yo-my there are only five children like her son in the whole of russia in our studio love kerteeva. hello, how does your son differ from other children; he ages 8-10 times faster than everyone else. this is the rarest progeria disease in 8 million people for your son. he is small and has not yet developed outwardly. he

resembles a child. here are three or four years, they do not grow even younger than their age. yes, but on his face, his skin is so thin, not elastic, so to speak, not taut, as if it were a small piece, but internal organs. in which one does he condition at this time? we are lucky with his organs, corresponding to his age so far at the turning point. no this moment. it may simply come when we don’t see, we don’t know, we don’t feel, that is, it can arise spontaneously. yes, any nervous, there may be some kind of surge, any trauma of emotions can lead to this point. aging internal organs intensively quickly and irrevocably, this will lead to our very result to a

fatal outcome. no perversions can not say. what is your son preparing for? it's rare disease. began to appear from the first days of his life. no, he was born a completely normal child. he was born, however, small 2.800 50 cm, he was given 8-9 points. that is, he was an ordinary calm child, developed up to a year. he grew up, intensively gaining weight, nothing, as it were, foreshadowed trouble. after a year, his growth began to slow down, and he began, er, to gain less weight, but the doctors reassured me, saying that well, this happens. well, what matters is what he eats. uh, cheerful sociable does not get sick, somewhere, probably in age 3.5 years. and we've got silver russell

syndrome, if they're wrong. what is this syndrome? this is when just a small child, that is, he develops normally, he does not grow up. it's very tall or something healthy. well, just don't come little ones, no. we were diagnosed with progeria this year. you were diagnosed with kettlebell at your hospital. no, we were forced to travel to other specialists in another republic, because here, uh, we have not even heard of such a disease. what republic do you live in? balkaria, we generally ended up in the hospital with another. he abruptly began to refuse food, began to vomit very strongly and stopped walking. he wanted to lie down all the time. ah, peace and quiet. in 2 weeks, he lost weight to 9 kg, and weighed as much as

eleven, but these 11 kg were very difficult for us . as such, they do not have a layer and he eats food, he does not absorb full-fledged, naturally, and weight gain. with us, these 100-200 g can take a month or two. how were you diagnosed? we went to the hospital at we spent 2 weeks in gastroenterology, where you were diagnosed at the genetic center in stavropol territory, stavropol territory. yes, when we just came in, and he is young, a doctor, he told me the diagnosis. i began to sob, as if i probably understood that this was something terrible. we passed tests in october and in january. we've got it confirmed. i asked him what it is. he told me that at this time medicine does not have any exact data on

this disease, because it is enough rare only now some developments are starting. i don't know how to say survey. he showed me the book and said, you don’t see that the child that is depicted here is yours, and not something similar. i see with my mind. i understand that there is something, but as a mother i cannot accept it. naturally, doctors have cured this disease? yes, these are incurable options. no, 13 14 years old. this is the most. there is a dangerous age for them , yes, they live longer, but this is already right with the treatment. exception is a turning point when it will be clear will the child live on no, the most crucial moment comes from the age of

5 to 7 years, but again this is an individuality, and 13-14 years old is when the moment when you already have to wait for the worst, that is this, if 13 years old is an ordinary child, then my child, and at 5 years old, a turning point. in what it should manifest itself it will not be seen. that's how we constantly have to be examined every six months a year. if possible, of course, more often monitor his health. first of all, the heart joints. in general, everything that adult older people are concerned in the first place, this should pay attention. if we pay attention in time that something has gone wrong, there is a possibility that we can heal a little and thereby increase his life, at least for a

little bit you need to study not even children's diseases, but the diseases of the old people to understand , what is happening with your child and how to treat him . recently, problems with the joints have appeared, but for now, hmm, swimming is physical training. that's all, but it can slightly relieve the momentum of specific and serious for now we have no violations, when you found out that your case is one in eight million. and when you realized it, what did you feel? well, it's like before and after that's the day when they said, yes, we are, it's like before and after, when you realize that your child is doomed? this is a completely different story, different feelings and understanding, in general, everything that happens. you understand that you will outlive your son. to be

honest, i can’t even imagine what a mother can experience after giving birth to a long-awaited child. suddenly learns about such a terrible diagnosis and every day, maybe the last, when they wait , thank you, that one more day he sleeps with you. he sleeps in the middle of our morning. and our day ends with caresses, he asks to stroke and scratch his back and kiss and hug , he won’t fall asleep until one of us lies with him. and these actions are 15 minutes until he falls asleep, despite

