The Rare Life

Epizodes

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  Why Asking for Help Feels So Hard (Summer Mini #7) 23.07.2026 35min

  As parents taking care of disabled and medically complex kids, we could probably use a little more help and support than the average person... But that doesn’t make it easy to ask for it.From guilt to societal pressure to simply not having anyone you can trust for support, we’re digging into why help is just so hard to ask for. A huge thank you to our sponsor for this summer season, Real Food Blends! Real Food Blends are the only 100% real food meals thatare ready-to-feed for people with feeding tubes. Offering 8 different meals and 1 snack for adults & kids, it's the closest thing to homemade blenderized tube feeding. Learn more at realfoodblends.com!Links:Fillout our contact form to join upcoming discussion groups!Join The Rare Life newsletter and never miss an update!Follow us on Instagram @the_rare_life!Donate to the podcast or Contact me about sponsoring an episode. 
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  Sexual Health for Disabled Youth w/ Jill Arneson & Amanda Griffith-Atkins (Summer Mini #6) 16.07.2026 29min

  As our disabled and medically complex children grow and mature, caring for and navigating their sexual health can be a tricky topic. From appropriately navigating sexual activity, consent, basic hygiene and even more complicated topics like birth control and how puberty can bring about new health complications, we’re breaking down a ton of different sexual health aspects in this episode.A huge thank you to our sponsor for this summer season, Real Food Blends! Real Food Blends are the only 100% real food meals thatare ready-to-feed for people with feeding tubes. Offering 8 different meals and1 snack for adults & kids, it's the closest thing to homemade blenderized tube feeding. Learn more at realfoodblends.com!Links:Fill out our contact form to join upcoming discussion groups!Join The Rare Life newsletter and never miss an update!Follow Amanda on Instagram @amanda.griffith.atkins!Follow Jill on Instagram @jill.arneson!Follow us on Instagram @the_rare_life!Donate to the podcast or Contact me about sponsoring an episode.
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  Clinical Trials | Should I Enroll my Disabled Child in One? (Summer Mini #5) 09.07.2026 24min

  Clinical trials are so important. They’re how new therapies and treatments and cures are developed for diseases, and how we update our medical knowledge. At the same time, they aren’t without risk for our kids and our families. So, how do you decide whether it’s worth it? We’re breaking down that question with pros, cons, and personal experiences.A huge thank you to our sponsor for this summer season, Real Food Blends! Real Food Blends are the only 100% real food meals thatare ready-to-feed for people with feeding tubes. Offering 8 different meals and 1 snack for adults & kids, it's the closest thing to homemade blenderized tube feeding. Learn more at realfoodblends.com!Links:Fill out our contact form to join upcoming discussion groups!Join The Rare Life newsletter and never miss an update!Follow us on Instagram @the_rare_life!Donate to the podcast or Contact me about sponsoring an episode.
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  How Time in Nature Impacts Disability Parents (Summer Mini #4) 02.07.2026 26min

  Nature can be healing. But when you have a disabled or medically complex child, getting outside can also be complicated.Today, we’re talking about the ways nature grounds us, the grief that can come up when it is not accessible to our kids, and the small, beautiful ways our families still find their own version of outside.A huge thank you to our sponsor for this summer season, Real Food Blends! Real Food Blends are the only 100% real food meals that are ready-to-feed for people with feeding tubes. Offering 8 different meals and 1 snack for adults & kids, it's the closest thing to homemade blenderized tube feeding. Learn more at realfoodblends.com!Links:Fill out our contact form to join upcoming discussion groups!Join The Rare Life newsletter and never miss an update!Follow us on Instagram @the_rare_life!Donate to the podcast or Contact me about sponsoring an episode.
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  Traveling with Disabled Kids Tips and Tricks (Summer Mini #3) 25.06.2026 1h 24min

  For most of us, traveling with medically complex and disabled children can feel daunting, scary, or maybe even impossible. But while not necessarily easy or simple, if travel is a priority for your family, it is possible with the right planning and preparation.In today’s episode, we share the best tips and tricks from The Rare Life community. We cover everything from general planning to airplane specific tips (there are a ton!) to finding the best accommodations and more. We even have a few tips for camping with medically complex kiddos!Plus, we also dive into the big feelings that can come up for us around traveling with our kids and why it’s okay if that’s not a priority for your family right now. If you really want to take your disabled children on a trip, there are many ways to do it, but we also recognize that travel still isn’t feasible or accessible for many.Thank you to everyone who submitted tips, tricks, hacks, and ideas to this episode! And don’t forget to check our website and YouTube channel (linked below) for articles linking our favorite travel items, carriers, and tips, plus images of all the setups and devices parents in our community use.Links:Visit our Youtube channel to see thevideo version of this episode with photos of all the items mentioned and captions so you can read along!Listen to Ep 118: Organization Hacks for helpful devices when packing andtraveling.Listen to Ep 66 with Falesha Johnson on how she travels with her daughter Cali, who was machine dependent at the time.Follow us on Instagram @the_rare_life!Fill out our contact form to join upcoming discussion groups!Join The Rare Life newsletter and never miss an update!Donate to the podcast or Contact me about sponsoring an episode.
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  The Forgotten Fathers | To The Dads Who Hold It All Together w/ Lizzie (Summer Mini #2) 18.06.2026 18min

