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    Kids & Family

    Inside the Children’s Hospital

    Inside the Children’s Hospital shares real stories from parents, caregivers, and pediatric healthcare professionals navigating the emotional realities of caring for a hospitalized child with honesty, compassion, and hope.

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    Latest Episodes:
    Episode 15 | Alexis' Story - Ear tubes surgery and how to support your child through surgery Mar 12, 2018
    Show notes

    Today's episode features two women. First, we will hear from Alexis whose son went through a fairly common surgery, ear tubes, and she will talk about what their experience was like. However, as child life specialists and parents we know thate despite how "common" or "routine" a surgery may be, those words don't begin to cover all the emotions and experiences that come along with these "common" surgeries. You can follow Alexis through her business or her blog.

    As a part of celebrating child life month, after Alexis' story we will hear from Liz Anderson, a certified child life specialist who has spent a bulk of her career working in with children and families going through surgery. If you are a parent you will definitely want to stay tuned so you can hear great advice and suggestions for parents whose children have upcoming surgeries. If you are listening to this as an aspiring child life specialist or as a current CCLS, Liz shares a lot of useful information about her experiences and also how she created a program to help children with autism going through surgery.


    Episode 14 | Shani's Story - An interview with Child Life Mommy Mar 05, 2018
    Show notes

    In honor of March and the fact that is Child Life Month, this episode features Shani Thornton from Child Life Mommy.

    Shani shares her entrance into the child life field and how she chose to move forward in the field as a community-based child life specialist.

    Along with being the author of the children's book "It's time for your check up: What to expect when you're going in for a doctor's visit," Shani is a big voice in the child life world as she has her own blog and shares valuable resources for parents and child life specialists on Facebook, Instagram and Twitter.

    In today's episode, you will hear her talk about her child life career, current private practice, and how she's involved with the ACLP and community-based programs. Shani talks about her current role with the Standish Foundation, and my favorite part of the episode is when she gets real about finding the balance in her roles as "mom" and child life specialist.


    Episode 13 | Nina's Story - A son with craniosynostosis Feb 26, 2018
    Show notes

    In this first episode of the second season of this podcast, we hear from a self-proclaimed "crunchy granola mom" Nina, whose fourth child was born with what she calls "a funny shaped head."

    Nina goes on to describe her son's first few weeks of life and her appointments with her pediatrician and an osteopathic doctor. With little to no help from the osteopathic doctor, she trusted her instincts and returned to her pediatrician who then referred her to a surgeon at Children's National Medical Center in Washington D.C. and would learn that her son had craniosynostosis.

    Nina then discusses their surgical journey and all that in entailed. In addition to the stress of building a new business and homeschooling three other older children, Nina talks about the challenges and emotions that she felt at that time. She also talks about how her view of what a hospital is like has changed and how she talked to her older children about what Cohen was going through.

    She attributes the help of her friends and church congregation to helping her family cope with this experience.

    If you would like to follow along with Nina and her family, you can find her on Instagram or through her family's wellness business, True Whole Human.


    Episode 12 | Season 1 Finale Dec 07, 2017
    Show notes

    This episode closes out Season 1 of the Child Life On Call Podcast. This podcast went from a dream to a reality thanks to the help of the all the courageous families who came forward to share their stories about having a child with medical needs. Season 1 covered the spectrum in illnesses, diseases and conditions, and all episodes had a similar theme: children are resilient and teach us more about the world and ourselves than we could ever imagine.

    Katie gives life updates and talks about her need to bring to Season 1 to a close, but gives a preview of what is to come next season. In Season 2, you can expect to hear more brave parents come forward and share their inner most thoughts and feelings. We will talk about routine surgeries and the stress they can bring, as well as not-so-routine surgeries that can be life changing. We will hear from a parent whose daughter spent months of her life in the NICU after a scary delivery at 25 weeks, and we will hear from parents whose children have chronic health issues. Regardless of the diagnosis, each of these parents have an important message and story to share.

    In this finale episode, you will also get brief updates about how Season 1 families are doing now.

    A big thank you to all those who listen, share, and enjoy this podcast. We are always looking to record and share more stories, and if you are interested in doing so, you can contact Katie at info@childlifepodcast.com.

    Another big thank you to all the photographers who took photos of these families... you have given them and the world a gift that can never be replaced!


    Episode 11 | Susan's story - A son with Crohn's disease Oct 19, 2017
    Show notes

    At just six years old, Susan's son began complaining of belly pain along with other alarming symptoms. After a trip to the doctor, they were quickly sent to meet with a Pediatric Gastroenterologist and would eventually learn the news that one of her sons, Preston, had Crohn's disease. Susan shares personal details about their journey, procedures, and treatments that are associated with Preston's experience with Crohn's. She discusses how she and her family cope with living with this disease. Susan is honest, articulate and gives priceless advice to parents who may be going through similar situations.

