Marti Hines public
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MS Warrior, Brain Surgery Survivor, Trigeminal Neuralgia Warrior, Filmmaker, CEO. Join me as take on this wild journey called life. Living with Chronic Illness: It's not just about the tough days, but also about the triumphs, big and small. I'll share my stories, the highs, the lows, and everything in between. From personal struggles to unexpected joys, it's all here, raw and unfiltered. Searching for Grace: How do we find grace in the chaos? Together, we'll explore strategies to cope, ways ...
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In this episode, I open up about my personal fertility journey, sharing the challenges and emotional decisions I've faced. From freezing my eggs to navigating IVF, and the complexities of finding a sperm donor, I discuss it all. I'll also touch on how my health has influenced my path and the tough choices I've had to make. Join me as I explore the …
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In this episode, I reflect on my three-month podcast journey and the joy it has brought me. I share my recent travel experiences, revealing how I managed to fly first class for most of my flights using points and miles. I emphasize the importance of understanding the points game and provide valuable resources and tips for maximizing travel rewards.…
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In today's episode, I dive deep into how turning 40 has reshaped my relationships and the way I navigate friendships, especially in light of my journey with multiple sclerosis (MS). I'll share the challenges I've faced in maintaining these connections and why setting boundaries has become essential for my well-being. We'll explore the importance of…
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As I dive into the latest headlines, I'm hit hard by the news of Harvey Weinstein's overturned verdict. It's a gut-wrenching reminder of the uphill battle survivors face. Sharing my own story of assault, I confront the power imbalances and systemic hurdles within the entertainment world. Through the pain, I find solace in the notion of self-forgive…
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Come along with me for a heartfelt conversation with Hillary Lofton-Mosley, where we dive into her journey with multiple sclerosis (MS). From the whirlwind of diagnosis to unexpected surprises like a surprise pregnancy, Hillary shares her story with honesty and a sprinkle of humor. We'll laugh, we'll cry, and we'll navigate the twists and turns tog…
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In this heartfelt chat, my sister Alisha and I dive deep into the impact of my MS diagnosis on our sisterhood. We go back in time and reflect on the rollercoaster of emotions we've experienced, from denial to acceptance, and how it's reshaped our relationship. Through laughter and tears, we share the little moments of understanding and support that…
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In this episode, I share a journey that's close to my heart—MS Awareness Month. It's a time filled with activities and events I'm deeply involved in, all aimed at raising awareness for Multiple Sclerosis (MS), a condition that's part of my life. I'm incredibly thankful for the support I receive; it means the world to me. Yet, I won't shy away from …
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Curious about life with narcolepsy? Join me in an eye-opening conversation with my dear friend Lauren Thomas. We unpack her journey living with Narcolepsy Cataplexy, from navigating treatment to her unforgettable experience speaking at the White House. Tune in as we explore the importance of advocating for sleep equity and the personal challenges o…
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In this chat, I get real with my friend Kyle about our wild ride with multiple sclerosis and how we tackled the Run Disney Marathon together. Picture this: we met during those crazy pandemic times, thanks to a friend who thought we’d hit it off – and boy, were they right. Kyle spills the beans on what went down when he first got his diagnosis and w…
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In this episode, I open up about the silent battles with MS pain and its sneaky way of messing with friendships and daily life. I touch on the tricky bits of explaining what this pain feels like and the extra stuff you've got to juggle when you're living with a chronic illness. It's a bit about the loneliness and the guilt trips, too, and those hid…
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In this episode, I'm letting you in on a journey that turned my world upside down. It's about my fight with trigeminal neuralgia, a term that was as foreign to me as the unimaginable pain it brought into my life. This isn't just a story about physical pain, though. It's about hitting roadblocks when you're desperately seeking help, making tough cho…
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Navigating the dating world in 2024 with a chronic illness is like embarking on an unpredictable journey, where every interaction feels like stepping onto uncharted territory. Gone are the days of swiping right for me; now, it's about finding genuine connections in real-life encounters. Deciding when to reveal my illness is a delicate dance, akin t…
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Just wrapped up the first month of 2024, and honestly, it's been a struggle. After enduring 17 long months filled with pain and feeling like no one really got what I was going through, I've finally gotten some answers. But now, I'm left wondering, "What comes next?" It's like standing at a crossroads after a long, tiring journey, trying to figure o…
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Welcome to my very first podcast episode! Who am I? I'm just like you – someone navigating the unpredictable waves of life but with a little twist. I live with a chronic illness, a companion that's as challenging as it is enlightening. In this debut episode, I'm throwing open the doors to my world, inviting you to join me on a journey that's as rea…
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