Transposition of the Great Arteries (TGA): Life After TGA Surgery - CHOP (6 of 6)

TGA, a complicated, possibly lethal disease, can be turned into a manageable disease.

More information at heart.chop.edu.

Transposition of the Great Arteries (TGA) is a severe congenital condition in which the body's largest arteries are incorrectly attached to the chambers of the heart. Learn how pediatric experts from the Fetal Heart Program and Cardiac Center at The Children's Hospital of Philadelphia identify TGA during pregnancy, support the baby's delivery, and provide cardiac surgery and comprehensive care after birth.

Category:

Science & Technology

Tags:

• tga
• surgery for TGA
• pediatric cardiology
• pediatric cardiac surgery
• cardiothoracic surgery
• pediatric
• surgery

[photoj1102]

I was born in late 85, and had TGA in 86. Went to CHOP a few years ago to have a small hole/leak in my aortic valve repaired. I've been doing great ever since. It's nice to know there is a community out there. Awesome video's.

[kellydiffer]

I was born in may 1993 with TGA, i had surgery at two days old at children hospital Boston with Dr. Blume, i dont do sports much but they have told me I have no limitations, this summer they told me that the low pressure value was leaking more than it was last year but an MRI prove other wise. i have never talked to someone else to have TGA so i would welcome anyone who want to contact me. fallen2611@yahoo.com kelly :)

[megodude]

I was born with TGV in 1964 I had the mustard surgery ,. In 1967 , Had first pacemaker in 1985. I am now 46 years old and have had A great and full life. I plan on 46 more years. I even have two grandkids ages 7 and 8 .You can live a full life . You will not get picked in P E for sports teams

I Had the surgery done at childrens hospital of Los Angels

To all the parents and kids live life and enjoy

If you have any question just e mail me at

Megodude@charter.net

Kurt

[mbuenafranco]

@LittrellCarterLover Glad to hear you are doing well. My son Oliver was born with d-TGA last year - just turned a year old. Makes me happy to learn others are doing well in your age group. God Bless!

[mbuenafranco]

@soudenm84 My son Olive was born on July 6, 2009 with d-TGA. He is now 1 yr old and doing well. We are concernced about what the future may hold. I'd love to learn if you'd be willing to share. Much appreciated. Martin

[soudenm84]

I was born in Wellington Hospital, New Zealand in 1984. I was born with TGA and I had this surgery, at the time I was the youngest person to ever have this surgery. My dr was Dr Aitken from Greenlane Hospital in Auckland. Im now 26 years old and although I cant play sports and am limited to what jobs I can do ie no heavy lifting etc, Im doing ok. Thanks Dr Aitken for saving my life.  Anyone worried about this op can send me a message via youtube and ill tell you about my limitations etc.

[LittrellCarterLover]

I was born on April 9, 1993 and was then diagnosed with TGA. I had surgery at only 10 days old at Childrens Hospital of Philadelphia. I had the two best doctors in the world Dr. Norwood and Dr. Jacobs. I'm a healthy 17 year old. I go to a gym, have my license, going to be a senior in CBW in doylestown pa. i am very greatful for having a great hospital in my state. i go see my cardiologist. Im like any normal 17 year old.

[Celiecinema1]

That's some defect!

[norder69]

My son has had the switch operation done in Germany in 2003 and he is doing great - so if any you are about to go through this ordeal - keep you cool, it will be just fine.

[theeei]

Our daughter was born on May 7th, 2008 with TGA. She seemed fine right after birth, but soon after it became clear she had a serious problem. They operated her on her 10th day, a day I will never ever forget. Seeing her afterwards with all those tubes and monitors, a moment that will stay engraved. We will soon celebrate her 2nd birthday: she is a very lively and happy little girl with a very strong character. I deeply thank the medical staff who took care of her for saving our daughters life.