World Breastfeeding Week (WBW), held in the first week of August every year, is a global campaign supported by the World Health Organisation and UNICEF and many Ministries of Health and civil society partners on the protection, promotion and support of breastfeeding. This initiative was started in 1992 to encourage mothers to breastfeed their children and build a support community for new mothers who face any difficulties in breastfeeding.

Why Did We Need An Awareness Week?

Gynaecologist, obstetrician and founder of Baby Soon Fertility and IVF Center, Dr Jyoti Bali with 26 years of experience says, “A reason why some mothers stopped breastfeeding was because of the increased marketing of formula as a convenient solution compared to breastfeeding.”

Experts agree that women undergo physical changes in their bodies during their pregnancy and while breastfeeding too, however, these have been exaggerated. “Breastfeeding can lead to temporary changes in breast size and shape, but these changes are typically normal and revert to baseline after weaning. Perceptions about breastfeeding causing long-term body changes are often unscientific or exaggerated,” says Dr Rao.

These were some of the reasons why women stopped breastfeeding and thus an initiative like World Breastfeeding Week was started. This also aims to highlight the health benefits to the mother and the child on breastfeeding.

Benefits of Breastfeeding on Mother

Rao says that for the mother, it helps in faster postpartum recovery, reduces the risk of certain cancers, and can help with postpartum weight loss.

“Breast Feeding helps the mothers to shed their pregnancy weight more quickly because the production of milk requires the burning of calories,” agrees Dr Bali.

Other health benefits to mothers are postpartum healing, bonding with the baby and a decrease in the risk of ovarian cancer, mentions Dr Bali.

Breastfeeding Benefits on Baby

There are also nutritional values that help a preterm baby in his or her development. “For example, breast milk's higher protein content makes it easier for premature babies to absorb and digest than formula, which encourages better weight gain. Premature babies often have specific nutritional needs due to their early birth. Breast milk provides a tailored balance of proteins, fats, and carbohydrates that support their rapid growth and development. The composition of breast milk adjusts to meet the changing needs of a preterm infant, including higher levels of certain nutrients,” says Dr Goel.

Dr Bali also points out that breast milk contains antibodies, probiotics and DHA and ARA, a kind of fatty acids that are required for brain development. Thus, a baby can benefit a great deal from breastfeeding.

Health Risks When Not Breastfeeding

Poor breastfeeding practices in infancy and early childhood, resulting in malnutrition, contribute to impaired cognitive and social development, poor school performance and reduced productivity in later life.

Sarwa points out that psychological factors like stress, anxiety, postpartum depression, poor latch due to anatomical issues or improper positioning, and other medical conditions are the common reasons for this. “Identification and management of the specific cause, appropriate counselling by a healthcare provider, support (emotional and workplace both) and alternative feeding options,” he says.

Unable To Breastfeed Your Child? Here is What You Can Do

Do not be worried about its safety, Dr Rao says that donated milk is screened, pasteurised, and distributed to ensure safety and nutrition.

Are You a Working Mother?

“Purchasing a superior electric breast pump can increase the effectiveness of the procedure. Maintaining a consistent pumping schedule—ideally, every three to four hours—helps keep the milk supply steady. Pumped milk can be refrigerated for up to four days if stored in sterile containers or bags that have been labelled with the date and time. Milk can be frozen and thawed for extended storage,” suggests Dr Goel.

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.

"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

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.