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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.

    Advertise
    • Apple Podcasts
    • Google Play
    • Spotify

    Latest Episodes:
    PANDAS (Pediatric Autoimmune Disorder): Recognizing the Signs Feb 09, 2022
    Show notes

    Today's guest, Elizabeth, had never heard of PANDAS (Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal Infection) when her son was diagnosed with it. PANDAS is a tough diagnosis, because some doctors believe in it while others do not. Having a child with this diagnosis that only some doctors believe in is incredibly hard to navigate, to say the least. PANDAS is an autoimmune disease closely related to infections, so you will hear Elizabeth talk a bit about how her son's ear infections seemed to lead to PANDAS.

    Elizabeth also shares her thoughts about how society does not judge kids with colds, cancer, or appendicitis, but society tends to look down on you when your child suffers from neuropsychiatric symptoms. There are misconceptions that these symptoms are related to bad parenting, violence in the home, poor role models, lack of discipline, or just being a "bad child". Parents of children with PANDAS have a lot to carry on their shoulders, and I am so glad Elizabeth is here to share her story.

    In this episode, we talk about…

    [2:46] Elizabeth's family and background

    [5:17] Elizabeth's son's first symptoms of PANDAS

    [9:01] Getting the diagnosis of an acute onset of PANDAS

    [12:33] Being discharged from the hospital

    [16:28] More strep, different symptoms

    [23:38] Juvenile court and the path to treatment

    [33:58] Searching for the source of PANDAS with medical testing

    [43:58] How Elizabeth's son and family are doing after medical treatment

    [45:09] Elizabeth's book: What's Wrong With My Child?

    Connect with Elizabeth:

    Website

    Book: What's Wrong With My Child?

    When parents feel empowered, everyone wins – kids thrive and the care team excels!

    Links and Resources:

    • SupportSpot Website
    • Download SupportSpot iOS or Android
    • 85% of users report high satisfaction, appreciating the SupportSpot app's comprehensive resources and user-friendly interface.
    • 92% of parent users say the SupportSpot app's helped them understand medical procedures and treatment better.
    • 80% of parents believe the SupportSpot app's has contributed to better health outcomes for their child.
    • 73% of parent users believe the SupportSpot app's has made them feel more empowered to advocate for their child in healthcare

    Learn more here.

    Meet the host:

    Katie Taylor is the co-founder and CEO of Child Life On Call, a digital platform designed to provide parents, kids, and the care team with access to child life services tools and resources. She is a certified child life specialist with over 13 years of experience working in various pediatric healthcare settings. Katie is the author of the children's book, and has presented on the topics of child life and entrepreneurship, psychosocial care in the hospital, and supporting caregivers in the NICU setting both nationally and internationally. She is also the host of the Child Life On Call Podcast which features interviews with parents discussing their experiences throughout their child's medical journey. The podcast emphasizes the crucial role of child life services in enabling caregivers both at and beyond the bedside.

    Instagram.com/childlifeoncall

    The Child Life On Call Podcast is for informational and educational purposes only. The content shared in each episode, including stories, discussions, and interviews, is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay seeking it because of something you heard on this podcast. The views and opinions expressed by guests on the Child Life On Call Podcast are their own and do not necessarily reflect those of Child Life On Call. Child Life On Call does not endorse any specific medical treatments, procedures, or opinions shared in the podcast. If you or your child are experiencing a medical emergency, call 911 or seek immediate medical attention. By listening to this podcast, you acknowledge that Child Life On Call and its affiliates are not responsible for any decisions made based on the information provided.

    Facebook.com/childlifeoncall

    linkedin.com/in/kfdonovan


    Helping Children Cope After Disasters: Child Life Strategies Feb 02, 2022
    Show notes

    Today's 12 minute talk became a 20+ minute talk, and Cara Smith and I discussed how parents can connect with their children after a disaster. Cara is an amazing pioneer in the child life field, and she has valuable tips both for child life specialists as well as for parents in the wake of a natural disaster, a pandemic, or any other stressful event.

