As bad as any mental disability can be, I have to say that from looking at these smiling faces, I feel this is the best of the worst. I know hardships wait these people at all crossroads... but it can't hurt to approach those roads with a smile and jublient personality.
My son Jordan has WS. He's 12 1/2 and had 22 hours of open heart surgery. Seven heart catheterization's 14 teeth pulled. Hernia surgery. (oh 4 more teeth in april) I'd say the 6 million dollar man has nothing on him. For peps with young WS children...its quite a ride. But having a special child has made me a better person. GL and fasten your seat belt...your in for quite a ride!
Jordan Hallmark 12 yrs old...My hero!! Been dealing w/ this for over twelve years now...very scary not knowing the future. One thing for sure he has touched more lives than most of us will if we live to be 100! To all WS parents, i know your pain for sure..hang in there and try to enjoy every second ya can w/em. peace
Thanks for showing the brighter, happier side of this sad disease. We too are trying to help bring cures to rare disease to the people they effect. In conjunction with the Children's Rare Disease Network we are giving away a rare disease registry worth $50,000 to the winner of a video submission contest and the organization of their choice. Visit RemedyMD's website under the "About" section to learn more about this partnership. Have a great day.
my little girl molly ann has williams syndrom she is a gift from heaven , you can see her singing romany rye and brown girl in the ring on my chanel shes so lovely :) all these children are pure angels and we are blessed to have them :)
my best friend has williams syndrome and once i knw what he had i wanted to learn more about him he loves music and loves to smile and hug.... i love u clayton!!!!
Hi My Daughter Phoenix is 9 she has Williams Syndrome. She makes this world a brighter Place with her smile and her happy outlook on life. All these fab WS Kiddies look so alike. X
My nephews baby is having test for williams syndrome,may i ask do babies with this condition have a whoop when breathing similar to a hic cup,i,m asking as my nephews baby does this most of the time,he,ll still be loved just as much but we are hoping the test will be negative,i imagine it will be very tough for them as its there first baby,thanks for this beautiful video
My son probably has it, he has to be diagnosed first, but I don't care, Its just the love that I have for him, he is just about 4 months now, but I have loved him all my life
my sister has williams syndrome. they are amazing. she attends the berkshire hills music academy and has a band with other kids with williams syndrome...probably the most talented kids i have ever met! anyone watched the new show on MTV "hows your news", it features kids with williams syndrome!
I am very interested in WS and I am looking for Spanish children with william's. I am actually doing a researching work about WS in school, WSA in Spain, WS Music Camps, etc. So if someone has some information about that I would be glad to read it, and also if you know children with WS and you want to share your experiences with them or if you know any books about the WS (specially in Spanish), ... anything you would know and want to share with me, I would apreciate it so much. Thank you :)
Hi i was very moved by your clip. The children are beautiful! I have a 31month old daughter who also has Williams Syndrome. So it was great to see all the children
mi hermanito omar tiene 21 años y tiene sindrome de williams,eslo q mas amo en este mundo!!desde el dia q nacio a hecho mi vida la mas feliz!!los niños especiales son una bendicion de Dios!!
Thanks to all williams guys for a wonderful video and a shining smile watching the video I have tried a strong emotion thinking my daughter Eleonora 3 years old WilliamS
Grazie a tutti i ragazzi williams per il meraviglioso video, e per gli splendidi sorrisi nel vederlo ho provato una forte emozione pensando a mia figlia eleonora di 3 anni con la sindrome di Williams
Gracias a todos los williams por el maravilloso video y por las sonrisas maravillosas, en ver el vido he tenido una fuerte emocion pensando a mi hija Eleonora de tres años con el Sindrome de williams
My 1st grandbaby was diagnosed with Williams when she was 6 weeks old. She's now 9 weeks old. She's still undergoing test on her kidneys and heart. But she a beautiful precious baby girl.
We have just found out our 31 month daughter has WS. We have been told that it cannot be passed down or genetic. Just a one in 25,000 chance. Could you please tell me more if you don't mind
Our daughter, who is now 17, was diagnosed at age 4 with WS. It is my understanding that there is a very high chance of a person who has WS passing it along to their child. But as far as you having another child with WS, it would be very rare to have it happen twice in one family. I believe the only record of that happening is in the case of identical twins born with WS.
Lovely kids!!!! they are very social and cheerful ones!! Nicely put up Ispinney.
poojamehta21 3 months ago
As bad as any mental disability can be, I have to say that from looking at these smiling faces, I feel this is the best of the worst. I know hardships wait these people at all crossroads... but it can't hurt to approach those roads with a smile and jublient personality.
