Family Testimonials

I am Tahsin Alinin’s mother, my son has down syndrome and autism diagnosis. Although we went to many special education and sports centers, my teacher Koray and his teachers solved many things that they could not solve. Your behavior has improved, he used to live in his own world but now he is with us.

As we approach the 2nd year of my daughter Gülce’s adventure, what we experienced today with my esteemed teacher Koray and teacher Baturay was beyond imagination. My daughter was able to start kindergarten with her peers just in time. At the age of 3, this journey we started together has given us its fruits. Of course, it was not as easy to plan and program this as I am writing now, I thank them very much for their efforts. They came to school with me and helped me choose a school and they are still interested in her adaptation to school. At the same time, we continue to hear new words and sentences in my daughter who has language development retardation. Yes, it is very difficult to be on this path, but it is wonderful when the right education and the right institution meet the child. The common denominator of what we have experienced in these 2 years is the child and believe me, family is everything, being one in the education of the child is everything. As I say to everyone who comes to this institution, you are in good hands, there has never been a day when I asked the question and did not get an answer. If we can only know how to treat our children right, they already do. We cannot thank you enough for being a light on our path. The Güleryüz family owes a lot to this team.

Hello there;
I am the father of İbrahim Orhan, we have made great progress although it has only been 5 months since we started moving special education.İbrahim Orhan’s diagnosis is mental deficiency, language and speech deficiency.There are also symptoms of autism.We saw that our son was thinking after we started here for the first time.May Allah be infinitely grateful to my teacher Koray.I have never seen another team so loyal to their profession.I would like to thank the whole team, especially my teacher Koray and my teacher Baturay.

Hello, I’m Ayaz’s mom. Ayaz is now exactly 31 months old. Ayaz was diagnosed with mild autism when he was 20 months old. We immediately started private education in Manisa, the city where we lived, but unfortunately we were not very satisfied. Then we went to another private education in Izmir, we went for about 5 months, but there was something that didn’t sit well with me there either. I found Koray teacher and Baturay teacher with my researches and I am glad I did. My wife came to meet with Koray teachers at my request and Koray teacher asked us to come for only 8 hours and see the change in the child. And Ayaz started to form sentences with four words in just 1 week. After that day, we left special education and started only active education. We saw serious improvements in my son within 6 months and when we went to see our psychiatry doctor, we were very happy when he said that my son’s diagnosis was no longer diagnosed and all the symptoms of autism disappeared. I am glad that we had the chance to meet my Koray teacher, Baturay teacher and your beautiful teams. Thank you very much to my teacher Koray, my teacher Baturay and your beautiful team. Thank goodness you are our beautiful teachers

Hello, I am Demet, the mother of Enes, we met my teacher Koray and my teacher Baturay on the recommendation of our psychiatrist when we could not see the expected development in our child from the special education center that diagnosed our child with stimulus deficiency and we went to for about 1 year. We observed a serious improvement in our son even before a year. We were very happy to hear from our doctor that our son no longer has developmental retardation due to lack of stimuli. I would like to thank my teacher and his team for their selfless work. Especially communicating with each child and following his development week by week, contacting our child’s daycare center when necessary, enabled Enes to progress quickly. I’m glad we met, I’m glad you exist.

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Hello, I’m Zeynep Baby’s mother, we were diagnosed with developmental delay + Atypical autism at 15 months old. Everyone who reads this knows that fear due to fingertip pressing and eye contact limitation… my research brought me here. First of all, the fact that my teacher Koray talked to me like an older brother and patiently explained me for a long time made me very comfortable, especially when he first saw Zeynebi, why don’t you make her wear shoes? With the right choice of shoes, toe pressing has decreased to the point that it is said to be over, she started to walk 🙂 gestures, mimics increased, words started to come out and of course, those caring behaviors that they love and care more like their own children than educators… I can’t thank you enough, they are in my prayers every night… the right place, the right approach, the right time, we have come a long way, thank God you are here

This is an update message. My son South is 3.5 years old and it has been 2 months since I left special education. He started half-day kindergarten. We had no difficulty in the adaptation process. He is very happy doing the activities and activities in kindergarten. Güney now objects when there is a situation he does not want, chooses his own clothes, says where he wants to go, our toilet training is now complete, he obeys the rules of the house, he can play and play alone, he makes his toys talk, his imitation skills are very good, he learned to share, he says the names of his classmates. The process of adapting to kindergarten was much easier thanks to mobile special education. I will never forget the support of my teachers Baturay and Koray on the first day of kindergarten and afterwards. Knowing that they will not leave us alone in the future when I cannot find a solution for Güney makes me feel very peaceful and safe. We are constantly ringing your ears 🙂 We love you very much.

