My Grandfather George was born a blue baby in 1911. The doctors stated he wouldn’t live through his teen years. He lived to be 37. He grew up, got married, had my Mom and my Aunt. My Mom was 11 when her Dad died. They didn’t know how to fix his heart back then. I’m sure they know now.
My husband was born with ToF in 1957. His 1st surgery was done in Cuba in 1959, 2nd in Miami 1977 and the last one in 2006 at Mayo Clinic Rochester mn. He has been an owner operator since age 17 traveling all over the US driving his Big Rig, has seen his 3 children grow up, and is in the process of being the best Grampa possible to his now 3 grandkids... Oh, and will be retiring in Sept at the ripe age of 66-1/2...Yes miracles do happen🎉❤
Good video explaining vsd. My son , now 39 and healthy was born in 1983 with a vsd, he wasn't a blue baby. It was discovered when he was 4 months old. He had a minor infection/ cold and the doctor heard a murmer. Diagnosed with a small vsd and said they would monitor his health over 2 years and would do surgery if it worsened. We were told that small ones sometimes heal up as the child grows. This was in South Africa. Back in the UK now and he's been fine. I still worry. I am so sorry to hear of those who have lost their child to this defect.
My late BF passed away from this. This was the first video I saw or bothered to look up because the cause of death on the certificate hunts me. Now I understand what they supposedly fixed. Just now gotta find out how it was "fixed" and what can fail 28 years later.
When I was five, I had a Patent Ductus repair, and my hospital roommate was an orphaned baby named Regina who had Tetralogy of Fallot. I remember she was blue. I’ve always wondered what happened to her. She would be about 55 if she survived.
This is 100% my daughter’s heart condition. It’s so devastating from the parent aspect. I’ve watched my little girl recover from heart caths, open heart surgeries and many, many hospital stays. She is doing very well considering what she has been through. I’m very grateful that technology has improved and my baby is alive.
Some babies have what is called “Pink Tet” it’s when they still have the tetralogy, but, instead of having a bluish hue, they will be pink..which means that more oxygen-rich blood is able to circulate throughout their bodies but they are poor feeders, tachypneic, can be diaphoretic at times, and tend to be febrile. So, with both pink and blue tetralogy, Surgical intervention is absolutely necessary. Wonderful video again Nucleus Media
I was born a blue baby, my dad was told by a Sister that I wouldn't survive the night, imagine what he felt, I can only imagine as he never talked about it. Still 58 and nearly 59 years later, I am still here. What caused me to be born like this is important to me. To all born blue, hope you all are well and living a nice life. 😃🇬🇧
I was taken away to be worked on according to Mom. 10-15 mins later I was returned. I have sleep apnea. 89 episodes p/h. I use a cpap machine to help me sleep otherwise I would not be capable of a lot of anything.
Wow sobre que la tetralogia de Fallot es muy peligrosa y necesita intervención de cirugía de inmediato, creo que otra característica es los dedos en forma de tambor y radiografía de esa zona tiene una forma extraña me encanta las animaciones de este canal ❤️❤️❤️❤️👌👌👌
Tengo una niña de 5 años con (VSD) ventricular septal defect nacio sin nungun problema, lleva una vida normal; como cualquier otro niño; corre brinca grita etc… cada año visita a su cardiologo para checar que todo marche bien, nos dijo que una persona con ese defecto puede vivir toda su vida sin ningun problema.. pero tambien hay veces que no es asi, que puede llegar el momento enq ella necesite una pequeña cirugia dependiendo el problema que se presente o asta un transplante de corazon… entre hermanos hay un 90% a que no se herede; tube mi segundo bebe que tiene un año y gracias a Dios nacio bien de su corazon.. confio en Dios que siempre estara con mi niña y el cuida de su corazon ❤️..
Oh my lord. So this was the reason my nephew died.. Ya allah, she was only 2,5 years old at that time, she was born with pale blue color, she was having a bad faver that night, she had a problem with her heart and it wss difficult for her to breath, after 1 days 1 night in a local hospital, finally she has return to the almighty 🙏. She's smilling when she passed away. I can't hold my tears that night, remembering all the memories we had been throught together 🤧. Will see you soon in jannah insya allah. " Annisa nur fatimah ".