    In this episode, we talk about…

    [1:41] Cara's background

    [4:18] Burnout as a child life specialist

    [6:44] Cara's experience working with children in the wake of a traumatic event

    [14:13] Supporting caregivers after a disaster

    [21:39] Giving children the tools to be resilient

    [24:29] Learning more about working as a child life specialist in disaster relief

    Connect with Cara:

    Website

    Instagram

    Facebook

    When parents feel empowered, everyone wins – kids thrive and the care team excels!

    Links and Resources:

    • SupportSpot Website
    • Download SupportSpot iOS or Android
    • 85% of users report high satisfaction, appreciating the SupportSpot app's comprehensive resources and user-friendly interface.
    • 92% of parent users say the SupportSpot app's helped them understand medical procedures and treatment better.
    • 80% of parents believe the SupportSpot app's has contributed to better health outcomes for their child.
    • 73% of parent users believe the SupportSpot app's has made them feel more empowered to advocate for their child in healthcare

    Learn more here.

    Meet the host:

    Katie Taylor is the co-founder and CEO of Child Life On Call, a digital platform designed to provide parents, kids, and the care team with access to child life services tools and resources. She is a certified child life specialist with over 13 years of experience working in various pediatric healthcare settings. Katie is the author of the children's book, and has presented on the topics of child life and entrepreneurship, psychosocial care in the hospital, and supporting caregivers in the NICU setting both nationally and internationally. She is also the host of the Child Life On Call Podcast which features interviews with parents discussing their experiences throughout their child's medical journey. The podcast emphasizes the crucial role of child life services in enabling caregivers both at and beyond the bedside.

    Instagram.com/childlifeoncall

    The Child Life On Call Podcast is for informational and educational purposes only. The content shared in each episode, including stories, discussions, and interviews, is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay seeking it because of something you heard on this podcast. The views and opinions expressed by guests on the Child Life On Call Podcast are their own and do not necessarily reflect those of Child Life On Call. Child Life On Call does not endorse any specific medical treatments, procedures, or opinions shared in the podcast. If you or your child are experiencing a medical emergency, call 911 or seek immediate medical attention. By listening to this podcast, you acknowledge that Child Life On Call and its affiliates are not responsible for any decisions made based on the information provided.

    Facebook.com/childlifeoncall

    linkedin.com/in/kfdonovan


    Clubfoot Treatment: One Family's Experience with Casting and Surgery Jan 26, 2022
    Show notes

    Today's guest is Maureen, and she found out at her 20 week ultrasound that her daughter had clubfoot. She shares what families have to endure when confronted with a child with clubfoot. You'll hear about B and B (boots and bar), serial casting, surgeries, doctors' visits, and the amount of parent intervention that has to take place in the first four to five years of these kids' lives.

    In this episode, we talk about…

    [2:07] Maureen's family and background

    [4:53] Getting a clubfoot diagnosis in utero

    [11:39] Processing her daughter's clubfoot diagnosis

    [13:28] Medical treatment for clubfoot

    [17:14] Handling the stress of her daughter's diagnosis

    [23:32] The parental workload involved with clubfoot maintenance and treatment

    [26:34] Maureen's advice for other parents going through the boots and bar scenario

    [30:05] Sleep challenges related to clubfoot

    [31:52] Treatment since the boots and bar

    [34:35] Maureen's book: Clubfoot Chronicles

    [40:27] What Maureen's daughter has taught her through this experience

    Connect with Maureen:

    Website

    Instagram

    Podcast

    When parents feel empowered, everyone wins – kids thrive and the care team excels!

    Links and Resources:

    • SupportSpot Website
    • Download SupportSpot iOS or Android
    • 85% of users report high satisfaction, appreciating the SupportSpot app's comprehensive resources and user-friendly interface.
    • 92% of parent users say the SupportSpot app's helped them understand medical procedures and treatment better.
    • 80% of parents believe the SupportSpot app's has contributed to better health outcomes for their child.
    • 73% of parent users believe the SupportSpot app's has made them feel more empowered to advocate for their child in healthcare

    Learn more here.

