When you sustain a spinal cord injury, seeking help with activities of daily living becomes a necessary task in life. Personal care can be a challenging job, whether one is caring for a disabled family member or for people with disabilities in facilities or private homes.
Experiencing burnout is common among caregivers.
Caregiver burnout is a state of physical, emotional and mental exhaustion that happens while you’re taking care of someone else.
Caregiver burnout especially threatens those caring for family members in the home because they often lack outside support they need.
Fatigue is more than chronic tiredness and lack of energy. It can causes headaches, dizziness, sore muscles, muscle weakness, slowed reflexes and responses, and even impaired decision-making and judgement.
Family caregivers often report high levels of anxiety. Anxiety manifests in physical ways too. Caregivers experiencing burnout may experience nausea, headaches, trouble sleeping, restlessness, irritability and depression.
Spinal cord injury changes our lives so much. Both the injured and the family caregiver experience loss and sacrifice. Experiencing burnout exacerbates depression. A family caregiver may experience apathy, guilt, hopelessness, loss of interest or pleasure in activities, or mood swings. A depressed caregiver may lack sleep, appetite, and the ability to concentrate.
A fatigued, anxious, depressed caregiver cannot perform their job efficiently, which puts you at risk. Burnout can also put family relationships at risk.
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