Encourage active range of motion (ROM) exercises
🔷 Active ROM exercises are appropriate in ALS because they help maintain joint mobility, reduce stiffness, and support function for as long as possible.
🔷 ALS is a progressive motor neuron disease that causes muscle weakness, but sensation is usually preserved.
🔷 Gentle exercise and stretching can help delay contractures and improve comfort when tailored to the client’s ability.
🔷 The nurse should encourage activity that avoids exhaustion because overfatigue can worsen weakness.
🔷 This intervention supports mobility and quality of life in the early and middle stages of the disease.
Encourage high-calorie, soft foods
🔷 High-calorie, soft foods are appropriate because clients with ALS often develop dysphagia and increased effort with eating, which can lead to weight loss and poor nutrition.
🔷 Soft foods are easier to chew and swallow, while calorie-dense intake helps maintain energy and body weight.
🔷 Preserving nutrition is especially important because progressive muscle weakness can increase the work of eating.
🔷 The nurse should also monitor for aspiration risk as swallowing becomes more impaired.
🔷 This intervention helps support both safety and nutritional status.
Plan for early ventilatory support discussions
🔷 Early discussions about ventilatory support are appropriate because ALS can progressively weaken the respiratory muscles.
🔷 Advance planning allows the client to express preferences about future respiratory care before communication becomes more difficult.
🔷 These conversations support autonomy and improve preparation for expected disease progression.
🔷 Early decision-making also helps the family understand options such as noninvasive ventilation and long-term support choices.
🔷 Planning ahead is an important part of high-quality, client-centered ALS care.
Delay appointing health care proxy until late stage of disease
🔷 This is inappropriate because advance care planning should begin early, while the client can clearly communicate preferences and make decisions.
🔷 Delaying a health care proxy may leave critical decisions unresolved as the disease progresses.
Expect sensory loss as disease progresses
🔷 This is incorrect because ALS primarily affects motor neurons, not sensory pathways.
🔷 Clients usually experience progressive weakness, not major sensory loss.