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For Love & Life No Ordinary Campaign
⏲ 2:39 👁 80K
'It was Very SWEET!' - One-and-a-half-year-old girl meets newborn baby brother for the 1st time
⏲ 1:2 👁 495K
Mum told she was “cruel” for having her son after he was born with severe cleft lip
⏲ 2:20 👁 60K
Catherine, Princess of Wales is \
⏲ 1:42 👁 5K
Understanding Broken Heart Syndrome - Guide to Diagnosis, Treatment, and Prevention
⏲ 3:38 👁 5K
LIFE & STYLE PODCAST: Living with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is out NOW!
⏲ 1:17 ✓ 12-May-2024
For Love & Life: No Ordinary Campaign | Official Trailer (2024)
⏲ 2:27 ✓ 11-May-2024
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_for-love-amp-life-no-ordinary-campaign.jpg "For Love & Life No Ordinary Campaign Documentary Movie Trailer HD - Plot synopsis:<br/>FOR LOVE & LIFE: NO ORDINARY CAMPAIGN is an emotionally gripping documentary illustrating the power of love and determination in the face of adversity.The film follows the life of Brian Wallach and his wife Sandra in the aftermath of his ALS diagnosis at age 37.Exemplifying bravery, inspiration and hope, Brian and Sandra, continue to fight against a broken system for their own future, while seeking to build a brighter one for countless others.<br/> <br/>FOR LOVE & LIFE: NO ORDINARY CAMPAIGN is presented by Amazon MGM Studios, a LIMA CHARLIE PRODUCTION in association with THE CHAN ZUCKERBERG INITIATIVE.")
_39it-was-very-sweet39-one-and-a-half-year-old-girl-meets-newborn-baby-brother-for-the-1st-time.jpg "The irresistibly endearing first meeting between a one-and-a-half-year-old girl and her newborn baby brother is captured in this video. <br/><br/>\")
_mum-told-she-was-cruel-for-having-her-son-after-he-was-born-with-severe-cleft-lip.jpg "A mum who was told she was “cruel” for having her son after he was born with a rare severe cleft lip says it has never held him back.<br/><br/>Zac Coates, now 18, was born with Tessier cleft lip and palate – a condition which is caused by facial tissues not joining up properly during development.<br/><br/>It left Zac with severe facial disfigurement on his ride side and he had no eye lid which left him blind in his right eye.<br/><br/>Mum, Joanne Lythgoe-Frank, 58, was “shocked” when she first saw her son but raised him to accept his differences.<br/><br/>Zac has undergone 16 surgeries to help restructure his face and is now a happy and healthy 18-year-old who is hoping to go to university to study film production in September.<br/><br/>Zac, who lived in Cyprus for 17 years, has dealt with stares and comments such being called a “monster” – but he hasn’t left his difference hold him back.<br/><br/>Joanne, a part-time receptionist, living in Faringdon, Oxfordshire, said: “My initial reaction was shock at the extent of it. <br/><br/>“It was different to what I expected – a lot more severe.<br/><br/>“I’ve never hidden Zac away to be an over protective mother.<br/><br/>“I tried to instil in Zac – ‘you are different but to embrace it and be proud of your differences’.<br/><br/>“It’s made him into a confident young man.<br/><br/>“On TikTok I was told how cruel a mum I was because I let my child be born.<br/><br/>“Zac lives a normal life. He’s educated, confident his differences haven’t hindered him in life.”<br/><br/>Joanne, who is originally from Manchester, was living in Cyprus when she fell pregnant with her second child Zac.<br/><br/>At 22 weeks pregnant she was told he had a cleft anomaly and asked if she wanted an abortion.<br/><br/>She said: “That for me was never an option.”<br/><br/>Joanne started getting a high blood pressure and developed severe preeclampsia at 24 weeks along.<br/><br/>She was rushed for an emergency C-section and Zac was born on February 24, 2006, weighing 1lbs 5oz.<br/><br/>Joanne said: “I remember being told ‘your little boy isn’t going to survive – he’s got issues. Maybe it’s better he doesn’t’.<br/><br/>“I came round hours later and got taken down to see him.<br/><br/>“Zac’s face was all bandaged up.<br/><br/>“It was deemed something you hide away in Cyprus.”<br/><br/>Joanne was told Zac had a 20 per cent chance of survival and she didn’t see her little boy properly until she was able to get him flown over the UK two weeks later.<br/><br/>There he was diagnosed and Joanne was able to hold him for the first time.<br/><br/>She said: “I didn’t see him without bandages until I came back to the UK.<br/><br/>“They offered for me to hold him. My instincts were he was about to die.<br/><br/>“They put him down my bra and he was there for hours.”<br/><br/>Zac was discharged after six months in hospital but had his first surgeries at nine months old to repair his palate and his lip.<br/><br/>Since then he has been back and forth to the UK for further surgeries to reconstruct his face.<br/><br/>He had a recent surgery in October 2023 to reconstruct his cheek – by using bone from his skull.")
