Kaidence Stephenson got sick when she was just a baby. Her and her family's lives changed quickly as Kaidence's heart began to fail. See how Kaidence's other family up at Primary Children's Medical Center, a Children's Miracle Network Hospital, prolonged her life. A last minute gift came that would save Kaidence's life.
5 г. назад
Incredible story of shaken baby syndrome survivor Lola Bernicky and call for justice! Sign petition here: https://www.change.org/petitions/waukesha-county-prosecute-the-attacker-of-our-daughter-5-mo-old-lola-bernicky www.Facebook.com/LolasHopeStopSBS www.LolasHope.com Song credits: Miqz - 'Never Forget'
8 г. назад
Audrey Jean was born 15 weeks early at just 25 weeks gestation due to severe pre-eclampsia and severe IUGR. At birth she weighed only 12 ounces (350 grams) and was 10 inches in length. The doctors gave us very little hope in her survival. But the minutes turned into hours and hours into days. She surpassed all expectations. After 93 days in the NICU, we brought our beautiful, healthy baby girl home. This video is a photo journal capturing our journey with Audrey from birth through her first 8 months of life! Her journey is truly remarkable. Enjoy!
1 г. назад
AHMAD ROMANSYAH , BALITA USIA 10 BULAN , LAHIR NORMAL , MENDERITA PENYAKIT HIDROSEFALUS,MESKI KEPALANYA SEMPAT DI OPERASI ,NAMUN KONDISI MUKANYA MIRIP MANUSIA PLANET..SEMOGA SAJA KEDUA ORANG TUANYA YANG BERASAL DARI PADANG LAMPE ,KABUPATEN LUWU , SULAWESI SELATAN , YANG KINI HARUS MENGONTRAK RUMAH DI MAKASSAR , DEMI MENYEMBUHKAN BUAH HATINYA YANG MEMBUTUHKAN ULURAN TANGAN PEMERINTAH DAN DERMAWAN DI BERI KETABAHAN .
8 г. назад
http://kayleighannefreeman.blogspot.com/ I do not own this video. Kindly visit the above site to know more about Kayleigh Ann Freeman. As a mother, my heart aches to see how the child is fighting for her life. I can feel how hard it is for her mother to see her daughter undergoing all those surgeries and daily struggle. The song Title is "Amazing" The morning cold and raining, dark before the dawn could come How long in twilight waiting longing for the rising sun ohoh ohoh Oh ooh You came like crashing thunder breaking through these walls of stone You came with wide eyed wonder into all this great unknown ohoh ohoh Ohoooh Oohh Hush now don't you be afraid I promise you I'll always stay I'll never be that far away I'm right here with you [Chorus] You're so amazing you shine like the stars You're so amazing the beauty you are You came blazing right into my heart You're so amazing you are... You are You came from heaven shining Breath of God still flows from fresh on you The beating heart inside me Crumbled at this one so new ohoh ohoh Oooh ooohhh No matter where or how far you wander For a thousand years or longer I will always be there for you Right here with you [Chorus] You're so amazing you shine like the stars Find More lyrics at www.sweetslyrics.com You're so amazing the beauty you are You came blazing right into my heart You're so amazing you are... I hope your tears are few and fast I hope your dreams come true at last I hope you find love that goes on and on and on and on and on I hope you wish on every star I hope you never fall too far I hope this world can see how wonderful you are [Chorus] You're so amazing you shine like the stars You're so amazing the beauty you are You came blazing right into my heart You're so amazing... You're so amazing you shine like the stars You're so amazing the beauty you are You came blazing right into my heart You're so amazing you are... You are
2 г. назад
At age six, our daughter Mila was diagnosed with Batten Disease—a rare fatal disease with no cure... yet. With your help, we can fund necessary research and clinical trials to give the hundreds of children like Mila a second chance at life. For more information, please visit STOPbatten.org. UPDATE: Since launching this video, we learned that Azlan does not have Batten Disease. Such joy amidst the pain. Please continue helping us in #SavingMila and other children suffering from Batten— gofundme.com/savingmila.
7 г. назад
This video was created for showing during intermission at the Michael Allen Harrison benefit concert for Alena Marek on April 16th, 2011. It is a summary of the suffering she experienced from her diagnosis on March 15, 2010, through one year of treatments. She handled this trial with dignity, grace, courage, and love. At the time of this video, she was finished with treatments, in complete remission, and the future looked very good for her. I'm sorry to report that the cancer returned late in 2011, and Alena peacefully passed away on Christmas Day. She will always be loved, treasured, and missed.
