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1158 Videos  
page 1 / 58
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  my name is the healthy boy au mondo biza...
my name is the healthy boy au mondo bizarro à rennes, le 15 mars 2007. my name is the healthy boy au mondo bizarro à rennes, le 15 mars 2007. my name is the healthy boy au mondo bizarro à rennes, le 15 mars 2007.
  my name is the healthy boy au mondo biza...
my name is the healthy boy au mondo bizarro à rennes, le 15 mars 2007. my name is the healthy boy au mondo bizarro à rennes, le 15 mars 2007. my name is the healthy boy au mondo bizarro à rennes, le 15 mars 2007.
  my name is the healthy boy au mondo biza...
my name is the healthy boy au mondo bizarro à rennes, le 15 mars 2007. my name is the healthy boy au mondo bizarro à rennes, le 15 mars 2007. my name is the healthy boy au mondo bizarro à rennes, le 15 mars 2007.
  the healthy boy - all over the seas
live footage by makiz'art @nantes/live bar/oct-27-2006 live footage by makiz'art @nantes/live bar/oct-27-2006 live footage by makiz'art @nantes/live bar/oct-27-2006
  my name is the healthy boy au mondo biza...
my name is the healthy boy au mondo bizarro à rennes, le 15 mars 2007. my name is the healthy boy au mondo bizarro à rennes, le 15 mars 2007. my name is the healthy boy au mondo bizarro à rennes, le 15 mars 2007.
  my name is the healthy boy au mondo biza...
my name is the healthy boy au mondo bizarro à rennes, le 15 mars 2007. my name is the healthy boy au mondo bizarro à rennes, le 15 mars 2007. my name is the healthy boy au mondo bizarro à rennes, le 15 mars 2007.
  healthy boy
music video for david tranaman's song entitled music video for david tranaman's song entitled music video for david tranaman's song entitled
  the healthy boy
we are never healthy. this is guinness, nyquil, and crushed tums. song: 'track 3' - soul position we are never healthy. this is guinness, nyquil, and crushed tums. song: 'track 3' - soul position we are never healthy. this is guinness, nyquil, and crushed tums. song: 'track 3' - soul position
  106 - a healthy baby boy
owned by www.droversrun.web-log.nl owned by www.droversrun.web-log.nl owned by www.droversrun.web-log.nl
  bye bye birdie video blog: day 7:healthy...
and we're already at day 7! wow. this is going by fast. i'm almost a third of the way done... but no time for that now! i have a message: some people have already started pointing out small problems in these dailies. that's a good thing. at this point in the project, i can still fix problems. after i finish the dvd, the odds of me fixing anything are one in a million. like, there'd have to be a crippling problem with the movie, not someone missing one line. but for now, if you notice someone's hair magically change, be sure to let me know! i'm still open to constructive criticism. well, enough public service messages. i have math homework to finish and an english project to film. enjoy healthy normal american boy and the introduction of albert's obnoxious madre. and we're already at day 7! wow. this is going by fast. i'm almost a third of the way done... but no time for that now! i have a message: some people have already started pointing out small problems in these dailies. that's a good thing. at this point in the project, i can still fix problems. after i finish the dvd, the odds of me fixing anything are one in a million. like, there'd have to be a crippling problem with the movie, not someone missing one line. but for now, if you notice someone's hair magically change, be sure to let me know! i'm still open to constructive criticism. well, enough public service messages. i have math homework to finish and an english project to film. enjoy healthy normal american boy and the introduction of albert's obnoxious madre. and we're already at day 7! wow. this is going by fast. i'm almost a third of the way done... but no time for that now! i have a message: some people have already started pointing out small problems in these dailies. that's a good thing. at this point in the project, i can still fix problems. after i finish the dvd, the odds of me fixing anything are one in a million. like, there'd have to be a crippling problem with the movie, not someone missing one line. but for now, if you notice someone's hair magically change, be sure to let me know! i'm still open to constructive criticism. well, enough public service messages. i have math homework to finish and an english project to film. enjoy healthy normal american boy and the introduction of albert's obnoxious madre.
  bye bye birdie - healthy normal american boy
hicksville high school production of bye bye birdie 2008 hicksville high school production of bye bye birdie 2008 hicksville high school production of bye bye birdie 2008
  mae peterson/ healthy normal american bo...
this is a scene from jerry gibson summer theater's production of bye bye birdie performed in july 2007. i am in this scene as mae peterson =] also included is healthy normal american boy. this is a scene from jerry gibson summer theater's production of bye bye birdie performed in july 2007. i am in this scene as mae peterson =] also included is healthy normal american boy. this is a scene from jerry gibson summer theater's production of bye bye birdie performed in july 2007. i am in this scene as mae peterson =] also included is healthy normal american boy.
  healthy boy 2
ang likot ni aj ngayon, eto ang pruweba. ang likot ni aj ngayon, eto ang pruweba. ang likot ni aj ngayon, eto ang pruweba.