    Meet the host:

    Katie Taylor is the co-founder and CEO of Child Life On Call, a digital platform designed to provide parents, kids, and the care team with access to child life services tools and resources. She is a certified child life specialist with over 13 years of experience working in various pediatric healthcare settings. Katie is the author of the children's book, and has presented on the topics of child life and entrepreneurship, psychosocial care in the hospital, and supporting caregivers in the NICU setting both nationally and internationally. She is also the host of the Child Life On Call Podcast which features interviews with parents discussing their experiences throughout their child's medical journey. The podcast emphasizes the crucial role of child life services in enabling caregivers both at and beyond the bedside.

    Instagram.com/childlifeoncall

    The Child Life On Call Podcast is for informational and educational purposes only. The content shared in each episode, including stories, discussions, and interviews, is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay seeking it because of something you heard on this podcast. The views and opinions expressed by guests on the Child Life On Call Podcast are their own and do not necessarily reflect those of Child Life On Call. Child Life On Call does not endorse any specific medical treatments, procedures, or opinions shared in the podcast. If you or your child are experiencing a medical emergency, call 911 or seek immediate medical attention. By listening to this podcast, you acknowledge that Child Life On Call and its affiliates are not responsible for any decisions made based on the information provided.

    Facebook.com/childlifeoncall

    linkedin.com/in/kfdonovan


    Episode 103 | A Talk with an Expert: Kat Harrison on Living with Medical Challenges, Disability, Mental Health, and Chronic Illness Jan 19, 2022
    Show notes

    For today's 12 minute talk, I'm speaking with Kat Harrison. At the end of 2021, I shared Kat's episode (episode 99) in which she talked about what it was like being a teenager with chronic illness. During that episode, we touched on what helped her the most when she was a teenager in the hospital and how to support adolescents coping with different medical or mental challenges. I'm so excited to share this talk with you today so you can be more prepared when you're talking to your own teenager or working in the field with adolescents.

    In this episode, we talk about…

    [2:46] Kat's background

    [3:19] How parents can empower their teens living with medical and mental health challenges

    [5:26] Planning for appointments

    [8:17] Preventing a diagnosis from becoming an identity

    [10:02] Mental health

    [11:41] Asking your teen how they want to be supported

    [13:04] Kat's books

    Surgery on Sunday

    Migraine and Mia

    Connect with Kat:

    Website

    Instagram

    Have you heard? The Child Life On Call mobile app for parents, kids and their care team will be available in 2022. Sign up to stay informed here.

    Child Life On Call is a community of parents and professionals that share ideas, stories and resources to help YOU navigate your child's unique experiences. We give you strategies to support yourself and your family through life's challenges. We are so glad you are here.

    Website: childlifepodcast.com

    Merch: bonfire.com/store/childlifeoncall

    Instagram: instagram.com/childlifeoncall

    Facebook: facebook.com/childlifeoncall

    Twitter: twitter.com/childlifeoncall

    YouTube: https://www.youtube.com/channel/UCnh95T1MOYtbpBxJaZqg7rg


    HIE (Hypoxic Ischemic Encephalopathy): Finding Hope After Birth Injury Jan 12, 2022
    Show notes

    Today's guest is Betsy, from an organization called Hope for HIE (Hypoxic Ischemic Encephalopathy). HIE refers to brain injury in an infant, and Betsy will share more specifics about the condition and her family's experience with it in our discussion. I originally learned about this organization through working in the NICU here in Texas, and it is a wonderful source of support for parents struggling in completely unknown territory with their babies.

    In this episode, we talk about…

    [1:19] HIE: Hypoxic Ischemic Encephalopathy

    [2:29] Betsy's family

    [3:02] The beginning of the HIE journey

    [11:36] Brain cooling (therapeutic hypothermia)

    [15:10] Seeing your baby in the NICU

    [24:06] Warming after therapeutic hypothermia

    [24:41] MRI day and diagnosing the severity of HIE

    [30:58] Leaving the NICU

    [36:01] Moving forward with career and family as parents of a child with HIE

    [41:20] A current update on Betsy's son and family

    Connect with Betsy:

    Website

    Instagram

    Facebook

    When parents feel empowered, everyone wins – kids thrive and the care team excels!