  The dads deserve a village too.In this Father’s Day mini episode, Madeline talks with Lizzy of Wonders of Wally about her poem, The Forgotten Father, and the quiet, crushing ways dads are often expected to carry everything without being seen.A huge thank you to our sponsor for this summer season, Real Food Blends! Real Food Blends are the only 100% real food meals that are ready-to-feed for people with feeding tubes. Offering 8 different meals and 1 snack for adults & kids, it's the closest thing to homemade blenderized tube feeding. Learn more at realfoodblends.com!Links:Listen to Ep 146: The Dad Perspective.Fill out our contact form to join upcoming discussion groups!Join The Rare Life newsletter and never miss an update!Follow Lizzy on Instagram @wonders_of_wally!Follow us on Instagram @the_rare_life!Donate to the podcast or Contact me about sponsoring an episode.
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  Summertime Feels, Disability Ed. (Summer Mini #1) 11.06.2026 21min

  It’s summer! But when you have a disabled or medically complex kids, this season can bring with it many, many mixed feelings. Today, we’re digging into all of that: how we feel about summer, what makes summer uniquely hard for our families, and the parts of summer we still love anyway.A huge thank you to our sponsor for this summer season, Real Food Blends! Real Food Blends are the only 100% real food meals thatare ready-to-feed for people with feeding tubes. Offering 8 different meals and 1 snack for adults & kids, it's the closest thing to homemade blenderized tube feeding. Learn more at realfoodblends.com!Links:Fill out our contact form to join upcoming discussion groups!Join The Rare Life newsletter and never miss an update!Follow us on Instagram @the_rare_life!Donate to the podcast or Contact me about sponsoring an episode.
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  228: Season 13 Finale | Biggest Impacts, Hardest Listens, + A Special Guest 28.05.2026 33min

  Season 13 is coming to a close, and this season covered a lot of heavy, but necessary ground.In this finale episode, Madeline and Alyssa are joined by Caitlyn, a listener and mom to Miles, to look back on the episodes that were the hardest, most impactful, and most validating to hear. We’re also sharing listener reflections, talking through the clips from all 14 episodes, and discussing why this season felt especially deep for our community.And finally, we’re sharing a few personal and behind-the-scenes updates, including Madeline preparing to become a foster parent, Alyssa editing with a broken foot, and a peek at the summer mini episodes coming next.Thank you for listening, sharing your stories, and being part of The Rare Life community. We’re so grateful you’re here.Links:Join The Rare Life newsletter and never miss an update!Fill out our contact form to join upcoming discussion groups!Follow us on Instagram @the_rare_life!Donate to the podcast or Contact me about sponsoring an episode.Follow the Facebook page. Join the Facebook group Parents of Children with Rare Conditions.Access the transcript on the website here. And if you love this podcast, please leave us a rating or review in your favorite podcast app!
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  227: Abuse and Neglect Safeguards | Who We Can Trust + How to Protect Our Disabled Children 21.05.2026 34min

  Most of us can’t be with our children 24/7. At some point, we often must hand off care of our children school staff, nurses, therapists, hospitals, family members, etc to help care for our disabled and medically complex kids. And honestly? That can feel terrifying.In this episode, we're exploring one of the hardest topics parents in this community navigate: preventing abuse and neglect for children who may not be able to fully communicate what happened to them. We talk about the fears parents carry, missed medical care and hospital concerns, building trust with other caregivers, red flags families watch for, and the real-life strategies parents use to try to keep their children safe.If you’ve ever wondered how to balance protection with independence, trust your gut when something feels off, or navigate the reality that you can’t always be there, we hope this episode gives you a little guidance to get started.Links:Fill out our contact form to join upcoming discussion groups!Join The Rare Life newsletter and never miss an update!Follow us on Instagram @the_rare_life!Donate to the podcast or Contact me about sponsoring an episode.
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  226: Should I Be Raising Awareness About My Child’s Diagnosis? 14.05.2026 48min

