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Nerves & brain
Motor Neurone Disease
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Diagnosis :
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Living with MND :
Mobility, arm and leg weakness
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Personal care and care support
Speech and communication
Eating, swallowing and breathing
Tiredness, pain and discomfort
Forgetfulness and thinking
Emotional lability, depression and low mood
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Impact on family carers
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Motor Neurone Disease
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Nerves & brain
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Motor Neurone Disease
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Personal care and care support
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Personal care and care support
Personal care and care support
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Nerves & brain
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Motor Neurone Disease
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Rarer forms - PMA (progressive muscular atrophy)
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Paul - Interview 09
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He uses a ventilator most of the time, which enables him to speak normally. He has adapted well to it, but can't be left alone for too long.
Paul's diagnosis of progressive muscular atrophy was confirmed 2 years ago (2004) after several years of leg pain and weakness. Now unable to walk and he has limited arm movement. Uses a ventilator, but his speech is not affected. He worked until 6 months ago.
Nerves & brain
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Motor Neurone Disease
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Carers
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Bev - Interview 47
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She felt worried and unprepared for dealing with her mother's PEG. To be feeding the person who had always nurtured her seemed a strange role reversal
Bev's mother died about a year after developing speech and swallowing difficulties and being diagnosed with bulbar onset MND, aged 72. Her family were unhappy with many aspects of the care received.
Nerves & brain
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Motor Neurone Disease
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Personal care and care support
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Personal care and care support
Personal care and care support
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