    Links and Resources:

    • SupportSpot Website
    • Download SupportSpot iOS or Android
    • 85% of users report high satisfaction, appreciating the SupportSpot app's comprehensive resources and user-friendly interface.
    • 92% of parent users say the SupportSpot app's helped them understand medical procedures and treatment better.
    • 80% of parents believe the SupportSpot app's has contributed to better health outcomes for their child.
    • 73% of parent users believe the SupportSpot app's has made them feel more empowered to advocate for their child in healthcare

    Learn more here.

    Meet the host:

    Katie Taylor is the co-founder and CEO of Child Life On Call, a digital platform designed to provide parents, kids, and the care team with access to child life services tools and resources. She is a certified child life specialist with over 13 years of experience working in various pediatric healthcare settings. Katie is the author of the children's book, and has presented on the topics of child life and entrepreneurship, psychosocial care in the hospital, and supporting caregivers in the NICU setting both nationally and internationally. She is also the host of the Child Life On Call Podcast which features interviews with parents discussing their experiences throughout their child's medical journey. The podcast emphasizes the crucial role of child life services in enabling caregivers both at and beyond the bedside.

    Instagram.com/childlifeoncall

    The Child Life On Call Podcast is for informational and educational purposes only. The content shared in each episode, including stories, discussions, and interviews, is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay seeking it because of something you heard on this podcast. The views and opinions expressed by guests on the Child Life On Call Podcast are their own and do not necessarily reflect those of Child Life On Call. Child Life On Call does not endorse any specific medical treatments, procedures, or opinions shared in the podcast. If you or your child are experiencing a medical emergency, call 911 or seek immediate medical attention. By listening to this podcast, you acknowledge that Child Life On Call and its affiliates are not responsible for any decisions made based on the information provided.

    Facebook.com/childlifeoncall

    linkedin.com/in/kfdonovan


    Childhood Osteosarcoma (Bone Cancer): A Mother's Story of Strength Jan 05, 2022
    Show notes

    As we kick off the new year, my guest Christiana is sharing the story of her son's osteosarcoma. Nathaniel has passed away, but his family created Nathaniel's Childhood Cancer Foundation in his name and legacy. Christiana walks us through his experience with osteosarcoma from the beginning, and she shares details about his battles with childhood cancer.

    In this episode, we talk about…

    [1:27] Introducing Christiana and her family

    [3:09] The beginning of Nathaniel's story with osteosarcoma

    [11:49] Nathaniel's osteosarcoma diagnosis

    [14:32] How Nathaniel reacted to these sudden life changes

    [18:52] What was helping Christiana through her son's cancer battle

    [21:02] Health insurance and hospitals

    [23:01] Nathaniel's experience after amputation

    [28:06] Finding out that Nathaniel's cancer had spread

    [32:13] Getting fitted for a prosthetic and accessing video games post-amputation

    [35:11] Treatment after radiation

    [36:19] Nathaniel's last days

    [40:28] Nathaniel's Childhood Cancer Foundation

    Connect with Christiana:

    Website

    Instagram

    Facebook

    When parents feel empowered, everyone wins – kids thrive and the care team excels!

    Links and Resources:

    • SupportSpot Website
    • Download SupportSpot iOS or Android
    • 85% of users report high satisfaction, appreciating the SupportSpot app's comprehensive resources and user-friendly interface.
    • 92% of parent users say the SupportSpot app's helped them understand medical procedures and treatment better.
    • 80% of parents believe the SupportSpot app's has contributed to better health outcomes for their child.
    • 73% of parent users believe the SupportSpot app's has made them feel more empowered to advocate for their child in healthcare

    Learn more here.