  For many parents of disabled and medically complex children, “raising awareness”, especially on social media, can start to feel like another responsibility sitting on top of an already overwhelming life. Post more. Educate people. Share your child’s diagnosis. Explain disability better. But what actually changes when we do that… and what are we giving up in the process?In this episode, Alyssa and Madeline explore the tension many caregivers feel between wanting the world to better understand disability and wanting to protect their child’s privacy, energy, and family life. They talk about awareness versus advocacy, the pressure social media creates to constantly educate others, the guilt parents carry when they don’t share publicly, and how many families’ relationships with awareness evolve over time.If you’ve ever wondered whether sharing your child’s story is helping, hurting, healing, or just exhausting, this episode will give you a lot to think about.Links:Fill out our contact form to joinupcoming discussion groups!Join The Rare Life newsletter andnever miss an update!Listen to Ep. 100: Raising Awareness | DisabledChildren Don't Owe Society Anything!Listen to Ep. 219: Handling Questions fromStrangers About My Disabled Child!Follow us on Instagram @the_rare_life!Donate to the podcast or Contactme about sponsoring an episode.
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  225: Schooling Options for Disabled Kids | Advocacy, Access + Emotional Toll of Navigating Tough Choices w/ Rachel Redmond 07.05.2026 52min

  For many families of disabled and medically complex children, school is rarely a simple decision. It’s a constant balancing act between medical needs, safety, transportation, therapies, staffing, inclusion, and what your child can realistically access.In this episode, Alyssa is joined by Rachel, a special education professional and fellow disability parent, to talk about the realities of navigating school options for medically complex kids. The types of schooling options available, the differences between these options, support shortages, IEPs, inclusion, and the emotional toll of having to constantly fight for the support your child is legally entitled to.If you’ve ever felt overwhelmed trying to figure out the “right” educational setting for your child, this episode is here to offer you some hope and clarity!Links:Fill out our contact form to joinupcoming discussion groups!Join The Rare Life newsletter andnever miss an update!Listen to Ep. 222: Intellectual Disabilities!Follow us on Instagram @the_rare_life!Donate to the podcast or Contactme about sponsoring an episode.
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  224: Emergencies & ER Visits | Making the Call, Coping with “What Ifs” + Survival Tips 30.04.2026 1h 5min

  For most people, a trip to the ER is unexpected. But when your child has medical complexities, it’s often an inevitable and rhythmic part of life.Every time something seems off and feels like it’s progressing, you’re forced to make a gut-wrenching call: do we handle this at home, or do we go in?In this episode, we’re unpacking what those moments actually look like. From the fear that sits in the background of every illness, to the reality of navigating ER teams who don’t know your child, to the emotional whiplash of being hyper-focused in the moment and unraveling later. We talk about how these decisions evolve over time, what experience teaches you (and what it doesn’t), and why “better safe than sorry” doesn’t even begin to capture the full picture.And a big thank you to Functional Formularies, our sponsor for this episode.Links:Learn more about Functional Formularies!Join The Rare Life newsletter andnever miss an update!Fill out our contact form to joinupcoming discussion groups! Listen to Ep. 185: Medical Parent Trauma!Listen to Ep 170: Hospitalizations!Follow us on Instagram @the_rare_life!Donate to the podcast or Contactme about sponsoring an episode.
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  223: Noelle’s Story | A Terminal Diagnosis, Making Decisions Without a Roadmap, + Longterm Advocacy 23.04.2026 43min

  Before Logan’s diagnosis of Sanfilippo syndrome, Noelle assumed they’d figure out what was off... and then fix it. She never imagined that her family would be facing a progressive, terminal disease that no one, including their doctors, knew much about.In this episode, Noelle shares how they navigated those early decisions, including choosing a high-risk stem cell transplant when it felt like the only option, and what it’s been like to live with that choice as the disease continued to progress. We also talk about what advocacy actually looks like long-term: fighting the same systems over and over again, pushing back when care is taken away, and the strange mix of exhaustion and purpose that comes with it.This is one episode you won’t want to miss!Links:Join The Rare Life newsletter andnever miss an update!Fill out our contact form to joinupcoming discussion groups! Listen to Ep 180: Does It Get Easier?Follow Noelle on Instagram @love_logan07!Follow us on Instagram @the_rare_life!Donate to the podcast or Contactme about sponsoring an episode.
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  222: Intellectual Disabilities | Complicated Grief, Stigma, and Shifting Perspectives w/ Amanda Griffith-Atkins, Madeline and Alyssa 16.04.2026 1h