LennyWeen 4 months ago
Leurs sourires sont magnifiques. Leurs yeux nous parlent. Que Dieu les bénisse. Mon Amour les accompagne
rentajo 5 months ago
They are so cute :D
nxtdoorgirl 7 months ago
These children are adorable!
MamaMacabre 8 months ago
My son, Cameron has WS. He is 24 years and the most beautiful, loving and caring person in the world. I am very blessed to have him.
agustinalaura8 8 months ago
How I love these Special Kids!! :) My Love goes out to everyone with Williams!! :)
Pierre4452 9 months ago
i have williams syndrome im in the uk
skodas 11 months ago
My son Jordan has WS. He's 12 1/2 and had 22 hours of open heart surgery. Seven heart catheterization's 14 teeth pulled. Hernia surgery. (oh 4 more teeth in april) I'd say the 6 million dollar man has nothing on him. For peps with young WS children...its quite a ride. But having a special child has made me a better person. GL and fasten your seat belt...your in for quite a ride!
irclittlee 1 year ago
Jordan Hallmark 12 yrs old...My hero!! Been dealing w/ this for over twelve years now...very scary not knowing the future. One thing for sure he has touched more lives than most of us will if we live to be 100! To all WS parents, i know your pain for sure..hang in there and try to enjoy every second ya can w/em. peace
irclittlee 1 year ago
Is there any chance of these children going to college?
MicahLuvFun26 1 year ago
Thanks for showing the brighter, happier side of this sad disease. We too are trying to help bring cures to rare disease to the people they effect. In conjunction with the Children's Rare Disease Network we are giving away a rare disease registry worth $50,000 to the winner of a video submission contest and the organization of their choice. Visit RemedyMD's website under the "About" section to learn more about this partnership. Have a great day.
RemedyMD 1 year ago
I work with children with Williams syndome that these children remind me of. They have the sweetest personalities.
StarWarsVSTMNT 1 year ago
very cute
PopeOnArope123 1 year ago
WOW, the most beautifull eyes I've ever seen 0:53
ElizeCeline 1 year ago
Normal faces!!!
111Ardo 1 year ago
Well, I don't see what's different! I see kids happy and smiling like everyone else!
Great pics :)
fegoras 1 year ago
my brother inlaw has william syndrome and it's a handfull alright but so spacialy kind and lovable!!! guess is part of the gift that comes with it
JENNYBRAKON 1 year ago
my little girl molly ann has williams syndrom she is a gift from heaven , you can see her singing romany rye and brown girl in the ring on my chanel shes so lovely :) all these children are pure angels and we are blessed to have them :)
MsRosielee 1 year ago
my son was recently dignosed with a formof williams syndrome thats new and non syndromic ....
marisab38 1 year ago
I've seen this video lots of times, and I will never be tired of seeing it... It's fantastic, they are fantastic, and their faces are full of life...
loquitatu 1 year ago
hello from the uk i have it to wre on Facebook there are loads of us on there
skodas 1 year ago
very inspirational! Thanks for sharing:)
amandavandergriff5 1 year ago
my best friend has williams syndrome and once i knw what he had i wanted to learn more about him he loves music and loves to smile and hug.... i love u clayton!!!!
soccergrl412 1 year ago
i cry with joy everytime i hear and view this video. my son is 2 and has WS, he's so cute!
jimh16 1 year ago
i cry with joy everytime i hear and view this video. my son is 2 and has WS, he's so cute!
jimh16 1 year ago
That was delightful! Thanks!
Gimmer3 1 year ago
:') made my day
chubu 1 year ago
moving video, these kids look so happy. Do you know where I can get this version of the song? I love it!
poppylv21 1 year ago
What beautiful children!
amayasmum 2 years ago
Hi My Daughter Phoenix is 9 she has Williams Syndrome. She makes this world a brighter Place with her smile and her happy outlook on life. All these fab WS Kiddies look so alike. X
PaulaPink13 2 years ago
@PaulaPink13 the children I work with, that have WS love music. Does your daughter?
StarWarsVSTMNT 1 year ago
my half-brother has williams sydrome and does have an interest in music and an obsession with cars
swords983 2 years ago
I have Tourettes syndrome. Diagnosed at 5 yr old.
grabba73 2 years ago
my brother has is, he's only 7 months...
can anyone help us...please...we don't know what to expect from this...
i will affect him too much?
for me he's normal,more than normal...you should see his smile...and hear his laughing
thank you
great job
cera22sela 2 years ago
i have william sydrome
mponekov 2 years ago
what is the williams syndrome?
grindfuckernms 2 years ago
God bless you!
tanechka32 2 years ago
My nephews baby is having test for williams syndrome,may i ask do babies with this condition have a whoop when breathing similar to a hic cup,i,m asking as my nephews baby does this most of the time,he,ll still be loved just as much but we are hoping the test will be negative,i imagine it will be very tough for them as its there first baby,thanks for this beautiful video
tazzarman 2 years ago
my daughter has williams sydomre, she's so amazing, beautiful, lovely and happy child
Mistroher 2 years ago
My daughter has williams sydrome and she's amazing and so beautifl, lovely and happy...