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My son Ahlas is 2 years old and we searched for many places due to the suspicion of Autism Spectrum Disorder and Developmental Delay. We came across Koray Uygur Sports Club on the occasion of Instagram. In such cases, unfortunately, we as parents do not know what to do and what path we should follow. As soon as I had a meeting with Mr Baturay, everything he said made sense to me and they asked us to come to only 8 lessons and said that if there was no positive change or progress, you could leave. The education process with Ahlas started on 6 September We noticed changes in our son before 8 lessons. There was no eye contact, he did not look when he called his name, he always slept on the swings in the park, he did not go to anyone, he had stopped talking months ago, if he wanted to eat or drink something, he could not tell if he wanted to eat or drink, there was no command taking, there was no clapping, waving, kissing. It has only been 3 months since I started there and all of them are there now, my son is about to catch up with his peers. Now he started to speak slowly. If he wants to eat or drink something, he brings it and gives it to us, we open it and give it to him. He wants to eat his own food.His perception has opened up a lot. When he sees the parks, he immediately goes to run and play. We can now enter the playgrounds. Ahlasda loves his teachers very much, they spend a very nice and productive time. Many other skills that I cannot write more have come back. Please, as a mother, if you have a child in a similar situation, go to Koray Uygur Sports Club before rehabilitation centres. Change must first start with us as parents. The more conscious people we want to move forward, the more beneficial we can be for our children. I come from Torbalı and I am glad we are a part of this family. Your sincerity, sincerity, the approach of the teachers towards our children is wonderful. May God bless Koray Hocam-Baturay Hocam and the whole team behind them. You are super… I am glad you are here…

It’s been 6 months since we crossed paths with you. There is no trace of Ata when we first arrived. Ata was a child who had very little eye contact, did not look at his name, did not speak, and was an irritable child. At our first doctor check
Thanks to you, we made 7 months of progress in 2 months. Thanks to your efforts, we managed to hold hands and walk with Ata and this happened in our first 1 week. Our son communicates with us and his environment. He plays games with his peers, even takes a step to play, our word digit is constantly increasing. Our imitation ability has increased greatly. Koray Teacher and Baturay Teacher, who do their job properly, your place for us is very different. We are very grateful to you for your efforts, sharing your knowledge with us, listening to us one by one from the heart, guiding us and ensuring that our hope is not lost. Thank goodness you are here.

Hayal is a 12-year-old child with autism, shouting, fear of public transport, no speech, no speech, a child who was irritable, all of them have been lifted for 1 year since we started here, and now he is at school and around us, his teachers said that Hayal is doing very well, his doctor told us to reduce his medication anymore, he is very good now, thanks to Koray Teacher, Baturay Teacher and the whole team.

Since we started Mobile Special Education, Yağmur has improved a lot, I wish we had met earlier, I wish we had met earlier, when we first came here, there was a walking disorder in the rain, she couldn’t express herself, because she came here with love and desire, people around me are asking where are you going, there has been so much improvement in the rain, I would like to say that I recommend it to everyone, I would like to thank all my teachers and the Koray teacher and the Baturay teacher for their contributions.

Hello, I am Emir Taylan Karaeşin’s mother, we have been coming to Koray Uygur Sports Club with my son for 8 years, when we first came, my son had distraction, balance problem, lack of self-confidence, There were many things such as muscle problems and inability to express themselves, my son’s diagnosis was serabral palsy and mild mental retardation, we overcame all of these, and now I still bring my son here because he has scoliosis that develops later and because this is a reliable place, and I will continue to bring my son because he needs to do sports for life anyway, thanks to the support and friendliness of this place, my son comes here willingly and willingly.