Video yükleniyor...

Video Yüklenemedi

Ana Sayfaya Dön

A day to remember for young Hibee Sam Millar… 💚 Sam is eight years old and suffers from a rare condition called Duchenne muscular dystrophy. After hearing his story on the news last week, we invited him down to HTC to meet his heroes! 🥬

HibernianFC's profile picture

Hibernian Football Club

116,942 subscribers

40,855 görüntüleme • 1 yıl önce •via X (Twitter)

Sağlık & İyilikSporHaberler & Politika
LIVE

Anya Rossi• Live Now

Private livecam show

11 Yorum

JackGillies1875🇩🇪💙🏴󠁧󠁢󠁳󠁣󠁴󠁿 profil fotoğrafı
JackGillies1875🇩🇪💙🏴󠁧󠁢󠁳󠁣󠁴󠁿1 yıl önce

Always love seeing stuff like this 👏🏻💚

Propertee profil fotoğrafı
Propertee1 yıl önce

Pour yourself some Swiftea and reminisce on every era ☕✨. From ‘Debut’ to ‘Midnights,’ this mug is the ultimate Taylor fan gift! 😉 Shop now👉🏻

𝓙𝓮𝓷𝓷𝓲𝓯𝓮𝓻 🎀 profil fotoğrafı
𝓙𝓮𝓷𝓷𝓲𝓯𝓮𝓻 🎀1 yıl önce

Love that Dwight let him sit in his car! Memories he will cherish forever 💚

Gee_Hibs profil fotoğrafı
Gee_Hibs1 yıl önce

Nice one again Hibs... Sam will have enjoyed this... 💚

Muscular Dystrophy UK profil fotoğrafı
Muscular Dystrophy UK1 yıl önce

Brilliant to see @HibernianFC inviting Sam to meet the team. Moments like this mean so much, especially when Sam and his family work hard to raise awareness around the difficulties in accessing much needed treatments.🧡

Michelle profil fotoğrafı
Michelle1 yıl önce

💚💚👏

Mamma_Lairdy profil fotoğrafı
Mamma_Lairdy1 yıl önce

Sam I hope you told Dwight the Hibbies want him to hang around for one more season..... Please 🙏🙏🙏🙏🇳🇬💚🇳🇬🤍🇳🇬💚🇳🇬🤍

Tony Cervi profil fotoğrafı
Tony Cervi1 yıl önce

💚💚💚

Mark Jones profil fotoğrafı
Mark Jones1 yıl önce

Nice one Sam, good choice with Dwight! 🇳🇬

Ross profil fotoğrafı
Ross1 yıl önce

Class 🥬

Fabrav 🇳🇬🏴󠁧󠁢󠁳󠁣󠁴󠁿🇾🇪⚽️⛳️ profil fotoğrafı
Fabrav 🇳🇬🏴󠁧󠁢󠁳󠁣󠁴󠁿🇾🇪⚽️⛳️1 yıl önce

👏👏👏👏🇳🇬🇳🇬

Benzer Videolar

Let's get Eli to Glastonbury. 15 year old Eli Crossley is living with Duchenne Muscular Dystrophy and has trialled a new piece of technology he hopes will one day let him play with Sam Fender. Sam Fender Glastonbury Festival
0:56

Let's get Eli to Glastonbury. 15 year old Eli Crossley is living with Duchenne Muscular Dystrophy and has trialled a new piece of technology he hopes will one day let him play with Sam Fender. Sam Fender Glastonbury Festival

BBC Breakfast

66,650 görüntüleme • 3 yıl önce

Meet Henri, a Stoke City fanatic with an incredible story full of courage and generosity. We invited him for a special day at Clayton Wood to spend some time with his heroes.
11:25

Meet Henri, a Stoke City fanatic with an incredible story full of courage and generosity. We invited him for a special day at Clayton Wood to spend some time with his heroes.