Mistroher 2 years ago
Thank you for sharing your lovely children!
MonicaHWWT 2 years ago
Beautiful
Thank you
mimimanah 2 years ago
Very nice - as cute as buttons!
Morecake2 2 years ago
I have a 6 month olg with william syndrome and ... when I saw this video .. it's just great,,,, i love the song
arianita88 2 years ago
My son probably has it, he has to be diagnosed first, but I don't care, Its just the love that I have for him, he is just about 4 months now, but I have loved him all my life
Icecoldhard 2 years ago
my sister has williams syndrome. they are amazing. she attends the berkshire hills music academy and has a band with other kids with williams syndrome...probably the most talented kids i have ever met! anyone watched the new show on MTV "hows your news", it features kids with williams syndrome!
08ackleyr 3 years ago
Wow thats funny. I didnt know their was so much information on the internet about williams syndrome. My brother also attend BHMA!!
italianlilckicka 2 years ago
I like the video very much! I can see the happiness in these faces. And the song is lovely!
loquitatu 3 years ago
we ARE often very happy, =]
Marduk077 2 years ago
I am very interested in WS and I am looking for Spanish children with william's. I am actually doing a researching work about WS in school, WSA in Spain, WS Music Camps, etc. So if someone has some information about that I would be glad to read it, and also if you know children with WS and you want to share your experiences with them or if you know any books about the WS (specially in Spanish), ... anything you would know and want to share with me, I would apreciate it so much. Thank you :)
dejedi 3 years ago
This video is so touching beautiful :) I love it, they seem so happy, they are so special, blessing, and beautiful.
dejedi 3 years ago
I love this Video!! My 19 yr old sister has Williams. Anyone who knows someone with williams know what a Blessing they are! :)
Darah316 3 years ago
my cousin has willams you would never know he has anything I LOVE ZYOU JORDAN
superbecky96 3 years ago
Read the book "The language instinct" From steven Pinker, they speak of this syndrome in it
muggluh 3 years ago
Hi i was very moved by your clip. The children are beautiful! I have a 31month old daughter who also has Williams Syndrome. So it was great to see all the children
freyasmumanddad 3 years ago
I almost cryed
Ityler94 3 years ago
mi hermanito omar tiene 21 años y tiene sindrome de williams,eslo q mas amo en este mundo!!desde el dia q nacio a hecho mi vida la mas feliz!!los niños especiales son una bendicion de Dios!!
niduskita 3 years ago
Thanks to all williams guys for a wonderful video and a shining smile watching the video I have tried a strong emotion thinking my daughter Eleonora 3 years old WilliamS
Grazie a tutti i ragazzi williams per il meraviglioso video, e per gli splendidi sorrisi nel vederlo ho provato una forte emozione pensando a mia figlia eleonora di 3 anni con la sindrome di Williams
lelelud0507 3 years ago
Gracias a todos los williams por el maravilloso video y por las sonrisas maravillosas, en ver el vido he tenido una fuerte emocion pensando a mi hija Eleonora de tres años con el Sindrome de williams
lelelud0507 3 years ago
My 1st grandbaby was diagnosed with Williams when she was 6 weeks old. She's now 9 weeks old. She's still undergoing test on her kidneys and heart. But she a beautiful precious baby girl.
dmgodfrey 3 years ago
Williams kids r sooo beautiful my baby nephew has williams.....they r sooo special in many ways!!!!!!
sexyjamieky2002 3 years ago
I think that they have such beautiful facial characteristics.
natatatt 3 years ago
These williams people are special.
My wife and my son has williams syndrome and theres still a lot for us to learn about the syndrome.
wurzelmanone 3 years ago
We have just found out our 31 month daughter has WS. We have been told that it cannot be passed down or genetic. Just a one in 25,000 chance. Could you please tell me more if you don't mind
freyasmumanddad 3 years ago
Our daughter, who is now 17, was diagnosed at age 4 with WS. It is my understanding that there is a very high chance of a person who has WS passing it along to their child. But as far as you having another child with WS, it would be very rare to have it happen twice in one family. I believe the only record of that happening is in the case of identical twins born with WS.
pctputertutor 3 years ago
well, when she's older, she'll probably LOVE music. and maybe play an instrument.
Marduk077 2 years ago
solo puedo decir que son personas muy especiales
i just can say that they are very special people.
god bless them forever and ever. bye
AJMU26 4 years ago