Finding Strength in Our Reactions with Myasthenia Gravis

Greg Olsen

in

Living with Myasthenia Gravis (MG) means navigating a landscape of unpredictability. Each day can bring new challenges—sometimes subtle, sometimes overwhelming. Fluctuating muscle strength, unexpected fatigue, and the ever-present uncertainty about how we’ll feel tomorrow are all realities we share. While it’s easy to wish for more control over the circumstances we face, the truth is that many aspects of life, and of chronic illness, are simply beyond our grasp. There exists a profound truth, however, that lies inside each one of us: we may not control what happens, but we can choose how we respond.

Myasthenia Gravis doesn’t ask for permission before it disrupts our plans or changes our bodies. It can be frustrating, even heartbreaking, to realize we can’t always predict or prevent a symptom flare, no matter how careful or prepared we are. Understanding and accepting this lack of control is not the same as giving up. Instead, acceptance allows us to redirect our energy away from self-blame or resentment and toward more meaningful actions like managing our reactions, seeking support, and caring for ourselves with compassion.

  • Relief from Self-Blame: When a symptom flares despite doing everything “right,” it’s easy to turn inward, critiquing ourselves for not doing more. Acceptance helps us release this burden.
  • Energy for What Matters: By letting go of what we can’t change, we free up emotional energy to invest in what we can—our mindset, our self-care, and our community.

We often underestimate our own strength in choosing our response to life’s challenges. We often don’t realize how strong we actually are. When MG brings an unexpected hurdle like having to cancel plans due to fatigue, adjusting medications, or facing a difficult medical appointment, our reaction defines us far more than the event itself.

Choosing our reaction doesn’t mean denying difficult emotions. It’s normal to feel anger, grief, or frustration. Giving ourselves permission to feel these emotions is healthy; what matters is what comes next. Do we get stuck in the spiral of negativity, or can we gently shift our focus to what’s within our reach?

  • Pause and Breathe: When a setback occurs, take a moment. Breathe deeply. Allow yourself to acknowledge the disappointment or worry before moving forward.
  • Reframe the Narrative: Instead of dwelling on what’s lost or changed, try to see what you still have or what new opportunities might arise. “I can’t join that outing today, but I’ll enjoy some much-needed rest and connect with friends tomorrow.”
  • Seek Support: Connect with others who understand—family, friends, or the MG community. Sharing our experiences often lightens the load and brings new perspectives.
  • Practice Self-Compassion: Speak to yourself as kindly as you would to a loved one. Remember, living with MG is tough; you deserve empathy and patience, especially from yourself.

It’s easy to feel powerless when faced with a chronic illness like Myasthenia Gravis, but within every situation lies a choice. We can’t control our situation, but we can control how we choose to react to it and that’s where our strength shines through and our freedom lies.

While we can’t choose the challenges that come our way, we can always choose hope, kindness, gratitude and courage as our response. Sometimes that’s all we need. Sometimes that makes all the difference.

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