Bringing your child home is just the beginning. Here's what you need to know about their health, growth, development and learning in the months and years ahead.
The paediatrician plays a vital role in the physical and emotional well-being of your child, setting them on the path to becoming a thriving, contributing member of society.

For most families, the paediatrician is the first point of contact - and the first source of reassurance — when a child is brought in for a medical check. Over time, this grows into a continuing relationship between the paediatrician and the parent. The medical community can also help adoptive and prospective parents dispel myths and address medical concerns around adoption.
This care and attention becomes even more important for children in the initial years after adoption, sometimes because of gaps in care during the gestational period, post-natal care, or time spent in an adoption home. Paediatricians who bring a child-centric approach, along with compassion and empathy for parents, make a real difference given the many unknowns and variables in the early adoption journey.
A complete general physical examination gives your paediatrician a clear picture of your child's health at the time of adoption, and forms the baseline for everything that follows.
Two screening tests are commonly used to check a child's hearing:
If medical documentation about the biological parents is available, it's worth focusing on:
| Area | What to Check |
|---|---|
| Birth history | Full term or preterm, vaginal or c-section delivery (and indication, if c-section), post-delivery complications such as jaundice or respiratory distress/ICU admission |
| Mother's obstetric history | Previous childbirths, history of congenital anomalies, history of abortions |
| Parents' medical history | Anaemia, thyroid or psychological disorders, teratogenic medication use, HBsAg/HIV status, familial diseases (sickle cell, haemophilia, thalassemia), blood groups, tuberculosis, asthma, diabetes, hypertension, seizure disorders, and breastfeeding history |
The best way forward is a complete, thorough head-to-toe examination of the child along with all the required blood investigations. On the immunisation front, a catch-up schedule can be followed based on the child's age, after which the usual immunisation guidelines apply.
Basic screening tests that should be done at the time of adoption:
Additional tests, including those recommended in high-risk areas:
Serological tests such as HIV and hepatitis screening are especially important in a country like India, where the prevalence of these infections is high. Consider performing these at the time of adoption if documentation is unavailable.
Understanding your child's vaccination status — and how to fill any gaps — is one of the first practical steps after adoption.
Catch-up immunisation is a blanket immunisation schedule given when vaccination records are unavailable, or when a child begins the immunisation process later than usual.
You can check the number of vaccines your child should have received by their age against the National Immunisation Schedule published by the Indian Academy of Paediatrics.
Immunisation is available at any primary, secondary or tertiary health care centre. Most hospitals and nursing homes with a paediatric facility are equipped for vaccination under the National Immunisation Schedule. That said, it's always better to go to a known paediatrician who can assess your child and make sure the process — and future follow-ups — stay simple and consistent.
Child development is the complete set of changes that carry a helpless newborn to a walking, talking child and, eventually, adult. In the usual sequence, this is a one-way process that unfolds largely on its own — provided the brain and body are supported, protected and given a good environment.
The challenge with adoption lies in providing that right support and environment, and then allowing the natural process to unfold. The intrauterine period and the earliest days after birth may not always have been ideal environments for adopted children — though, of course, the same can be true for biological children too. Fortunately, the brain has a remarkable ability to change, repair and rewire itself given enough time and space, at any point in life. This "neuroplasticity" is the key to developmental success, and harnessing it is something every parent — adoptive or otherwise — learns as they go along.
Physical: Nutritional gaps can leave a child underweight or stunted, with common deficiencies in iron, calcium and vitamins. The encouraging news is that nutrition is one of the easiest things to remedy — even months or years of malnutrition can recover in a matter of weeks to months with adequate care.
Developmental milestones: Both intrauterine and early-life environments matter for a child's development, and gaps here can show up as delays — most commonly in gross motor milestones (rolling over, head control, sitting, standing, walking) and in language, since language depends heavily on a consistent primary caregiver. Children in group-care settings often miss out on this one-on-one interaction, and in India, a change in the language spoken to the child around the time of adoption can add to the delay.
The good news: most of these delays can be rectified, even at later stages. The majority of adopted children catch up with their peers within months to years, and go on to reach the same developmental potential as any other child. What they need is opportunity and time — both of which lie in the hands of the parent. Development in an adopted child follows the same natural path as in biological children, just with a somewhat higher chance of initial delays that patience and support can close.
