This is very informative but impossible to read. I hope you'll redo it so the information will be available to those who do wish to become informed. (I realize how repetitive that came across)
My nephew is 21 w Duchennes & this cause is very important to me.
tiny.cc / ukpolitics <<<<< this one , you have to TYPE the URL in to the IE browser
JUST look at this subliminal advertisement, fall for stem cell fictions trap , HOW STUPID can new generation of mothers be -- - or family -- illiterate !!
for great indian treatment for nerve and bone diseases just click once at our blog ===> successful-treatment.blogspot.com or contact us : successmd.india@gmail.com
my nephew is 6.5 years (may 2011). he started showing up the sign. kindly suggest me what to do ? is there any cure? i am totally out of my mind..can not even think properly..
@121nafees best thing you can do is get everyone to vote ron paul 2012. fda is holding among other government barriers are holding things up. ron paul will fix.
I Thomas E Ichim, am the senior author of the publication in which this (adult stem cells) was performed in a human with Duchenne...since youtube doesnt let me put up links, if you search Ichim T on pubmed you will find paper
so far i dont have any serious problems with my heart and lungs... i am just worried or bothered why im still strong coz i know the usual dmd patient is losing their ability to walk at age of 12...
@ladyanatsu im already 18. no, i havent taken some serious treatments... it is just that i made myself independent on everyday happenings of my life especially in school... since i can still walk
@dilan678 That is truly amazing that you can still walk without taking treatments. The doctors told me my son would most likely end up in a wheelchair if he doesn't get Exon Skipping Treatments. Keep in mind he is only 6 months old but I have to think of his future.
I'm 28 years old and I have Duchenne. I am alive and still living strong! So there is hope. The process for finding a cure is slow because of politics and the FDA. About religion, I'm Catholic but I don't share all of the Church's beliefs. I support any stem cell research and I'm not ashamed by it. I want people to live normal happy lives. It makes me sad that people are against research that will help improve the quality of people's lives. They would rather protect a cell! That is ridiculous!
Damnation for the living, let them suffer, but save the fetuses so that they too might be damned by "Ethics". Is it more ethical to ignore those diagnosed or is it more ethical to ignore those yet to be diagnosed? I'm all for protecting life but how about saving whats left of the lives of those already in need of help. Living the life of a person with Duchennes Isn't much of a life to live and all hope possible is needed. I don't get how people can be so cruel as to try to stop such research.
i've got DMD i'm 23 years old and what they are saying on this video does not make me feel hopeful of ever getting out of my wheelchair but ill never give into the illness that's why i'm still here the doctors don't know what part of my gene is missing but i'm getting a lot weaker these days it scares me i wish i know more about what the government are doing too help.
Im sure people in a fucking wheel chair getting ready to die would not mind having a chance of a normal life. They got it to work in a dog so why not a human? They just want to be cautious so they cannot be sued.
cause of christianity it is the church who attempt to deny all of biological research in the first place. they believe on;y god can deside the life span of human, can human do not own the right to control their fate. so human still have long way to go if we can't get away from these ridiculous religious belief.
PS: pretty much of christian population still believe ridiculous resurrection and after-life. but remember these stupid god-belief are all came from fucking middle east.
My brother has it and he's 14 years old. He's getting weaker and we really want to see him get stronger. My uncle died from it when he was 18 years old. It's a horrible disease to have. I want this disease to go away forever.
I probably should have had an argument about it. I realize what i said was odd. Testing will maybe work. Im in a different study for treatment so i have heard wrong opinions. I have read about it lately and now know the secret behind it, no one knows yet what will happen with this stem cell research. I am hopeful that more people will read and understand this research before they point fingers.
hi im doing a school project on duchenne and i came across this video. i didnt know that there were any potential tratments for it. I posted this comment to wish everyone with any muscular dystrophy the best of lucks and never to stop fighting cause its not over
This has been flagged as spam show
This is very informative but impossible to read. I hope you'll redo it so the information will be available to those who do wish to become informed. (I realize how repetitive that came across)
My nephew is 21 w Duchennes & this cause is very important to me.
Godspeed-
530BigBen 2 months ago
all the illiterate people are I
tiny.cc / ukpolitics <<<<< this one , you have to TYPE the URL in to the IE browser
JUST look at this subliminal advertisement, fall for stem cell fictions trap , HOW STUPID can new generation of mothers be -- - or family -- illiterate !!
rTVstation 4 months ago
This has been flagged as spam show
for great indian treatment for nerve and bone diseases just click once at our blog ===> successful-treatment.blogspot.com or contact us : successmd.india@gmail.com
varma4md 6 months ago
my nephew is 6.5 years (may 2011). he started showing up the sign. kindly suggest me what to do ? is there any cure? i am totally out of my mind..can not even think properly..
121nafees 8 months ago
@121nafees best thing you can do is get everyone to vote ron paul 2012. fda is holding among other government barriers are holding things up. ron paul will fix.