the fact that such warmth. tell me, i see that and your eyes are tears. we are every day. so i don't let myself relax sour, because my baby he doesn't need you, the stronger. i am the more likely that i can help him in some way, which means that i can somehow make his life easier, or something? or maybe even let it be a day or two weeks to increase his eyelid, so let's say small it is very difficult. yes. can you imagine what a young mother is experiencing this terrible disease. with this outcome. this is a disease. the basis of this disease is a gene mutation that is responsible for protein synthesis, which in turn controls the

state of the nucleus in the cell. and this defective protein does not allow this nucleus to be found, so to speak. a balanced state, as a result of which the cells of the whole organism mow down, today in america a drug has been created that possibly prolongs life there by 17-18 months. i understand that every day this is for mom, and we ourselves must understand that this is a minute of a second. this is a lot, it means anyone. did you know about this drug, about which jamila speaks, we have been drinking it for almost 2 months. yes, we went to the doctor. as a matter of fact, we got through the mother, whose girl also suffers from this disease. she was this doctor's first. we were second. she 's negotiating directly with boston, who supplies us with this drug. and how does this drug help such children, does it slow down and

prevent the accumulation of this defective protein in the cells as a result of what? they don’t grow old and die like that, let’s say, tests were carried out on animals, for example, and the cardiovascular system responds to this drug in 90%, a medicine has been created that helps and there are all prospects that this medicine will not only support, but in principle, it will cure into remission, because even without drugs there were such people who lived with this form up to 45 years. that is, if such precedents are being actively researched in sweden now, accordingly, there is a possibility that, with the successful development of these studies, the disease will generally be curable love. so you say, your son is already old on the outside, but in terms of his character development, he differs from others who lose children. he's such a good solar mover. yes, he is very active

he runs and sees a step in front of him on novyas stepping over with two legs. only then will it move on. he is very smart, a distinctive feature of this particular form of progeria they have one kind, but mentally they are ahead of their peers, love this son is our firstborn. my first child. well, it turned out as unexpected, or what? at first i was in shock, in the same shock. i told my husband and now, only then the two of us were delighted. especially because of the four children that my parents have. i'm the youngest myself. this is the first one. well he has never been defined by the love of such a child , it is impossible not to love the support. here is the one that i can get from my loved ones, it costs another. and how did your husband react to this terrible diagnosis? when we were driving from the clinic, and he

asked me why you were crying. and i went on the internet and began to read, in principle, what it is. i just got to 13 years old. i just told them the number and he just sobbed, because astema is my father's son. here they are all the time together without each other at all. let's invite your an amazing son and dad there, aslan and the mirtiyevs are visiting us. hello hello world. tell me, what city did you come to us from? i don't know you all so much say indulges. in general, your

son is a sociable boy. well, yes, with peers with small children, they always play friendly, i hug the boy. steamer, what kind of toy do you say? it is impossible to take your eyes off him, he is unusual and looks like his dad, in my opinion, aslan, your sons play with each other. yes, of course, just as they love the other, they fight too. that is, at them the usual kid games. maybe we 'll let assmir go so that he doesn't get tired. well

, a really unusual child and amazing and, probably, lyuba attracts a lot of attention on the street , both children and adults. well, the reaction is different. now we see more and more, here are some views that are so oblique and more condemning, and i’m not justing them, i probably just can understand because a person, when something is unknown, he is afraid of it. he tries to bypass his parents, they abruptly took his children away, and and aloud. saying a phrase to you, so that there is no one else to play with. you know, people used to watch the same thing because they didn’t know what the essence of the problem is, that these are children on the contrary, but now, in recent years, after ah, all this data has been popularized, on the contrary, everything

people began to respect and burned out, too, this is a disease, in fact. well, sunny, this is a man with a broken watch inside, imagine, they just work faster than they should. i am sure that after today's broadcast, for sure. well millions people will treat you in a completely different way, this ignorance said correctly. eh, a misunderstanding of a person, he immediately gets lost a little bit afraid of something. and now this program. i think everyone will watch it. and, of course, everything will be fine. i'm just sure that this is how it will be anatoly. you let his six-year-old child go far away to play with the system, without even thinking. see what kind of fish we could learn from. this relationship between the husband was alarming when they knew about some problems with the health of their son. we have

