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Sometimes growth looks like taking the first step into a new experience. And sometimes, it looks like staying just a little longer.
In this episode of Medical Mama, I’m sharing a recent family outing that reminded me just how many years of practice can sit behind one seemingly simple moment. We’ll talk about honoring our children’s communication while still holding loving boundaries, helping them feel safe through discomfort, and recognizing when they may be ready to stretch beyond what feels familiar.
Because the goal isn’t to push our children before they’re ready. It’s to keep building the skills, trust, and confidence that make more of the world accessible to them even when getting there takes years.
If you’re still in the season of short outings, early exits, or wondering whether all of this practice is making a difference, this episode is for you. Sometimes the progress we’ve been working toward quietly shows up when we least expect it.
For many medical and special needs families, even a simple outing can require planning, preparation, flexibility, and a whole lot of courage.
In this episode of The Medical Mama Podcast, I’m sharing what we’ve learned about gently expanding Benjamin’s world in ways that make sense for him — from preparing for new experiences and setting realistic expectations to recognizing that sometimes simply walking in and walking back out is a win.
We’ll also talk about something that can quietly keep families home: the fear of being watched, judged, or misunderstood. Our children deserve opportunities to experience their communities, take up space, and participate in the world around them — even when that participation looks a little different.
You don’t have to make their world bigger all at once. Sometimes, you just make it a little bigger today than it was yesterday. 💛
Challenging behaviors can be some of the hardest moments to navigate as a parent—especially when you’re trying to understand what your child needs while managing your own emotions, too.
In this episode of The Medical Mama Podcast, I’m sharing what we’re learning in a season of challenging behaviors with Benjamin and why these moments call for curiosity, regulation, and connection rather than simply trying to make the behavior stop.
We’ll talk about staying regulated when your child is struggling, looking beneath the behavior for what might be driving it, recognizing when changes may warrant a closer look, and activating your child’s team to help identify patterns and build supportive strategies.
Because challenging behavior is hard—but it’s also information. And sometimes the most important question we can ask isn’t, “How do I stop this?” but, “What is my child trying to tell me?”
Time is something we all live by but understanding what “five more minutes” actually means isn’t always so simple.
In this episode of The Medical Mama Podcast, I’m sharing how one simple recommendation to introduce a visual timer became a surprisingly transformative tool for our family. What started as a way to help make transitions and expectations more concrete opened my eyes to something much bigger: we all benefit when we can understand how much time we have, what’s coming next, and when something will end.
We’ll talk about visualizing time, creating structure without rigidity, supporting transitions and big feelings, and how some of the tools we discover through raising children with different needs can teach us something about the way all of our brains thrive.
Sometimes a little more predictability can create a whole lot more peace. ❤️
As medical parents, we’re often willing to explore anything that might help our children grow, connect, communicate, or experience more joy. There’s beauty in that hope and openness—but there’s also wisdom in bringing discernment along with us.
In this episode, I’m sharing our family’s experience with nontraditional therapies, including the role music therapy has played in our boys’ lives, as well as some of the lessons I’ve learned while exploring other approaches along the way.
This isn’t about labeling therapies as “good” or “bad.” It’s about asking thoughtful questions, being mindful of big promises, and remembering that there is rarely one magical intervention that changes everything.
More often, the real beauty happens through consistency, relationship, practice, and time.
You can be hopeful. You can stay curious. And you can ask questions, too. 🤍
What if a psychological evaluation wasn’t about putting a label on your child—but about understanding them more deeply?
In this episode, I explore the important role psychologists play in a child’s developmental journey and why a comprehensive evaluation can become one of the most valuable tools for families navigating diagnoses, therapies and educational planning. We unpack common misconceptions, talk about what these evaluations are really designed to do, and discuss how they can provide clarity, direction and confidence as your child grows.
Whether you’re considering an evaluation for the first time, wondering if it’s time for an updated assessment, or simply wanting to better understand this often misunderstood part of the care team, I hope this conversation leaves you feeling more informed, encouraged and empowered.
Because every child is more than a diagnosis—and sometimes understanding them more fully is one of the greatest gifts we can give them.
This week, I’m sharing a simple moment from a trip to our neighborhood pool that reminded me just how powerful children can be.
A group of kids noticed my son Benjamin, asked thoughtful questions, and then did something beautiful, they included him in a way that honored exactly where he was. They simply led with curiosity instead of fear.
In this short episode, we talk about how parents can model simple, respectful language for children, why genuine curiosity is something to celebrate rather than discourage, and how small moments of inclusion can leave a lasting impact on every child involved.
Whether you’re raising a child with medical complexity or simply want to help your children grow into compassionate, welcoming people, I hope this conversation encourages you to embrace curiosity, ask kind questions, and make room for connection.
Sometimes the smallest interactions become the moments we remember most.
Therapy can be one of the greatest gifts we give our children—but it was never meant to become their entire life.
In this episode, I share what I’ve learned over eight years of navigating therapies with our sonshines, from the importance of early intervention to finding a healthy balance between pursuing support and protecting the joy of everyday childhood. We talk about why therapy is such an important cornerstone of development, how our children’s needs evolve over time, and why it’s okay for families to embrace different seasons along the journey.
Most importantly, I share one piece of wisdom from Benjamin’s geneticist that completely transformed the way I think about progress: life is therapy.
If you’ve ever wondered whether you’re doing enough, doing too much, or simply need the reassurance to trust the process, this episode is for you.
A child’s diagnosis doesn’t just change life—it changes a marriage. In this episode, I share the lessons Ben and I have learned while navigating medical parenthood together. We talk about grief, teamwork, communication, and why it’s so important to remember that you’re grieving beside each other, not against each other.
Inspired by a beautiful conversation with my husband—and a remarkable 100-year-old banyan tree—we explore what it means to grow deep roots that can withstand life’s storms. Whether you’re raising a child with medical complexities or simply walking through a difficult season together, I hope this episode reminds you that while the journey is hard, your relationship can continue to grow with intention, grace, and love.
Because sometimes the strongest marriages aren’t the ones that avoid storms—they’re the ones that keep growing new roots.
One of the questions we’re asked most often is, “How is Bane doing with Benjamin?” It’s a thoughtful question—and one that opens the door to an even bigger conversation about intentionally nurturing sibling relationships when one child has significant disabilities.
In this episode, I share the practices that have helped our family create space for genuine connection between our boys. From family adventures and individual one-on-one time to having honest, age-appropriate conversations about disability, we talk about what it looks like to cultivate curiosity, celebrate each child’s unique strengths, and build a home where differences are embraced rather than feared.
I also address common questions about future caregiving, why Ben and I have made future planning a priority, and how we hope to give both of our sons the freedom to build a relationship rooted in love—not obligation.
Whether your children have disabilities, different personalities, or simply unique interests, this episode is filled with practical encouragement for helping siblings—and all relationships—grow through acceptance, shared experiences, curiosity, and intentional connection.
As always, we don’t have all the answers. We’re simply sharing what we’re learning along the way and the beautiful fruit we’re seeing as our boys grow together.
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