ULTRASOUND at 32 weeks of GAMMAS ROSE MIRACLE WHIPCREAM. ..
8 г. назад
Billy and I had the best time with Brayley. If you are in doubt I want you to know we absolutely do NOT regret a thing. She lived for a wonderful 7 hours. She touched so many lives. I do recommend contacting a NOW I LAY ME DOWN TO SLEEP person, Stephen caught our memories perfectly. Thank you to everyone who supported us. RIP baby girl, mommy and daddy are so so so proud of you and love you forever. I can't wait to hold you in heaven.
11 г. назад
Child Foundation supports children worldwide born with birth defects. Meet Baby Miracletina from Samoa. She was born September 1, 2007 and not expected to live for more than a few hours. Her parents would not allow her to slip away and were able to sneak milk to her and she became strong enough to go home to her loving family and Samoan community. Since arriving in the US, Miracletina has defied odds that were against her from the beginning and is now facing her first round of multiple life changing surgeries. Miami Children's top surgeons will donate their services, but it is up to Miracle's supporters to raise the hundreds of thousands of dollars needed to provide her with the necessary hospital expenses involved in such delicate and life saving surgeries. Please visit our website for more information and how YOU can support this precious "Miracle" that we are honored to provide assistance to. www.childfoundation.com You can make a difference and show this loving child that she deserves the quality of life that ALL children deserve. http://childfoundation.com
2 г. назад
This video is dedicated to every baby with Anencephaly. No matter how brief their lives may be, they matter, they are loved and they make a huge impact in this world and in the hearts of so many. Their names will be spoken and we will never forget them. #SayTheirName Music Credits: Selah - I Will Carry You Dominic Balli - Just a Little Bit Longer Soaring Through Skies - Itty Bitty Beats Danny Gokey - I Will Not Say Goodbye I'll See You Again - Westlife All Of Me - Matt Hammitt www.facebook.com/groups/anencephalyhope www.anencephaly.info
8 г. назад
Although they are two completely separate people, these accomplished teens share a body and have just two arms and legs between them. Born in 1990, the girls have been brought up in a small, tightly knit community in Minnesota, almost completely protected from prying eyes and inquisitive stares. To their friends and family, they are distinct people with very different personalities, needs, tastes and desires. But to the outside world they are a medical mystery -- particularly given the fact that they can do virtually all the same things as their friends, including playing the piano, riding a bike, swimming and playing softball "Their personalities make them inspirational," says their mother Patty. "They never give up; anything they want to do, they go out and do it." The medical world is keen to find out how two separate brains and nervous systems can work in such a perfectly co-ordinated way, but the twins and their family have always resisted non-essential medical tests. "The family want to treat them as though they are just like everyone else," says Joy Westerdahl, the girls' doctor, who admits that it is a mystery how their unique physiology functions. As they enter adulthood, the twins are likely to leave the haven of their home town and face the wider world. In preparation for that time, they have taken part in this intimate documentary to show the world what it is like to be joined for life. http://en.wikipedia.org/wiki/Abigail_and_Brittany_Hensel
7 г. назад
History of the pregnancy of Quesia e Arthur. They had an anencephalic baby and named her Esther. She has born on 29-june-2011 and left to the eternity 40 minutes after the birth. It was 36 weeks of happiness and hopefulness. All family could fell the wonderful experience of having a anencefalic baby. A true history. Read the birth report: http://www.nucleobemnascer.com.br/relato-de-partos/esther-english-version
7 г. назад
* I know this is something we have never done on the channel but this story inspired us so very much we wanted to spread the word about this amazing story and journey. This was also a project for school and we wanted to share the story with you. *A short film about a boy who has been diagnosed with Microcephaly. His name is Jayden and is fighting for his life. He is an example for many kids out there diagnosed with the same disease or even anyone out there fighting for their life. LoneStarGamingForU decided to make a short-film for him to spread his message. Enjoy. Check out the links below. News Article-http://www.komu.com/news/microcephaly-versailles-boy-needs-seizure-dog-training/ Zayden's Website!- http://www.wix.com/raylfamily/zayden
5 г. назад
this video is in memory of my beautiful daughter who was taken away from us from a disorder called Anencephaly if you would like to donate please go to http://www.gofundme.com/Raylee-Jo-Foundation or message us at www.facebook.com/RayleeJoFoundation we also have tshirts and bracelets for sale big thanks to everyone who is supporting us in this time of need also big thanks to Suzette Clark Brady for taking all of these wonderful pictures www.facebook.com/sbrady03?fref=ts Rainy May and much much more