  the healthy normal patriotic american boy
conrad birdie conrad birdie conrad birdie
  the boy who can never grow old
this programme follows 19-year-old stuart wickison, who is refusing to let the debilitating condition duchenne muscular dystrophy (dmd) stop him from going to university. dmd is a rare degenerative condition that affects boys, gradually robbing the sufferer of the ability to use all his muscles. born healthy, boys with dmd will later begin to have problems standing up. as teenagers they will need wheelchairs and soon become effectively trapped inside their bodies. the incurable condition gets progressively worse until the sufferers heart and lungs stop functioning altogether, resulting in death. young men with dmd do not live long into their 20s. incredibly, faced with this prognosis, 19-year-old stuart wickison has decided to go to university. despite the fact that he is nearing the end of his life, stuarts determination to live as a normal teenager has never been stronger. he has decided to leave the comforts of treloar college, a hampshire college with a high level of specialist care for severely disabled young people, to study art. im not here to suffer, he says matter-of-factly. im here to make an impact. going to university will be a huge step for stuart. at treloars he has 24-hour medical support, can call upon physiotherapists at any time, and lives in an environment where people are accustomed to his needs. this support enables stuart to live, so organising his care for university is a matter of life and death. the treloars staff, with whom stuart has become close during his three years at the college, are encouraging him to go and helping him prepare for this next step. however, when stuart leaves treloars he will also be saying goodbye to four friends with dmd: jonathan, harry, ben and tyran. the five boys lost another friend, david, to dmd last year and have been campaigning for greater medical research funding to find a cure something which scientists are coming closer to achieving. the boys head up to london to lobby parliament, and meet families from all over the country who have been affected by dmd. the campaign is now in its fifth year and has made great advances in raising awareness and funds for research. at the forefront of the research is professor dominic wells, who has been involved in pioneering, cutting-edge research into gene transfer therapy. unfortunately, developing a cure will be a long and complicated process and stuart knows that it is unlikely to happen in his lifetime. however, the campaign has given him a sense of shared purpose and the knowledge that it could eventually help the younger generation of dmd sufferers. back at treloars, the students are getting ready for the end of term. while his friends head out for a night on the town, stuart must study: he has an a-level exam in a few days and a university open day to attend. however, staff are concerned as stuarts health is deteriorating: his ability to swallow is getting weaker and he is losing weight. four days before he is due to begin university, stuart has to have an operation to place a feeding tube in his stomach but the doctors say that he can still start university as planned. stuarts first day is a momentous one for him, as well as his mother, mandy. hes been through a lot to get here, she says proudly. stuart is excited about taking the next step in his education and development. its made me realise that theres more to me than suffering, he explains. its enlightening to walk into a place and everyones looking at you and valuing you as an equal to everyone else which ive never had before. this programme follows 19-year-old stuart wickison, who is refusing to let the debilitating condition duchenne muscular dystrophy (dmd) stop him from going to university. dmd is a rare degenerative condition that affects boys, gradually robbing the sufferer of the ability to use all his muscles. born healthy, boys with dmd will later begin to have problems standing up. as teenagers they will need wheelchairs and soon become effectively trapped inside their bodies. the incurable condition gets progressively worse until the sufferers heart and lungs stop functioning altogether, resulting in death. young men with dmd do not live long into their 20s. incredibly, faced with this prognosis, 19-year-old stuart wickison has decided to go to university. despite the fact that he is nearing the end of his life, stuarts determination to live as a normal teenager has never been stronger. he has decided to leave the comforts of treloar college, a hampshire college with a high level of specialist care for severely disabled young people, to study art. im not here to suffer, he says matter-of-factly. im here to make an impact. going to university will be a huge step for stuart. at treloars he has 24-hour medical support, can call upon physiotherapists at any time, and lives in an environment where people are accustomed to his needs. this support enables stuart to live, so organising his care for university is a matter of life and death. the treloars staff, with whom stuart has become close during his three years at the college, are encouraging him to go and helping him prepare for this next step. however, when stuart leaves treloars he will also be saying goodbye to four friends with dmd: jonathan, harry, ben and tyran. the five boys lost another friend, david, to dmd last year and have been campaigning for greater medical research funding to find a cure something which scientists are coming closer to achieving. the boys head up to london to lobby parliament, and meet families from all over the country who have been affected by dmd. the campaign is now in its fifth year and has made great advances in raising awareness and funds for research. at the forefront of the research is professor dominic wells, who has been involved in pioneering, cutting-edge research into gene transfer therapy. unfortunately, developing a cure will be a long and complicated process and stuart knows that it is unlikely to happen in his lifetime. however, the campaign has given him a sense of shared purpose and the knowledge that it could eventually help the younger generation of dmd sufferers. back at treloars, the students are getting ready for the end of term. while his friends head out for a night on the town, stuart must study: he has an a-level exam in a few days and a university open day to attend. however, staff are concerned as stuarts health is deteriorating: his ability to swallow is getting weaker and he is losing weight. four days before he is due to begin university, stuart has to have an operation to place a feeding tube in his stomach but