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後天性異常族群AAC (ALS
肌萎縮性脊髓側索硬化症 (symptom (weakness 肌肉無力, upper-extremity (arm…
後天性異常族群AAC
ALS
肌萎縮性脊髓側索硬化症
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Progressive, degenerative disease
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ALS介入模型
初期
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第2階段
select AAC options, purchase AAC technology & instruct person who will rely on AAC and facilitators
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中期
Assess, recommend, Implement
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(4) Selecting low-and high-tech AAC options that will meet current and future needs 選擇可以符合目前及未來需求的AAC
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後期
Adapt & accommodate
provide effective communication options in response to changing communication needs capabilities, and living situations
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格林巴利綜症
progressive destruction & subsequent regeneration of myelin sheath of peripheral nerve axons 周圍神經細胞軸突的髓鞘
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Communication
disorders
:lips:Flaccid dysarthria(弛緩性吶吃)
:lips:Anarthria(complete loss of speech完全喪失語言能力)
:lips:Severe weakness often requires ventilator support through oral intubation or tracheostomy
介入
Middle phase
prolonged speechlessness, spontaneous recovery of speech
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Early phase
deterioration phase, loss of speech
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