tv Documentary RT February 3, 2013 8:28pm-9:00pm EST
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say a nato have caused mass instability that has allowed the seeds of terrorism to grow when the justification for most of the actions in the muslim world is to stop evil dictators who harbor terrorists or spread chatting to mock recy if libya would have been left alone algerian terrorists wouldn't be getting any weapons from it now this is like an exterminator accidently or maybe on purpose actually feeding the roaches in your basements that there are ten times more of them and then saying that he has to keep working because he's the only one who can get rid of the roaches people like hillary clinton who support funding brutal jihad as rebel groups to overthrow governments to somehow bring about stability and democracy are either dismally stupid or consciously running a very brutal con game but that's just my opinion. speak your language not advance the. programs and documentaries and spanish
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what matters to you breaking news a little turn into the angles keep the stories. spanish find out more visit. to lose it was born doctors told us she had multiple fractures they also said lisa would be a difficult child to handle she was bedridden the first. she had to eat and sleep on a cushion because she would cry when we touched her. yes i probably fell from the chair and i from the sofa and that didn't hurt at all but then i fell off the arm chair and i broke my leg. i
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cried for a while. and then at those sleep. but why why why why did it have to be us. but. she. needs a simpler factor is one of the most common congenital bone disorders affecting children if we're talking about those that are present from birth to believe are supportive of the sufferers have brittle bones and are at risk of multiple fractures but they are mineral metabolism is in good order the ailment is due to faulty college information. as the main protein in connective tissue college and is
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the basis of the human skeleton more. to portman wiley's even some adults don't become aware of the fact that they are affected until they give birth to a child that suffers from a more severe form. of the disease in its worst form it changes the shape of the child's chest to build fractures make their arms and legs shorter and in this state even something as light and insignificant as a blanket can cause fracture as. there's a swelling beneath the eye here did you hit something new is hamper out there you can hear her mate with fooling around well well here we have a person that we can already send to the anesthesiologist.
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now we're going to have an orthopedic surgery most likely it's going to be done on the left but strictly speaking both should be operated on but then will begin with the left one simply because it's so deformed that it prevents her from resting on both feet. lisa is determined to walk she can already stand on her feet she's trying her best but she can't walk because of these deformities we hope that she's going to learn little by little to begin she's going to have to start using a walker we think that everything will work out in the end we'll be keeping our fingers crossed for her. a good morning i just know of how you doing. but since the patients he elizabeth elisa oestrogen this is simple fact she wouldn't wear planning surgery for today that they missed to fix the deformities with flexible titanium pins to remedy angular to from
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much as my father suffered from brittle bone disease but he could walk using crutches. my mother left us because she felt the problem was too much for. that my father had to take on her role in the house too. i made some progress after being taught to walk by one time the wheelchair turned over to a mishap as a result of both my thighs fractured at the same time that morning when the doctor arrived he said just don't touch him don't touch him and that's how much childhood came to an abrupt end with. the will of god is omnipotent. and the initials which i found my soul mate. the woman who'd shares my interests and principles. god willing we will go through life together richard. if
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we have to enjoy our trials and tribulations well so be as good as he is but then you don't need to give. us our first child was born on the first step february two thousand and three. when i was fifteen weeks pregnant my child was diagnosed with a do. you. know that unfortunately there was no internet at the time so i was not aware of how serious the condition actually is. that just says to his. in the challenge of our sin he said to me you had been warned about everything it was stupid decision to i think you ought to terminate the pregnancy. my second pregnancy was out of the blue none of us could figure out when it could have happened. just staring at each other and shrugging our shoulders that's how
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teenagers behave in similar situations. is our second child. we have been under a great deal of pressure not to have a second child especially considering that my wife. would be running the risk of dying during childbirth. be all you want was simple it was this. should she leave this world there'd be no telling what might happen to the first child but thank goodness that never came to pass. was the disease to me by any chance to carry on with a cure like playing with kittens i didn't pick up the disease. you didn't. know you were a didn't either but i did and i pass it on to maria and i say that's how it is. in the overwhelming majority of cases the failure of just one gene is enough for
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all stewed genesis imperfecta to be inherited. the risk of those impacted passing the disorder on to their children. i read french as when she was still in the womb the first months was the most difficult period for me she spent it all in an intensive care. and fractures. both arms. have fractured twice. oh happened when they were messing around at the time i wasn't being attentive enough i didn't stop them and they're playing around. like that when i began chasing the cat she lost her balance fell over and broke. that incident to lay the treatment they even said that further treatment might be pointless but if
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none was provided immediately then she'd be back to square one. if this kept happening over and over again then we would all of found it very difficult to deal with. this is born is a very painful. so what does it do. you. here. that's where it's supposed. to heard yesterday to remember now ok it's best to forget about it. came with me to the lift. and that was that then they took me away. and after that i didn't feel anything.