_catherine-princess-of-wales-is-92.jpg "Prince William has revealed that his wife is \")
_understanding-broken-heart-syndrome-guide-to-diagnosis-treatment-and-prevention.jpg "Understanding Broken Heart Syndrome: Guide to Diagnosis, Treatment, and Prevention. <br/>Ever felt like you’re having a heart attack after a tough situation? It could be broken heart syndrome, also known as stress-induced cardiomyopathy. This condition mimics heart attack symptoms, such as chest pain and shortness of breath, and can be triggered by emotional or physical stressors. Whether you’ve experienced a loss or undergone a major life event, understanding the signs, triggers, and treatment options is crucial. Here’s a detailed look at what you need to know. <br/><br/>References:<br/>https://www.webmd.com/heart-disease/diagnosing-echocardiogram<br/>")
_life-amp-style-podcast-living-with-mayer-rokitansky-kster-hauser-mrkh-syndrome-is-out-now.jpg "Nur Syazwani Abdul Rahim’s journey to her Mayer-Rokitansky-Küster-Hauser (MRKH) diagnosis was nothing short of confusion. Only after countless consultations did one doctor uncover the truth: she was born without a uterus. But there's more to her story - she shares it in the latest episode of the Life & Style podcast out now.<br/><br/><br/><br/>#Podcast #MRKH #RareDisorder #Motherhood #Health #SinarDaily")
_for-love-amp-life-no-ordinary-campaign-124-official-trailer-2024.jpg "For Love & Life: No Ordinary Campaign is an emotionally gripping documentary presented by Amazon MGM Studios, a Lime Charlie Production in association with The Chan Zuckerberg Initiative.<br/><br/>The film follows the life of Brian Wallach and his wife Sandra in the aftermath of his ALS diagnosis at age 37. Exemplifying bravery, inspiration, and hope, Brian and Sandra, continue to fight against a broken system for their own future, while seeking to build a brighter one for countless others.<br/><br/>For Love & Life: No Ordinary Campaign is directed by Christopher Burke and produced by Tim Rummel and Christopher Burke. Executive producers for the film are Jeff MacGregor, Katie Couric, Phil Rosenthal, Brian Wallach, and Sandra Abrevaya.<br/><br/>For Love & Life: No Ordinary Campaign is releasing on May 28 on Amazon Prime Video.")
_for-love-amp-life-no-ordinary-campaign.webp "For Love & Life No Ordinary Campaign Documentary Movie Trailer HD - Plot synopsis:<br/>FOR LOVE & LIFE: NO ORDINARY CAMPAIGN is an emotionally gripping documentary illustrating the power of love and determination in the face of adversity.The film follows the life of Brian Wallach and his wife Sandra in the aftermath of his ALS diagnosis at age 37.Exemplifying bravery, inspiration and hope, Brian and Sandra, continue to fight against a broken system for their own future, while seeking to build a brighter one for countless others.<br/> <br/>FOR LOVE & LIFE: NO ORDINARY CAMPAIGN is presented by Amazon MGM Studios, a LIMA CHARLIE PRODUCTION in association with THE CHAN ZUCKERBERG INITIATIVE.")
