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Andrew Borge
Registrace 25. 07. 2006
The Cricketers of Redbourn Summer 2018 menu
The Cricketers of Redbourn Summer 2018 menu
zhlédnutí: 253
Video
CDLS The Rollercoaster Ride
zhlédnutí 23KPřed 6 lety
This film takes you on a journey into the world of Cornelia de Lange Syndrome. Understanding the ups and downs for people affected by this rare genetic disorder is brought home by frank and open interviews with parents, carers , professionals - and people who themselves have CdLS. The film also introduces the work of the CdLS Foundation UK & Ireland and shows how the organisation helps families...
The Armed Forces Memorial
zhlédnutí 138Před 11 lety
This film was made to interest potential donors to give money towards the building of the Armed Forces Memorial. The Armed Forces Memorial is the first national memorial dedicated to the 16,000 men and women of the United Kingdom Armed Forces, both Regular and Reserve, killed on duty or as a result of terrorist action since the Second World War. In those six decades, not a year has gone by with...
Targa Florio in a Mercedes-Benz 220 CDI
zhlédnutí 304Před 15 lety
Targa Florio in a Mercedes-Benz 220 CDI
If you can detect in the womb, a choice of aborting should be offered.
Very cute, sweet children.
Should connect with parent's in the U.S. with CDLS children
God bless you all ❤
Loving and being loved is what's most important
Besides that, you will need a LOT of health insurance, something in the USA a lot of people DON'T have.
@@janmac218he would qualify for assistance..
May God bless all families and children that are effected by this illness, l wish them lots of strength and courage and joy in their journey of life ❤
My cousin David had CDLS . He was born in 1958, and was non verbal, intellectually impaired, and physically aggressive. My Aunt took care of him at home until he passed.
I saw a child with this illness and it was so sad to see the poor child. Terrible illness.
A minha filha até os 10 anos de idade, era muito doente comesou a falar com 6 anos, ainda é difícil mas a questão da saúde melhorou ficou mais forte, mais resistente, faz ainda tratamento para os brônquios, e toma medicamentos para comtrolar as convulsões, já está com 27 anos, é linda sempre criança, 😉😉😉😉😉😉😉😉😉Maria Irene Santos, esse é o canal dela, parabéns pelo belo trabalho, obrigado 👍😉
Oi posso postar esse vídeo no canal da minha filha que também é portadora da simdrome, Cornélia de lange, me responda por favor, obrigado 😉👍
I know a boy named Thomas who has CDLS and he is very similar to the Thomas in this video. He has some hearing loss and loves music especially playing the piano