there is a tradition after one year of children, uh, shaving baldly and after that his hair began to grow badly, well, he has alopecia there, that he does n’t have hair at all, in my opinion, light shows there yes , really such kids, they are born completely ordinary . they will have a hairline, but gradually with each month they noted a deterioration in the part of the hair and somewhere by 10-12 months. usually this already manifests itself from two to three of these children, the eyebrows of the cilia may gradually disappear and indeed in the scalp may to remain already light fluff, that is, terminal pigmented hair. there will already be plants there, because, in principle, in such patients, in such people, they do not have much subcutaneous fat , and without this. the medications he takes for him cause alopecia, but after

the withdrawal of these drugs, some begin to grow hair much stronger than before the study. it started only a year ago aslan, do you remember that you experienced it when your wife first told you about your son’s illness, it was very painful to hear that our child has such a disease. yes , in general, something like this disease exists, and there is no cure for it. and the average age of life. you must have been horrified. i can't put it into words. it would be better if i felt it on myself than on my child, that some medicine would come up with something that would cure him and help him. eh, now the science of medicine is at a high level and i think there are all the possibilities for this and i wish that all this would

help us in the future, children with this syndrome. they are could radiate to your son that he is not like everyone else? no, he never understands this when he is little. and uh, he doesn't see any looks at the moment when he has questions about his appearance. you will find the right words. in this case , there is. i will tell. come on, well, the main thing is that you are the living future. you don’t tell him that someone will do it for you in a very harsh manner. i

want my child to live fully here and now, and if every second one will be for him, he says, yes, you are a person of the future, you are an alien. but if i was told that, it would hurt me, but sometimes they tell me that i am an alien. although i don't look like an alien. i take it as a compliment when people talk about my son. this is my own. this is a little bit different. i want to say e love islam is great. thank you for putting all your strength into the final transmission. and you, probably, still , uh, imagine what you did for all of us here, you know, millions of people will watch programs and draw some kind of parallel between what you have and your own, some small, disorderly and maybe they will stop paying attention and become kinder and about. here is a sentence you know 10 years ago, somewhere i knew that there is still such a problem, lopezia, that cannot be treated. i knew that i needed

to make a fund. i sat down and opened it. we have many children in this fund in moscow. brilliant children. we call yes and we have a brilliant brilliant community. maybe not just outside. you can be inside . this is a shining soul. we are glad to everyone, come to us when we are going to do an event. we are not talking about disease. we won't ask anyone why and even more so there will be no reaction of some kind told. we are going to play sports. we live a good full life. do you want to invite? event and time for those i would like to give, i am friends with diana gurtskaya until the moment when i was not in a children's, but a specialized boarding school. she did not know that she was blind, and her sighted brother ran around the house with her and her parents never said that she was not like everyone else and the girl grew up in love. and we see

what she has become, you can just say that everything kids are different. it seems to me that while the child is with you, you need to give him maximum love and confidence, and then, maybe, he himself will tell you the answer. he 'll be fine. well, we always say that you are our best favorite. it's generally local. absolutely. he loves himself so much when a film crew came to us. they film him . he began to imagine when we go out into the street, he will spin in front of the mirror up to the teeth. can you look and see what kind of he he is constantly in this ball, happiness that whether? here in this love, never for a minute, never. we didn't let him doubt that he is everything new for us, wonderful parents, great great

happiness to become a mother. few. this happiness is given and more and more women who cannot give birth to a child already have an experimental let. even a little, a drug that delays, let's say, the expected results, and there may be some kind of breakthrough genetically in any case. it seems to me that you really need to live in joy every day that is released and in general none of us of all people who are born on this planet knows. how long or short is this path? why does love doubt the result? a test based on the results of which her son was given a rare diagnosis. i am sitting in the kitchen. i tell my husband we will retake. and about this and how astemir's mother protects her son from adults who are not shy in expressions at the sight of an old boy. children can, uh, say, it’s not your

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the icon medallion on a chain matrona of moscow for only 999 rubles. but if you call us right now, you will receive a second icon of medallions as a gift limited offer beyond the limit this is beyond the limit of a five-year-old ozdemir. kirteev. from nalchik, a year of life is 10 years due to rare genetic progeria disease, the boy is rapidly aging even at the age of 5. he is physiologically older than his parents lyubov and aslan kerteev, twice his biological age now. troops of the world 60 years old, first of all, his organs begin to age. elastic joints the elasticity of the skin is all disturbed by the world's thin and flabby, like an elderly person's hair does not grow on his head, and his muscles do not develop his body does not absorb protein,

