Parents often put parental controls for their kids and keep an eye on their media consumption at all times but often neglect their own usage by a mile. When you are telling kids to not do certain things and then proceed to do it yourself, you send a hypocritical message to kids. They start believing that you are making up rules and they are not that important, because if they were you yourself would’ve been following it! While you may not think that your media usage should be your kid’s business, a new study shows that it has a direct effect on your kids. Not just their mentality, but also what your screen hours show them that the internet is a safe place where they can explore whatever content they want. It is very easy for kids to override the age rule and get access to mature content, which lead to them consuming these videos and media from an early age! A new study looked at how parents' phone use might affect whether their kids see inappropriate content. Researchers found that when parents spend a lot of time on their phones and don't have clear rules about media use at home, their kids are more likely to watch R-rated movies or play video games meant for adults. The study talked to over 10,000 kids aged 12 and 13.

What Did The Study Reveal?

A recent study published in the journal BMC Pediatrics has revealed a potential link between parents' phone habits and their children's consumption of inappropriate content. The researchers wanted to learn more about how parents can help their young teens with media use. They explained that while there's advice for younger kids and older teens, there's not much for this age group. These young teens are in a tricky stage, they're not little kids anymore, but they're not quite teenagers either. The study wanted to see how what parents do and the rules they make affect what kind of content young teens are exposed to.

Parents answered questions about their own phone use, like how often they try to limit their screen time around their kids. The kids also answered questions about how often they watch R-rated movies or play mature video games. The study found that the more time parents spent on their phones, the more likely their kids were to consume mature content. Things like using phones during meals or in bedrooms seemed to be especially linked to kids seeing this type of content.

Why Should Parent’s Mobile Usage Be A Concern?

Experts say it's important for parents to be aware of their own phone habits, because kids often copy what they see. They suggest that parents should "practice what they preach", if they make a rule about no phones at the dinner table, they should follow it too. Experts also recommend that families create a media plan together with clear rules, like limiting screen time during meals and before bed, talking about what they see online, not using screen time as punishment, and using it as a reward for good habits. Basically, the study shows that what parents do with their phones can really influence what their kids are doing online.

How You Can Reduce Your Screen Time?

First, see how much you're using them and set small goals to cut back. Make some areas and times in your house phone-free, like during meals and before sleep, this is a great chance to connect with your family. Turn off notifications you don't need and find fun things to do instead of being on your phone, maybe even things your family can do together. Put your phone away so it's not always tempting and think about why you're picking it up. Tell your family you're trying to use your phone less, and maybe they'll join you! If it's tough, think about taking a break from all screens for a bit. It takes time, so be patient with yourself and enjoy the extra time you have with your family. This not only benefits you but also sets a positive example for your children.

The birth of a child is often filled with joy, hope, and dreams for the future. But for some families, that journey also begins with an unexpected diagnosis — Down syndrome.

According to health experts, while the news can initially feel overwhelming, understanding the condition and accessing the right support can help children with Down syndrome lead fulfilling and meaningful lives.

Down syndrome, also known as Trisomy 21, is a genetic condition caused by the presence of an extra copy of chromosome 21. Instead of the usual 46 chromosomes, individuals with Down syndrome are born with 47. This additional chromosome can affect physical growth, learning, speech, and overall development.

Speaking to HealthandMe, Neurologist Dr. Rahul Chawla from ISIC Multispeciality Hospital says families often struggle emotionally after hearing the diagnosis, but understanding that Down syndrome is a genetic condition — and not a disease — can gradually help them move toward acceptance.

He noted that children with Down syndrome may learn and develop differently, but with proper medical care, therapy, emotional support, and inclusive education, many go on to study, work, play sports, and live independently with support.

How The Condition Is Diagnosed

Dr. Sweta Singla, Consultant and Head of Movement Disorder & Neurology at Manipal Hospitals, Dwarka, explained to HealthandMe that the condition can often be identified during pregnancy through screening tests such as blood tests and ultrasounds, and confirmed through diagnostic procedures like amniocentesis. After birth, genetic testing helps confirm the diagnosis.

The experts emphasized that early intervention plays a major role in improving quality of life.

"Physiotherapy, occupational therapy, and speech therapy started during infancy can help children develop communication and motor skills more effectively," Dr. Sweta said.

The experts warned that regular medical check-ups are important because children with Down syndrome may be more prone to conditions such as congenital heart defects, thyroid disorders, hearing difficulties, and vision problems.

Every Child Is Different

Children with Down syndrome present distinctive facial features, low muscle tone, delayed developmental milestones, short stature, and mild to moderate intellectual disability. Hearing and vision problems may also occur.

However, all children with Down syndrome have their own personalities, strengths, talents, and emotions, Prof. (Dr.) Brig. Ashok Saxena, Director of Neonatology and Paediatrics at ShardaCare–Healthcity, told HealthandMe.