Timb0NZ 3 months ago
I Thomas E Ichim, am the senior author of the publication in which this (adult stem cells) was performed in a human with Duchenne...since youtube doesnt let me put up links, if you search Ichim T on pubmed you will find paper
this indeed is a very fascinating area
Tom
cellmedicine 1 year ago
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Tea Baggers will do thier best to put an end to it here. Voting has consenquences.
Rainiermec1 1 year ago
Tea Baggers will do thier best to put an end to it here. Voting has consenquences.
Rainiermec1 1 year ago
so far i dont have any serious problems with my heart and lungs... i am just worried or bothered why im still strong coz i know the usual dmd patient is losing their ability to walk at age of 12...
dilan678 1 year ago
How old are you? Did you have other treatments?
ladyanatsu 1 year ago
@ladyanatsu im already 18. no, i havent taken some serious treatments... it is just that i made myself independent on everyday happenings of my life especially in school... since i can still walk
dilan678 1 year ago
@dilan678 That is truly amazing that you can still walk without taking treatments. The doctors told me my son would most likely end up in a wheelchair if he doesn't get Exon Skipping Treatments. Keep in mind he is only 6 months old but I have to think of his future.
ladyanatsu 1 year ago
i have a dmd too... but at my age of 17 i might say that im still strong coz i can still WALK or moving around the house INDEPENDENTLY...
dilan678 1 year ago
@dilan678 ya me too
jubinjibin 1 year ago
I'm 28 years old and I have Duchenne. I am alive and still living strong! So there is hope. The process for finding a cure is slow because of politics and the FDA. About religion, I'm Catholic but I don't share all of the Church's beliefs. I support any stem cell research and I'm not ashamed by it. I want people to live normal happy lives. It makes me sad that people are against research that will help improve the quality of people's lives. They would rather protect a cell! That is ridiculous!
tealfinatic 2 years ago 2
Damnation for the living, let them suffer, but save the fetuses so that they too might be damned by "Ethics". Is it more ethical to ignore those diagnosed or is it more ethical to ignore those yet to be diagnosed? I'm all for protecting life but how about saving whats left of the lives of those already in need of help. Living the life of a person with Duchennes Isn't much of a life to live and all hope possible is needed. I don't get how people can be so cruel as to try to stop such research.
Pitraptor 2 years ago
i've got DMD i'm 23 years old and what they are saying on this video does not make me feel hopeful of ever getting out of my wheelchair but ill never give into the illness that's why i'm still here the doctors don't know what part of my gene is missing but i'm getting a lot weaker these days it scares me i wish i know more about what the government are doing too help.
Electrome 2 years ago 3
Why a decade?
Im sure people in a fucking wheel chair getting ready to die would not mind having a chance of a normal life. They got it to work in a dog so why not a human? They just want to be cautious so they cannot be sued.
jc1pick 2 years ago 6
why a decade? what's holding up the process?
DarkRain9000 2 years ago 8
cause of christianity it is the church who attempt to deny all of biological research in the first place. they believe on;y god can deside the life span of human, can human do not own the right to control their fate. so human still have long way to go if we can't get away from these ridiculous religious belief.
PS: pretty much of christian population still believe ridiculous resurrection and after-life. but remember these stupid god-belief are all came from fucking middle east.
blueuser4000 2 years ago
you are so wrong!!
middle east is not against that to find medical for people who need it,because God gave us a brain to think about everything,tallk ect .
so we have brain and we can use it,God gave to people some sicknes but also He gave a medical for it so on us people is to find it...
and church is agains that because they think that people playing with God
thats stupid!
and one PAPA have no right to think in the name of milions sick people and to stop their opportunity to live normal life
ilepile26 2 years ago
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@DarkRain9000 its the fda, vote ron paul 2012 to fix
Timb0NZ 3 months ago
This has been flagged as spam show
Respond to this video... its the fda, vote ron paul 2012 to fix
Timb0NZ 3 months ago
My brother has it and he's 14 years old. He's getting weaker and we really want to see him get stronger. My uncle died from it when he was 18 years old. It's a horrible disease to have. I want this disease to go away forever.
missyS92 2 years ago 4
Comment removed
cooldit1 3 years ago
Well if you were disabled you wouldn't say that.
Stem cells aren't taken from feotuses anymore if that's what you mean.
CapriceK 3 years ago 4
i happen to have duchenne muscular dystrophy.
I probably should have had an argument about it. I realize what i said was odd. Testing will maybe work. Im in a different study for treatment so i have heard wrong opinions. I have read about it lately and now know the secret behind it, no one knows yet what will happen with this stem cell research. I am hopeful that more people will read and understand this research before they point fingers.
Just saying, i am hopeful it may work.
cooldit1 3 years ago 2
i also got duchenne so i hope im still there when if there is an medicin who recors.
SecretYoungLink007 3 years ago 2
hi im doing a school project on duchenne and i came across this video. i didnt know that there were any potential tratments for it. I posted this comment to wish everyone with any muscular dystrophy the best of lucks and never to stop fighting cause its not over
damnationandaday2003 3 years ago 2
Please please please hurry and thank you soo much for your effort!
Luchik33 3 years ago 2
Hurry up!
StuBakerComedy 3 years ago 2