her guard can often misunderstand things but the administration of the school seems to be no smarter than six year olds immediately going into total panic mode guess what this is hardly the first time that something like this has happened remember the kid who pointed a piece of chicken at a teacher and said bang the thing is that the real terrorism of the event is that the mental sleeves of fear propaganda that work at these schools are raising a generation of children to be just like their own somebody shoot me with a bubble gun just my opinion. speak your language. programs in documentaries in arabic in school here on. the world talks specifically ip interviews intriguing story for you. to find out more visit arabic.

and was born don't just 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. yeah i probably fell from the chair and i've been on the sofa and that didn't hurt at all but then i felt the arm chair and i broke my leg. i cried.

for a while. and then at those sleep. but why why why why did it have to be. part. of. the cheat. to simper 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 i suppose the sufferers have brittle bones and are at risk of multiple fractures but there mineral metabolism is in good order the ailment is due to faulty college information. as the main protein in connective tissue college in is the basis

of the human skeleton more. 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 make their arms and legs shorter and in this state even something as light and insignificant as a blanket can cause fractures. there's a swelling beneath the eye here did you hit something you always have brother can hit her they were fooling around well well here we have a person that we can already send to the anesthesiologist.

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. with 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 a sion and restore the limbs to

a normal links creations. ok. you sell one why would a big girl. didn't think i was an outsider going in which my elder twin brother is a totally healthy get. my younger brother is ok too. in the election

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 to. which you could use i made some progress after being taught to walk by one time the wheelchair turned over due 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 what could you not tell my child it came to an abrupt end with. the will of god is omnipotent. in the initial thoughts i found my soul mate. the woman who'd shares my interests and principles. god willing we will go through life together and it should he ended with a thought if we have to enjoy our trials and tribulations well so be. but then you've

given. us our first child was born on the first to february two thousand and three. when i was fifteen weeks pregnant my child was diagnosed with a disc. but unfortunately there was no internet at the time so i was not aware of how serious the condition actually is. geneticist who was in the challenge of our sin he said to me you had been warned about everything it was a decision to i think give or to terminate the pregnancy. my second pregnancy was out of the blue none of us could figure out when it could have happened we went through just staring at each other and shrugging her shoulders that's how teenagers behave in similar situations.

because our second child is ok 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. the argument 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 did i. didn't. know you were a didn't either but i did i pass it on to maria and i said that's how it is. in the overwhelming majority of cases the failure of just one gene is enough for

all stuart genesis imperfecta to be inherited. the risk of those affected passing the disorder on to their children. had french as when she was still in the womb the first months was the most difficult period for me she spent it all in intensive care. and fractures. both arms. have fractured twice. 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. was that when they began tracing the camp she lost her balance fell over. that incident to lead treatment they even said that further treatment might be pointless but if 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 what is a very painful. so what does it do. you. know here here. that's where it's supposed. to heard yesterday to remember. 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. but i slept 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 the operation was successful but of course it's hard to look at a child off to be honest but it's a little. i didn't want to feel old 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 there had to be another fracture. oh are you. ok here i've got a present for you it's a russian doll this time too but it is of

a different kind it's made of crystal. you think you want to describe 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. dr natalia below has spent years treating children afflicted with the disease 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 for those

parents. but i did to me if i knew that sharing my knowledge with others wouldn't be much of a burden to me. so i volunteered to have their so see. two months of the operation we're going to remove the costs today. i want it i can see only part of this bone this is all they've been moved it. all together. it was almost center 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 unlikely to be. if they sense that the parents are also uncomfortable with that

idea i mean psychologically a. scam. 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 right do the same with the other hand do you need to rest against it closer to those now it's like a yogi exists. when the child was born i couldn't understand it was wrong with her she was like jalen her burns was soft and flexible. we didn't temp i was helen's they just fixed and each time he got threat shirt she was in plaster for

six weeks at a time she was simply fall down and break. muscles don't support his spine throw. by half hour walk is not to make a spine show through the process of compression. i do exercises with. one so i think she feels more comfortable when by her side. what's most difficult is making her realized that she must help herself by getting stronger through exercise. you grace. the board with the warmest of the children tain in the courtyard bowl it's good they complained that it arms length then i can't take part in simple i games because there aren't enough

goes 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. they're asked to. listen i want to invite you to attend the event 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. grey it's helen seen each other for a long time you miss him. very much.