_39it-was-very-sweet39-one-and-a-half-year-old-girl-meets-newborn-baby-brother-for-the-1st-time.webp "The irresistibly endearing first meeting between a one-and-a-half-year-old girl and her newborn baby brother is captured in this video. <br/><br/>\")
_mum-told-she-was-cruel-for-having-her-son-after-he-was-born-with-severe-cleft-lip.webp "A mum who was told she was “cruel” for having her son after he was born with a rare severe cleft lip says it has never held him back.<br/><br/>Zac Coates, now 18, was born with Tessier cleft lip and palate – a condition which is caused by facial tissues not joining up properly during development.<br/><br/>It left Zac with severe facial disfigurement on his ride side and he had no eye lid which left him blind in his right eye.<br/><br/>Mum, Joanne Lythgoe-Frank, 58, was “shocked” when she first saw her son but raised him to accept his differences.<br/><br/>Zac has undergone 16 surgeries to help restructure his face and is now a happy and healthy 18-year-old who is hoping to go to university to study film production in September.<br/><br/>Zac, who lived in Cyprus for 17 years, has dealt with stares and comments such being called a “monster” – but he hasn’t left his difference hold him back.<br/><br/>Joanne, a part-time receptionist, living in Faringdon, Oxfordshire, said: “My initial reaction was shock at the extent of it. <br/><br/>“It was different to what I expected – a lot more severe.<br/><br/>“I’ve never hidden Zac away to be an over protective mother.<br/><br/>“I tried to instil in Zac – ‘you are different but to embrace it and be proud of your differences’.<br/><br/>“It’s made him into a confident young man.<br/><br/>“On TikTok I was told how cruel a mum I was because I let my child be born.<br/><br/>“Zac lives a normal life. He’s educated, confident his differences haven’t hindered him in life.”<br/><br/>Joanne, who is originally from Manchester, was living in Cyprus when she fell pregnant with her second child Zac.<br/><br/>At 22 weeks pregnant she was told he had a cleft anomaly and asked if she wanted an abortion.<br/><br/>She said: “That for me was never an option.”<br/><br/>Joanne started getting a high blood pressure and developed severe preeclampsia at 24 weeks along.<br/><br/>She was rushed for an emergency C-section and Zac was born on February 24, 2006, weighing 1lbs 5oz.<br/><br/>Joanne said: “I remember being told ‘your little boy isn’t going to survive – he’s got issues. Maybe it’s better he doesn’t’.<br/><br/>“I came round hours later and got taken down to see him.<br/><br/>“Zac’s face was all bandaged up.<br/><br/>“It was deemed something you hide away in Cyprus.”<br/><br/>Joanne was told Zac had a 20 per cent chance of survival and she didn’t see her little boy properly until she was able to get him flown over the UK two weeks later.<br/><br/>There he was diagnosed and Joanne was able to hold him for the first time.<br/><br/>She said: “I didn’t see him without bandages until I came back to the UK.<br/><br/>“They offered for me to hold him. My instincts were he was about to die.<br/><br/>“They put him down my bra and he was there for hours.”<br/><br/>Zac was discharged after six months in hospital but had his first surgeries at nine months old to repair his palate and his lip.<br/><br/>Since then he has been back and forth to the UK for further surgeries to reconstruct his face.<br/><br/>He had a recent surgery in October 2023 to reconstruct his cheek – by using bone from his skull.")
_catherine-princess-of-wales-is-92.webp "Prince William has revealed that his wife is \")
_understanding-broken-heart-syndrome-guide-to-diagnosis-treatment-and-prevention.webp "Understanding Broken Heart Syndrome: Guide to Diagnosis, Treatment, and Prevention. <br/>Ever felt like you’re having a heart attack after a tough situation? It could be broken heart syndrome, also known as stress-induced cardiomyopathy. This condition mimics heart attack symptoms, such as chest pain and shortness of breath, and can be triggered by emotional or physical stressors. Whether you’ve experienced a loss or undergone a major life event, understanding the signs, triggers, and treatment options is crucial. Here’s a detailed look at what you need to know. <br/><br/>References:<br/>https://www.webmd.com/heart-disease/diagnosing-echocardiogram<br/>")
_life-amp-style-podcast-living-with-mayer-rokitansky-kster-hauser-mrkh-syndrome-is-out-now.webp "Nur Syazwani Abdul Rahim’s journey to her Mayer-Rokitansky-Küster-Hauser (MRKH) diagnosis was nothing short of confusion. Only after countless consultations did one doctor uncover the truth: she was born without a uterus. But there's more to her story - she shares it in the latest episode of the Life & Style podcast out now.<br/><br/><br/><br/>#Podcast #MRKH #RareDisorder #Motherhood #Health #SinarDaily")
_for-love-amp-life-no-ordinary-campaign-124-official-trailer-2024.webp "For Love & Life: No Ordinary Campaign is an emotionally gripping documentary presented by Amazon MGM Studios, a Lime Charlie Production in association with The Chan Zuckerberg Initiative.<br/><br/>The film follows the life of Brian Wallach and his wife Sandra in the aftermath of his ALS diagnosis at age 37. Exemplifying bravery, inspiration, and hope, Brian and Sandra, continue to fight against a broken system for their own future, while seeking to build a brighter one for countless others.<br/><br/>For Love & Life: No Ordinary Campaign is directed by Christopher Burke and produced by Tim Rummel and Christopher Burke. Executive producers for the film are Jeff MacGregor, Katie Couric, Phil Rosenthal, Brian Wallach, and Sandra Abrevaya.<br/><br/>For Love & Life: No Ordinary Campaign is releasing on May 28 on Amazon Prime Video.")
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