  From an early age, most of us are taught that being “smart” matters. It’s tied to the way society measures and views success, independence, and worth.So what happens when you're raising a child with an intellectual disability in that world? In this episode, Alyssa, Amanda, and Madeline get honest about all of it: the grief that's hard to express, the fear that you won't be able to connect with your child, and the ways people with intellectual disabilities get left out, even within disability spaces.Plus, they dig into the nuance behind "presume competence," the disability hierarchy often felt in the backdrop of these conversations, and what radical acceptance actually looks like in lives like ours.Links:Join The Rare Life newsletter andnever miss an update!Fill out our contact form to joinupcoming discussion groups! Listen to Ep 19: Katie's Story!Listen to Ep 166: Nonspeaking Child!Follow Amanda on Instagram @amanda.griffith.atkins!Follow us on Instagram @the_rare_life!Donate to the podcast or Contactme about sponsoring an episode. 
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  221: Equipment for Our Medically Complex Children | Grief, Gratitude, and Everything In Between 09.04.2026 52min

  At face value, our kid’s equipment is just stuff. It helps our kids move, eat, hear, breathe, communicate, and more. But when that “stuff” feels like it’s taking over our lives (and homes), complicated feelings can come up.In this episode, Madeline and Alyssa talk about the emotional, logistical, and financial reality of living with medical and mobility equipment. From the grief that can show up when a new piece of equipment arrives, to the frustration of a system that makes you fight so hard to get something your child may not even like, there's so much more to this topic than it seems on the surface.We get into the design problems that make managing equipment harder, the disagreements that come up when one partner is ready to try everything and the other isn't, the comments from other people that land all wrong, and what it actually looks like to embrace your child’s equipment in whatever way you can.Whatever your relationship with your child's equipment right now, this episode has something for you.And a huge thank you to our sponsor, MOOG Medical for making some parts of managing our children’s equipment a little easier with their 24/7 helpline and for making this episode possible!Links:Visit MOOG’s website to see themany ways they support families like ours!Join The Rare Life newsletter andnever miss an update!Fill out our contact form to joinupcoming discussion groups! Listen to Ep 125: Traveling with Medically ComplexKids.Listen to Ep 153: Hurtful Things Loved Ones Say.Listen to Ep 214: Relocating for Our MedicallyComplex Kids.Follow us on Instagram @the_rare_life!Donate to the podcast or Contactme about sponsoring an episode.
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  220: Robin’s Story | Preparing for the Worst, Staying Present, + Embracing a Different Type of Fatherhood 02.04.2026 40min

  Before his daughter was born, Robin thought he had a sense of what it meant to be a dad. But after a prenatal diagnosis of Trisomy 13, that understanding started to unravel.In this episode, Robin reflects on what it was like to face a future filled with uncertainty, including the possibility that his daughter might not live long and might require a completely different kind of parenting than he had imagined. He shares how that uncertainty led him to emotionally distance himself early on, the role grief and fear played in that response, and how his connection to his daughter has grown and changed over time.This conversation also touches on learning to be present, understanding your role and strengths as a parent, and how isolating this life can feel, even as you look for connection with others who get it.This is one you can’t miss.Links:Join The Rare Life newsletter andnever miss an update!Fill out our contact form to joinupcoming discussion groups!Listen to Ep 146: The Dad Perspective.Listen to Ep 151: Finding Other Disability ParentFriends.Listen to Ep 197: Difficulty with Making DisabilityParent Friends.Follow Robin on Instagram @thedadadays!Follow us on Instagram @the_rare_life!Donate to the podcast or Contactme about sponsoring an episode 
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  219: How Do I Handle Questions from Strangers About My Disabled Child? w/ Disabled Author James Catchpole (UPDATED) 26.03.2026 55min

  As parents of medically complex kids, we’ve all been there. We’re at the park or the grocery store with our kid, and someone we don’t know walks up to us and starts asking questions about our child. You might be so put off that you don’t know what to say. Or you might just start saying whatever pops into your head, which can devolve into unintentional oversharing, because we’re often under the impression that it’s rude NOT to answer a question.But if you’ve ever wanted permission to just not answer invasive questions from strangers, this episode is here to validate you. I’m talking with James Catchpole, author and publisher, about his experience as a disabled adult and how he deflects or simply (but politely) refuses to answers questions from strangers about his disability. He also shares about his experience as a disabled child and how his parents were able to set a helpful example for how on how to navigate questions about his disability as he grew older. Whether your child will eventually be able to advocate for themselves or if you as the parent will be their advocate indefinitely, this episode will give you lots to think about when it comes to dealing with uncomfortable and invasive questions about your child’s disability or medical status.2026 Update: We’re resharing this always relevant episode that was originally published in 2023 with our updated thoughts at the end. We hope you enjoy!Links:Listening to Ep 100 on Raising Awareness.Get a copy of James’ book “What Happened to You?”Read a collection of parenting essays written bydisabled parents (including a chapter by James and his wife Lucy.)See more of James’ work and writing on hiswebsite!Follow James on Instagram!Follow us on Instagram @the_rare_life!Join The Rare Life newsletter andnever miss an update!Fill out our contact form to joinupcoming discussion groups!Donate to the podcast or Contactme about sponsoring an episode
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  218: Moms vs. Dads in the Medical System | Dismissal, Assumptions + the Cost of Not Being Trusted w/ Kyrie Herman 19.03.2026 54min