Stoke City FC

134,399 görüntüleme • 2 yıl önce

POWERFUL: 21-year-old Sam Schulz fulfills his dream at Michigan State💚 Schulz, a lifelong Spartan fan, is battling epidermolysis bullosa (EB), a rare genetic condition that causes the skin to blister and tear very easily. As his health declines, one of his biggest wishes was to spend time in East Lansing. Thanks to former MSU basketball player Tum Tum Nairn, that dream became a reality. Sam got to meet the team, spent time with Coach Izzo, tour the facilities, and receive a team-signed Michigan State jersey. Fred Heumann of News 10 Lansing with this story
2:29

POWERFUL: 21-year-old Sam Schulz fulfills his dream at Michigan State💚 Schulz, a lifelong Spartan fan, is battling epidermolysis bullosa (EB), a rare genetic condition that causes the skin to blister and tear very easily. As his health declines, one of his biggest wishes was to spend time in East Lansing. Thanks to former MSU basketball player Tum Tum Nairn, that dream became a reality. Sam got to meet the team, spent time with Coach Izzo, tour the facilities, and receive a team-signed Michigan State jersey. Fred Heumann of News 10 Lansing with this story

Michigan State Content

38,925 görüntüleme • 1 ay önce

A 3-year-8-month-old boy from Kurnool has been diagnosed with Duchenne Muscular Dystrophy (DMD), a rare genetic disorder. Doctors say he needs a life-saving injection costing Rs 26 crore within 4 months to survive. His parents have appealed #AndhraPradesh government and the public for help to save their child. Lokesh Nara N Chandrababu Naidu
1:46

A 3-year-8-month-old boy from Kurnool has been diagnosed with Duchenne Muscular Dystrophy (DMD), a rare genetic disorder. Doctors say he needs a life-saving injection costing Rs 26 crore within 4 months to survive. His parents have appealed #AndhraPradesh government and the public for help to save their child. Lokesh Nara N Chandrababu Naidu

Ashish

102,618 görüntüleme • 6 ay önce

Making Harley's dream come true 🤍 James Maddison recently invited young fan Harley, who suffers with a rare genetic condition impacting his spine, to a @PremierLeague match, surprising him at half-time for a cup of tea and custard cream ☕
4:11

Making Harley's dream come true 🤍 James Maddison recently invited young fan Harley, who suffers with a rare genetic condition impacting his spine, to a @PremierLeague match, surprising him at half-time for a cup of tea and custard cream ☕

Tottenham Hotspur

324,936 görüntüleme • 6 ay önce

Carolynn and I have known Sam Altman for his whole career. In fact it was Sam who introduced us. So today's Social Radars is a special one. Join us as we talk to Sam about the inside story of his journey from Stanford sophomore to AI mogul.
10:36

Carolynn and I have known Sam Altman for his whole career. In fact it was Sam who introduced us. So today's Social Radars is a special one. Join us as we talk to Sam about the inside story of his journey from Stanford sophomore to AI mogul.

Jessica Livingston

642,386 görüntüleme • 1 yıl önce

Inside the NBA aired #SCFeatured's ‘For Hannah’ last night - a story that hit especially close to home for Ernie Johnson, whose son Michael lived with Duchenne muscular dystrophy. Shaq, Chuck and Kenny shared an emotional reaction. Mitchell Widmeier
2:23

Inside the NBA aired #SCFeatured's ‘For Hannah’ last night - a story that hit especially close to home for Ernie Johnson, whose son Michael lived with Duchenne muscular dystrophy. Shaq, Chuck and Kenny shared an emotional reaction. Mitchell Widmeier

Bea Panitz

32,437 görüntüleme • 3 ay önce

We’d like you to meet Frazer, our eight year-old fan. He is blind after going through 64 operations to try and save his eyesight, but he is still full of joy 💛 We wanted to give him the best day of his life. 🫶 Young Wolves x Mario Lemina
9:10

We’d like you to meet Frazer, our eight year-old fan. He is blind after going through 64 operations to try and save his eyesight, but he is still full of joy 💛 We wanted to give him the best day of his life. 🫶 Young Wolves x Mario Lemina

Wolves

5,340,669 görüntüleme • 3 yıl önce

Andrew Palmer, who has Duchenne muscular dystrophy, lost the ability to walk after breaking his leg in sixth grade. His family surprised him with a power wheelchair, restoring a sense of freedom he had long lost. His emotional reaction was captured on video as he realized he could finally move around his home on his own again.
0:47

Andrew Palmer, who has Duchenne muscular dystrophy, lost the ability to walk after breaking his leg in sixth grade. His family surprised him with a power wheelchair, restoring a sense of freedom he had long lost. His emotional reaction was captured on video as he realized he could finally move around his home on his own again.

NOLLY

11,542 görüntüleme • 3 ay önce

The old delivery driver, who went viral for delivering DoorDash to make ends meet after his wife lost her job, talks to a local news network about the GoFundMe set up in his name. What a great story to end the week!
0:55

The old delivery driver, who went viral for delivering DoorDash to make ends meet after his wife lost her job, talks to a local news network about the GoFundMe set up in his name. What a great story to end the week!

