Understand the diagnosis fully
We take time to explain the condition, its implications, and the range of possible outcomes – so you can make decisions from a place of understanding, not confusion.
Receiving a diagnosis of a fetal anomaly can be overwhelming. You may have many questions, fears, and decisions to make – all while navigating the medical system. Fetal anomaly counseling provides a dedicated, compassionate space to understand your baby's condition, explore your options, and create a plan that honours your values and your family's needs.
Our counseling is provided by a fetal medicine specialist with deep experience in supporting families through complex diagnoses. We take time to explain the medical facts in clear, understandable language – what the condition means, what the prognosis is, and what options are available for testing, management, and care. We also address the emotional and practical aspects: how to cope, who to involve, and how to prepare for the future.
At Amytri, we believe that every family deserves not just accurate information, but genuine support. We coordinate with genetic counselors, neonatologists, pediatric surgeons, and mental health professionals to ensure you have access to a full multidisciplinary team. You will never have to face this alone.
When you receive a fetal diagnosis, the way you receive the news and the support you receive afterward can profoundly affect your emotional wellbeing and your ability to make the best choices for your family.
We take time to explain the condition, its implications, and the range of possible outcomes – so you can make decisions from a place of understanding, not confusion.
We help you build a realistic, step‑by‑step plan – from additional testing to delivery and neonatal care – so you are prepared and in control.
We provide a compassionate space to express your fears, ask difficult questions, and receive support – not just medical advice, but genuine care for your emotional wellbeing.
Our fetal anomaly counseling is not a one‑size‑fits‑all approach – it is personalised to your unique situation, values, and needs.
We break down complex medical information – what the condition is, how it develops, what it means for your baby's health, and what the long‑term outlook may be. We use visual aids and clear language to ensure you fully understand.
We review all test results – including imaging, NIPT, amniocentesis, or CVS – and discuss the genetic basis of the condition, the likelihood of recurrence, and the implications for future pregnancies.
We explore all available pathways: prenatal interventions (if any), timing and mode of delivery, neonatal intensive care, surgical options, and palliative or supportive care. We help you weigh risks and benefits.
We connect you with a team of specialists – neonatologists, pediatric surgeons, genetic counselors, and mental health professionals – so you have all the expertise you need in one coordinated network.
We provide a safe, non‑judgmental space to express grief, fear, anger, or hope. We can connect you with counselling services, support groups, and resources to help you cope.
We help you think through difficult decisions – about further testing, pregnancy continuation or termination, delivery preferences, and postnatal plans – respecting your values and cultural beliefs.
Your obstetrician or fetal medicine specialist refers you. We gather all your medical records, images, and test results to prepare for a comprehensive discussion.
We review your case thoroughly, often with the multidisciplinary team, to ensure we have the most accurate understanding of the condition and its implications.
We meet with you (and your partner) in a private, unhurried setting. We explain the condition, explore your options, answer your questions, and provide emotional support.
You receive a written summary of the discussion and a personalised care plan. We remain available for follow‑up questions and coordinate with your obstetrician and other specialists.
If you have received a diagnosis of a fetal condition – or if you are at high risk – this service is designed to support you.
Any significant finding – cardiac, brain, spine, abdominal wall, or skeletal – warrants a dedicated counseling session to understand the implications.
If NIPT, amniocentesis, or CVS has revealed a trisomy, microdeletion, or other genetic condition, we help you understand the condition and plan accordingly.
If you've had a previous pregnancy affected by an anomaly, counseling can help you understand recurrence risks and plan surveillance for the current pregnancy.
If your combined screening or NIPT shows increased risk, counseling can help you decide whether to pursue invasive testing and prepare for possible outcomes.
If you have a family history of genetic or congenital conditions, counseling provides risk assessment and guidance for reproductive options.
Even if you are not sure what you need, if a diagnosis has been made and you are struggling to process it, counseling can provide clarity, support, and a way forward.
Dr. Abhishek has extensive experience in fetal anomaly counseling – not just in the medical facts, but in the art of communicating difficult news with compassion and clarity. He understands that behind every diagnosis is a family with hopes, fears, and values. He takes time to listen, to explain, and to support you through every decision.
Fetal anomaly counseling is a difficult but important conversation – having your partner with you can make it more manageable and ensure you both hear the same information.
We strongly encourage partners to attend. We create a safe, private environment where both of you can ask questions, express concerns, and make decisions together. If you have other family members or a support person you would like to bring, we welcome them too.
It is a dedicated, compassionate service for parents who have received a diagnosis of a fetal condition. It provides medical explanation, emotional support, and help with decision‑making, coordinated with a multidisciplinary team.
Typically, a referral from your obstetrician or fetal medicine specialist is helpful, but you can also request a counseling session directly. We will coordinate with your care team.
Please bring all ultrasound images, reports, genetic test results, and any other medical records. If you have questions written down, bring those too – we want to make sure we address everything.
No – it covers medical, emotional, and practical aspects. We address your fears, help you cope, and support your decision‑making in a way that respects your values.
We do not make decisions for you – we provide all the information, options, and support you need to make the best decision for your family. We are here to guide, not to judge.
Yes. We coordinate with neonatologists, geneticists, pediatric surgeons, and mental health professionals to ensure you have a full team behind you.
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