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    pulmonary_atresia

    Explore "pulmonary_atresia" with insightful episodes like "Living with a Single Ventricle Heart, But No Fontan", "Aging Care of a Fontan Patient", "Getting to Know Keith Flynn: A Heart Transplant Hopeful!", "Living with a Bi-Directional Glenn Heart" and "Difficulties Growing Up with a CHD" from podcasts like ""Heart to Heart with Anna", "Heart to Heart with Anna", "Heart to Heart with Anna", "Heart to Heart with Anna" and "Heart to Heart with Anna"" and more!

    Episodes (9)

    Living with a Single Ventricle Heart, But No Fontan

    Living with a Single Ventricle Heart, But No Fontan

    How can a 30-year-old Heart Warrior single ventricle survivor live without the Fontan? What special considerations need to be made when moving from Egypt to Canada? What are the biggest concerns when you fall out of cardiac care?

    Ellen Banoub was born in Egypt 30 years ago. She is a Heart Warrior, diagnosed with a hypoplastic left ventricle, transposition of the great arteries (TGA), pulmonary atresia, and dextrocardia. Ellen has had two surgeries, a shunt operation at one year of age, and a half-Fontan when she was 11 years old. She moved to Canada in 2013. She is studying social services and academic English and hopes to study social work to help others with social and medical problems. She has three heart-healthy siblings. Her older sister is a doctor who takes care of Ellen's health. Ellen recently became an aunt to Molly, who was born in early 2022. Aside from studying and spending time with family, Ellen enjoys acting, watching movies, listening to music, and reading.

    Ellen talks with Anna about how she was born with a single ventricle heart and had surgery abroad since she was unable to have the surgery in her homeland (Egypt). Ellen talks about how she eventually moved to Canada where she has been able to get the care she needed for her heart. She shares how she came to study social work and how working in this field is her new purpose in life.

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    Aging Care of a Fontan Patient

    Aging Care of a Fontan Patient

    Texas Reardon is a Heart Warrior. Whitney is his wife of 10 years. Born with a host of congenital heart defects, Texas explains to Anna, in this episode of "Heart to Heart with Anna," about his complicated medical history, and some consequences he's had to face due to falling out of medical care for years. Whitney shares her story, with Anna, about the adjustments she's had to make to help her husband live optimally given his condition. Tune in to hear about the kinds of consequences Texas has endured and the advice he has for others so they won't suffer his same fate.

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    Getting to Know Keith Flynn: A Heart Transplant Hopeful!

    Getting to Know Keith Flynn: A Heart Transplant Hopeful!

    Keith Flynn was born in 1975 and shortly after birth, he was diagnosed with Ventricular Septal Defect, Double Inlet Left Ventricle, Pulmonary Atresia, and Hypoplastic Right Ventricle. He had two Blalock-Taussig shunts at age 6 months and 5 years, and a modified Fontan procedure when he was 15. Despite experiencing atrial arrhythmias in early adulthood, Keith received limited cardiac care in his 20s and early 30s. 

    In his 30s, Keith started experiencing syncopal (or fainting) episodes, and on one occasion was rescued by his wife after fainting while swimming. As a result of these episodes, Keith received a pacemaker and recording device and was treated with Sotalol, a beta-blocker. However, Keith had also begun to experience fluid retention related to heart failure, and doctors told him that he would need a heart and liver transplant. He is currently undergoing the required testing to be listed for both organs. 

    Over the years, Keith worked for a variety of retail and restaurant businesses, before working his way up to managing and owning businesses. He also started doing stand up comedy. Most recently, he has worked in the health and disability rights fields and earned his Bachelor’s degree in Accounting. He met his wife in 2003 and currently lives in Baltimore.

    In this episode, Keith will share more about his life -- living with a congenital heart defect -- with Anna. He will also explain how he has come to need to be listed for two different organs. He will also share with Anna what he believes keeps him going, even when the going gets rough.