so the boy almost does not gain weight and quickly gets tired of physical exertion, not that he starts to pinch. that is, he starts. here in his joints of his bones, changes occur, there are cries. mom of the world with the help of aging drugs. you can only slow it down, but even with constant therapy, her son, according to medical forecasts, will live, at best, only up to 14 years old, the worst thing, when do you understand? and where do you realize yourself inside? that the name is the day when all parents will understand that every day of their son can be the last and they give him all the love and care, too, was there at the time of the announcement terrible up to seven diagnoses in our studio rustam evloev. to the hospital with love and aslan, they were very

worried beyond words. how parents care about their child. well, either to the last, she hoped that the diagnosis would not always be confirmed from her, lyuba , a strong person, heard it from her until the last, she keeps in herself, we cried with her. i don't know how any other person would react in her place, but their love and care is better. i don't know who would. it's just a matter of seeing a second child, no one in the family. they have a difference of a year and 10, and at that time we did

n’t know anything, but even if now i had the opportunity to give birth, i would give birth, because firstly, the likelihood that this will happen again in our family is very small . we are genetically healthy parents. we also took tests and we don’t have any disorders, that the doctors say why this manifested itself in asti of the world to us the doctor said that well, now specifically no one can answer this question. just in the very early stages of pregnancy. well something went wrong so, maybe, she had arvi, there is something else. well, some little thing and all. the child is absolutely healthy album book of the first year of the life of the world.

or every month with a cake for the first year and aslan kerteev did not sleep for several nights in a row, it is very much written that children die in their sleep. so, as it were, well, they were very afraid, of course, and overslept in the middle of the night and listened to how he breathes at all, does not adhere to a strict diet, gluten is contraindicated for him. flour fried sweet. all this from the boy's diet. mom ruled out even buckwheat for her son. she cooks, peeled green. ordinary buckwheat contains particles of gluten, which, when it enters the liver. they begin to destroy the son to eat children's cottage cheese. i understand that it is impossible, but

once there 10 days. just then, we have consequences for the physical form of the stimmer. dad plays football with his son and teaches him to pull himself up for medical reasons. doctors advise to move a lot. ah, then, uh, i highly recommend swimming, like everyone else, boys of his age timir loves outdoor games, loves cars and with with pleasure dissects on one of them his beloved in the apartment. but, unlike his peers from temir, half an hour of active games gets tired very quickly and the boy needs a break. my milan wow, dimochki has arrived. love is recognized by the son always sees her cheerful, joyful energetic, but as soon as she is left alone with her thoughts, she is no longer able to restrain anxiety and

pain. no matter how strong he is, active , something is wrong inside, you can’t do anything, it ’s impossible to prepare for this, it’s impossible with come to terms with this. when next to your wife share some of your feelings about the future of your son. yes? of course, we talk about him very often, and well, we still try to somehow not think about the bad, there is still

some hope. well, something good will be all the same. and how do you draw in your dreams his future. i would like to see him athletes, good athletes. and, of course, that he had healthy children. and would also like to see his grandchildren sports people. this is where your father taught some kind of physical preparation to run horizontal bars, stretch, do push-ups. these are the moments that you yourself are self-developing your body and useful all the same for your body - this is good, can football, for example, with your peers? yes, we take a sports town to the playground, and there they also play football with the children, there they pull themselves up on the horizontal bars and

it’s good for the walkers, well, it gets up and runs on them. here, he is a very active boy, mobile and his legs work well. and by the way, he has a lot friends. yes, and he has friends with whom he is good. the kids probably all run around the sharp world mostly. yes, because magic comes from him, like a magnet. he attracts. when my mother was in the hospital, the last time the entire floor of the children was constantly in our ward. he is in the center of attention, yes, he attracts. here are the views. here he is, as if beckoning, or something to himself, and mothers in your yard, seeing the world, react like that. here, well, now that's all, they treat him as an equal, or something, no, no and the children play with him and we visit each other

neighbors, you told these women about the disease, but there are those who know, of course, who supported us, who were nearby. well, since 2015-16 we live in the neighborhood and are friends. that is, before this case was put, of course, i saw how tall he was, he was an ordinary child. that is, we communicate with families. i also have a child of the same age as dima. he calls him dim dimych for up to a year, the child did not have any changes in appearance, he was active, but he constantly smiled. contact. but, and when he was diagnosed with this, you immediately learned about him. yes, of course, anyone called. she was very upset, she decided, then she came to moscow to double-check, but

