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.
1 г. назад
Please SUBSCRIBE, Like, Comment and SHARE! Music: https://www.youtube.com/watch?v=3jKb5jwBqrc Instagram: @whealthbyslaiman Facebook: https://www.facebook.com/WhealthbySlaiman Twitter: @whealthslaiman Snapchat: @whealthslaiman Mail Address: PO Box 988, Toowong DC, QLD 4066, Australia.
1 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
7 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
11 г. назад
HI RES FOR BEST VIEWING. A tribute to Joshua Sams, born with a neural tube defect and gone to heaven on 3/15/08 at 67 days of age.
1 г. назад
sponsor my hard work https://www.patreon.com/missionhandy This video shows how a family handles a very dificult situation when they have a baby born with birth defects and brain development problems and the mom unable to pay for the surgery she has to live him as He is. He was given three months to live and its being 3 1/2 year later please to see the update on baby Isac click for newest video 2018 https://youtu.be/m5g54gCgmto help us in our next baby care outreac goal https://www.patreon.com/missionhandy -~-~~-~~~-~~-~- Please watch: "Understanding adoption laws and procedures in mexico cps #adoptions" https://www.youtube.com/watch?v=wV6dHOxVxRw -~-~~-~~~-~~-~-