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but i slap i woke up and then that was it i didn't feel anything it was like magic i was worried about some technical aspects rather than the operation itself anything could have happened so gratian was successful but of course it's hard to look at a child after being interest but it's a little. i didn't want to feel all the forms registering her as disabled until she was three years old. i felt unworthy of society because my child was disabled i didn't want to me that she was an invalid but whenever i rolled the promo with or lying flat on her belly everybody knew they had to be and not the fracture. oh are you. ok here i've got a present for you it's
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a russian doll this time too but it is of a different kind it's made of crystal. thank you water it's quite heavy yeah i have a year then my cast. i wish. as a rule i come here to meet the parents of other children suffering from auster genesis imperfecta first and last. god when our daughter was born we had no idea what would become of her doctors predicted a very poor outlook but they said the child was unlikely to be able to walk and faced a very bleak future with dr natale below has spent years treating children afflicted with the disease is what she was the one who came up with the idea of sitting up in the. parents with such children. by the time this is in clinical psychology realized that some simple methods could make life much easier
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for those parents. but i did to meet if i knew that sharing my knowledge with others wouldn't be much of a burden to me. so i volunteered to had this so see. every two months of the operation we're going to remove the costs today. i want to i can see only part of this bone this is on dave removed it. all together. it was almost ten to right angle. and had to be fixed somehow you. understand from my contact with children and their families but most parents need support and encouragement. because i noticed children are
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unlikely to be teased if they sense that the parents are also on a comfortable but i didn't i mean psychologically. our bush bush bush. world more or. less a push against. her but don't overdo it go it would be gentle. you . kill you through with the salk. can you reach out to me. and all of our rights to do the same with the other hand do you need to rest against it closer to those now it's like a yoga exercise. when the child was born i couldn't understand was wrong with her she was like john and her burns were soft and flexible. we didn't tamper with her
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limbs they just fixed and each time he got thread chert she was in plaster for six weeks at a time she would simply fall down and break. weak muscles taut supported spine. by a half hour walk is not to make her spine show through the process of compression. but i do exercises with her. and i think she feels more comfortable when i am by her side. what's most difficult is making her realized that she must help herself by getting stronger through exercise if. you grace. the board with the warmest of the children taint in the courtyard bowl it's a good they keep it to arms length then i can take part in simplied games because
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there aren't enough girls around she doesn't need contact with other people i see that she wants to to communicate. the world that. she has she has admirers and that's a source of inspiration. there at the below. listen i want to invite you to attend the events you've been looking forward to the place is called the museum of intertainment science all of us will be there in saturday. by the way coming to. graduates balancing this all the long time you miss him in which larry much.
