Tracy is living with MND and her husband Iain is her main carer. They talk openly about their challenges with social care, communicating with eye gaze and voice banking. Tracy focuses on, “It’s important to me to have my own voice on the eye gaze because I don't want to sound like a robot or lose my individuality.”
See Tracy and Iain's interviews below.
1. Access to healthcare
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2. Communicating
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3. Eating and drinking
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4. Tube feeding
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5. Emotional and psychological support
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6. Social care
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7. Equipment and adaptations
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8. Carer and family support
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9. End of life decisions and planning ahead
Page last updated: 10 April 2026
Next full review: April 2027