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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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    • Apple Podcasts
    • Google Play
    • Spotify

    Latest Episodes:
    Episode 5 | Karen's Story - A nicu stay after undected gestational diabetes Jul 31, 2017
    Show notes

    Karen had a typical pregnancy up until the last few scary days when she was unable to feel her daughter move. After following her mother instinct, Karen went to the hospital and quickly learned she would need an emergent c-section. As emergencies go, everything was unexpected.

    In this episode, Karen walks us through what her daughter's birth and subsequent NICU stay was like. She talks about the unknown's of her daughter's health as well as how difficult it was to be away from her in those first 48 hours.

    Karen shares with us how her husband and a dear friend who stayed at the hospital with her until 2 a.m. helped her cope, and encourages other mothers going through similar situations to know that they are not alone.

    If you would like to personally reach out to Karen, you can do so via Facebook or Instagram.

    Interested in sharing your story with our listeners? Get in touch with Katie here. Visit our website and connect with us on Facebook, Twitter and Instagram.


    Episode 4 | Abigail's story - a son diagnosed with Spina Bifida and Hearing Loss Jul 17, 2017
    Show notes

    After arriving at her 20 week ultrasound, Abigail, her husband and mother were anxiously awaiting to hear the news of their first child's gender. However, the appointment took a turn when they learned that their son would be born with Spina Bifida. Abigail talks to us about that experience and their journey since that life changing moment. They'd come to learn that their son also had hearing loss and she talks about the challenges associated with it.

    Abigail expresses her feelings about Teak's diagnosis, talks about the incredible six (AND A HALF) year-old boy that he has become, and gives great advice to parents facing similar challenges. You can follow along and connect with Abigail through her blog, www.theheadhouseatx.com.

    She recommends connecting with a Spina Bifida group on Facebook, she specifically has benefited from meeting other parents here. She also spent a lot of time on BabyCenter's Spina Bifida group when Teak was born.

    Abigail also recommends the following resources:

    www.hearingloss.org

    https://www.livebinders.com/play/play?id=1666786 (This is the Texas Regional Day School for the Deaf and Hard of Hearing programs that Abigail referenced in her interview)

    If you would like to connect with Abigail, you can find her on Instagram or Facebook. She also blogs here and at Austin Moms Blog.


    Episode 3 | Kim's Story - A son born with Microtia Atresia and hearing loss Jul 10, 2017
    Show notes

    In this episode you will hear Kim talk about her experience in finding out that her son had Microtia Atresia, the interesting link to their family history and how that has affected her journey, and the tough decision about how and when to move forward with surgery.

    Microtia is a congenital deformity where the external ear is underdeveloped, and Atresia is the absence or closure of the external auditory ear canal. The malformation of the middle ear bones may be affected including the narrowing of the ear canal. This is a birth deformity that occurs in about 5,000 to 7,000 births.

    Kim recommends the following resources:

    • Microtia.net
    • Earcommunity.org
    • Microtiasurgery.com
    • Pedient.com

    If you'd like to connect with Kim, you can do so through her blog, The Hill Country Woman, through social media sites Facebook and Instagram, and she also blogs for Austin Moms Blog.

    A big thank you to the incredible photographer, Laura Morsman Photography for her beautiful pictures of Kim and her family for this episode. If you live in Austin… book Laura Morsman Photgraphy NOW.

    Take a look at the world's first swaddle for hospitalized infants, Woombie Med Pods, from Barski Vail Designs.


    Meningoencephalitis Leads to a Coma in the PICU Jul 03, 2017
    Show notes

    Michelle's story is one that took place over 15 years ago, and this is the first time she has spoken about it publicly. At the age of two, Brynn started developing inexplicable fevers which concerned her mother, an Emergency Room nurse. After trusting her gut that "something was wrong," Michelle brought her daughter in the middle of the night to the ER and shortly after was diagnosed with meningoencephalitis and in a coma for over a week.

    Michelle brings a unique perspective on relationships with healthcare providers, given the fact that she is and has been a nurse for over 18 years. You'll hear her talk about the benefits of building a trusting relationship with your child's pediatrician. She gives great advice about how to find that specific provider, and also talks about the importance of following your parental instincts.

    If you would like to connect with Michelle, you can do so here, Michelle on Facebook or through her email, mlbrahaney@gmail.com.

    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


    Goldenhar Syndrome and Caudal Regression: Living with Multiple Diagnoses Jun 26, 2017
    Show notes

    After a long pregnancy on hospitalized bedrest, Kelli describes the birth and first year of her twin girls, one of which was born with two genetic conditions, Caudal Regression Syndrome and Goldenhar Syndrome. The journey to diagnose these conditions was a long one, and Kelli talks about what that process was like, and what is like to have a child with these two syndromes.

    Kelli recommends a several resources, www.isacra.com and the Goldenhar Syndrome Facebook group.

    Kelli also recommends rarediseases.org's network for a community of support and information on Goldenhar syndrome.

    If you would like to connect with Kelli personally, you can follow her on instagram at @kelita83, on her blog at www.babygruens.wordpress.com and at Austin Moms Blog.

    If you would like to share your story or have questions about this podcast, you can email childlifeoncall@gmail.com or submit your information on childlifepodcast.com.

    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 May 11, 2017
    Show notes

    This is the first promotional episode for the Child Life On Call Podcast. If you would like to share your story, email us at childlifeoncall@gmail.com, visit our website at www.childlifepodcast.com, or find us on Instagram @childlifeoncall.

    The first official podcast episode will launch in June 2017. Subscribe to be updated on our most recent episodes.


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