Red flag: No smile by 20 weeks
Red flags: Poor head control by 6 months; consistently preferring one hand while reaching; no sounds at all
Red flags: No attempt at sitting with support by 9 months; no attempt to crawl or move; no single syllables by 9 months
Red flags: No sitting by 10 months; no pulling to stand by first birthday; doesn't wave or follow instructions; no stranger anxiety or recognition
Red flags: Not walking by 18 months; can't point to common objects when asked; still mouthing objects; poor eye contact; no meaningful words by 18 months
Red flags: Fewer than 50 words by 2nd birthday; doesn't follow single-step directions or point to common objects/body parts; unable to scribble; toe-walking after 2nd birthday
Red flags: Fewer than 100 words by 3rd birthday; doesn't follow 2-step directions; no attempt at bowel control
Red flags: Not talking in sentences by 4th birthday; unable to draw lines/shapes; clumsiness, tremors or unsteadiness; poor pronunciation by 5th birthday; no bladder/bowel control; unable to manage self-care tasks; not interested in playing with other children; unable to sit in a classroom for 30 minutes by 5th birthday
A growth chart is used by paediatricians and other healthcare providers to track a child's growth over time, built from observing large numbers of typically-developing children.
Your child's height, weight and head circumference are compared to expected parameters for children of the same age and sex, to check whether growth is on track. Because children tend to maintain a fairly constant growth curve, these charts can also help predict expected adult height and weight — and any deviation from a child's established curve usually prompts further investigation.
Abnormal growth on a chart is only a sign of a possible problem — your doctor will determine whether it points to an actual medical issue, or simply needs watching over time.
Gaps in developmental milestones and nutritional benchmarks are common among children through adoption. These gaps vary from child to child — often wider in older children and those with special needs — but in time, they can be bridged and deficiencies circumvented.
Much depends on what the birth mother experienced during the gestational period and after delivery, since many come from economically disadvantaged circumstances. Understanding the extent of these gaps — especially within the "golden 1,000 days" from conception until the child turns two — is important.
Children may have minor to major deficiencies. Micronutrient deficiency refers to a lack of vitamins and minerals such as calcium, folate, iron, iodine, zinc, vitamin A, vitamin B12 and vitamin D (leading to rickets). Macronutrient deficiency refers to a lack of carbohydrates, protein and fat — the nutrients needed in larger amounts for normal growth — and can cause stunting, wasting and other childhood health complications.
Fortunately, most of this is treatable and within your control — nutritional gaps in adopted children are among the easiest challenges to bridge.
Catch-up growth is a faster-than-normal rate of weight and length gain that happens when a child receives more calories and protein at home. It occurs in most adoptees and is especially critical for severely malnourished children.
Refeeding syndrome refers to fluid and electrolyte disturbances that can occur when a child is given too many nutrients too quickly. To avoid this in severely malnourished children, consult a paediatrician or dietician before ramping up intake.
| Test | What It Checks |
|---|---|
| CBC & differential count | Decreased levels may indicate anaemia (iron, folate or B12 deficiency), chronic illness, lead poisoning or nutritional deficiency |
| Serum ferritin / transferrin receptor | Checks iron stores and cellular iron status — can detect deficiency before anaemia sets in |
| Thyroid Stimulating Hormone (TSH) | Tests for thyroid hormone deficiency, often linked to iodine deficiency |
| 25-hydroxy Vitamin D | Assesses vitamin D levels and risk of rickets |
| Stool test for ova & parasites | Screens for gut infections that can inhibit nutrient absorption if untreated |
| Serum zinc | Deficiency raises risk of infectious disease and atypical cognitive development |
| Vitamin B12 | Deficiency raises risk of neuropsychiatric and neurologic complications |
| Standard anthropometric measures | Height/length, weight and head circumference — maintaining growth matters more than reaching a specific percentile |
The best way to accelerate growth is by adding calories and protein to foods your child already wants to eat — every bite counts for slow or picky eaters.
These non-commercial, scientifically-backed recipes from the National Institute of Nutrition are inexpensive, easy to prepare, and effective at bridging protein-energy malnutrition.
| Mix | Ingredients | Nutrition (per 100g) |
|---|---|---|
| Davengere Mix | Equal parts ragi, roasted bengal gram powder, roasted groundnut powder and jaggery syrup | 14g protein, 400 kcal |
| Hyderabad Mix | Whole wheat (40g), bengal gram powder (16g), groundnuts (10g), jaggery (20g) | 11.3g protein, 330 kcal |
| Besan Panjiri | Equal parts bengal gram powder and wheat flour, with jaggery and ghee | 9g protein, 500 kcal |
| Shakti Aahar | Roasted wheat (40g), roasted gram (20g), roasted peanuts (10g), jaggery (30g) | 11.4g protein, 394 kcal |
Need guidance on your child's nutrition plan? Contact us at adoptpadme@gmail.com to speak with a specialist.
Differently-abled children are generally not the first choice of prospective adoptive parents — yet they are often the ones most in need of a loving, supportive family to reach their full potential.
