mediately going into total panic mode guess what this is hardly the first time that something like this has happened remember that 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 slaves of fear propaganda that work at these schools are raising a generation of children to be just like the somebody shoot me with a bubble gun that's just my opinion. to leeds i 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 cried for a while. and then at those sleep. but why why why why did it have to be. what. she. needs 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 are 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. to court more 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 fracture as. there is a swelling beneath the eye here did you hit something and you always have brother can hit her mate with willing around well well here we have a person that we can already sent 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 is trying her best but she can't walk because of these deformities we hope

that she's going to learn a 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. but good morning i just tell you doing. with a patient 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 that information and restore the limbs to a normal links equations. ok well do you then sell one why would a big girl. didn't

think i was an outsider when you reached the elder twin brother totally healthy and asking. my younger brother is ok to. 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 would you announce how much childhood came to an abrupt end with. the will of god is omnipotent. in the initial thoughts i found my soul mates and a woman who'd shares my interests and principles. god willing we will go through life together in egypt he stands with the thought if we have to enjoy our trials and tribulations well but also be. but then you've given. us our first child was born on the first to february two thousand and three. is when i was fifteen weeks pregnant my child was diagnosed with a disk. that the fortunately there was no internet at the time so i was

not aware of how serious the condition actually is. geneticist who is in the challenge of our sin he said to me you had been warned about everything it was still 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. just staring at each other and shrugging her shoulders that's how teenagers behave in similar situations. is our second child. we had 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 us. was the disease to me by any chance to carry on with a care. 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 but i passed 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. back to 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 an 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 and broke. 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 bring to mind is the thank you. i hear here.

that's where it's supposed it's my duty 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 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 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 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. thank you. 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 austin a genesis imperfecta first and last. card 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 a bill over 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 on 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 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 all they've 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 unlikely to be. if they sense that the parents are also on a comfortable that 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.

for the right 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 it was wrong with her she was like jalen her burns was soft and flexible. we didn't tamper with helen's they just fixed and each time they got thread chert she was in plaster for six weeks at a time she would simply fall down and break its. muscles don't support a spine throw. a half hour walk is not to make a spine show through the process of compression.

i do exercises with her. so i think she feels more comfortable when i'm by her side . what's most difficult is making her realize that she must help herself by getting stronger through exercise. you grace. the board with the might be more menace to the children tain in the courtyard. they keep then they are missing. then i can't take part in simpler games because there aren't enough goals 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 for. the rest of though. 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 balancing this all the time you miss him. larry much. wealthier british style.

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both my parents were atheists it's the same 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 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. hurting his feelings would really not be a nice thing to do and most of i felt that i would offend him if i didn't join the orthodox church with them. his nation. look at that across here in this holy place of the what the law says see the entire family of royal musses was murdered in nineteen eighteen it is there and their holy

remains were. 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 dreadfuls 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. just like a film star 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 human 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 i had a dream but i want. to visits in petersburg a lot of the papers the public by nachiket for twenty five years i yearned to go that would give those 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 studying on my own would be boring i don't have any bad grades only good and great going into will 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'm 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 chases other children as she drives her wheelchair around the room she chimes in 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 stack 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 bad dream. only his 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 just as 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 and 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 broom powers 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 kid a syrian eat. while it's so beautiful. thanks you're welcome. when the kids and i first met had plenty to talk about always glad to read on that

there was somebody else like me. explain on line games. if i find a new game he placed with me was on the proceeds of. the going to sends me messages as soon as i am on the internet. but for sure doing things with children in wheelchairs i would love to means more people so that i could visit them for birthdays and other parties. gave birth to twins this kid would come from the kitchen carrying the baby bottle like just she would use it to feed them with my own. their good bit of the good but she was only three years old and already she was trying to help me. yeah

i knew. known as. i wish you happiness and health. i hope you'll be condoms and well behaved. i love you i love you. thank you. but then my husband where god the other children will take care of her no doubt about. the love of it's great to have such as. it is such a blessing of syria. 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 divel family may 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 news for the new entertaining things in this world chill has never faced a situation when nobody needs her. honestly if i had a child diagnosed with austere genesis perfect i wouldn't have 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 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 it interesting for the herders. and when it suffers. people do their best to help. but the distances are. and the roads are tough and unpredictable. will the roman need d.h.i. .

choose your language killing the killer the infidels going to stay still some. choose to use the consensus get to. choose the opinions that invigorating book. choose the stories that imply the life choose be access to your office.