Видео

Hi Pls my son needs help He has TOF of the heart n requires heart surgery but am not financially capable.Pls come to his rescue am ready to give u all his medical informations🙏

Heads will roll, because Teddy bears nead xtra attention

Hi Doctor My Son has TOF of the heart n He is 10yrs now.Am so worried about him help me pls🙏

Talon Gateway

Konopelski Pines

great innovation. Thank you Dr Rodefeld.

Your channel videos are very interesting and the thumbnail image is also very nice but it has some problems due to which the videos are not increasing in subscribers and views.

THANK YOU to The Children's Heart Foundation's 9th annual Red Tie Ball on another successful year's event. We HEART WARRIOR FAMALIES are also very grateful to all of our supporters & I look forward to attending net years ball!! ~S. Bason, Atlanta #TeamBrianna

Please my son has cyanosis since birth,he is 10yrs now and He has not gone for His heart surgery because I don't have the money.Pls we sincerely need your help🙏

My daughter is pregnant in Tampa FL. Her baby will be born in just a few weeks in November. I'm praying hard and getting ready to support both her and my grandson for the journey ahead. He will be having a Fontan procedure at some point in the near future. It's scary but I just sent her this video. Thank you for all the work you do. ❤🙏🏿🙏🏿🙏🏿

ruclips.net/video/OouV-FXk5bA/видео.html&si=UXPByeOB6g7GlEp-

My son was born with AVSD, PDA and coarctation

Unfortunately there is a flaw in this. It won't stop left ventricular failure

I wish the world understood.

This is amazing. The problem is people need this NOW. I hope one day this is an option to me so I can avoid a transplant myself. I have a lateral tunnel fontan

Need a real cure for heart disease Contact ( Dr imenherbal ) on channel for real and complete cure His herbs saved my life from this disease.....

I pray everyday

I have conginital heart deases

When I was a baby I had meningitis. It was then that they discovered a hole in my heart affecting all four chambers. Back in the seventies, they had to wait to do surgery because I wasn't big enough. At the age of two and a half, they couldn't wait any longer. I had a second surgery in 1990 at the age of seventeen. I get the comments, but that was years ago? What do you mean you're tired, you need to keep going. Why were your children both high-risk pregnancies? However, thanks to the wonderful doctors at Texas Children's in Dallas I have lived a pretty good life and am nearly fifty. I'm blessed beyond measure.

waiting for this great pump to be applied soon for fontaner 's it will relief liver congestion and fibrosis

When will it get tested in human??

Really great work. How often does it need to be changed? Do the parts wear out?

I was born with a congenital heart defects i am now 40 and have been living with heart failure. Over the years iv had 3 open heart surgeries for my aorta valve. The last sugary was to replace the valve in 2016 I have two bad values. I can feel my self going down every thing I do takes alot out of me. Everything I go to the er they say everything is normal. I can feel my heart straining..the way my rhythm changes from day to day I feel its not much longer. I'm always weak and its not fun but I still keep going no matter what. Because I am young I have to fight for SSI I don't look sick and people don't understand or really see the reality of heart failure in young people. Its a struggle 😪

I wasn’t born with heart problems but I had a heart condition last year an enlarged left atrium from having covid I had moderate covid and double covid pneumonia which effected my lungs and later on found out it effected my heart but I’m better now my heart is better too. I got healed last year on February 5th after being sick for 25 days I finally got to come out of quarantine snd was better it took me a while to get my strength back and my heart got better in I think July I got checked out because I was having chest pains

She’s so cute

Thank you Everyone! We truly appreciate each of You. #CHDAwareness #HeartWarriors #chdmoms #fundingresearch #Children'sHeartFoundation #AtlantaHeartWalk

Honestly when my Doctor told me I had Herpes virus I almost gave up in life because I was so afraid but then I came online and saw a lot of testimonies from people here in US talking about Dr IGUDIA on RUclips who has the natural herbs medication to cure Herpes virus infection once and for all. After ordering the herbs medication that was the end of my Herpes Virus infection.

Finally my wife got cured from cardiovascular disease using an herbal mixture from Dr. Gbenga, after 9 years of battling with this illness which almost claim the joy of our marriage, Get a permanent cure today using Dr. Gbenga herbal mixture.

Hellow I am from the Philippines and I am just hoping that you could help me with my son. He is currently confined here in the Philippines. Philippine heart center to be exact. They conduct open heart surgeryThey switched his great artery. We are having trouble financially and would really appreciate it if you could help me with that. Thank you so much. My baby boy name Jeremiah Dylann B. David Birthday June 02 2021 20 Days old I hope someone can reach me..godbless

I am a CHD survivor. I was born with a partial AV canal, which included a large septal atrial defect and a severe mitral regurgitation. My parents didn’t know anything about my condition until I went to heart failure at 11 months. I had my first open heart surgery when I was 14 months old; after surgery I had a complication called hemolysis... after 5 blood transfusion and 3 months in hospital, I went home. My mitral valve wasn’t completely repaired and I had my second open heart surgery at the age of 9. Now I am 31 years old and I am fine. Thank you for you video about CHD awareness. Hugs to you, Anna from Italy 🇮🇹

I have TOF/APV. I have had two open heart surgeries. I suffered a brain injury during my open heart surgery in 2013. I still have really stiff muscles in my legs that causes trouble with walking.

Thank you for all you do you ❤ #HeartsThatHope #CHDAwarness #HeartWarriors #HeartAngels #fundingresearch #GivingTuesday

My 8 weeks daughter passed away with CHD 😭

I am the mother of a 53 y/o CHD survivor. This documentary is marvelous and a good instrument to get the information out to the public. I know if many of my son's friends see this, they too will be interested along with family members who have been along for the ride for all these many years. Thank you so much for producing this. It certainly gives me more knowledge to explain CHD to my own friends who ask about it, or who would be interested.

GO MOM!!!!!!

That is Awsome!

We Love The Children’s Heart Foundation’s and will forever be volunteers because "I Have A Heart That Hopes" - Team Brianna, Atlanta

So proud of you, Chase! You’re AMAZING!

That's my son! That's our lives! CHF is our rock and always will be!

That's my boy! That's my son! This is his life and our lives!! CHF is our rock and always will be.

Every part of this is so fantastic! Thank you for sharing your stories!

Thank GOD for people who support them!

This channel NEEDS more viewers and subs

Fantastic documentary! I am a 28 year old CHD survivor and it was a joy to watch this awesome documentary!

I’m 39 and I have D-TGA. I had the Schumacher repair in 1980 (slightly different than the mustard and the sennings procedures). I have a hard time breathing, I have SVT’s and my heart function is at 35%. But I’m still hear. My doctors kept telling my parents she might only make it to age... it started to a max of 25.

I am 28 with CHD. I man medication for atrial tachycardia and heart function issues.

I also have a CHD, I am 11 now and I got a pacemaker when I was only a few weeks old

I am #1in100 I was born with a CHD I am now 32 but I have a pacemaker