065: It Takes a Village: How to Add a Child Life Specialist to Yours with Caitlin McNamara
Release Date: 05/02/2023
082: Bringing Peace & Joy to Families with Pediatric Cancer with Jenna Kmitch
Joy In The Journey
Caring for a newly diagnosed child going through a medical journey can be scary and overwhelming. Especially when finding resources meant to support you, like Child Life Specialists, requires extensive research and planning. This is why I am so grateful to our guest today, Jenna Kmitch, for courageously sharing what her process looks like beside her daughter Sydney, who was diagnosed with neuroblastoma just a few weeks after birth. Jenna is the founder of Love Smiles, an organization dedicated to bringing moments of peace and joy to families with pediatric cancer through...
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081: Insights on Communicating Effectively With Your Medical Team with Henry Rosh & Megan Keeler
Joy In The Journey
When you first enter the medical world as a caregiver, everyone around you hits the ground running. The nurses and doctors know exactly how to get started, and yet, you might be left feeling overwhelmed and powerless. This is what makes social workers so important: they support the family holistically, encourage communication, help bridge information gaps, and empower you to become an important member of your child’s medical team. My guests today, Henry Rosh and Megan Keeler, are both social workers at Lurie Children's Hospital of Chicago. Henry works with families who have extended...
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080: Discovering Unexpected Gifts in Times of Grief with Sara Ward
Joy In The Journey
After losing someone close to us we are usually told about the five stages of grief and how each of them will show up. But grief often shows up differently for everyone, skipping and cycling through stages in unique ways. My guest today is Sara Ward, and she knows a thing or two about grieving. After unexpectedly losing her father to a heart problem as a teenager, her 9-month-old adopted son was diagnosed with a rare and terminal disease and given a very short time to live. Instead of choosing to focus only on the hardships of grief, Sara committed to looking for unexpected gifts in her...
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079: The Glimpses of Joy You’ll Find When You Look For Them with Gina Prosch
Joy In The Journey
We’ve all experienced those days where it feels like we catch every red light on a busy commute and nothing seems to be going right. But what happens when we’re intentional about stopping to look for the small glimmers of joy, even in those heavier days? Allow me to introduce you to today’s guest to answer that question. Gina Prosch is a writer and teacher who has made it her mission to help children and adults find joy in even the most difficult days. Her childrens books are perfect for little ones who may be experiencing a harder season of life, and provide parents with inspiring ways...
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078: Offering Hope, Dignity and Holistic Care in Kenyan Hospice with Juli Boit
Joy In The Journey
Juli Boit is no stranger to helping those in need. She’s an author, family nurse practitioner, and international non-profit director of , dedicated to providing palliative care services to adults and children in western Kenya. After going through an adoption journey with her son Ryan, whose parents had recently passed, and consequently adopting his siblings, she found herself needing some help of her own when two of her kids required transplants far from their Kenyan home. These transformative experiences made Juli see her work through a different lens: that joy can be found in...
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077: Trauma & Anxiety: Going From “Why Me?” to “What Now?” with Sarah Falk
Joy In The Journey
Sarah Falk has received more than a few extremely scary cancer diagnoses in her life: the first one at only 17 years old (bone cancer) and the second at 40 years old (breast cancer). Naturally, she found herself asking, “Why Me”? But as you’ll hear, a better question to ask yourself is, “What now?” Sarah is a mom to 4 boys, a mental health therapist, an author, and 4-time cancer survivor. She has taken her traumatic experiences and used them as a source of deep understanding of the challenges these diagnoses come with. Having specialized in anxiety, panic, and trauma, her work is...
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076: Blooming Littles: Helping Parents and Caregivers Manage NICU Journeys with Katie Ross
Joy In The Journey
As today’s guest will tell you, “You become a NICU parent in the blink of an eye.” Katie Ross is the creator of and she’s doing incredible work in the NICU space as a certified neonatal occupational therapist. As a mom of a full-term NICU baby herself, she’s made it her mission to inform and empower parents by teaching them about the little things they can do that make a difference in their baby’s development and truly transform their NICU experience. By combining her doctorate with additional certifications, including neonatal massage and lactation support, her...
