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Explore practical tips, expert insights, and inspiring stories dedicated to supporting those affected by ALS. Rooted in the Deanna Protocol’s mission to empower families through holistic, science-backed care, our blog offers guidance on caregiving, managing symptoms like fatigue and muscle weakness, and staying strong—physically and emotionally—through the ALS journey.

  • When ALS Steals Your Voice

    Authored By Deanna May 08, 2025

    Losing the ability to speak is one of the most emotionally devastating symptoms of ALS. For many, it starts subtly—words get slurred, speech slows down—but over time, communication becomes nearly impossible. But here’s what you need to know: you are not powerless. While ALS does impact the brain and muscles, there are steps—technological and nutritional—you can take to maintain quality of life and keep connecting with the world around you. One patient’s journey offers a powerful glimpse into what this could mean for the future of ALS care.

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  • Caring for Someone with ALS

    Authored By Deanna April 02, 2025

    Being a caregiver for someone with ALS is one of the most selfless and challenging roles a person can take on. Whether you’re a spouse, family member, or friend, you’re stepping up in ways you never imagined—helping with daily tasks and offering emotional support through an unpredictable journey.

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  • Energy and ALS

    Authored By Deanna April 02, 2025

    Fatigue is one of the most frustrating symptoms of ALS. It’s more than just feeling tired—it’s an overwhelming, body-wide exhaustion that makes even simple tasks feel impossible. But why does it happen? And more importantly, what can you do about it? Let’s break it down in a way that makes sense, and talk about real strategies to help manage fatigue and improve daily energy levels. Why Do People with ALS Feel So Exhausted? At its core, ALS affects motor neurons, the nerve cells that control movement. These neurons need energy to stay alive and function efficiently and effectively. ALS disrupts…

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  • Muscle Weakness in ALS

    Authored By Deanna April 02, 2025

    Muscle weakness is one of the most challenging symptoms of ALS. It can start subtly—trouble buttoning a shirt, feeling unusually tired after walking short distances—but over time, it progresses, making everyday tasks harder. But here’s what you need to know: you are not powerless. While ALS does affect muscle function, there are steps you can take to help preserve strength, improve mobility, and support your body’s energy production. Let’s break down why ALS causes muscle weakness and what you can do to stay as strong as possible for as long as possible. Why Does ALS Cause Muscle Weakness?

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