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What are the 4 stages of PSP?

The four stages are: Early stage. Mid stage. Advanced stage.
...
End of life stage:
  • Severe impairments and disabilities.
  • Rapid and marked deterioration in condition.
  • Decisions with regard to treatment interventions may be required, considering an individual's previously expressed wishes (advance decisions to refuse treatment).
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What do the final stages of PSP look like?

Advanced stages

As PSP progresses to an advanced stage, people with the condition normally begin to experience increasing difficulties controlling the muscles of their mouth, throat and tongue. Speech may become increasingly slow and slurred, making it harder to understand.
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How quickly does PSP progress?

PSP typically begins in late middle age and worsens over time, with severe disability occurring within three to five years of onset. The disease can lead to serious complications such as pneumonia, choking, head injury, and fractures.
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Is PSP considered a terminal illness?

Although PSP isn't fatal, symptoms do continue to worsen and it can't be cured. Complications that result from worsening symptoms, such as pneumonia (from breathing in food particles while choking during eating), can be life threatening.
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What are the first signs of progressive supranuclear palsy?

The characteristic signs and symptoms of progressive supranuclear palsy include:
  • A loss of balance while walking. A tendency to fall backward can occur very early in the disease.
  • An inability to aim your eyes properly. You may not be able to look downward, or experience blurring and double vision.
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Following disease progression with clinical milestones in PSP and MSA

What is the life expectancy of someone with supranuclear palsy?

What is the life expectancy of someone with progressive supranuclear palsy? People with progressive supranuclear palsy typically die six to nine years after their diagnosis. But this can vary. PSP symptoms increase your risk of developing pneumonia, which can be fatal.
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What is the most common cause of supranuclear palsy?

What causes PSP? PSP occurs when brain cells in certain parts of the brain are damaged as a result of a build-up of a protein called tau. Tau occurs naturally in the brain and is usually broken down before it reaches high levels. In people with PSP, it isn't broken down properly and forms harmful clumps in brain cells.
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How do you care for someone with progressive supranuclear palsy?

Physical therapy and occupational therapy, to improve balance. Facial exercises, talking keyboards, gait and balance training also can help with many of the symptoms of progressive supranuclear palsy.
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Is progressive supranuclear palsy a form of dementia?

Progressive supranuclear palsy (PSP) is a frontotemporal dementia. It is characterised by difficulties with balance, movement, vision, speech and swallowing. It is caused by progressive damage to the cells in the brain that control eye movements.
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What personality changes occur with PSP?

Eye problems, such as keeping eye contact with another person, will get worse. PSP can also affect a person's ability to speak, and their voice may become soft and weak. Mood and behavior changes may occur. People with PSP may become irritable, forgetful, or depressed, and they may become less interested in things.
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Do PSP patients feel pain?

Pain was reported in 58 PD patients (89%), 17 MSA patients (81%), and four PSP patients (25%) (P < 0.01).
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Do people with PSP sleep a lot?

Poor sleep is common with PSP. It takes longer for patients to fall asleep, and they wake more frequently during the night, resulting in a shorter time asleep. Neuroanatomical areas affected in PSP are also the same areas of the brain that house the sleep/wake regulation system.
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Do PSP patients hallucinate?

Finally, 11% had hallucinations and 5% delusions. These behaviors pose a particular challenge in regards to patient management for caregivers of patients with PSP. Overall, there is significant neuropsychiatric morbidity in these patients who are primarily seen by movement disorder specialists and neurologists.
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Who died of progressive supranuclear palsy?

Neuroscience for Kids - Dudley Moore Dies of PSP. Actor and classically trained pianist Dudley Moore died March 27, 2002, of complications from a rare brain disease called progressive supranuclear palsy (PSP). He was best known for his starring roles in the 1979 movie 10 and the 1981 film Arthur.
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Does PSP run in families?

Most cases of progressive supranuclear palsy are sporadic, which means they occur in people with no history of the disorder in their family. However, some people with this disorder have had family members with related conditions, such as parkinsonism and a loss of intellectual functions (dementia).
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What activities can people with progressive supranuclear palsy do?

Structured exercises can improve strength, mobility, and balance in people living with PSP (9). Physical therapy (11) and physical activities, such as walking (12, 13), music-cued movement (14), dancing (15), and cycling (16), can also improve fitness, community ambulation, and social participation in parkinsonism.
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Why do PSP patients fall?

Nocturia in PSP relates to bladder instability and can also contribute to falls, especially if patients are trying to reach the bathroom or commode at night in low light, unattended, and without time to adjust to postural and thermal shifts on getting out of bed.
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What celebrity has supranuclear palsy?

A re-evaluation in late 2019 changed her diagnosis to the rare brain disorder, progressive supranuclear palsyopens in a new tab or window (PSP). Ronstadt told Cooper that her illness has had a major impact on her life: "Everything becomes a challenge.
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How many people in the US have progressive supranuclear palsy?

Progressive supranuclear palsy (PSP) is a rare brain disorder that causes dementia and problems with walking and balance. About 20,000 Americans — or one in every 100,000 people over age 60 — have PSP.
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Is PSP caused by stress?

Stress is associated with the development of neurofibrillary tangles via glucocorticoids. Hypertension is associated with an increased risk for PSP by inducing the aggravation of tau pathology and neuroinflammation. Inflammation may be associated with pathological tau accumulation and neurodegeneration.
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What medication is used for supranuclear palsy?

There are currently no medications that treat PSP specifically, but some people in the early stages of the condition may benefit from taking levodopa, amantadine or other medications used to treat Parkinson's disease.
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What are the traits of PSP?

As originally described, PSP was characterized by progressive supranuclear ophthalmoplegia, gait disorder and postural instability, dysarthria, dysphagia, rigidity, and frontal cognitive disturbance [1].
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Does PSP affect the eyes?

A person with PSP will begin to experience eye problems, such as difficulty opening and closing their eyes, blinking, blurry vision, or moving their eyes side to side or up and down. Later in the disease, people with PSP may feel increasing weakness in their limbs.
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Do people with PSP lose weight?

Weight loss begins in the early stage of PSP, whereas dopaminergic treatment may contribute to keep weight in the early stage of PD through reduction of energy expenditure and/or improvement in appetite.
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