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075: Exploring Growth Through Grief and Choosing Faith Everyday with Emily Ann Adams
Joy In The Journey
How are parents meant to believe that the loss of a child is all part of God’s plan? Grief is a difficult journey for everyone, but it can feel especially challenging when it’s accompanied by a feeling of losing yourself or your faith. My guest today, Emily Ann Adams, had this exact experience after the passing of one of her twin boys, Aidan. Faced with three little children under 5 to look after, including Aidan’s brother Alan who was born at 32 weeks, Emily made a courageous decision; to dive deep into her grief to understand it better. In the process, she helped dozens of other...
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074: Finding Community and Letting Love In on a NICU Journey with Meg Helgeson
Joy In The Journey
One of the only certainties about having children is uncertainty: we can’t find out beforehand how a pregnancy or birth experience will go, or who our children will grow up and become. Add in a premature birth, an illness diagnosis, and a NICU stay to the mix, and it can lead to overwhelming worry and anxiety. My guest today, Meg Helgeson, is certainly no stranger to this. Her twin girls Ellie and Leah, who are now healthy 12-year-old girls, had to be flown to the NICU at Comer’s Children Hospital at only 5 days old to receive a meningitis diagnosis. Looking back, Meg is now able to share...
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073: Learning To Flex Your “Joy Muscle” with Bekah Bowman
Joy In The Journey
When a parent learns that their child has been diagnosed with a serious illness or condition, it’s difficult not to be consumed with worst case scenarios. But as Bekah Bowman will tell you, you have two choices: either allow your past and future to steal joy from your present, or embrace joy in the present moment, no matter what it looks like. And Bekah is no stranger to this concept: her two boys, Titus and Ely, were both affected by a rare genetic disease (CLN2) that leads to the quick loss of skills and eventual passing in childhood. After her oldest son passed away...
info_outlineIf raising a child takes a village, parents can use all the help they can get when navigating a difficult medical journey. But between medical teams, family, friends, and all the different groups of people that come together in order to provide the care needed, a lot of informational gaps can get left behind.
From splitting time between the hospital and your family at home to preparing for discharge and transitioning home with (potentially new) medical equipment, it is quite easy to feel overwhelmed as a caregiver.
That’s why Child Life Specialists like Caitlin McNamara dedicate their career to helping families bridge those gaps: they walk along with them on the journey and assist whenever possible by providing guidance and advice that could otherwise be hard for caregivers to find.
And while we firmly believe that every hospital should have Child Life Specialists available, it’s unfortunately not the case yet. This is why Caitlin and her team created Child Core: an online coaching program dedicated to becoming an integral part of families’ support systems.
Today, Caitlin shares with us incredible advice on creating plans for difficult moments or transitions in your journey, finding your community, and understanding the uniqueness of each journey.
In the “Resources” section below, you’ll also be able to find Child Core’s free resources. These were designed to offload some pressure off of caregivers by providing guidance on using medical equipment, providing checklists to take to appointments, and much more.
Key Takeaways with Caitlin McNamara
- The benefits of adding a Child Life Specialist to your support team.
- Navigating a difficult medical journey with your child as a caregiver.
- The impact of the journey on caregivers, siblings, and the child.
- Advice on creating your “village” or community, and how to ask for help.
- Preparing for the complexities of a transition home (discharge).
- Free resources that can help parents who are feeling overwhelmed.
- Remembering that what worked for others may not work for you.
- How needs may change with time, and how to process these changes.
- Finding a balance between caring for your child, your family, and yourself.
Show Notes:
Get Full Access to the Show Notes by visiting: MatteasJoy.org/65.
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