hachi bu is not meant to be a restrictive eating approach. It promotes moderation and eating in tune with your body – not “eating less”.

When viewed as a means of losing weight, it risks triggering a harmful cycle of restriction, dysregulation and overeating – the very opposite of the balanced, intuitive ethos it’s meant to embody. Focusing solely on eating less also distracts from more important aspects of nutrition – such as dietary quality and eating essential nutrients.

This practice also may not suit everyone. Athletes, children, older adults and those living with illness often have higher or more specific nutritional needs so this eating pattern may not be suitable for these groups.

While often reduced to a simple “80% full” guideline, hara hachi bu reflects a much broader principle of mindful moderation. At its core, it’s about tuning into the body, honouring hunger without overindulgence and appreciating food as fuel — a timeless habit worth adopting.The Conversation

Aisling Pigott, Lecturer, Dietetics, Cardiff Metropolitan University

This article is republished from The Conversation under a Creative Commons license. Read the original article.

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Childbirth and Breastfeeding Can Reduce Breast Cancer Risk Shows New Study

– credit Leighann Blackwood

Scientists in Australia, which endures the highest rates of breast cancer in the world, have presented multiple lines of evidence to suggest that breastfeeding and childbearing reduces a woman’s risk for developing breast cancer.

The scientists started by first pointing out that as far back as 300 years ago, people noted that women who didn’t have children—nuns, in this case—suffered from the highest rates of breast cancer in society.

More modern research confirmed these early observations, but the mechanism behind why that might be remained hidden. While previously hypothesized to be the work of hormonal shifts, the answer now seems clear: breastfeeding works on the human immune system.

“Pregnancy and breastfeeding leave behind long-lived protective immune cells in the breast and the body, and these cells help to reduce risk and improve defense against breast cancer, particularly triple-negative breast cancer,” Professor Sherene Loi, a medical oncologist and lead author on the research, told ABC News Au.

Triple-negative breast cancer, one of several forms of the disease, is characterized by an absence of the three receptors commonly found on breast cancer cells. It’s common in younger women but is one of the less-common forms of the cancer, as well as the most lethal.


Cancer risk is determined by many factors, but Loi felt confidant is ascribing the decision by many modern women around the world to delay pregnancy and shorten, or even abandon breastfeeding, as contributing to cancer risk.

A study published last week in Nature found that women who had children and breastfed had more T cells in their breast tissue, which “act like local guards, ready to attack abnormal cells that might turn into cancer,” Loi said.

T cells are those which are activated to fight cancer in the Nobel Prize-winning treatment known as CAR-T cell therapy, and these were found to be more plentiful in the breast tissue of women who breastfed or had children, and that these elevated T cell counts were conserved for years and years after the mother had stopped breastfeeding.

To provide additional controls, Professor Loi and her co-authors performed a test with mice, implanting cancerous cells in the mammary fat of animals that had never reared offspring, that were rearing them, or who had had and finished rearing them.


Group 2 showed smaller tumor growth with a higher T cell count, while group 3—those who had reared and weened pups—showed the smallest tumors. To continue their tests, the scientists removed the T cells from the mammary tissue, and the cancer began to grow and spread unabated.

Lastly, the study presented an analysis on 2 papers totaling 1,000 women with triple-negative breast cancer to see if the effect in mice was replicated in humans.


“What we found is that women who had breastfed did better than those who had not breastfed, and their tumors actually had more immune cells … suggesting there was ongoing immune activation and regulation from the body against their breast cancer,” Professor Loi told ABC.

Though quantifying this protective effect is very nuanced, it seems that every child a woman has reduces her risk for breast cancer by 7%, and each 5 months of breastfeeding reduces it by an additional 2%.These are substantial differences when the average rate of breast cancer incidence is about 1 in 8 women Childbirth and Breastfeeding Can Reduce Breast Cancer Risk Shows New Study
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7 ways to teach little kids about body safety before they can talk

Danielle Arlanda Harris, Griffith University

Families with young children are yet again reeling after this week’s Four Corners investigation into abuse in the early childhood sector.