My second daughter was born with TOF and AVSD.. we've waited for total repair surgery when she will be one year old.. now she is almost 9 months.. she cannot sit on her own. but she can roll over and crawl..
Minha filha tem 2 meses e foi diagnóstica com T4F ... Tá sendo difícil o coração de uma mãe doei tanto...pois mãe nenhuma que ver seu filho sofrendo. Mais eu creio que Deus vai curar ela, pois Deus e o Deus do impossível 🙏
My son is also suffering from this..he is 5+. I don't know how to cure this. Doctrs said for multiple surgeries at high risk .can't understand what to do.
Am 21 week pregnancy now through anomaly scan we know that my baby has tetralogy fallots problem so doctor suggeste to remove the baby but I can't accept it what to do if i continue my pregnancy or remove the baby
Surgeons reroute arteries and veins to places they usually don't go, but will provide oxygenated blood to the body nevertheless. It's like adding shortcuts.
I lost my first and second child to this. Nina, my first daughter died at 7 month. My second daughter Kim, died at birth. My third daughter Luna; had the opportunity to do her practical at Grootte Schuur Hospital in Cape Town, where her siblings died. She was allowed a genetic test, to confirm, if she would have a child with the same defect. The result was 84% chance to have a baby with that defect. She and her husband decided not to have children.
We detected in anomaly scan and doctors asked to terminate the pregnancy...we aborted at 21 weeks my second baby it's a boy...I can't tolerate the pain still now
My Grandfather George was born a blue baby in 1911. The doctors stated he wouldn’t live through his teen years. He lived to be 37. He grew up, got married, had my Mom and my Aunt. My Mom was 11 when her Dad died. They didn’t know how to fix his heart back then. I’m sure they know now.
There's a good movie called Something The Lord Made that details how we got the solution to ToF
Dr Alfred Blalock and Vivien Thomas found the cure for this at the Johns Hopkins Hospital.
1944 they operated successfully the first one with blue baby syndrome..
@@QTinEP
Excellent movie.
Everyone must watch it
I have TOF and am 45. Had multiple surgeries. God has helped me.
Right at the end of the video, I felt my heart wrenching for the babies who go through this 😢
My 2 year son have tetralogy of fallot
@@lifewithmysuperheroshivans1954 I hope your son gets better.
I lost my daughter after one day of open heart surgery (Vsd and Tof) due to Dr's negligence.
My husband was born with ToF in 1957. His 1st surgery was done in Cuba in 1959, 2nd in Miami 1977 and the last one in 2006 at Mayo Clinic Rochester mn.
He has been an owner operator since age 17 traveling all over the US driving his Big Rig, has seen his 3 children grow up, and is in the process of being the best Grampa possible to his now 3 grandkids... Oh, and will be retiring in Sept at the ripe age of 66-1/2...Yes miracles do happen🎉❤
Good video explaining vsd. My son , now 39 and healthy was born in 1983 with a vsd, he wasn't a blue baby. It was discovered when he was 4 months old. He had a minor infection/ cold and the doctor heard a murmer. Diagnosed with a small vsd and said they would monitor his health over 2 years and would do surgery if it worsened. We were told that small ones sometimes heal up as the child grows. This was in South Africa. Back in the UK now and he's been fine. I still worry. I am so sorry to hear of those who have lost their child to this defect.
My late BF passed away from this. This was the first video I saw or bothered to look up because the cause of death on the certificate hunts me. Now I understand what they supposedly fixed. Just now gotta find out how it was "fixed" and what can fail 28 years later.
very sad to hear. let his soul be born again in a beautiful way.
I’m so sorry for your loss ☹️
I’m very sorry 😢
When I was five, I had a Patent Ductus repair, and my hospital roommate was an orphaned baby named Regina who had Tetralogy of Fallot. I remember she was blue. I’ve always wondered what happened to her. She would be about 55 if she survived.