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    If you enjoy this program and would like to be a Patron, please check out our Patreon page: https://www.patreon.com/HeartToHeart

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    Living with a Bi-Directional Glenn Heart

    Living with a Bi-Directional Glenn Heart

    Most people today (2019) with a single ventricle heart typically have one of two courses of treatment for their heart condition: 1) a series of surgeries culminating with the Fontan Procedure or 2) a heart transplant. That is not the case with our Guest in this episode. Born in 1970, returning Guest Laura Ryan, talks about what her life has been like growing up with a single ventricle heart palliated in a rather unusual way -- with a Potts shunt, a Waterston shunt and a Bi-Directional Glenn shunt. 

    In this episode she shares what it was like for her as a child and what her endurance was like. She talks about how she interacted with her siblings and friends. She then moves on to share what it was like for her once she decided she wanted to start her family. In this very candid interview, Laura shares some of the travails she endured and what helped to her make it through the difficult times.

    Finally, Laura shares how she feels pregnancy affected her body and her heart. She also shares her doctor's prognosis for her future, especially given her sequence of medical events thus far. Laura's story is one of inspiration and hope.

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    If you enjoy this program and would like to be a Patron, please check out our Patreon page: https://www.patreon.com/HeartToHeart

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    Difficulties Growing Up with a CHD

    Difficulties Growing Up with a CHD
    What is it like to grow up with critical congenital heart defects requiring surgery in the first year of life? How does having multiple surgeries through a person's life affect their career choices? How are two amazing adult survivors giving back?Support the show

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    Encore Presentation "Hope for Babies Diagnosed In Utero

    Encore Presentation "Hope for Babies Diagnosed  In Utero
    What should parents do if they're told their unborn children will be born with a heart defect? What professionals can help pregnant women who have babies with heart defects? Is there hope for babies born with broken hearts?Support the show

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    The Miracle of Giving Back

    The Miracle of Giving Back
    Those who have been through the trauma of having open-heart surgeries and dealing with all of the situations that accompany them have many choices. They can choose to be positive and to see the bright side, even when things get difficult or they can choose to feel negative and like what is happening to them is unfair. Survivors can choose to let their heart defects define them or they can choose to live a quality life despite their difficulties.Sometimes a person used her personal trauma to empathetically reach out to others. That's what this show is all about. Tune in to hear how a CHD Survivor has used her experiences to reach out to others -- specifically to children with learning and medical disabilities. Discover the miracles she has witnessed over the years and the good that can come of living a challenging life.Today's show, "The Miracle of Giving Back" features CHD Survivor and special education teacher Catherine Scavone.***Thanks to Stuart Miles of FreeDigitalPhotos.net for the illustration***Support the show

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    A Modern Medical Miracle

    A Modern Medical Miracle
    Miracles seem to be all around us, but some miracles are thanks to the great strides made in the field of pediatric cardiology. What kind of advances have been made over the years? What are some techniques being used that can save untold numbers of lives? How, exactly, are babies or children benefiting from the developments in pediatric cardiology?This show will feature the mother of two daughters who is grateful for the advances in pediatric cardiology and how those advances have personally affected her life. Tune in to hear how Sharisse Roberts feels she has a medical miracle living with her and the advice she has for others who find themselves being told their unborn child will be born with a congenital heart defect.Support the show

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    Hope for Heart Babies Diagnosed In Utero

    Hope for Heart Babies Diagnosed In Utero
    What happens when you are pregnant and go in for a routine ultrasound only to discover your baby has a heart defect? How do you handle the news? What options are you given? Even though congenital heart defects are the number one birth defect, there aren't many people who talk about it and it's not a widely known fact. Today we'll talk with three mothers who have been there -- who found out in utero, not only that their babies would be born with a heart defect, but that they would be born with critical congenital heart defects requiring surgery in their first year of life. (Thanks to David Castillo Dominici at FreeDigitalPhotos.net for the beautiful photo.)Support the show

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