    Meet the host:

    Katie Taylor is the co-founder and CEO of Child Life On Call, a digital platform designed to provide parents, kids, and the care team with access to child life services tools and resources. She is a certified child life specialist with over 13 years of experience working in various pediatric healthcare settings. Katie is the author of the children's book, and has presented on the topics of child life and entrepreneurship, psychosocial care in the hospital, and supporting caregivers in the NICU setting both nationally and internationally. She is also the host of the Child Life On Call Podcast which features interviews with parents discussing their experiences throughout their child's medical journey. The podcast emphasizes the crucial role of child life services in enabling caregivers both at and beyond the bedside.

    Instagram.com/childlifeoncall

    The Child Life On Call Podcast is for informational and educational purposes only. The content shared in each episode, including stories, discussions, and interviews, is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified healthcare provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay seeking it because of something you heard on this podcast. The views and opinions expressed by guests on the Child Life On Call Podcast are their own and do not necessarily reflect those of Child Life On Call. Child Life On Call does not endorse any specific medical treatments, procedures, or opinions shared in the podcast. If you or your child are experiencing a medical emergency, call 911 or seek immediate medical attention. By listening to this podcast, you acknowledge that Child Life On Call and its affiliates are not responsible for any decisions made based on the information provided.

    Facebook.com/childlifeoncall

    linkedin.com/in/kfdonovan


    Episode 100 | Thoughts about the Child Life Field Dec 22, 2021
    Show notes

    It's the 100th episode!

    Today I'm opening up a bit and letting you get to know more about me as well as more about what a child life specialist does. I will be sharing my thoughts about the holiday season, and then I will answer some questions about child life.

    In this episode, I talk about…

    [2:57] The child life perspective on dealing with holiday feelings

    [7:21] A commonly held belief about my role that I passionately disagree with

    [8:41] What I wish my younger self knew about being a child life specialist

    [9:22] What I would buy with ten times my current budget

    [10:35] Something everybody in my industry should start doing

    [12:11] The biggest challenge child life is facing today

    [13:37] How I self-educate

    [13:56] The topic of a book I would want to write

    [14:29] Wrapping up the year

    Have you heard? The Child Life On Call mobile app for parents, kids and their care team will be available in 2022. Sign up to stay informed here.

    Child Life On Call is a community of parents and professionals that share ideas, stories and resources to help YOU navigate your child's unique experiences. We give you strategies to support yourself and your family through life's challenges. We are so glad you are here.

    Website: childlifepodcast.com

    Merch: bonfire.com/store/childlifeoncall

    Instagram: instagram.com/childlifeoncall

    Facebook: facebook.com/childlifeoncall

    Twitter: twitter.com/childlifeoncall

    YouTube: https://www.youtube.com/channel/UCnh95T1MOYtbpBxJaZqg7rg


    Episode 99 | Kat's Story: Chronic Illness as a Teenager Dec 15, 2021
    Show notes

    My guest today, Kat, is sharing her story as a child and now as an adult with chronic illness. I think it's important for us to change our perspective a bit and hear what the patient has to say. Kat is the community manager at The Mighty, and she has also written two children's books: Migraine and Mia and Surgery on Sunday. She is such a creative spirit, and she gets really honest with us about what it was like being a teenager in the hospital. She shares what her parents did that worked well, what could have been done differently, and how to support teens with chronic illness.

    In this episode, we talk about…

    [1:25] Kat's background

    [2:28] The beginning of Kat's health issues

    [4:01] What helped Kat when she was in the hospital

    [5:51] Looking back on Kat's surgical experiences

    [7:36] Handling physical differences as a teenager

    [11:30] The vestibular system and its role in the body

    [13:02] How Kat's parents helped her deal with chronic illness as a teenager

    [16:57] Coping with pain

    [19:02] Kat's advice for herself as a teenager

    [20:30] Connecting with others in similar circumstances

    Connect with Kat:

    Website

    Instagram

    Have you heard? The Child Life On Call mobile app for parents, kids and their care team will be available in 2022. Sign up to stay informed here.