she was, of course, very upset about it. well, beyond words, how it was? well, of course, it hurts a lot, and in fact, when she was upset and now you can never say that she has something wrong with her child, that he is sick. that is, she is constantly in sight with him, we go to events together. there is no such thing that she is closed and this child did not take anywhere, there is no such thing, if only society would perceive him as an ordinary child, that he simply has problems with adjacency. not even children. they notice it. here's what i want to focus on. not children, adult parents, are trying to remove the child from him, so that, well, as if to show that he does not want problems with him, problems have long been known. on the example of children with down syndrome. we have to work with the community. our transmission, well contributes. yes, definitely there is some on the territory. why is our love for aslan program that's for this, to convey to society

that it is impossible, that he is an ordinary child there, he is healthy. in the brightest moment of this program was. this is the exit here of this unconditionally sunny person, from whom it was impossible to tear off and from whom even the name itself is consonant with two russian words grow and peace. i don't know what your child dreams about, but if he loves the camera, if he loves the mirror, if he loves to show off, we will accept the studio school. children of your child's cinema, without any payments there. he will definitely be there. to be among people among children who you will accept and who will understand lyuba do you think that mikhail's proposal will be astened to the little one, maybe this will interest him. i want the public to know and accept. i want to convey to everyone who does not understand that this can happen. in any family. it's not an infection. none of your children will get sick from him. he is the same as everyone else. i

really hope that someday he will go to school, and then college institute. there is another level. there are other people there. i want my child to live a full-fledged life and on medicine, its technology helps us to better monitor the condition of your child, somehow help him, let's say shunting for today, that is, if we see somewhere, atherosclerotic plaques that contribute there, let's say, uh, deterioration of the child’s condition, all this, so to speak, is removed surgically, invasively, in non-invasive ways. it all helps. uh, improving the quality of life of the child and its duration, for my part, i want to say, i understand what has passed quite a bit of time when you learned about the diagnosis. and no matter how they say, yes, you don’t have to cry, you can’t. no need to be sad, but not to do this. it is impossible, or any emotions that arise, they have a place to be, of course, we can not

always, but show them when dieting. if you need help, please, after the broadcast, and i will share my contacts. if you want, i will be happy to help you, who will fulfill the dream. five year old auster we have a surprise for you, we'll see you together in a couple of minutes. whose 35 plus anniversary concert live tomorrow at 23:20 on ntv vocal-criminal ensemble today at

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, if you call us right now, then osteo will be yours for only 4.99 rubles. call by phone or order on our website lemax.ru this is beyond love and the weak cry every night because a year ago doctors told them their five-year-old son and the world is one in 8 million. and with temir, he is rapidly aging due to a diagnosis of progeria and may not to live even to the age of majority girls who at his age have already suffered a stroke from someone. m-m joint disease someone a little bit older than him is already in a wheelchair, because the destruction goes to the joints. now the organism from temir, like that of a sixty-year-old, has thinned

pale skin, through which veins appear hair on the head does not grow, eyebrows and eyelashes are rare brittle, and for every 100 g of his weight, his parents fight for months, he is very hard to digest , he does not get better almost there he he can gain 100-200 g per month, and that's it, while he will be fine, eat great, eat love complains. many children are afraid of her son, and their parents only they add fuel to the fire, the ghost of an ordinary boy forbid to play with him people look at him as if he is right now before him , with some kind of shrillness, there are those who don’t play with them, but they can say and i just tried at first not to pay attention. and

now, uh, probably, just a little bit, i can answer love turned to our program to show the whole country they don’t deserve to be fled from him like a leper, so that when he went out into the street, to say oh this here is a suit, this is the same suit, this is the same world, but they didn’t say, god. it is that with him love cries he must spend in love and joy and grandmothers are also always with you. it’s closer to be something, to catch as many as possible these moments when he says some interesting phrases more and more to look at his development, but,

unfortunately, my dad couldn’t even you transfer it. he's gone, quite recently. it was a huge support for my stem child. they were right there as one. is not convey in words. he also has grandmothers, two grandfathers, great-grandmothers are still alive, and still he did not have such close feelings with any of them, as with my dad. they say that parents parents train. but already grandchildren are loved unconditionally with love, father. aslana is even afraid to imagine her life without her long-awaited grandson. yuri kerry is our guest. i want to say

that you are an amazing grandson. he charmed us all. you wake up and fall asleep with the thought of him, of course, and you know almost everything about his illness talk about it like that. so, when they found out their son's diagnosis, their attitude somehow changed among themselves, they began to respect each other better. this is noticeable, so i think that they cope when a person is sick in any case. and it is very difficult, but they do not cope with it. here you are, yuri , pampering your grandson in full, for sure. what he likes the most is cars fire trucks wow maybe he wants to be