Thanks to nucleus medical media for such important information 🙏
in this small amount of time you provide very deep knowledge with proper understanding 👍🙌
I didn't realize that the structural wall inside of the heart also gives an arrangement to the blood flow
I am preparing this topic for my mid term exam and appear the Topic with its Epic explanation.
Thank you Nucleus medical media
Good luck on ur exam🙌
You should watch more videos as this was poorly explained to interpret the entire scenario as there's a lot more to this
Goodluck for your exam
Tetralogy of falllot-
1)ventricular septal defect
2)overriding aorta
3)Pulmonary stenosis
4)Right ventricular hypertrophy
My one year old daughter had undergone this surgery 5 months ago at Narayana Institute of cardiac science. Now she seems to be fine.
Kitne din hospital rhi thi apki beti operation ke bad
Hello there
I would love to connect with you to understand more about it and your experience
Do you mind sharing your email or number ?😊
Nice video for every medical student i waiting for these video lot of time
Very Well Explained.
This is 100% my daughter’s heart condition. It’s so devastating from the parent aspect. I’ve watched my little girl recover from heart caths, open heart surgeries and many, many hospital stays. She is doing very well considering what she has been through. I’m very grateful that technology has improved and my baby is alive.
Great to hear that may God bless her...we aborted our baby at 20 weeks because of this condition doctors here said to terminate the pregnancy
Some babies have what is called “Pink Tet” it’s when they still have the tetralogy, but, instead of having a bluish hue, they will be pink..which means that more oxygen-rich blood is able to circulate throughout their bodies but they are poor feeders, tachypneic, can be diaphoretic at times, and tend to be febrile. So, with both pink and blue tetralogy, Surgical intervention is absolutely necessary.
Wonderful video again Nucleus Media
Three de (3D) digital illustration makes every hard to becomes easy
Thank you very much for the video with kindness and respect
Thank you
Very much helpful
Great animation 🔥
Crystal clearance about TOF..Before seeing this video , i had no idea about.. Thanks nucleus 🥰
Thank you so much sir for this kind of info ❤️
Great video ❤
It's really amazing sir 🔥😊
Subhan Allah Glorified is God The Almighty in His creation❤️I never heard of this before❤️May Allah God the Almighty protect and heal all
I was born a blue baby, my dad was told by a Sister that I wouldn't survive the night, imagine what he felt, I can only imagine as he never talked about it. Still 58 and nearly 59 years later, I am still here. What caused me to be born like this is important to me. To all born blue, hope you all are well and living a nice life. 😃🇬🇧
Can you tell me what procedure they did to you?my son is baby blue and his only 7months
I was taken away to be worked on according to Mom. 10-15 mins later I was returned. I have sleep apnea. 89 episodes p/h. I use a cpap machine to help me sleep otherwise I would not be capable of a lot of anything.
My daughter has 2 chambers 😢😢😢😢😢😢 i dont know what to do.
@@Andy13april64Have you had open heart surgery?
I have issues with the lungs but no open heart. I believe I was extremely lucky. I truly wish this never happens but it does.
you are the best tuitor sir.
My goal is to learning something new everyday. Goal reached for today
Wow sobre que la tetralogia de Fallot es muy peligrosa y necesita intervención de cirugía de inmediato, creo que otra característica es los dedos en forma de tambor y radiografía de esa zona tiene una forma extraña me encanta las animaciones de este canal ❤️❤️❤️❤️👌👌👌
Omg i studying now thx 🙏🏻
سبحان الله ، دقة وتنظيم بشكل خرافي
❤ Well explained thank u so much
Thank you for this video! Awesome!
Thank you so much sir, now i think I will never forget this topic ✌️🙌❤️❤️
Tengo una niña de 5 años con (VSD) ventricular septal defect nacio sin nungun problema, lleva una vida normal; como cualquier otro niño; corre brinca grita etc… cada año visita a su cardiologo para checar que todo marche bien, nos dijo que una persona con ese defecto puede vivir toda su vida sin ningun problema.. pero tambien hay veces que no es asi, que puede llegar el momento enq ella necesite una pequeña cirugia dependiendo el problema que se presente o asta un transplante de corazon… entre hermanos hay un 90% a que no se herede; tube mi segundo bebe que tiene un año y gracias a Dios nacio bien de su corazon.. confio en Dios que siempre estara con mi niña y el cuida de su corazon ❤️..
