ULTRASOUND at 32 weeks of GAMMAS ROSE MIRACLE WHIPCREAM. ..
10 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
6 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
4 г. назад
Today, (January 31st) is Omphalocele Awareness Day. We are taking this opportunity to share Sadie's story. Every journey with an Omphalocele (Exampholos) baby is different but this is ours. These babies are fighters! And Medical science and knowledge on Omphalocele's is developing rapidly. Our O warriors are strong, and they are certainly worth the fight! We were so blesses to have come into contact with the ever growing Mother Of Omphalocele (MOO) group during pregnancy. It is more than just Mothers, it is Dad's (Doo's) Grandparents (Goo's) and even some Adult Omphalocele survivors. There is such an amazing level of support, advice, triumphs, and sorrows shared among the group. I do not know how I would have made it through everything without my MOO family! But, while I once needed the group for support, and still do sometimes... It feels wonderful to have the opportunity now to offer support and advice to others. We were so blessed to have been seen during our pregnancy by the Minnesota Perinatal Physicians Staff, who were WONDERFUL and so helpful and supportive! They put us in contact with the Minneapolis Children's hospital and Mother Baby Center where our daughter was born, by a C section performed by Dr. Wagner from the Perinatal Physicians. While I had to recover in the Mother Baby Center, it was wonderful that our daughter was treated in the NICU just down the hall, and an elevator ride away. So, even though, we had to recover in separate places for a couple of days, I could still go down as often as I wanted to visit her before I was discharged. (I had some wonderful nurses in the Mother Baby center who helped me get to the NICU when needed, and allowed some flexibility so that I could spend time with my baby during the day) Our daughter was treated at that same Children's Hospital in Minneapolis. Our Doctor (Dr. Swenson), Surgeon, (Dr. Feltis), the nursing staff, social worker, lactation consultants, and the entire hospital were absolutely helpful and amazing!
11 мес. 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
2 г. назад
When Dan and Jenna were told their baby boy, Shane, would not live for long after birth, they decided they would bring him on a 'bucket list' of adventures - before he was born. He became known as the 'bucket list baby' and his story was followed by millions worldwide. The courage and love in their beautiful story together touched hearts everywhere, and changed how we see babies like Shane, precious and important and deeply loved, however short anencephaly makes their lives. Read his story here: http://www.everylifecounts.ie/stories/shane-haley/ Watch and Share his video
6 г. назад
This is in honor of the Walker family and their little hero. The Walkers were told that Grayson had anencephaly and sweet Grayson was born on 2-15-2012 at 10:00am and lived for 8 beautiful hours. God certainly provided the strength and peace for the parents thru this whole journey. There is a blog following their journey at http://www.oursweetboygraysonjames.blogspot.com. Music credit belongs to Jenn Bostic and the track is titled Jealous of the Angels.