Why patients cannot work living with myasthenia Gravis

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  • เผยแพร่เมื่อ 8 ก.ย. 2024
  • Patients with myasthenia gravis (MG) may find it difficult or impossible to work due to several factors:
    1. **Fluctuating Symptoms**: The unpredictable nature of muscle weakness and fatigue can make it hard to maintain a consistent work schedule.
    2. **Physical Limitations**: Weakness in the arms, legs, neck, and respiratory muscles can hinder the ability to perform job-related tasks, especially in physically demanding roles.
    3. **Cognitive Effects**: Fatigue can affect concentration, memory, and overall cognitive function, making it challenging to stay focused on tasks.
    4. **Medical Appointments**: Regular doctor visits and treatments can take time, leading to absences from work.
    5. **Exacerbations**: Periods of increased weakness (exacerbations) may require extended time off for recovery.
    6. **Stress and Fatigue**: The demands of a job can exacerbate symptoms, leading to increased fatigue and stress, which can further impact health.
    7. **Support Needs**: Some individuals may require accommodations or assistance that are not feasible in all work environments.
    These factors can lead many patients to reconsider their employment options or seek disability support.

ความคิดเห็น • 2

  • @imgm94
    @imgm94 หลายเดือนก่อน +1

    I work. I found something that accommodates my myasthenia gravis. It's not easy, but it's possible. Of course, before I was stable, I could not work. I was too sick. Everyone is different. We know our bodies and do what we can 😊

    • @jenniferdailey2540
      @jenniferdailey2540  หลายเดือนก่อน +1

      @@imgm94 I absolutely agree about everyone being different. I have been on disability for sometime now since being diagnosed with myasthenia Gravis . I used to be a CNA and enjoyed working and actually miss the work I used to do. Unfortunately I suppose it’s impossible for me to go back working as a nursing assistant. It’s been rough throughout these 9 years because I have generalized MG and my symptoms recently returned last December after being in remission for 4 years. I desperately want to do something part time but I’m afraid it will trigger my symptoms.