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"Each child with Down syndrome is different – they all have their personalities, strengths, talents, and feelings," he said, adding that while some may take longer to learn speech, movement, or social skills, many are affectionate, emotionally expressive, and socially engaging.

Dr Ashok noted that a diagnosis of Down syndrome can be a very emotional and stressful time for parents.

"It can also be frightening, confusing, and filled with a lot of questions. It is important to keep in mind, though, that a diagnosis of Down syndrome doesn't mean a child's life ends. Children with Down syndrome can live a full and happy life with a loving family and appropriate medical treatment, emotional support, early therapies, and an inclusive environment," he said.

Breaking Stigma And Building Inclusion

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Inclusive education and social acceptance are also considered essential.

The doctors noted that supportive teachers, accessible opportunities, and community awareness can help children gain confidence and independence.

Families are also encouraged to seek counselling and support groups to cope with emotional stress, fear, guilt, or social stigma that may accompany the diagnosis.

Medical professionals say that awareness around Down syndrome has improved significantly over the years, alongside advancements in healthcare and therapies that have enhanced life expectancy and quality of life.

Pediatric hematological malignancies, specifically leukemia and lymphoma, constitute some of the most frequently observed forms of cancer in pediatrics.

Pediatric cancers make up almost 7.9% of all cancers that are diagnosed in India, according to figures released by the Indian Council of Medical Research (ICMR).

Leukemia is responsible for almost half of all pediatric cancers in children under 14 years old.

Why Early Detection Matters: Common Symptoms

Healthcare professionals assert that early detection is essential in enhancing treatment success. Nevertheless, the symptoms are often mild and can be easily misdiagnosed as other childhood conditions.

Parents need to carefully observe any symptoms such as recurring fever, fatigue, susceptibility to infections, inexplicable bruising, and gum and nose bleeds. Pain in bones and joints, swelling in the lymph nodes, rapid weight loss, pale complexion, and protracted weakness are some other red flags that must not be overlooked.

Parents usually think these symptoms are associated with infections during the changing season or lack of nutrients in the body; however, if such symptoms do not subside within two weeks, medical attention is vital.

How Blood Cancer Affects The Body

The origins of blood cancer are found in bone marrow, causing problems with blood cell development. Symptoms can include anemia, which causes a low hemoglobin level, as well as low platelet levels and immune problems.

According to experts, a child suffering from blood cancer may also experience symptoms like fatigue and poor appetite.

Awareness Can Save Lives

Fortunately, good progress has been made in terms of survival rates for pediatric blood cancers through early diagnosis and new treatment techniques.

Research and professional opinions indicate that a significant number of kids who suffer from ALL, which is the most prevalent type of blood cancer among children, are able to enter long-lasting remission.

The importance of awareness among parents cannot be understated. Not every fever and bruise indicates cancer; however, symptoms that are seen are inexplicable and must always be taken into consideration. It is critical to consult an expert on time; this will definitely make a difference in treatment and recovery.

Many people carry the thalassemia gene without knowing it because they may not have any symptoms. A simple carrier screening test before pregnancy can help couples understand risks and make informed decisions while planning parenthood.

Importance of Genetic Screening

Parenthood planning today is not only about financial preparation or healthy lifestyle changes, but also about understanding genetic health risks that can impact the child’s future. And one such condition that tends to go unnoticed is thalassemia carrier status.

Did you know? Many individuals discover they are carriers only after facing difficulties during pregnancy or after the birth of a child with thalassemia major.

What Is Thalassemia?

Thalassemia is an inherited blood disorder that affects the production of hemoglobin, the protein in red blood cells that carries oxygen throughout the body. People who are carriers usually live normal and healthy lives and may not experience major symptoms. Because of this, many remain unaware of their carrier status for years.

However, it becomes a matter of concern when both partners are carriers of the thalassemia gene. In such cases, there is a huge risk that the child may inherit thalassemia major, a severe condition that may require lifelong blood transfusions, regular hospital visits, medications, and continuous medical care.

Why Thalassemia Often Goes Undetected

These are some of the challenges faced by families: So, challenges are that the thalassemia carrier status is often detected very late. Mild tiredness or anemia may be ignored or mistaken for iron deficiency, and many will not seek help.

So, couples do not consider genetic testing before marriage or pregnancy because they feel healthy and have no family history of the disease. When a child is born with thalassemia major, families may face stress, anxiety, repeated hospital visits, financial burden, and long-term treatment responsibilities. The condition can also affect the child’s growth, immunity, and overall quality of life.

The Need For Awareness And Early Action

This is why screening is important for couples: Carrier screening is a simple blood test that helps identify whether a person carries the thalassemia gene. If one partner tests positive, the other partner is advised to get tested as well.

Early screening before pregnancy helps couples understand their risks and explore available options with proper guidance. Thalassemia carrier screening is a small step that can make a major difference in parenthood planning.

Increasing awareness and encouraging timely testing can help families make informed decisions and reduce the burden of severe thalassemia in future generations. So, it is imperative to go for timely screening as advised by the expert and improve the quality of life.