A child with special needs is one who can benefit most from the individualised care and resources that adoptive parents can provide, more than an institution ever could. From a parent's point of view, every child is a source of happiness, love, meaning and learning — children with special needs are no exception.
| Physical | Mental / Developmental |
|---|---|
| Epilepsy / convulsions / seizures | Autism |
| Paralysis | Intellectual disability |
| Multiple sclerosis | Speech impairment |
| Neurological disorders | Conditions requiring psychiatric treatment |
| Severe learning disability |
Most academic learning takes place during school years, delivered by a teacher or facilitator. When a child shows large gaps in learning and understanding, it's worth examining where those gaps come from — and how to address them.
Specific Learning Disabilities (SLD) is an umbrella term describing several kinds of learning difficulties. SLD should not be confused with learning issues that stem from economic, cultural or social disadvantage, intellectual disability, delayed childhood milestones, emotional trauma or physical handicaps. Its underlying cause is neurologically-based processing difficulty in the brain, affecting basic academic skills like reading, spelling, math and writing. There is no single identifiable cause — most research points to a combination of genetics and environment. Importantly, children with SLD typically have average or above-average intelligence, but struggle to perform on tests and in the standard academic system.
A child who struggles is too often labelled lazy, diffident, or "dumb." The first step is realising that isn't so. A proper assessment — usually involving a paediatrician, special educator and psychologist or counsellor together — helps distinguish SLD from other conditions. The earlier this is done, the earlier a child can be helped with strategies to cope and close the gaps in learning.
There is no "cure" for SLD, because it isn't a disease — but remedial education is essential. This means teaching in the style that works best for each child, helping close skill gaps, and building strategies for independent functioning, all with the goal of minimising the effect on the child's social, emotional and intellectual life, now and as an adult.
SLD affects children across every background — economically privileged or disadvantaged, urban or rural, biological or adopted — and is now believed to be equally common in boys and girls. In children through adoption, some pre-adoptive history of stress, genetics or trauma may be unknown, which can make differential diagnosis more complex. That said, a child benefiting from the supportive home environment that adoptive parents typically provide is often well positioned to receive and respond well to remediation.
A food allergy happens when a person's immune system treats a substance — an allergen — as an inappropriate invader. Signs to watch for include:
Lactose intolerance happens when the body doesn't produce enough lactase, the enzyme that breaks down lactose in dairy products. It's rare in young children and usually develops after age 3, though it may persist for some children while others adjust.
You can meet your child's calcium needs with lactose-free or lactose-reduced milk, along with:
Vitamin D intake may also be inadequate in this case, so speak to your physician about supplementation.
PICA is the persistent eating of non-nutritious substances, often a sign of nutritional deficiency and potentially harmful to the child. It's common for young children to put non-food items in their mouths out of curiosity — sand being a typical example — but in children with PICA, that curiosity becomes a compulsion.
Commonly ingested items include sand, ice, paint flakes, glue, chalk, powders and soap; more dangerous items include glass, stones, metal objects and faeces. PICA is often linked to iron, calcium or zinc deficiency, and can also stem from worm infestation, developmental disorders, or psychosocial concerns.
Managing PICA: for some children, it resolves with simple behavioural strategies; others need a more advanced, professional approach. If symptoms persist beyond a month, consult your paediatrician. Helpful steps for parents include improving communication with your child, creating a "PICA box" of edible alternatives, and using positive reinforcement when your child avoids the behaviour.
Baby formula is the next best substitute for breast milk, and most milk-based formulas are designed to act as alternatives to it. Commonly available options in India include Similac Advance, Lactogen, Enfamil A+, Farex Stage 1 and Nutricia Dexolac.
When choosing a formula, check its form, the type of protein and carbohydrate it contains, and its full ingredient list. Choose one that dissolves easily in boiled water without leaving lumps, and always check with your paediatrician for milk allergies before starting. An iron-fortified, cow's-milk-based formula is generally recommended for the first 9–12 months. Always follow the packaging instructions carefully — adding more or less formula than directed can make an infant ill.
Iron is a mineral babies and children need for good health and development. Red blood cells contain haemoglobin, a protein that carries oxygen throughout the body, and the body needs iron to make it. Without enough iron, red blood cells become small and pale and can't carry enough oxygen to organs and muscles — this is anaemia.
Treatment depends on the type and severity of the deficiency. Consulting a physician is important to close the gaps caused by lack of nutrients — with the right treatment and diet plan, symptoms usually resolve over time.
Yes, some children find this difficult in the early stages. It's useful to consult a paediatrician or dietician to guide the transition, especially for children who were severely malnourished before adoption.
Our adoption-specialist paediatricians and counsellors are here to support you through every stage of your child's growth and development.
Contact Us Today