wealthier british style. markets why not. find out what's really happening to the global economy because a report on. download the official application to yourself choose your language stream quality and enjoy your favorite touch if you're away from your television well it just doesn't matter how would your mobile device if you could watch ati any time anyway.

live. live. live . live

live. live . you.

know. why. both my parents were atheists if they were among those people who built a savior to union realty 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 and that's when i was twenty six years old. it was abundantly clear to me that if i had a guardian angel who was looking over me and protecting my. own hurting his feelings would really not be a nice thing to do and most of it i felt that i would offend him if i didn't join the orthodox church with them. fish nation.

look at that across here in this holy place that the what the law says see the entire family of royal mottoes was murdered in nineteen eighteen it is there and their holy remains with. those of alexei the heir apparent and his sister as. that's why this is a holy place any more they pray for us to understand. i

don't have the worst husband and the wild mind children on two problematic either. things on said 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 from them the thing is that because see life as something beyond your rachel is something you can't cope with but but if you're a human being in the proper sense of the word like healing almost anything is within your powers but i just feel i may have become somewhat braver when i chose to rely on god's will again me here i had a dream that i want. to visit some petersburg at the parish the public by nurtured

it for twenty five years i yearn to go that would give the wealthy finally my dream came true that if you abandon yourself to god's will and 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 just staying at home and studying on my own would be boring i don't have any bad grades only good and great . i don't like reading or writing writing takes too much

time and since 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'm going to be an artist the worst thing is because drying that's what i like most of all. the children understand that d.s. is not like that they know they'd better not pass to her and leave her alone to avoid unnecessary problems. but she does try to join in. some times she even chases other children as she drives her wheelchair around the room she chimes then when the boys or girls are discussing something that she has friends and a certain fifth forms as well as her own. i discovered she copes

pretty well without me sometimes she asks me to stir pick up books because she finds a disappointment just desserts and i 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 i sensed that their problems provided me with a host of opportunities for reassessing my values. now i communicate with an 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 the elite in 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 linda has a bit of a crush on the kids a searing heat. wallow

it's so beautiful. thanks you're welcome. when nikita and i first met had planted to talk about always glad to read on that there was somebody else like me with a lie explained on line games. if i find a new game he placed with me was on the proceeds of. the sends me messages as soon as i am on the internet. love you shouldn't since with children in wheelchairs i would like to meet more people so that i could visit them for birthdays and other parties. of that easy this gave birth to twins this kid would come from the kitchen carrying

the baby brought to legislate she would use it to feed them with my own. their good bit of the blue to be sure as any three years old and already she was trying to help me. yeah i knew. no not of the. hour i wish you happiness and health. i hope that you'll be condoms and well behaved. and i love you i love you. thanks. my husband when we're gone the other children will take care of her no doubt about. the love of it's great to have such as. it is said to blessing of syria.

some kids don't move much but there's no stopping her she one sits in five minutes . and says all we're doing this concerns both the state of health and this is day to. day think we can convention eight house to house and told her that she can have a good life. and she knows that does a good deal of interesting useful and entertaining things in this world she was never faced a situation where nobody needs and. honestly if i had a child diagnosed with all stewed genesis perfect i wouldn't have a problem with that i 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 with any parent has to be proud of such a child i just wish that there were no tears and there was no pay. here the reindeer is interesting for the herders and when it suffers

people do their best to help. but the distances are. and the roads are. unpredictable. sigrid laboratory to mukherjee was able to build a new most sophisticated robot which all unfortunately doesn't give a darn about anything tim's mission to teach the creation of life should care about humans and world this is why you should care only on the dog.