    Susan says that reaching out to her own doctor and support system was invaluable in helping her cope with a child who has an illness. She and her husband face each challenge with trusting fully in her sons health care team, leaning on each other, and prayer.

    If you would like to connect with Susan, you can follow along with her on Instagram or Facebook. She recommends the Crohn's section on kidshealth.org and researching your child's specific medication in order to feel empowered.

    If you would like to share your story, you can message Child Life On Call's Twitter, Facebook or Instagram or submit your information on childlifepodcast.com or email info@childlifepodcast.com


    Episode 10 | Roxanne's Story - A son with viral encephalitis and epilepsy Sep 11, 2017
    Show notes

    Episode 10 features an interview with Roxanne, a mom of three from San Antonio, Texas. Just after entering high school and an outstanding performance in a football game, Roxanne's eldest child, Rueben, began having high fevers and flu-like symptoms. After about a week, his parents found him having a seizure and rushed him to the emergency room. They would soon learn that Rueben was diagnosed with viral encephalitis.

    Roxanne tells the story of their stay in the Pediatric ICU, what it was like balancing being there for Rueben in the hospital while having a newborn and another child at home, and how family played a major role in getting through some of their darkest times.

    Rueben's seizures continue after he returned home from the hospital, and during his sophomore year he was diagnosed with epilepsy which led to four invasive brain surgeries. Roxanne talks about what a critical role basketball was in Rueben's life prior to acquiring viral encephalitis and how he continues to show his determination in finding purpose while dealing with his illness.

    Roxanne wants parents to know that it is ok to vent, it is ok to ask questions and know that you are not alone. Roxanne and Rueben are advocates and aim to bring awareness to the rare disease that is encephalitis. Roxanne is currently in the works to bring an encephalitis walk to raise awareness in San Antonio.

    Roxanne says that Chris Maxwell has been instrumental in helping Rueben cope with his illness. She also suggests that families visit EncephalitisGlobal.org.

    If you would like to connect to Roxanne and follow along with Rueben's Journey, you can do so here on Facebook or Instagram. If you'd like more information or to share your own story, please email info@childlifepodcast.com.


    Episode 9 | Liz and Jamie's Story - A daughter acquires HIV after a blood transfusion during cardiac surgery Aug 28, 2017
    Show notes

    Episode 9 features an interview with Liz and Jamie. Shortly after Jamie was born, she developed a heart murmur and began passing out. Her mom, Liz, walks us through what it was like to witness such terrifying scenarios and how she began to become an advocate for her daughter. Despite being told that nothing was actually wrong with Jamie, Liz pushed harder and demanded tests that led them eventually to her diagnosis, Tetralogy of Fallot, a rare and serious heart defect.

    Years after the surgery to correct the defect, they'd come to learn that Jamie had been infected with HIV during a blood transfusion. Throughout this episode Liz talks about how she made some of her toughest parenting decisions: how to tell her child that she had the AIDS virus and how much information to give her. She talks about how she coped with not knowing how long her daughter would live for, experts had guessed it would be about two years. Unlike most childhood diseases and illness, there were no support groups for children with HIV and the stigma associated with it provoked fear in the public who didn't know much about the disease.

    Liz provides incredible insight on how she dealt with news that could have easily darkened her world and every day life - She says to think about the worst case scenario and be thankful for the here and now and to choose hope.

    Jamie shares her own experiences and memories surrounding how she kept her HIV a secret from her friends and classmates, and how her experiences at Hole in the Wall Gang Camp were a game changer for her and her confidence.

    Liz and Jamie live with a glass-half-full mentality and talk about their most personal conversations, their hardest experiences and how they find joy in the small celebrations and challenges of life.

    Jamie is the Child Life Director at Inova Children's Hospital and pursued the career based on the fact that her own experiences led her to want to support other patients and families going through their own medical journeys.

    Liz's advice to other parents going through their own experiences would be to advocate for your child, you know your child the best and you are the first line of defense.

    Jamie tells children and adolescents to ask questions and tell people what you need, build your support team, and become an advocate for yourself.

    Jamie credits her mom to being the reason she is alive today and says that without her, she wouldn't be loving life, living with her husband and talking about what she wants to do in her retirement. Liz tells us that Jamie chose hope. Medical science can leap frog over you, but choosing hope is what will get you through.

    I have excellent news for you, and that is if you wish you knew MORE about Jamie's experience about growing up with HIV, she has written a book! It is called "Surviving HIV: Growing Up a Secret and Being Positive" and you can buy this book on Amazon.

    Please follow along with Child Life On Call wherever you like to check your social media, Facebook, Instagram or Twitter, and if you have any questions you can always write to me at info@childlifepodcast.com.