  For most of us who have spent years inside the medical system with a complex child, the experience of being mom in an exam room can feel very different from the experience of being dad. Sometimes that means being dismissed while your husband gets taken seriously. Sometimes it means the opposite — dad gets treated like wallpaper while mom is assumed to be the only one who knows anything. Either way, those dynamics have a way of wearing on a family over time.In this episode, Kyrie joins The Rare Life to talk about the gap between how mothers and fathers can be received by medical providers, and what it costs families when those assumptions go unchecked. We get into the emotional toll of having to manage how you come across just to be believed, the medical trauma that quietly changes how we show up over the years, and the way this can play out differently depending on your family — including the families where it's dad who feels dismissed and overlooked.If you've ever felt like you had to work harder than your partner just to be heard, or wondered why the same concern lands so differently depending on who's saying it, this one will resonate.Links:Join The Rare Life newsletter and never miss an update!Fill out our contact form to join upcoming discussion groups! Follow us on Instagram @the_rare_life!Follow Kyrie on Instagram @kyrieherman!Donate to the podcast or Contact me about sponsoring an episode.
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  217: The NICU Experience | The Shock, Fear, and Emotional Rollercoaster of Navigating the Unknown w/ Madeline 12.03.2026 1h 32min

  For many disability parents, medically complex life begins in the NICU. In those early days, everything feels heightened: the machines, the uncertainty, the helplessness of watching doctors care for your tiny baby while you stand nearby unable to help.In this episode, Alyssa and Madeline unpack the NICU experience through stories from the Rare Life community, covering the shock of having your baby taken away after birth, the grief over early parenting moments you miss, and the emotional toll of leaving the hospital without your child. We also explore why the NICU can feel so uniquely overwhelming: when the future is unclear, it becomes incredibly hard to imagine that anything good could be waiting on the other side. And a big thank you to one of our long-time sponsors MOOG Medical.And a huge thank you to our sponsor, MOOG Medical, for making this episode possible!Links:Visit MOOG’s website to see the many ways they support families like ours!Listen to Ep 161: Having a Non-disabled child after their disabled child.Listen to Ep 140: Alyssa’s Story.Listen to Ep 26: The NICU Experience with Madeline.Follow us on Instagram @the_rare_life!Join The Rare Life newsletter and never miss an update!Fill out our contact form to join upcoming discussion groups!Donate to the podcast or Contact me about sponsoring an episode.
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  216: Cindy's Story | Survival Mode, Unexpected Grief + Navigating Inclusion and Accessibility 05.03.2026 53min

  When you’re raising a child with complex medical needs, the early years can feel like one long stretch of survival mode. Hospital stays, surgeries, therapies, and constant uncertainty loom large over everything.For Cindy, that uncertainty started before her son Thoren was even born. After a routine ultrasound raised concerns, her family began a medical journey that would eventually reveal not just one rare condition, but a genetic mutation so uncommon that Thor was one of the first documented cases in the world. In this episode, Cindy shares the story of Thor’s early years: surgeries shortly after birth, years of hospitalizations, and learning how to advocate for his medical needs again and again. She also talks about the emotional side of caregiving: the grief that shows up in unexpected moments, the challenges of navigating medical systems, and the complicated transition that happens when survival mode finally begins to ease. Plus, she shares her thoughtful perspectives on the importance (and difficulty) of including Thoren in as many places as possible and why that can prove to be so difficult sometimes.Finally, a big thank you to our sponsor for today’s episode, Huckleberry Hiking! Learn more about how they can help make hiking more accessible for your disabled kiddo here!Links:Visit Huckleberry Hiking’s website.Listen to Ep 180: Does Disability Parenting EverGet Easier?Connect with Cindy on Instagram @montanareinhard!Follow us on Instagram @the_rare_life!Join The Rare Life newsletter and never miss an update!Fill out our contact form to join upcoming discussion groups!Donate to the podcast or Contact me about sponsoring an episode.