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Living with Congenitally Corrected Transposition of the Great Arteries

Living with Congenitally Corrected Transposition of the Great Arteries

FromHeart to Heart with Anna


Living with Congenitally Corrected Transposition of the Great Arteries

FromHeart to Heart with Anna

ratings:
Length:
32 minutes
Released:
Dec 15, 2014
Format:
Podcast episode

Description

The most common cyanotic congenital heart defect that presents in the first month after birth is transposition of the great arteries (TGA) -- dextro-TGA (d-TGA) and levo-TGA (l-TGA) or congenitally corrected TGA (also known as cc-TGA). Because cc-TGA is rarer than d-TGA, it's not often spoken about. In this episode, we'll have two adult survivors with cc-TGA talk about what it's like living with cc-TGA, how it's affected their lives and what advice they have for parents of babies with cc-TGA.The episode opens with Carol Raimondi. Carol Raimondi was born in 1975 with levo-transposition of the great arteries, pulmonary stenosis, atrial septal defect, ventricular septal defect (or VSD) and dextrocardia. Her first surgery at age 5, repaired her VSD and widened her pulmonary artery. Soon after that, she required a pacemaker. She has had 3 more open-heart surgeries – at ages 12, 21 and 31, and numerous pacemaker surgeries.David Franco was born on December 19, 1966. His heart defect was not detected until 6 weeks after birth. David’s parents were given very few options and David was sent to the University of Alabama, Birmingham to have his VSD closed by Dr. John Kirklin. He received a pacemaker during the operation.David had a second OHS at 27 to replace his pulmonary valve and add a pulmonary conduit allowing more oxygenated blood to go through his body. The surgery was successful but David suffered a stroke during the procedure. He also received an implanted cardioverter defibrillator — or an ICD.Please take a moment to follow and like us on your preferred social media platforms:Apple Podcasts (https://itunes.apple.com/us/podcast/heart-to-heart-with-anna/id1132261435?mt=2)Facebook  (https://www.facebook.com/HearttoHeartwithAnna/)YouTube  (https://www.youtube.com/channel/UCGPKwIU5M_YOxvtWepFR5Zw)Instagram  (https://www.instagram.com/hugpodcastnetwork/)If you enjoy this program and would like to be a Patron, please check out our Patreon page  (https://www.patreon.com/HeartToHeart)In this clip, Anna thanks listeners of "Heart to Heart with Anna" and asks them to keep the comments on the podcast episodes coming!Support the showAnna's Buzzsprout Affiliate LinkBaby Blue Sound CollectiveSocial Media Pages:Apple PodcastsFacebookInstagramMeWeTwitterYouTubeWebsite
Released:
Dec 15, 2014
Format:
Podcast episode

Titles in the series (100)

"Heart to Heart with Anna" is the longest-running podcast devoted to the congenital heart defect (CHD) community. Our shows feature Survivors, family members, medical professionals and others in the CHD community who wish to share their stories, expertise, and advice. This show is devoted to empowering, educating and enriching the lives of members of the CHD community.