the doctors say that he can still start university as planned. stuarts first day is a momentous one for him, as well as his mother, mandy. hes been through a lot to get here, she says proudly. stuart is excited about taking the next step in his education and development. its made me realise that theres more to me than suffering, he explains. its enlightening to walk into a place and everyones looking at you and valuing you as an equal to everyone else which ive never had before. this programme follows 19-year-old stuart wickison, who is refusing to let the debilitating condition duchenne muscular dystrophy (dmd) stop him from going to university. dmd is a rare degenerative condition that affects boys, gradually robbing the sufferer of the ability to use all his muscles. born healthy, boys with dmd will later begin to have problems standing up. as teenagers they will need wheelchairs and soon become effectively trapped inside their bodies. the incurable condition gets progressively worse until the sufferers heart and lungs stop functioning altogether, resulting in death. young men with dmd do not live long into their 20s. incredibly, faced with this prognosis, 19-year-old stuart wickison has decided to go to university. despite the fact that he is nearing the end of his life, stuarts determination to live as a normal teenager has never been stronger. he has decided to leave the comforts of treloar college, a hampshire college with a high level of specialist care for severely disabled young people, to study art. im not here to suffer, he says matter-of-factly. im here to make an impact. going to university will be a huge step for stuart. at treloars he has 24-hour medical support, can call upon physiotherapists at any time, and lives in an environment where people are accustomed to his needs. this support enables stuart to live, so organising his care for university is a matter of life and death. the treloars staff, with whom stuart has become close during his three years at the college, are encouraging him to go and helping him prepare for this next step. however, when stuart leaves treloars he will also be saying goodbye to four friends with dmd: jonathan, harry, ben and tyran. the five boys lost another friend, david, to dmd last year and have been campaigning for greater medical research funding to find a cure something which scientists are coming closer to achieving. the boys head up to london to lobby parliament, and meet families from all over the country who have been affected by dmd. the campaign is now in its fifth year and has made great advances in raising awareness and funds for research. at the forefront of the research is professor dominic wells, who has been involved in pioneering, cutting-edge research into gene transfer therapy. unfortunately, developing a cure will be a long and complicated process and stuart knows that it is unlikely to happen in his lifetime. however, the campaign has given him a sense of shared purpose and the knowledge that it could eventually help the younger generation of dmd sufferers. back at treloars, the students are getting ready for the end of term. while his friends head out for a night on the town, stuart must study: he has an a-level exam in a few days and a university open day to attend. however, staff are concerned as stuarts health is deteriorating: his ability to swallow is getting weaker and he is losing weight. four days before he is due to begin university, stuart has to have an operation to place a feeding tube in his stomach but the doctors say that he can still start university as planned. stuarts first day is a momentous one for him, as well as his mother, mandy. hes been through a lot to get here, she says proudly. stuart is excited about taking the next step in his education and development. its made me realise that theres more to me than suffering, he explains. its enlightening to walk into a place and everyones looking at you and valuing you as an equal to everyone else which ive never had before.
  hilarious crank that soulja boy abc7 kid...
is this what they teach kids nowadays? notice how every kid is jumping up and down like some animal blowing their ears with this c(rap) music. i agree with getting them healthy and i really like this program, but when i heard that hideous song....it just ruined it... tags: hilarious crank that soulja souljah boy abc7 kid healthy 3/12/2008 crank dat that soulja boy abc7 healthy kid kids hip hop rap g-unit 50 cent crap music dat soulja boy spongebob souljaboy spongebob crap crap crank dat soulja boy spongebob superman superman superman souljah girl girl girl souljagirl souljagirl souljagirl bad music music musica musica r.i.p rest in peace blah blah boring music videos video funny comedy hilarious hysterical renowned stuff soldierboy soldier correct way of spelling it tags tag youtube you tube kan check 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 0 is this what they teach kids nowadays? notice how every kid is jumping up and down like some animal blowing their ears with this c(rap) music. i agree with getting them healthy and i really like this program, but when i heard that hideous song....it just ruined it... tags: hilarious crank that soulja souljah boy abc7 kid healthy 3/12/2008 crank dat that soulja boy abc7 healthy kid kids hip hop rap g-unit 50 cent crap music dat soulja boy spongebob souljaboy spongebob crap crap crank dat soulja boy spongebob superman superman superman souljah girl girl girl souljagirl souljagirl souljagirl bad music music musica musica r.i.p rest in peace blah blah boring music videos video funny comedy hilarious hysterical renowned stuff soldierboy soldier correct way of spelling it tags tag youtube you tube kan check 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 0 is this what they teach kids nowadays? notice how every kid is jumping up and down like some animal blowing their ears with this c(rap) music. i agree with getting them healthy and i really like this program, but when i heard that hideous song....it just ruined it... tags: hilarious crank that soulja souljah boy abc7 kid healthy 3/12/2008 crank dat that soulja boy abc7 healthy kid kids hip hop rap g-unit 50 cent crap music dat soulja boy spongebob souljaboy spongebob crap crap crank dat soulja boy spongebob superman superman superman souljah girl girl girl souljagirl souljagirl souljagirl bad music music musica musica r.i.p rest in peace blah blah boring music videos video funny comedy hilarious hysterical renowned stuff soldierboy soldier correct way of spelling it tags tag youtube you tube kan check 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 0
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