At first I hesitated to post this article, because it seemed to expose someone who is disabled is a gift from the Almighty, but when I think of profound postitif aspect and I think again, there are many things that many can we take lessons and learn from her This little. It was not strong enough to not tear dripping, try to explore and try to position themselves in the mirror of life itself, a little innocent fun and spontaneity in humor the boy. He is Juliana Wetmore, a little girl who was born with the condition of the body is not perfect as friends of his age. According to sources ruanghati.com Juliana was born in 2003 with a rare genetic disorder (craniofacial) better known as (Treacher Collins syndrome).
in infancy
Yuliana Wetmore, Although such conditions are not born peers, Yuliana remained optimistic and cheerful
The girl who does not have literal face because he lost 30-40 percent of the bones and jaw bones of his face. According to doctors who handle cases Yuliana is one of the rare cases in the world, until now Yuliana had undergone facial plastic surgery 20 times for more help perfecting his face. Doctors understand that it is very difficult and even impossible to provide such a face off or a new face for Yuliana, but at least they tried to help so that it can do better than that now. To better able to bring the girl to have Yuliana more confidence to interact with others. Yuliana is a little girl who has a pretty good intelligence, so said his parents. This girl has a pretty exciting potential of the intellectual side. God is Just and Wise.
By looking at the condition masihkah Yuliana we do not feel grateful at what the Lord Give it to us today?One thing that makes me a disturbed conscience of Yuliana, that is, with such a condition this girl can still optimistic and cheerful, and why we are given God's completeness perfect body and face were less grateful. Would not God has created us are born into this world by being as perfect as possible. Glory to God, indeed we often do not realize and forget about perfection that God has given us. Many of us are willing to spend up to a very expensive cost for plastic surgery because we are not satisfied with the condition of the actual face was created by God with a good and perfect. Is it not enough to make us give thanks to Him.
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15 comments:
Just an UGLY little SLUT
so which skull bones are there? I understand that such a child would have at least the occipital, parietal, frontal, etc to house the brain. Otherwise these children would be severely mentally handicapped and unlikely to reach a year of age.
Anyway, as long as there is a foundation of skull structure, a plastic surgeon should be able to build a prosthetic face once the skull bones have finished growing. The real question would be how much original tissue would the patient, parent or doctor be willing to sacrifice for her to have a social life and unobstructed airway.
Also, are these patients blind?
wow whoever is the anonymous commment you are really an asshole...this poor little girl was born this way and she has enough confidence to b e happy with herself. You should be able to learn from her because clearly you are a sad sick person..I feel very sorry for you..My prayers go out to Julianna and her family..Keep Smiling Sweetie! :)
to joseph- in the documentary following her development, after an operation her eyes 'swelled up so she couldnt see', but she recovered, so i'm assuming she can see normally.
well the anonymous comments show the very example of the difference between good and demented people.
that was a sick and inhuman comment, you need help.
stay strong Julianna =]
lol i feel sorry for you. you pray.
Dear Joseph, really you need help. Or may be you don't deserve to be a part of mankind . Julianna is a god gifted child. And we all see that she is recovering .... And one day she will be okay 100%. Our prayers are with this little child. god Bless you....
you are beautiful to me baby, be happy and keep smiling... wish you all the best :-*
What a moronically blind parent, oh sure let me keep a child alive whos going to be shunned by society her entire life, who will never love, who will live all alone when her parents die, yes what a "miracle"...
Never heard about Paul Stanley? The singer of "Kiss"...He also has face deformity (called microtia). So what? Smart, talented, famous...It doesn't matter how you look, it matters how and what you think and what you do.
Good luck little girl!
DEAR BLOGGER(S)
YOUR GRASP OF ENGLISH IS COMPLETELY AWFUL. PLEASE STAY OFF THE INTERNET.
THANK YOU
to the anonymous bastard who commented 'just an ugly little slut' should perish
Oh My Gosh, This Is Very Sad. Not To Make FUn Of the girl or anything but Some Kids are sad and they dont have this disease and they feel left out. Why Would they want her to grow up and not be happy with the way she looks. I♥Her and shes not something little and freaky. Shes One of Gods Most Beautifulest& Unique Child.♥
All Of you making fun of her arent any better of judging. Shes the same as us, a Human and god. Give her respect she needs.-__-. The 1st Comment saying 'Just an ugly little slut.' You Arent any better.
That Little girl she is with is SO Adorable(:.♥
my daughter was born almost 4o years ago and i have just realised after watching the program about Juliana that this condition is what she has. i was unable to have a scan and as nobody that i know of has been born in the UK with the degree of severity my child has and so was never given a name for my child's condition. when i saw juliana it was like seeing my child at birth all over again. she has had over 30 corrective surgery operations. she has much scar tissue and is partially sighted in her right eye, has no nasal passages at the back and mass bone missing from eyelids to jaw. her upper pallet was malformed. most of this has been corrected to an acceptable level for her acceptance. she has lived a full active life, has married and had children. all of whom have been born without this condition. it has not been easy as there was not many aids to help in her younger years but to let Juliana know that all will be well and to put her trust in the doctors, we wish her well and would like to keep in touch via facebook if you would like. Alison Holmes.
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