In this episode, we’re chatting about the tools, tech, and everyday resources that make life easier for me as I navigate multiple sclerosis from my power wheelchair. I share how smart home features, accessibility upgrades, and supportive resources help me conserve energy, maintain independence, and feel more comfortable in my own space—from running my home with a voice command to relying on extra sets of eyes, hands, and paws when needed. It’s a relaxed, real-life conversation about making your home work for you, whether you live with MS, use mobility aids, or simply love smart solutions that simplify daily life.

If you’re curious about the tools and essentials I use to make daily life easier, I’ve gathered them all in one place here: https://linktr.ee/Shesahazard

In this holiday episode, Brad and Mallory share an honest look at traveling without a power wheelchair, managing Foley catheters on the road, attending the Abilities Expo, and balancing fatigue during the holidays. They wrap up the conversation with their New Year’s resolution focused on physical fitness, strength, and sustainability—real life, real challenges, and real hope.

Brad and Mallory share the real, everyday rhythms of their life as an interabled couple. Mallory lives with multiple sclerosis and uses a power wheelchair, and together they navigate love, accessibility, and the strength of partnership.

What does it mean to invite a neurotoxin into your body—not to erase lines, but to soften pain, quiet spasms, and reclaim movement? In this episode, Mallory explores the strange duality of muscular Botox: a substance designed to disrupt, yet often used to restore. Through personal reflection, and a dose of irreverent honesty, she unpacks the emotional and physical terrain of living in a body that resists control—and the unexpected ways Botox can offer relief.

This is not a beauty story. It’s a story about adaptation, autonomy, and a body that refuses to behave.

Living with MS means navigating a healthcare system that often feels like a labyrinth. In this episode, Mallory dives into the real cost of chronic illness: the doctors, the shifting diagnoses, and the ever-growing list of medications. If you’ve ever felt overwhelmed by managing your own treatment plan, you’re not alone—and this episode is for you.

💉 Bladder Botox: strange name, powerful impact. This episode breaks down the procedure, the purpose, and the patient perspective you won’t find in a brochure.

Join Brad & Mallory as they pull back the curtain on their interabled marriage, sharing the raw, real, and intimate moments that shape their life together. From navigating accessibility to confronting societal assumptions, this episode is a candid celebration of love, partnership, and the power of showing up for each other. Whether you’re disabled, nondisabled, partnered, or solo, you’ll find comfort, insight, and connection..

In this episode of She’s a Hazard to Herself, Mallory guides listeners through a journey that’s been anything but linear. For starters—she flew. Really flew. Gliding through open air gave her something she hadn’t realized she’d been craving: the sensation of freedom, untethered and whole.

Back on the ground, life has been tough—but the tides are shifting. After seven relentless months of roadblocks, appeals, and endless phone calls, she’s secured access to medication that should never have been this hard to get. She’s landed a PCP, which feels like a win in a healthcare game she never signed up to play. A home remodel may be on the horizon too—accessibility, function, and fierce optimism are the vibe.

So buckle up—this episode is equal parts turbulence and triumph, with a whole lotta heart.

In this episode of ‘She’s a Hazard to Herself’, Mallory shares the daily routines that help her stay comfortable while navigating life with Multiple Sclerosis. 🦽✨ From the benefits of assisted stretching 🧘‍♀️ to the effects of gym time 🏋️‍♂️, she talks about how gentle movement helps contribute to overall well-being. Plus, she discusses the support chiropractic care provides—helping with alignment and keeping discomfort at bay. Whether you’re living with MS or simply looking for ways to enhance your comfort, this episode is full of thoughtful insights and self-care tips to support your journey. 🧡

Motherhood is a dynamic and ever-evolving experience, and for moms living with multiple sclerosis (MS), it presents unique challenges that require resilience, adaptability, and unwavering determination. In this episode, I’ll explore the complexities of parenting while managing MS—discussing the realities of fluctuating energy levels, mobility adjustments, and the ongoing pursuit of accessibility and independence. Through personal insights, I’ll highlight how parenting from a power wheelchair is not a limitation but rather an opportunity to redefine strength, connection, and capability.

Weather affects life with Multiple Sclerosis in surprising ways. In this episode, we explore how temperature, humidity, and seasonal shifts impact symptoms—from the draining heat to the stiffening cold. Through real-life experiences, we examine the connection between climate and MS, helping you better understand and adapt to these changes.