Vince Langman

15,695 görüntüleme • 5 ay önce

I'll always love and respect Sam Darnold. But remember Week 7 last season, Sam had a chance to make a 3rd down throw to essentially ice the game vs the Lions. He did not convert. JJ McCarthy did.
0:22

I'll always love and respect Sam Darnold. But remember Week 7 last season, Sam had a chance to make a 3rd down throw to essentially ice the game vs the Lions. He did not convert. JJ McCarthy did.

Purple FTW! Podcast

212,667 görüntüleme • 10 ay önce

Best thing you’ll see today 💯 72-year-old Sam became the first in his family to earn a college degree 🎓🙌🏻 On his graduation day, his 99-year-old mother came to watch and support him 🥹
0:22

Best thing you’ll see today 💯 72-year-old Sam became the first in his family to earn a college degree 🎓🙌🏻 On his graduation day, his 99-year-old mother came to watch and support him 🥹

Restoring Your Faith in Humanity

41,080 görüntüleme • 5 ay önce

The Players Trust is honored to announce Rhys Hoskins as this year's Philanthropist of the Year! ❤️ Rhys will receive a $25K grant from the Players Trust, which he will use to send those with muscular dystrophy to summer camp. His lasting impact in the community and support for Muscular Dystrophy Association continues to inspire us day in and day out. Milwaukee Brewers | FOX Sports: MLB
1:36

The Players Trust is honored to announce Rhys Hoskins as this year's Philanthropist of the Year! ❤️ Rhys will receive a $25K grant from the Players Trust, which he will use to send those with muscular dystrophy to summer camp. His lasting impact in the community and support for Muscular Dystrophy Association continues to inspire us day in and day out. Milwaukee Brewers | FOX Sports: MLB

MLBPA

67,703 görüntüleme • 1 yıl önce

#Habs Kent Hughes on Samuel Montembeault “Sam is in Laval to get a break from here and find his confidence. We've all seen him in the last 3 years and we know he's a good goalie. The question is whether it will take next week, two weeks, in a month, and we're trying to find ways to accelerate it" (Translated from French) #GoHabsGo #NHL #Hockey Rick Stephens / Rocket Sports
0:35

#Habs Kent Hughes on Samuel Montembeault “Sam is in Laval to get a break from here and find his confidence. We've all seen him in the last 3 years and we know he's a good goalie. The question is whether it will take next week, two weeks, in a month, and we're trying to find ways to accelerate it" (Translated from French) #GoHabsGo #NHL #Hockey Rick Stephens / Rocket Sports

Chris G

37,769 görüntüleme • 8 ay önce

This video is from 2019. A 4-year-old Palestinian prisoner on his way to attend his hearing. 4 years old!
0:57

This video is from 2019. A 4-year-old Palestinian prisoner on his way to attend his hearing. 4 years old!

The Resonance

257,468 görüntüleme • 24 gün önce

Our Co-Founder & CTO, Jesse Levinson, invited his eight-year-old nephew, Noah, for a spin and made history in the process. We recently lowered our rider age minimum from 13 to eight, making Noah the youngest person to ever ride in a purpose-built robotaxi. 💚
0:59

Our Co-Founder & CTO, Jesse Levinson, invited his eight-year-old nephew, Noah, for a spin and made history in the process. We recently lowered our rider age minimum from 13 to eight, making Noah the youngest person to ever ride in a purpose-built robotaxi. 💚

Zoox

34,096 görüntüleme • 1 yıl önce

Humanitarian Appeal Ameen Attallah, 10 years old, suffers from partial paralysis on his left side. His family is appealing for help to enable him to travel for treatment. +972592674687 Mother of Ameen
1:25

Humanitarian Appeal Ameen Attallah, 10 years old, suffers from partial paralysis on his left side. His family is appealing for help to enable him to travel for treatment. +972592674687 Mother of Ameen

Eye on Palestine

42,214 görüntüleme • 1 yıl önce

.Secretary Kennedy: “I’m proud to announce today that I’m approving the addition of duchenne muscular dystrophy and metachromatic leukodystrophy to the Recommended Uniform Screening Panel…if we detect the children very early on who suffer from these diseases, we can save them from a shortened life of misery.”
1:06

.Secretary Kennedy: “I’m proud to announce today that I’m approving the addition of duchenne muscular dystrophy and metachromatic leukodystrophy to the Recommended Uniform Screening Panel…if we detect the children very early on who suffer from these diseases, we can save them from a shortened life of misery.”

HHS Rapid Response

103,304 görüntüleme • 8 ay önce