The program identified almost 150 childcare workers who had been convicted, charged, or accused of sexual abuse and inappropriate conduct.

System-wide changes are needed to improve standards and safety in the early childhood sector. But parents may also be wondering what they can do in the home to teach their kids about body safety.

There is increasing awareness of how to talk to children about body safety. This includes teaching kids that adults should not ask them to keep secrets and to tell a trusted adult if something feels wrong.

But what about babies and younger children who have not yet learned to talk?

According to Swiss psychologist Jean Piaget, children under two can understand language and even communicate before they develop speech. It is never too early to teach them about body autonomy, normalise safety, and model trustworthiness in relationships.

How can parents and caregivers do this?

1. Use the correct words

When you’re talking to a child about their body, you may want to use “baby talk”.

But it is important to use the correct anatomical words for their genitals, the same way that we teach them about other parts of the body.

This reduces shame and normalises body boundaries. It also ensures children grow up being able to describe any experiences clearly if there is a problem.

2. Narrate what you are doing

We teach older children that people should not touch their penis, vagina, or bottom.

But obviously for younger children, parents and carers need to touch their genital areas at nappy changes.

When changing a nappy, you can talk to little children in straightforward language and narrate what you’re doing in simple and easy steps. This is so they understand what a “normal” nappy change looks like.

For example,

I’m going to pick you up now. We need to change your nappy. We change your nappy when it’s dirty. First, I’m going to get a new nappy out of the drawer. Now I’m going to take off your pants. Remember, we only touch your bottom when we need to clean it.

3. Would you like to go to Tickletown?

You can normalise consent around touching from the beginning.

For example, teach consent around tickling. Practice using language that invites them to respond: “Would you like to go to Tickletown? Would you like me to tickle you?”

Then teach and demonstrate “yes/no” or “happy/sad” with a smile/frown, or thumbs up/thumbs down.

As they get older this can develop into having a safe word or modelling safe touch and unsafe touch.

4. Respect ‘push-away’ body language

Even very young children can send clear messages when they don’t want to be touched or held.

Where possible, respect their “push-away” body language such as pushing back, turning away, wriggling to get down, or arching their back. This teaches them they have autonomy of their bodies.

You can say things like: “Do you want to be put down? Your body belongs to you”.

5. Don’t force affection

Family and friends may be eager to hug or kiss your child, especially if they don’t see them often.

Resist the temptation to force your child to hug or kiss adults (“go on, give Grandad a kiss”) – even if it is a special occasion or visit. This teaches children about body boundaries and lets them know they can make decisions about their own bodies

6. What if a child doesn’t want a nappy change?

The “my body, my rules” message can be complicated when a child does not want a bath or when they don’t feel like having their nappy changed.

If you meet resistance during these times, calmly explain and narrate what you are doing and why. It will help form a foundation for them to understand healthy and necessary touching and recognise if someone is touching them inappropriately.

For example,

we need to have a bath to wash off all the dirt from the park. Let’s put some soap on your feet where they went in the sandpit.

7. Recognise nonverbal signs of distress

Preverbal children communicate through gestures and behaviour. Parents can learn to recognise nonverbal cues that might indicate signs of general distress.

In preverbal children such signs might include increased meltdowns or tantrums, withdrawal, unexplained genital pain or redness, changes in appetite, regression in toileting or sleeping, sudden fear or dislike of people or places, and even sudden mood changes or changes in personality.

Learning these signs can improve parent-child interactions and make it easier to recognise early signs of abuse.


If this article has raised issues for you, or if you’re concerned about someone you know, you can call 1800 Respect on 1800 737 732, Lifeline on 131 114, Kids Helpline on 1800 55 1800, or Bravehearts (counselling and support for survivors of child sexual abuse) on 1800 272.The Conversation

Danielle Arlanda Harris, Associate Professor in Criminology and Criminal Justice, Griffith University

This article is republished from The Conversation under a Creative Commons license. Read the original article.

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