    Episode 8 | Part Two of Mandy's Story - A son born with a rare genetic condition Aug 21, 2017
    Show notes

    Episode 8 is Part 2 of Mandy and Nolan's story. If you haven't listened to Part 1, head on over to Episode 7 so you have a better understanding and appreciated for Mandy's story. I mentioned that Nolan was scheduled for surgery and I'm sure you're interested in an update… and this is directly from Mandy: The doctors were able to perform a scope of his airway to identify the obstruction that is causing the apnea; however, after getting a closer look at just how constricted his airway is, they decided they could not safely proceed with the surgery. We are now discussing a more involved approach to the surgery and exploring other options all together. We are disappointed but thankful to be working with a team of doctors so dedicated to finding solutions for our one in a billion patient.

    On this week's episode, we learn how incredible Mandy and Nolan are and how MadB does not define him as a child. Mandy talks honestly and candidly with us about what it's like to live with a child like Nolan and how the experience parallels emotions that she had in high school when she lost her mom to cancer. Mandy shares real stories about how others treat and react to Nolan, and she also talks about how incredibly adorable Nolan is and some of his favorite things: trucks, books, and a Bob Marley song.

    Mandy also gives incredible advice about what she and her husband do to cope and gives these suggestions for other families feeling isolated by an illness or diagnosis:

    1) Go hug your child and keep loving them - the diagnosis doesn't define your child.

    2) Try not to get too focused on the future, focus on making the most out of the present.

    3) Don't go through it alone.

    4) Learn everything you can about your child's diagnosis so you know that you've made the best decision you can.

    If you would like to reach out to Mandy, please message me and I will get you in touch with her through email.

    Thank you to Gruene Photography for the beautiful pictures of Mandy, Nolan and their family. We can't thank you enough for taking the time to give Mandy and her family these gorgeous photos that they will keep forever. If you are near New Braunfels or Gruene, Texas, go book Gruene Photography. Follow her on Instagram or Facebook.

    Thank you to Stephanie Sobic Gauthier for help in the storyline editing of this episode.

    Please subscribe to the Child Life On Call Podcast and leave a review on iTunes. If you would like to share your story or have questions about this podcast, you can email info@childlifepodcast.com or submit your information via the website childlifepodcast.com.


    Episode 7 | Part 1 of Mandy's Story - A son born with a rare genetic condition Aug 14, 2017
    Show notes

    Episode 7 features the first part of Mandy's story. Her son, Nolan, was born five weeks early with a host of symptoms which led them to find that he was diagnosed with a condition that only four other people are currently living with. Nolan is the ninth person in the history of medical science that has been diagnosed with Mandibuloacral Dysplasia Type B (Mad B).

    In part one of Mandy's story, she talks to us about how doctors and specialists eventually came to diagnose Nolan. It ended up being an unsuspecting doctor appointment with a Dermatologist who had studied Progeria in medical school who wrote the diagnosis on a sticky note that led them to this rare condition.

    Part two of Mandy's story will be available next Monday morning when she talks about what living with a child who has Mad B is like, how undeniably amazing Nolan is, and how she and her family cope with it.

    Thank you to Gruene Photography for the beautiful pictures of Mandy, Nolan and their family. We can't thank you enough for taking the time to give Mandy and her family these georgeous photos that they will keep forever. If you are near New Braunfels or Gruene, Texas, go book Gruene Photography. Follow her on Instagram or Facebook.

    Thank you to Stephanie Sobic Gauthier for help in the storyline editing of this episode.

    Please subscribe to the Child Life On Call Podcast and leave a review on iTunes. If you would like to share your story or have questions about this podcast, you can email info@childlifepodcast.com or submit your information via the website childlifepodcast.com.


    Episode 6 | Tricia's Story - A daughter diagnosed with Rolandic Epilepsy Aug 07, 2017
    Show notes

    Episode 6 features Tricia, a mama who lives in the southwest suburbs of Chicago. Tricia bring a unique perspective and understanding of child development in her experience based on the fact that she has her masters in early childhood development and education, is currently an adjunct faculty member at Depaul University and is also a doula.

    In this episode, you'll hear Tricia talk about the fight of a lifetime to find a diagnosis for her daughter, Cora, who is now 13 years old. After four and a half years of countless doctors and very little sleep, Tricia learned that her daughter has Rolandic Epilepsy.

    If you are going through a similar experience, Tricia recommends getting in touch with the Epilepsy Foundation and finding a local chapter in your area. If you happen to live in the greater Chicago area, she also recommends Danny Did and Equip for Equality. If you'd like to get in touch with Tricia, you can do so via her email, Facebook or Twitter.

    Please subscribe to the Child Life On Call Podcast and leave a review on iTunes. If you would like to share your story or have questions about this podcast, you can email info@childlifepodcast.com or submit your information via the website childlifepodcast.com.


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