An interview with child psychiatrist Yurii Stratovych about working with children with special educational needs, belief in miracles, daily work and love for the world.
Mr Stratovych, could you tell us about the specifics of your practice?
The years 2014-2015 were a turning point for me, when I finalised a new approach. It didn’t happen by chance – back in 2002, I studied in the United States and became familiar with the system that focused on the individual, rather than the state or institutions. That’s when I realised: everything must serve the individual – not laws or bureaucracy, but the family. Since then, I’ve been implementing this philosophy in my work. For over 10 years now, I’ve been engaged in behavior management of parents. This niche has been a real breakthrough for me. I realised how crucial it is to support parents. They need to hear that they’re doing the right thing, to build their confidence. After all, when parents feel supported, it immediately reflects on a child: parents genuinely want to help, but they often just don’t know how to do it right.
Were there any particular cases that would help our readers understand children’s potential?
One of the most striking examples is the story of this 13-year-old girl diagnosed with anorexia nervosa. It was one of the most difficult cases, but we worked tirelessly, and the outcome exceeded expectations. First, there was no relapse. Second, this girl is now a pediatrician and is planning to become a child psychiatrist. Can you imagine? The same kid who once battled her own problems – and won – is now helping other children.
In another case, I worked with a 2-year-old boy with severe autism, then didn’t see him again for 15 years. His mother had initially rejected the diagnosis – which is a typical reaction, by the way – but still diligently followed all of my recommendations. Years later, she told me that her son is now a coding genius who gets invitations from different countries – at the age of 17! Everyone talks about his incredible potential. This made me once again reconsider the possibilities of a child’s brain.
I also recall a case of a Ukrainian family that moved to Denmark. Their son, who has ASD, started kindergarten there at the age of 4. The Danish system simply amazed me: the educators immediately identified someone in the group – another four-year-old girl – to support and help him adapt. Not an adult, but another child! These inclusive peer groups are so important, because they help develop empathy and promote the acceptance of diversity. Another fascinating detail: the kindergarten has this special “friendship hut” on the playground. When a child wants to play with someone or needs support but is too shy to ask, he or she just goes into this hut – others notice and quickly join in. I dream that such a practice will take root in Ukraine, and I already see a lot of progress in tjis regard.
You mentioned that a mother initially rejected her child’s diagnosis – and said that’s a typical reaction. Can we talk about that? How to help parents move from “Why my child?” to acceptance?
This is the hardest part of my work, but also the most meaningful. The first step is always the same – to remove the sense of guilt. You see, nearly all disorders are genetic in nature: it’s just the way it is, and it’s no one’s fault. But parents often blame themselves instead of channelling their energy into helping the child.
Acceptance of a diagnosis by the family is a very difficult process. When I talk about ADHD or ASD, parents often get mad at me because I seem to have brought bad news. At first, that reaction surprised me: I want to help, but they perceive me as an enemy. Over time, I understood why this happens and have come to accept these reactions. The main thing is for parents to start working with the child; they quickly see results, and this changes everything.
I always explain a simple principle to parents: the past causes depression, the future brings anxiety, but we need to live in the present. If you’re constantly thinking about what happened or worrying about what might be, you’re not doing anything for your child right now.
What are the most common myths that get shattered in your office?
The biggest myth I come across every day is the belief that prognoses are set in stone. Parents often come in thinking that if a doctor says, “your child will never be able to…”, that’s a life sentence. But the brain is incredibly plastic! Making definitive predictions just doesn’t work. It’s far more effective to work every day, and the results will come. I believe in it, I see it, and I try to support it.
Another common myth is that working only with the child, taking him or her to specialists is enough, while the rest of the family can continue life as usual. This is fundamentally wrong. Success only comes when there is support from everyone – both parents, grandparents, godparents, friends – absolutely everyone. I often hear, “Dad earns money, and Mom takes care of the child”. But real success is 50% Mom plus 50% Dad. And it doesn’t matter if the parents live together – the main thing is that they work as a team.
What changes would you like to see in society’s attitude toward children with disabilities or special educational needs?
The biggest problem in Ukraine is that parents are ashamed of their kids’ diagnosis and try to hide it. We need to do the opposite and speak openly: “My child has ASD,” or “My child has hyperactivity”. It’s just necessary to talk about it, because that’s how trust is built, and people begin to sympathise and empathise.
When parents openly talk about their child’s diagnosis for the first time, they take a huge burden off their shoulders. And you know what? People are much better than we think they are. That’s my observation and my belief. When people understand a family’s needs, they start helping. I think we need to break this culture of silence and be open with neighbours, doctors, teachers. After all, it’s not the family’s fault. There are many children like this, and there is nothing to be ashamed of.
Do you believe children with special educational needs have a mission? That everything in this world happens for a reason?
Absolutely! As I’ve already mentioned, when such a child shows up in a kindergarten or school, other children automatically start learning compassion, develop empathy. Perhaps, it is through such interaction that one of these children will become a doctor or social worker one day. Kids are much more flexible than adults and have fewer biases. Of course, adults should supervise the process, but give children space to love, make friends, and accept.
In Israel, there’s a beautiful tradition: when a child with special educational needs is born, the state congratulates the family, because this requires a whole new level of family functioning. And it is true: such families become stronger, wiser, kinder.
How has the war affected the mental health of children with disabilities or SEN?
War is a complex stressor for everyone, but especially for children with SEN. On the one hand, it’s a huge challenge, especially when families are forced to leave. But I’ve also noticed something remarkable: under stress, children sometimes gain new skills, learn to adapt faster, and go through any other adaptation more easily. As they say, what doesn’t kill us makes us stronger.
I currently consult Ukrainian families that have moved to all corners of the world – New Zealand, the United States, Germany, France and the UK. I see how they adapt to new mentalities and cultures. True, it is stressful for both adults and children, but it also gives a powerful push for growth.
I always advise parents to stick to the routine, even during wartime: plant flowers, read books, bake favourite pies – follow familiar daily rhythms as much as possible. Yet we need to understand that in stressful situations, long-term planning becomes impossible. At best, plan a month ahead. Ideally – a week.
What would you say to parents who have just received a diagnosis?
First of all, don’t wait. Early intervention is absolutely critical. Usually, parents notice changes around the age of one, hope it will “go away” by the age of two, and only start seeking help at the age of three. This is a loss of precious time.
Remember, I said that the brain is very plastic! If you invest enough in a child, there’s a strong chance of active development. What children need most are independence and adaptive skills – these will help them far more in adult life than any academic knowledge.
One more crucial point: a child is not the same as his or her diagnosis. When working with children with special educational needs, we must always separate the condition from the child’s personality. Unfortunately, even professionals sometimes forget this rule.
What inspires you the most in your work?
My rule in life is to never give up. No matter how difficult the case is, I do everything I can. And I get energy from the results. When I see children change – some in a month, others in seven years – but they do change, and that’s incredibly inspiring. Helping kids with mental disorders is the highest level of spirituality one can imagine, and I try to follow this path every day and develop myself to be able to help even more.
How do you keep your emotional balance?
My family, sports, and travelling – seeing new cities, new cultures – help me keep my balance. I try not to obsess over age or how much time is left for me. Instead, I focus on making the right choices here and now – helping people, especially children.
Rich experience also brings stability: it helps me avoid mistakes I made in the past. Back in 2011, I started one of the first state centres in Ukraine for children with SEN based in a psychiatric hospital. We had a true multidisciplinary team, including speech therapists, special educators, psychiatrists, psychologists, and more. Families had to wait up to 18 months to get in. Being a pioneer is always difficult, but that experience now helps me influence change in the country and support new initiatives.