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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:
    Episode 46 | Pediatric Pain with the Meg Foundation Sep 30, 2020
    Show notes

    Katie, Certified Child Life Specialist, talks with Jamie Gentille, Director of Child Life Services at Inova Children's Hospital and Dr. Jody Thomas, from the Meg Foundation for Pain, in this episode.

    Dr. Jody Thomas is a licensed clinical psychologist, and specialist in pediatric medical illness and trauma and the founder of the Meg Foundation for Pain. She discusses the mission of their organization which addresses pain in children head-on. Listeners today will walk away with a better understanding about why children shouldn't be in pain if there are ways to reduce it as well as tangible tools the foundation is working on to support parents and children.

    Jamie adds her own perspective as someone who has spent her life in the medical world, personally and professionally. Jamie's stories show the reality of how the trauma of pain in childhood has effected her to this day.

    Child Life On Call | Instagram | Facebook | Twitter


    Episode 45 | Amrita's Story - A son with GERD and feeding aversion Sep 23, 2020
    Show notes

    Spit up, and even reflux, can be a common problem for infants, but what happens when it's more than that?

    In this episode, Amrita shares with Katie, Certified Child Life Specialist, about what happens when a child's reflux became severe and leads to a three-week hospitalization, a feeding tube, and ongoing support from developmental therapists. This is the reality of severe gastroesophogeal reflux disease.

    Listen to Amrita's story to hear how she has coped with this experience and how her son is now thriving with love and support from his amazing parents.

    Listen to more stories and get resources to support your children at www.childlifepodcast.com

    Child Life On Call | Instagram | Facebook | Twitter


    Sickle Cell Anemia in Children: A Mother's Advocacy Journey Sep 16, 2020
    Show notes

    In this episode, Katie interviews Lisa, mom to Riley. Sweet Riley is a spunky and sweet two-year-old living with Sickle Cell Anemia.

    Lisa talks about how they knew it would be a possibility while she was pregnant due to the trait being passed down, but they had hoped and prayed to avoid it like they did with their first born, a son who is now nine years old.

    She says that she can handle the frequent trips to the ER, but watching her daughter in pain is a feeling no mother should have to experience. Lisa attributes prayer, family, and educating herself helps her cope with the realities of her daughter's condition.

    If you'd like to follow along with Lisa, you can find her on Instagram at @thelisasykes.

    Child Life On Call | Instagram | Facebook | Twitter

    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


    VACTERL Association: What Parents Need to Know About This Rare Diagnosis Aug 19, 2020
    Show notes

    Meet Ashlyn, momma to her sweet and smiley boy, Myles. Myles was born with a rare disease that effects his limbs and other parts of his body. These symptoms are known as VACTERL association.

    As a self-proclaimed "planner," Ashlyn talks about the difficulties of having so many unknowns during her pregnancy and how she coped... and is coping... with their journey. She attributes her strong partnership with her husband and prayer as key components to getting through difficult times.

    If you'd like to follow along with Ashlyn and Myles, you can follow their Instagram account at @_aboutlaw.

    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

    Child Life On Call | Instagram | Facebook | Twitter


    Down Syndrome: A Mother's Journey of Love and Advocacy Aug 12, 2020
    Show notes

    Meet Maura Senneff, mom to sweet Ryan. Ryan is a thriving 8-year-old boy who has Down syndrome. The amazing advocate by his side, his momma Maura, describes that "zooming out" and looking at things from wide lens helped them turn Ryan's health around.

    She talks about small changes and the "no limits" attitude their family lives by.

    If you'd like to follow along with Maura Senneff and her son, Ryan, you can follow their Instagram @Maurasenneff.

    Guest: Maura Senneff, Released: Aug 12, 2020

    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.