a fireman what he wants to be but he's had a love for big cars since he was a kid straight. he loves very much. he knows what they are called. we even had construction going on in our yard. this is my faucet. he said this is a concrete mixer. and who taught him to distinguish between these machines? no, which of us has never sat down and shown this, then this is just from conversations. then they often went. my husband and i would walk around this construction site, of course. he must have heard something and grasped it very quickly. uh-huh and now, as it were, i myself can ask him. what is my car? let's invite aslan and astemir to our studio again. what is your

interesting toy? the girl gave this balloon. sit down with dad. grandfather and mother just told us in secret that you love firefighters very much. ha ha ha, we have a surprise for you. look what happened. wow, here it is, this astemirchik car, we give it to you and

, of course, we are waiting in our later life in our ranks, because we don’t have enough people like that. highly. let's put this helmet on for you, come here. real pozharasochku let's get in the car. yes, you feel like a firefighter. yes, you can still drive . ivan make us a cap. yes i work in lyubertsy, moscow region, in the fire

department, of course. tomorrow waiting for tomorrow is all for now. you will go, of course, i am extremely grateful to everyone who supported us, any proposal that we heard here is very dear to us, these are the emotions that we received here today. they are priceless those words that we heard here, mmm, well, such support, we have not yet received and never heard. i'm so glad to see and just need to be kinder kinder to each other need to understand each other and very much in my opinion

and, probably, my character was influenced by the fact that there are situations worse than ours and when you think that it can be worse. you let it go and start living on, no matter what, you go on living, trying to make your child as happy as possible. i don't want my child to be some kind of superstar or superrich in the future is my wish. just his health lyuba it seems to me that you need to stop crying. stop it. you must be very positive and joyful, because he feeds all this energy to you. take the example of your spouse. he believes in medicine and does the right thing. i believe too. i believe that they will definitely find medicines and the boy will live your friend some kind of sad such a

difficult conversation, but in the end your love is your unity. your care, and the child has been transformed. here in such great love for you and thank god that this can be conveyed to society and thank god that there is such a transmission and i hope that people will see this and relations will already change gradually. this is all laid down gradually, so thanks to your transmission. at the fire station here yes more than austin big wheels and what other profession did the boy try welcome to school and here's a little schoolboy set, we'll find out in a matter of minutes. the husband demanded from his wife a dna test for a one-year-old son, the child simply does not look like me. the woman's mother sided with her

son-in-law, and the daughter said she had worked up her grandson. i want to know who is the father of my grandson's child? why didn't you help her? i sheltered in my apartment studied. what's the difference? how do you live? that's just a young mother fends off all the accusations his sister told him that i went with her friend to his mother for tea, and he thought that after that i cheated on him. so it was, because you slept there. you spent the night, beat me constantly. i filmed the beatings. are you lying, you are also the father of a one-year-old boy. and who will deal with it, i'll climb in, what kind of child are you. you yourself are the soul of a child, i open the envelope. dna today 17:55 on ntv sentenced premiere tomorrow at 21:45 on ntv pentalgin number one remedy for spasm and inflammation pain in

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us right now, you will receive a second medallion icon as a gift, the offer is limited beyond the bounds. it's over the edge. biological age five-year awn of the world. kertieva from nalchik is almost 60 years old, he has a rare genetic disease of progeria. this is when in a year of life the body ages by 10 years orcs. the elasticity of the skin, it's all broken in our studio world. love asks to tell the truth about their son to a million viewers. after all, parents. tired of the fact that nastya of the world is pointing a finger at strangers like that, as if he would touch them right now, and they all die, you know, with such squeamishness of some kind of temporary aging. at

the boy has no hair on his head, the muscles do not develop. and the skin is thin and flabby, like an old man 's appearance scares off strangers. but their ostema, the most ordinary child, parents say. he easily makes friends, takes part in games with pleasure and, like any boy, loves cars. i don’t know what is a tractor, what is an excavator, what is a dump truck? that is, he sort of understands this, probably more than his grandmother in our studio astemir. received as a gift a toy fire truck and an invitation to ride a real one straight from the studio all the families go on an excursion to the assimire fire station. look , it's a fire truck sitting here. our driver takes out to lie down in the composition of the world. he not only sees a fire truck up close, but also sits behind the wheel, and then tries his hand at being the head of the fire department of the world and is met at a theater school.

actor mikhail safronov invited the boy to take an acting course under his strict guidance. welcome to school. and here's a little schoolboy set for you.