    Child Life On Call is a community of parents and professionals that share ideas, stories and resources to help YOU navigate your child's unique experiences. We give you strategies to support yourself and your family through life's challenges. We are so glad you are here.

    Website: childlifepodcast.com

    Merch: bonfire.com/store/childlifeoncall

    Instagram: instagram.com/childlifeoncall

    Facebook: facebook.com/childlifeoncall

    Twitter: twitter.com/childlifeoncall

    YouTube: https://www.youtube.com/channel/UCnh95T1MOYtbpBxJaZqg7rg


    Episode 98| Checking in with Meg and Jess from Friends with Fros Dec 08, 2021
    Show notes

    Happy December! I'm changing things up a big this week, and sharing my discussion with Meg and Jess from Friends with Fros. I first interviewed them in June 2020, so please feel free to go back and listen to their anti-racism and diversity episode before enjoying this conversation. Meg and Jess host a podcast called Don't Worry 'Bout My Hair, and they also hold dual certifications as child life specialists along with rec therapy and nursing.

    In this episode, we talk about…

    [1:47] Life updates all around

    [6:19] Hospital experiences during the COVID-19 pandemic

    [12:24] Working as a child life specialist while pregnant

    [14:53] Processing difficult experiences

    [18:02] Cultural considerations for families coming from Afghanistan

    [24:11] Anti-racism in the child life field

    [26:35] Changes in care for diverse families

    Connect with Meg and Jess:

    Podcast

    Instagram

    Have you heard? The Child Life On Call mobile app for parents, kids and their care team will be available in 2022. Sign up to stay informed here.

    Child Life On Call is a community of parents and professionals that share ideas, stories and resources to help YOU navigate your child's unique experiences. We give you strategies to support yourself and your family through life's challenges. We are so glad you are here.

    Website: childlifepodcast.com

    Merch: bonfire.com/store/childlifeoncall

    Instagram: instagram.com/childlifeoncall

    Facebook: facebook.com/childlifeoncall

    Twitter: twitter.com/childlifeoncall

    YouTube: https://www.youtube.com/channel/UCnh95T1MOYtbpBxJaZqg7rg


    Episode 97 | Samarrah's Story: A Son with an Ependymoma Brain Tumor Dec 01, 2021
    Show notes

    My guest today, Samarrah, is sharing her story about her son being diagnosed with a brain tumor. I encourage you to be present as you listen to her story and take the wisdom she is offering.

    In this episode, we talk about…

    [1:49] Introducing Samarrah and her family

    [2:53] Getting the diagnosis of an ependymoma brain tumor

    [6:19] Processing the brain tumor diagnosis

    [8:44} Treatment for ependymoma

    [12:43] The role of parents in a child's cancer treatment

    [15:32] Finding support and community

    [19:13] How Samarrah's daughter handled the situation

    [23:21] What helped Samarrah to cope with her son's diagnosis and treatment

    [26:59] What Samarrah's son has taught her throughout this process

    [28:06] The importance of a high-quality hospital experience and medical team

    [29:43] How Samarrah plans to help her son process this experience

    [31:15] Life post-diagnosis

    [32:23] Samarrah's book and the foundation she and her husband created to support ependymoma research

    Connect with Samarrah:

    Instagram

    Facebook

    Twitter

    Have you heard? The Child Life On Call mobile app for parents, kids and their care team will be available in 2022. Sign up to stay informed here.

    Child Life On Call is a community of parents and professionals that share ideas, stories and resources to help YOU navigate your child's unique experiences. We give you strategies to support yourself and your family through life's challenges. We are so glad you are here.

    Website: https://childlifepodcast.com

    Merch: https://bonfire.com/store/childlifeoncall

    Instagram: https://instagram.com/childlifeoncall

    Facebook: https://facebook.com/childlifeoncall

    Twitter: https://twitter.com/childlifeoncall

    YouTube: https://www.youtube.com/channel/UCnh95T1MOYtbpBxJaZqg7rg


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