I have been Landau-Kleffner Syndrome since I was 2 1/2 to 11 years olds... I am now 21 1/2... I still have problem with english language but ASL ( american sign language) is much more easy for me to chat with my family and friends. I did not remember what happen between 2-11 of my ages... and I have become a better person as today.
my daughter has just ben diagnosed with this syndroime she is now age 3 and first showed signs at age one as she spoke alot then just slipt back and startd screaming and making funny noises and its hard 4me as my daughter is the only one in my country with this syndrome so i have no one to talk to about it so its cool that ppl can post things on you tube about it
My 11 year old has it, his started at the age of two, but wasn't diagnosed till he was four. I have a video of him and his parrotlet on youtube. He still can't carry a conversation with anyone, but he can speak enough to let you know what he needs or how he feels. Thats wonderful compared to how angry and fustrated he was for most of his life. Its a cruel syndrome.
I have the Syndrom and i'm glad to see a person who take a try to inform other's of the syndrom. I'm actually in a kind of way cured for the syndrom, but sometimes there are some sitiutions where i have problem to say the upcoming sentence and need time to say it right, but I'm talking like normal people do perfectly. so i still have it, but the problem is so tiny that people can't see it on me. is great thank you for the video, still you lips aren't follow the video.
I was diagnosed with the rare-form epilepsy at age 8 and didn't start recovering until around age 10.
Today, the only remains of the disease is a speech disorder. Unfortuneatly, due to the lack of income in my immediate family, I have not been able to receive any amounts of speech therapy.
I'm 20 years of age now, and still, I have not been able to receive any speech therapy.
This video is a good summary of the disease, describing the basic aspects of Landau-Kleffner. Good Job.
I have been Landau-Kleffner Syndrome since I was 2 1/2 to 11 years olds... I am now 21 1/2... I still have problem with english language but ASL ( american sign language) is much more easy for me to chat with my family and friends. I did not remember what happen between 2-11 of my ages... and I have become a better person as today.
casgirl02 11 months ago
I think you will find that LKS is less rare than people think, and is being under diagnosed , and is being confused by misdiagnosis of autism
slacker361 2 years ago
my daughter has just ben diagnosed with this syndroime she is now age 3 and first showed signs at age one as she spoke alot then just slipt back and startd screaming and making funny noises and its hard 4me as my daughter is the only one in my country with this syndrome so i have no one to talk to about it so its cool that ppl can post things on you tube about it
missrayne100 2 years ago
@missrayne100 what country do you lives in?
casgirl02 11 months ago
My 11 year old has it, his started at the age of two, but wasn't diagnosed till he was four. I have a video of him and his parrotlet on youtube. He still can't carry a conversation with anyone, but he can speak enough to let you know what he needs or how he feels. Thats wonderful compared to how angry and fustrated he was for most of his life. Its a cruel syndrome.
Batznblkcatz 3 years ago
I have the Syndrom and i'm glad to see a person who take a try to inform other's of the syndrom. I'm actually in a kind of way cured for the syndrom, but sometimes there are some sitiutions where i have problem to say the upcoming sentence and need time to say it right, but I'm talking like normal people do perfectly. so i still have it, but the problem is so tiny that people can't see it on me. is great thank you for the video, still you lips aren't follow the video.
braindamaged89 4 years ago
Thank you! My daughter has just been diagnosed with LKS.
It is nice to hear someone speak about it.
MelandGj 4 years ago
I was diagnosed with the rare-form epilepsy at age 8 and didn't start recovering until around age 10.
Today, the only remains of the disease is a speech disorder. Unfortuneatly, due to the lack of income in my immediate family, I have not been able to receive any amounts of speech therapy.
I'm 20 years of age now, and still, I have not been able to receive any speech therapy.
This video is a good summary of the disease, describing the basic aspects of Landau-Kleffner. Good Job.
AlgidMidnight 4 years ago