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least be told language. programs and documentaries in arabic it's all here on. reporting from the world's hot spots that will be our piece interviews intriguing story for you. then try. to find out more visit our big teeth dog called. you know how sometimes you see a story and it seems so you think you understand it and then you glimpse something else and you hear or see some other part of it and realized everything you thought
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cool cool cool cool cool cool. cool. both my parents were atheists is to say they were among those people who built the savior of the union to live and in those days it wasn't all that easy to express your faith here in the twentieth century. but when i started to live on my own then i was baptized that's what i was twenty six years old. i believe it was abundantly clear to me that if i had a guardian angel who was looking over me and protecting my. hurting his feelings
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would really not be a nice thing to do and most of the way i felt that i would offend him if i didn't join the orthodox church with them. i. fish nation. look at that across here in this holy place that the what the law says see the entire family of royal monsters was murdered in nineteen eighteen it is there and their holy remains with. those of alexy the heir apparent and his sister's. that's why this is a holy place for you more if they pray for us to understand. i
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don't have the worst husband and the wild mind children on two problematic either. things on say drug phones that i have to complain and weep on the time. they want is a tough place to live and i'd like the children to be more self-reliant without being dependent on other people. to set the front on the thing is that because see life as something beyond your rachel is something you can't cope with but that if you're
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a human being in the proper sense of the word like human almost anything is within your powers but i just feel i may have become somewhat braver but i chose to rely on god's will again again i had a dream that i want. to visit some petersburg glow at the cottage the public by nurtured it for twenty five years i yearned to go that would get the bills and finally my dream came true that if you abandon yourself to god's will in the belief that what ever happens will happen it's easier for you to achieve your goals. that gives you the courage to face unknown challenges. mama told me either we're going to go to school or study at home i said i'm going to go to school ok like all children. i don't know what to staying at home and
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studying on my own would be boring i don't have any bad grades only good and great going into. i don't like reading or writing writing takes too much time and. i am not particularly fond of reading mathematics is more interesting for you we do exercises and drug patterns in our math lessons new orleans. you get a yeah i am going to be an artist the worst thing is because drawing that's what i like most of all. the children understand that d.s. is not like that they know they better not pass to her and leave her alone to avoid unnecessary problems. but she does try to join in. sometimes she even
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chases other children as she drives her wheelchair around the room she chimes then when the boys or girls are discussing something she has friends and the certain fifth forms as well as her own also. discovered she copes pretty well without me sometimes she asks me to stir pick up books because she finds it difficult to go through my fear for his safety because she might fall from the chair she leans over the skin if i knew that somebody was taking good care of her school i'd get a job that's my injury. has turned my life around before she was born i wasn't aware of what the world is like for disabled people it really was beyond my perception that i sensed that their problems provided me with a host of opportunities for reassessing my values. now i communicate with an
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entirely different kind of people interesting people my life has taken quite a different turn and i like it very much. my first wish was to bring them together so that parents could see one another and children could realize they weren't the only ones suffering from that disorder is that they need to know that other children have been diagnosed with the same disease but delete a normal life all the same but here they can do. what they like it's very important for parents to know how they'd children feel they should allow them to move as much as they can. you run the risk by doing so but it's a risk worth taking because you know why you are taking it for. a new group ours they are friendly to one another more than that girls know communicate with boys for example i know that has a bit of a crush on the kids
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a searing heat. that wallow it's so beautiful. thanks you're welcome. when the kids and i first met and planted to talk about always glad to read on that there was somebody else like me. explain on line games here for him if i find a new game he placed with me was on the proceeds to the. local guy sends me messages as soon as i am on the internet. love to show doing things with children in wheelchairs i would love to meet more people so that i could visit them for birthdays and other parties.
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gave birth to twins this kid would come from the kitchen carrying the baby brought to life just she would use it to feed them with my own. they're a good bit of a good choice any three years old and already she was trying to help me. yeah i knew. known as. el al i wish you happiness and health care. i hope we'll be condoms and well behaved. i love you i love you. and those thanks. my husband where the other children will take care of her no doubt about. the love of
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a prey to have such as. it is said to blessing. some kids don't move much but there's no stopping her she once it's been five minutes. and says all we're doing this concerns both the state of health and this day develop. they think we can convention and house the house and told her that she can have a good life. and she knows that does a good deal of interesting years for the name detaining things in this world she was never faced a situation where nobody needs her. honestly if i had a child diagnosed with austere genesis perfect i wouldn't have
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a problem with. i'd be glad if it happened in my life it's because i know these children so well and they're full of optimism and i know that they're going to go very far in life that i did what any parent has to be proud of such a child i just wish that there were no tears and there was no pay. no longer represents the. people.
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