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April Aramanda Podcasts

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This episode dives into what it really looks like to support a spouse living with chronic illness. Matt shares the long, emotional journey to his MCTD diagnosis — from years of pain and self-doubt to finally finding answers. Latricia offers honest insight into the emotional weight of watching someone you love struggle and how she’s learned to liste…
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Entrepreneurship is often painted as hustle, consistency, and 5 a.m. mornings. But when you live with chronic illness, that version of productivity just doesn’t fit. In this episode, I pull back the curtain on what it really looks like to run a business when your body has other plans. From working in bed with a laptop tray to building flexible sche…
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In this conversation, Tina Marie Medlin opens up about 30+ years with Crohn’s disease, drug reactions, major surgeries (including an ostomy), and the spiritual warfare of not giving up—like enduring six days with an NG tube and a terrifying arterial bleed she faced fully awake. Through it all, Tina discovered a calling: Warrior Braids Ministry, per…
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When your labs say “normal” but your body says otherwise—Dr. Reeti Joshi shares advocacy tools, faith, and hope for chronic illness. What You’ll Learn Why “normal” labs can still miss real disease activity—and how doctors actually interpret results in context of your story Concrete ways to self-advocate (questions to ask, when to seek a second opin…
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This week’s episode is different. April shares from a place of grief, prayer, and reflection after the recent assassination of Charlie Kirk, the murder of a young woman on a train, ongoing school shootings, and other tragedies shaking our nation. Rather than diving into politics, this is a conversation about how Christians can process these events …
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This conversation follows Aubree’s seven-year search for a diagnosis, the emotional toll of not being believed, and the day-after prayer moment that led—miraculously—to answers. She explains CIRS in plain language, why her family had to walk away from their home and most possessions, and what rebuilding practically and spiritually looked like in th…
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This episode dives into the shame so many of us carry when we’re living with chronic illness and can’t do what others expect—or what we expect of ourselves. From the outside, it might look like we’re resting too much, avoiding responsibilities, or being inconsistent. But the truth? We’re fighting invisible battles every single day. April shares a p…
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What does it look like to navigate lupus, POTS, and motherhood—all while raising a medically complex child and building a platform to support others? In this conversation, I’m joined by Keyundra Thompson, author, advocate, and founder of Secrets to Serenity. Keyundra shares her powerful story of growing up with undiagnosed symptoms, walking through…
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This episode is for the ones holding faith in one hand and pain in the other. I share my honest journey of praying, believing, and still living with chronic illness—and the quiet shame, grief, and questions that come with it. Together, we’ll unpack the wrestle of faith when healing doesn’t come, the ways God still shows up in the waiting, and how t…
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In this candid conversation, Shedrica opens up about her lupus diagnosis journey, the mental and emotional battles of living with an invisible illness, and how faith has been her foundation. She shares how using a physical planner transformed her daily life—helping her track symptoms, manage her household, and create space for both rest and joy. We…
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This episode dives into the hidden emotional weight of starting over with chronic illness. What happens when you’ve finally made the leap—downsizing your home, embracing a new lifestyle—only to find that your body and heart haven’t caught up? I’m opening up about the day I broke down in our RV, what no one saw beneath the surface, and how guilt and…
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This episode dives into Rachel’s story of loving and losing her husband to ALS and how she helped him “end well” with dignity, faith, and joy. We talk about invisible illness, caregiving, grief, honoring someone’s choices in their final days, and what it really means to live abundantly even when life hurts. Rachel also opens up about her ministry, …
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If you’ve ever felt embarrassed to use a cane, walker, or scooter because of your age or how “healthy” you look—you are not alone. This week, we’re breaking down the shame, judgment, and internalized ableism around mobility aids. I share my own experience using a rollator for the first time, plus tips and encouragement for anyone on the edge of mak…
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⚠️ Trigger Warning:This episode contains discussion of medical trauma, near-death experiences, and infertility Summary Melissa Smith was born with cerebral palsy, lives with multiple chronic conditions, and has survived a life-threatening surgery. But her story isn’t about staying stuck in the pain—it’s about how she turned that pain into purpose. …