    Child Life On Call | Instagram | Facebook | Twitter


    Episode 41 | Dominique's Story - A daughter born three months premature Aug 05, 2020
    Show notes

    Katie talks to Dominique, mom to Mila, who shares her birth story and NICU experience. Born at just 1lb 11ounces at 26 weeks old, Mila has made tremendous progress thanks to proactive parents, therapies and her momma's un conditional love.

    Dominique talks about the fear that comes with being an African American pregnant woman in the healthcare setting as well as the impact that sharing her story and community has had on her ability to cope with their journey.

    You can follow Dominique Pompey through her blog www.dominiquepompey.com on Instagram and YouTube @dominiquepompey.

    Child Life On Call | Instagram | Facebook | Twitter


    Anti-Racism and Diversity in Child Life: An Important Conversation Jun 10, 2020
    Show notes

    Katie interviews Meg and Jess, two certified child life specialists who also have dual certifications in rec therapy and nursing! These two ladies host a podcast called Don't Worry Bout My Hair and they are your @friendswithfros!

    We tackle tough questions that are way overdue in the field of child life:

    • Have you received any feedback or comments from black families regarding challenges due to limited diversity of the hospital staff?
    • What's been the most challenging thing about being a black woman in a predominantly white profession?
    • While I know you do not represent your entire race, like I don't represent mine, do you have any things you'd like white clinical and hospital staff to know, hear, or change?
    • What vital resources and habits would you like to for share children's hospital, specifically, that promote anti-racism and diversity?

    This episode is also available on the Child Life On Call YouTube channel.

    Go listen to Jess and Meg's podcast and follow them on Instagram at @friendswithfros!

    Released: Jun 10, 2020

    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


    Autism Diagnosis: A Mother's Journey from Anxiety to Acceptance May 26, 2020
    Show notes

    In this episode, Katie, Certified Child Life Specialist, interviews Jessica, mom to two special needs children and one of which who is on the Autism spectrum. Jessica is also an adult clinical neuropsychologist and also hosts a podcast with her husband called, Thriving in the Midst of Chaos.

    Jessica discusses their journey to get a diagnosis, how they are coping with virtual therapy during covid19, and provides great resources and information about the Autism community.

    If you'd like to share your story on the Child Life On Call podcast, please send an email to podcast@childlifeoncall.com

    Child Life On Call | Instagram | Facebook | Twitter

    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


    When Your Child is Diagnosed with Leukemia: What to Expect Apr 27, 2020
    Show notes

    Elizabeth, mom to three girls, shares with us her experience of having a daughter with cancer. In just an hour and a half, her 9-year-old daughter went from a pediatricians office to a cancer ward. Elizabeth discusses her Elizabeth's "out of body" experience, how she was able to identify the "gifts" in each of her girls, and offers wisdom and compassion to others going through similar experiences.

    We also talk about how the global pandemic of Covid19 and subsequent quarantine has impacted their family. Elizabeth is a writer by trade and published a book called The Puddle Jumper's Guide to Kicking Cancer

    which is available in both English and Spanish. You can listen to the book on YouTube. To get in touch or follow along with Elizabeth, you can email her at elizabethbillups@gmail.com or see her Instagram @teachingkidsaboutcancer.

    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 37 | Meg's Story - A daughter with Idiopathic Thrombocytopenic Purpura (ITP) Apr 14, 2020
    Show notes

    Katie, Certified Child Life Specialist, talks with Meg Casano, mother to Ella who has Idiopathic Thrombocytopenic Purpura (ITP) and also created the nonprofit Medi Teddy which is a stuffed animal cover for intravenous medications.

    Meg talks about the journey to discover her daughter's diagnosis and how an initial prediction that Ella's ITP would only last six months but has turned out to be a life-long chronic illness. She discusses the financial and emotional challenges that exist when you have a child with a chronic illness, but she also talks about how a school project and a driven child can turn into a fully functioning nonprofit that helps other kids like Ella.

    Connect with Meg and Ella on Instagram or at www.Medi-Teddy.org

    Child Life On Call | Instagram | Facebook | Twitter


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