Rita Ralston, Charles George
Walking With Families Podcast |Hope & Inspiration |Weekly Interviews With Families & People Involved With Helping Critically Ill and Injured Children.Episodes
Episodes of Walking With Families Podcast |Hope & Inspiration |Weekly Interviews With Families & People Involved With Helping Critically Ill and Injured Children.
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Amy shares her son’s journey with congenital heart disease. She talks about when her son was first diagnosed during a fetal ultrasound, and the conflicting advice she received from the physicians. She shares the story of her son’s birth. She ta
Margaret started her congenital heart disease journey when her daughter was first diagnosed with CHD. Since then she co-founded an organization that delivers superhero capes to children around the world who have CHD. Plus, she organizes S
Brandi shares the story of her two children. She talks about when her daughter was first diagnosed with congenital heart disease and her stay in the hospital with her for 6 months after she was born. She talks about their time in the hospital
Jodi shares her story about her teenage son who was born with congenital heart disease. Jodi shares her experience about when her son was first diagnosed with CHD. She talks about the delivery and the first two heart surgeries. Jodi talks abou
On this episode of the podcast, Kristine talks about her journey with her son who has CHD and how this has inspired her to become an organizer of the Super Hero Heart Run in Virginia. Kristine talks about her pregnancy and when the doctors firs
On this podcast, Kelli talks about how after both of her children were born that they both spent time in the NICU. Kelli shares how when her son was born he was hospitalized in the NICU for about 4 months. She talks about her and her son's expe
Amanda and Patrick talk about their son who has been through two heart surgeries and a heart transplant. They talk about their son being born and how they were unaware that he had congenital heart disease. They talk about the first 24 hours in
Kelley talks about her son, Mason, who was first diagnosed with cancer at age 5 and how his passing at age 11 inspires her to help other families and children in the hospital. She talks about her son's experience with cancer along with what ins
On this podcast, Alyssa shares her story of having 2 biological children and then adopting 6 other children. Alyssa shares the frightening story of when her first biological son coded after he was born and then experienced seizures. She a
On this episode of the podcast, Kelly shares her story and why she is so passionate about helping other families, fundraising, and doing anything she can to spread awareness about congenital heart disease! Kelly discusses the infertility issue
Tara shares her story about her daughter who has hypoplastic left heart syndrome. She talks about her pregnancy, when her she first learned that her daughter was going to have congenital heart disease, and the moments leading up to her daughter
48: Jolene Philo-How Trauma and PTSD Affect Children Who Experience Long Hospital Stays and Surgery.
Jolene talks about her journey with her son and how she discovered how his surgeries and hospital stays early in life affected his long-term development, causing trauma and PTSD. She shares the trauma her son experienced after birth, involving
On this podcast episode, Kayla shares her story about her daughter: born at 25 weeks in her pregnancy, her long 6 months stay in the hospital, being away from her family, and how her daughter has overcome all the odds and is now thriving and a
46: Melody Nutall- Anencephaly and Making The Most Out of Life To Help Other Children and Families. On this podcast, episode Melody shares her story about her daughter Lailah Joy Heaven who was born with Anencephaly. She talks about when she fi
On this week's podcast, Meagan Nash talks about her son, who has down syndrome and how both of them are changing people's perception in regards to children with special needs. Meagan talks about her pregnancy and when her son was first diagnose
On this podcast, Kathy talks about her son who has Cri du Chat Syndrome. Kathy talks about her pregnancy and how there were symptoms and risks during her pregnancy. She describes her son’s birth and his noticeable "cat-like cry". She talks abo
On this podcast, Celeste shares her story of how her daughter was diagnosed with Congenital Heart Disease (“CHD”) at the age of 3. She talks about the events that led up to her daughter being diagnosed with CHD. Celeste then describes how wit
On this podcast, Ellen Stumbo shares the story of her two daughters - one child who has Down Syndrome, and an adopted child who has cerebral palsy. Ellen talks about her daughter and how cerebral palsy has affected her. She discusses her daught
Kristie shares her journey and how she has overcome so many challenges living with a rare form of congenital heart disease known as Shone's Complex. Kristie shares: How she only had a 5% chance of surviving after her first heart surgery at sev
On this podcast, Dana shares her story about growing up with Tetralogy of Fallot and how all 3 of her children have congenital heart disease. She talks about growing up with CHD, her surgeries, and her experiences at the hospitals. Plus, she de
In this episode, Allyson Drake talks about helping parents and children through the grief process after losing a child or loved one. Alyson shares: What led her to starting her organization Full Circle Grief. What the 4 tasks of grief are that
On this episode of the podcast, Jenny Samuels shares her story about her son who has Type 1 Diabetes. Jenny talks about her son, his initial stay in the hospital, and how his he was diagnosed with juvenile diabetes. She talks about her daily
Amy shares her journey about what she does as a flight paramedic and how she transports children in critical condition via helicopter. She reveals the type of patients that she transports most often. She discusses some of the environmental ch
On this episode of the podcast Tammy shares her journey with CHD in regards to her son and how it led her to working with the Children's Heart Foundation. During this episode: Tammy shares her story about her 22-year-old son who has congenita
35: Jennifer DeBouver-Losing a Child to CHD and Helping Other CHD Parents Who Are Experiencing Loss!
This week on the podcast, Jennifer talks about losing her first child at 27 weeks in the pregnancy and then losing her second child to CHD. She talks about how the loss of her two children motivated her to help other families who have lost the
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