Brooke Greenberg is already 16 years old but she looks like a baby and thinks like a baby, and what she have are baby teeth. She's the child frozen in time. Doctors could not explain why she doesn't age like normal people.
TLC will show a documentary about Brooke, Child Frozen in Time, on August 9th, Sunday, 9 PM.
To me she is a adult baby and I think she have's and nice mind that no one should take away.god dose alot of nice that so we can be like other people and what that young teen she is a nice and loveing people like we all are in this world.
the story of Brooke Greenberg really hit home to me i'm from california and i have a son who is 4 years old that has many of the same features as her and the doctors don't know what to do much less what to think. he has chromezone deletions that haven't been heard of. thank you brittany hoagland from fresno, ca
i can relate brooke so much to my girlfriends sister. she is a twin 13years old, and like brooke in multiple ways. let me tell you she is the sweetest little girl i've ever met, she will chase me out the door just to say bye to me one more time lol she truely is the sweetest little girl ever! its amazing how aware she really is of what is going on around her. its really like she is a 13 year old girl trapped in a 3 year olds body.
i saw brooke on t.l.c she look's so sweet to me i whant to meet her so badlie but i am not where yall are i whant to see yall happy!!!!!!!!!!!!!!! yall sweet mom's and dad thack god she is alive
My child has the same problem. She is going to be 5 years old and still looks like a baby. She weighs 25lbs and measures in at 30 in. No doctor can tell me what is wrong. It is very frustrating. I am happy to see there is someone else like my Mya out there. She looks happy just like my baby is. I treasure her everyday.
i feel so bad for the family but the one thing i thing is totally ridiculous is the fact that the docters are pretty much using a child as an experiment to reverse the aging process or stop it.
I actually just seen the documentary of Brooke last night. I have a son that has DiGeorge Syndrome, a chromosome deletion. He has some similar features to her also. He is also very small. He will be two next month and only weighs 15 lbs. He is 30 inches also and is just very slender. He can stand on his own, and is well on his way to walking. I agree with the parents about not changing anything about our children's condition. We love them that much more.
I grew up all over Luzon because of the nature of my father’s work. I can remember Dagupan City, it has helped a lot in shaping my childhood, we stayed there for about 5 years. Then in one of the islands in Hundred Islands, I couldn’t remember how long. Then there was Los BaƱos Laguna, 7 colorful years there. And of course Mandaluyong City. Then from Luzon I came to Cotabato City where I experienced my first “culture shock”. But I later learned to love the people and the place and stayed there for two years. Now I’m here in General Santos City (the Pacquiao town) where I met my destined lifetime partner who is a Visayan who could speak Tagalog, English, and some Ilonggdo.
My father is Ilocano, my mother Ilonga, but I grew up speaking Tagalog because that was what my family use at home. I have a 3 year old gwapong long haired son named Joshua Daniel and for now my world and joy is almost inside my family lang, wife and mother muna. I studied in UPLB (Communication Arts Major in Theater Arts for Children) and Mass Communication at Ramon Magsaysay Memorial Colleges where I met my husband. He was teaching there part-time and I was in one of his Essay Writing classes. He encourages me to write and to blog. He majored in English but is so enamored with the language of computers. He takes care of the technical side of this blog and as much as possible does not get his hands wet with painting my emotions in my posts.
10 comments:
To me she is a adult baby and I think she have's and nice mind that no one should take away.god dose alot of nice that so we can be like other people and what that young teen she is a nice and loveing people like we all are in this world.
the story of Brooke Greenberg really hit home to me i'm from california and i have a son who is 4 years old that has many of the same features as her and the doctors don't know what to do much less what to think. he has chromezone deletions that haven't been heard of. thank you brittany hoagland from fresno, ca
i wacthed the documentary and it was unbeleivable
i can relate brooke so much to my girlfriends sister. she is a twin 13years old, and like brooke in multiple ways. let me tell you she is the sweetest little girl i've ever met, she will chase me out the door just to say bye to me one more time lol she truely is the sweetest little girl ever! its amazing how aware she really is of what is going on around her. its really like she is a 13 year old girl trapped in a 3 year olds body.
i saw brooke on t.l.c she look's so sweet to me i whant to meet her so badlie but i am not where yall are i whant to see yall happy!!!!!!!!!!!!!!! yall sweet mom's and dad thack god she is alive
My child has the same problem. She is going to be 5 years old and still looks like a baby. She weighs 25lbs and measures in at 30 in. No doctor can tell me what is wrong. It is very frustrating. I am happy to see there is someone else like my Mya out there. She looks happy just like my baby is. I treasure her everyday.
i feel so bad for the family but the one thing i thing is totally ridiculous is the fact that the docters are pretty much using a child as an experiment to reverse the aging process or stop it.
Her ears are growing. :o
brook is beautiful and was born in her own unique way she is our future.we all have a reason for being here. god bless her and her family.
I actually just seen the documentary of Brooke last night. I have a son that has DiGeorge Syndrome, a chromosome deletion. He has some similar features to her also. He is also very small. He will be two next month and only weighs 15 lbs. He is 30 inches also and is just very slender. He can stand on his own, and is well on his way to walking. I agree with the parents about not changing anything about our children's condition. We love them that much more.
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