2 г. назад
Watch the full testimony of Gabriella's story, here: https://youtu.be/XwqI2gsVbtw?t=17m42s Facebook Page: https://www.facebook.com/thenormalchristianlife/ Website: https://thenormalchristianlife.org More Episodes: https://www.youtube.com/thenormalchristianlife
2 г. назад
17/07/2016 News... Jenna and Jillian monoamniotic twins born holding hands still don't like being appart. Two peas in a pod! Twin sisters who were born holding hands are still inseparable two years after they defied the odds to survive. Jenna and Jillian were born May 2014 in one in 10,000 monoamniotic birth Mother Sarah Thistlethwaite spent 57 days on bed rest to minimize risks Ohio twins were born 45 seconds apart and held hands right afterwards Two years later, the sisters don't like to be separated to run errands Care for each other but also blame the other for their own misbehaviors. Twin sisters who held hands in the first seconds of their lives can't stand being away from each other, two years after their odd-defying birth. Jenna and Jillian Thistlethwaite were born on May 9, 2014 in Akron, Ohio after sharing the same amniotic sack - a condition that affects about 1 in 10,000 pregnancies and increases the chances of complications. Their mother Sarah had spent 57 days on bed rest to minimize the risks and was relieved to give birth to two healthy girls. The twins were born 45 seconds apart and as soon as the doctors held them close to each other, they clasped hands, stunning everyone in the delivery room. For More News Subscribe Our Channel.THANKS For WATCHING
8 г. назад
Katelyn "Katie" Olivia Connor was born December 27, 2005 to William & Christa Connor. Laura Beth (Katie's younger sister is also featured in this video. Katie lost her battle to Neuroblastoma on Thursday, August 5, 2010 after a valiant battle of 15 months. This video was made for the family shortly after Katie passed away as Katie's one fear was that she would be forgotten. This video is to celebrate her life and to let her know that ~ she will not be! Rest in Peace little angel! Enjoy playing with your Jesus! If you would like to read about Katie's life please visit her family's blog ~ www.ourturkey.blogspot.com "Heaven is the Face" was written by Steven Curtis Chapman shortly after the loss of his daughter Maria. You can purchase this music at: http://www.amazon.com/gp/product/B002SXXJ28/ref=dm_mu_dp_trk1 There is no intention for any gain in using this music or pictures. Music is noted and Pictures belong to the Connor family. Strictly for memorial purposes only. No intent to defraud.
3 г. назад
On January 25th, sweet Kycie started complaining of a headache. On Monday she said her tummy hurt and a little later she threw up. Her mom and dad figured she was coming down with the flu. She slept all day Monday. She was giving her sprite and water to help her tummy. She did not want any food. Tuesday there was no change, and her brothers started to complain of stomach aches and sore throats. Jamie took Daxton and Kycie to the doctor on Wednesday. They were given antibiotics for strep throat. By Thursday night, she was worse. On friday they went to the doctor and went to the ER at 1:00pm. By 5:00pm she was life flighted to Primary Children's Hospital with blood sugar of 1148. Her parents had no idea that sweet little Kycie had diabetes! Enroute to the hospital she had a seizure and another one right when they got to the hospital. She has been unresponsive ever since. At this point her blood sugars are under control. After reviewing her MRI the doctors said that she has extensive damage to the brain. The brain had herniated into the brain stem.They said if she survives to prepare themselves for her to be severely handicapped. They will do another MRI on Tuesday and at that point with decide if they should consider taking her off the breathing machines. The family is hoping for a miracle and knows that this little girl's life is in God's hands right now. You can show your support to the Terry family by keeping them in your prayers and donating to help with any financial expenses that they have. Let's join together to support this wonderful family! We love you Kycie! #kissesforkycie www.kissesforkycie.com
8 мес. назад
SUBSCRIBE to Barcroft TV: http://bit.ly/Oc61Hj This observational documentary looks at the worrying condition of extreme sleep disorders in children. Extreme sleep disorders in children can be frightening and disabling. Recurrent night terrors, head banging, insomnia, narcolepsy, chronic sleepwalking and sleep paralysis can shatter families. For kids suffering from these and many other sleep disorders, Evelina Children's Hospital Pediatric Sleep Disorder Unit is the last chance resort. Dealing with only the most extreme cases, and with a remarkable success rate, the doctors have transformed the lives of some of the most sleep-deprived families in the UK. CREDIT: Banijay Rights (Zodiak) Barcroft TV: https://www.youtube.com/user/barcroftmedia/featured Barcroft Animals: https://www.youtube.com/barcroftanimals/featured Barcroft Cars: https://www.youtube.com/user/BarcroftCars/featured For more of the amazing side of life: For the full story, visit BARCROFT.TV: http://www.barcroft.tv/ Like @BarcroftTV on Facebook: https://www.facebook.com/BarcroftTV Follow @Barcroft_TV on Twitter: https://www.Twitter.com/Barcroft_TV Check out more videos: https://www.youtube.com/user/barcroftmedia/videos Download Barcroft TV on iOS: https://itunes.apple.com/us/app/barcroft-tv/id1287734327?mt=8 Download Barcroft TV on Android: https://play.google.com/store/apps/details?id=com.recipe.barcroft&hl=en
6 г. назад
24 Oras is GMA Network's flagship newscast, anchored by Mike Enriquez and Mel Tiangco. It airs on GMA-7 Mondays to Fridays at 6:30 PM (PHL Time) and on weekends at 5:30 PM. For more videos from 24 Oras, visit http://www.gmanetwork.com/24oras.