Thank you so much.
Great 👍🩺♥️
Great and easy information
Oh my lord.
So this was the reason my nephew died..
Ya allah, she was only 2,5 years old at that time, she was born with pale blue color, she was having a bad faver that night, she had a problem with her heart and it wss difficult for her to breath, after 1 days 1 night in a local hospital, finally she has return to the almighty 🙏. She's smilling when she passed away.
I can't hold my tears that night, remembering all the memories we had been throught together 🤧.
Will see you soon in jannah insya allah.
" Annisa nur fatimah ".
RIP
Bellissima animazione!
Please do animation on left/right subclavian artery.
Wow 👍 great vedio
Great animation 👌
Looking at this video made me think that this was probably the condition my older brother had before he passed 3 days after birth
It's beautiful 💛
My second daughter was born with TOF and AVSD.. we've waited for total repair surgery when she will be one year old.. now she is almost 9 months.. she cannot sit on her own. but she can roll over and crawl..
How is baby
Hows your baby
Thanks for this information
I finally understood why I was operated on
Very informative
Subscribed!
Gives me gosebump
Impreesive informission
ventricular septal defect
overriding aorta
right ventricular hypertrophy
pulmonary artery stenosis
I have had heart problems like mostly of my life and I was born with a heart defect I ended up having surgery on my heart.
Stay strong dear...
More and more videos please
Look so good ❤️
Minha filha tem 2 meses e foi diagnóstica com T4F ... Tá sendo difícil o coração de uma mãe doei tanto...pois mãe nenhuma que ver seu filho sofrendo. Mais eu creio que Deus vai curar ela, pois Deus e o Deus do impossível 🙏
Thanks ❤
Very nice and neet vedio
0:57 Start
What is its diagnosis?
Please explain
thanks
My baby son had this problem....He passed away before birth in 37weeks of my pregnancy...3rd Fabruray 2022...
My son is also suffering from this..he is 5+. I don't know how to cure this. Doctrs said for multiple surgeries at high risk .can't understand what to do.
The baby may be too upset for a blue body like this. Sadly.
Why this problem happens?... I have lost my baby that he had this birth defect...
Am 21 week pregnancy now through anomaly scan we know that my baby has tetralogy fallots problem so doctor suggeste to remove the baby but I can't accept it what to do if i continue my pregnancy or remove the baby
My baby also affected by vsd 4.5mm
this is what Acacia Kersey’s daughter has 💔
Is it possible to be cured?
Probably via heart surgery or transplant
Surgeons reroute arteries and veins to places they usually don't go, but will provide oxygenated blood to the body nevertheless. It's like adding shortcuts.
@@QTinEP do they patch the hole in the heart?
Tetralogy of Fallot
سبحان الله.
sobhan ulkah
make a video about the rabies virus in humans
I lost my baby to this 🥺😭 .. if i could detect it in anomaly scan
I’m so sorry for your loss 😢
I lost my first and second child to this. Nina, my first daughter died at 7 month. My second daughter Kim, died at birth. My third daughter Luna; had the opportunity to do her practical at Grootte Schuur Hospital in Cape Town, where her siblings died. She was allowed a genetic test, to confirm, if she would have a child with the same defect. The result was 84% chance to have a baby with that defect. She and her husband decided not to have children.
So sorry my dear
We detected in anomaly scan and doctors asked to terminate the pregnancy...we aborted at 21 weeks my second baby it's a boy...I can't tolerate the pain still now
God is amazing creator.
Mery bety k ye masla tha last year death ho gai he was 3years old
😢 Surgery nhi karaye te?
Verb for Arabic?
Mampir Jakarta timur
👍
🤝👌
Hm
Allahu Akbar
Malekum salam
Indeed ❤ ☪
Speak louder
😳