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Faith isn’t always easy when your body won’t cooperate and your plans constantly fall apart. In this raw and personal episode, I’m sharing how chronic illness is teaching me to stop performing and start trusting. From years of self-reliance to finally learning how to rest in God’s strength, this is for anyone who’s ever whispered, “God, I can’t do …
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What does depression really look like? For Kristen Van Horn, it didn’t mean crying in bed or skipping daily routines—it meant anger, irritability, and feeling disconnected from a life that “should” have made her happy. In this honest conversation, Kristen shares how she finally got the support she needed, what it looks like to maintain her mental h…
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Thinking of canceling travel plans because of chronic illness? In this episode, we talk about how travel can still be possible—just differently. From pacing tools to packing smart, this one’s full of real talk, tips, and encouragement to help you see the world again—on your terms. Memorable Quotes: “You’re not broken. You’re just navigating life wi…
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I’m joined by JoBeth Polley, a certified grief recovery specialist who shares her own heartbreaking story and offers hope and healing for those grieving lives they didn’t choose. ⚠️ Trigger Warning: This episode contains discussion of terminal illness, infertility, and grief. In this raw and deeply moving episode, JoBeth Polley and I talk about the…
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In this episode of The Invisible Illness Club, we’re talking about the absolute worst combo—getting sick on top of your chronic illness. I’m sharing what it felt like when I got COVID this past February (spoiler: it was brutal), why being “extra sick” hits so much harder when you already live with limited energy, and what to actually do when you’re…
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What happens when the body you’ve always relied on breaks down? Jessica McGarvey knows this journey intimately. A former professional dancer turned Pilates instructor, Jessica opens up about her herniated disc injury, the long road to recovery, and how that season deepened her empathy for clients navigating invisible illness and postpartum healing.…
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If you’ve ever felt guilty for saying no, this one’s for you. Let’s talk about why living with chronic illness is a full-time job—and how setting boundaries can save your energy (and your sanity). Plus, I’ve got a brand-new resource to help: The Boundaries Reset Workbook. Memorable Quotes: “Chronic illness is a full-time job—with no PTO, no weekend…
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In this episode, I’m joined by Nicole Roth—a Health Restoration & Joy Coach and longtime autoimmune warrior—who shares how she reclaimed her health and joy after years of living with Hashimoto’s. We talk about the power of mindset, the role of boundaries in healing, and how faith and nervous system regulation helped her shift from seeing herself as…
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Let’s get real: not all entrepreneurs start their day with a latte and a color-coded calendar. Some of us start it from bed—with heating pads, pill bottles, and a to-do list that flexes with our energy. In this episode, I’m sharing how I run a business while managing chronic illness, why “business as usual” doesn’t work for spoonies, and how to cre…
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I know this wasn’t the most uplifting episode—but I also know how lonely it feels to sit with scary lab results, unanswered questions, and a body that’s just not cooperating. So if you’re there right now too, please know: I see you. You’re not broken. You’re not failing. And you don’t have to face the unknown alone. Whether your kidneys are flaring…
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Today’s episode is for the ones who miss their old selves—the energetic version who stayed out late, made spontaneous plans, and didn’t have to count spoons just to take a shower. Chronic illness brings a grief that no one prepares you for. It’s not linear, it’s not loud—but it’s real. We talk about what this grief looks like, why it comes in waves…
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Ever felt completely alone, even in a room full of people? This episode is all about that invisible ache—loneliness that isn’t about being physically alone, but about not feeling understood. When you’re living with a chronic illness, especially one others can’t see, that kind of isolation can run deep. I’m sharing a personal story that hit me hard …
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In this first episode, I share my journey to getting diagnosed with Ankylosing Spondylitis and Fibromyalgia after years of being dismissed. I also talk about why I started The Invisible Illness Club Podcast and what you can expect—real, honest conversations about chronic illness, faith, and finding joy in the hard moments. You’re not alone here! Me…
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In this episode, we’re talking about the power of gratitude—not as toxic positivity, but as a tool to find hope and joy even on the hardest days. You’ll learn how gratitude rewires your brain, helps shift your focus, and creates space for both the pain and the good. 💛 Memorable Quotes: “Hope and joy feel so out of reach sometimes. But gratitude doe…
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Are you feeling overwhelmed, unseen, or just plain exhausted from navigating life with a chronic illness? You’re not alone, and this podcast is here to remind you of that. Welcome to The Invisible Illness Club Podcast, a space where your struggles are acknowledged, your wins (big or small) are celebrated, and real-life solutions meet hope and encou…
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