#Pst nuclear time psp#

This can lead to pneumonia, which can be life threatening. It's a good idea to talk to your doctor about what you'd like to happen when the condition reaches this stage.ĭifficulty swallowing can cause choking or inhaling food or liquid into the airways.

#Pst nuclear time psp#

Good care and assistance can help someone with PSP to be more independent and enjoy a better quality of life, but the condition will eventually put them at risk of serious complications. There's currently nothing that can be done to stop PSP gradually worsening, although research into new treatments gives hope that this may be possible in the future. feeding tubes to help manage dysphagia and avoid malnutrition or dehydration.Botox (botulinum toxin injections) or special glasses to help with eye problems.occupational therapy to help improve the skills needed for daily activities.speech and language therapy to help with speech or swallowing problems.physiotherapy to help with movement and balance difficulties.medication to improve balance, stiffness and other symptoms.Treatment will be tailored to meet the needs of each individual and may include: Treatment currently focuses on relieving the symptoms while trying to make sure someone with PSP has the best possible quality of life.Īs someone with PSP can be affected in many different ways, treatment and care is provided by a team of health and social care professionals working together. There's currently no cure for PSP, but research is continuing into new treatments that aim to relieve symptoms and slow down the progression of the condition. This will usually be a neurologist (a specialist in conditions affecting the brain and nerves). The diagnosis must be made or confirmed by a consultant with expertise in PSP. You may need to have a brain scan to look for other possible causes of your symptoms, as well as tests of your memory, concentration and ability to understand language. The large number of possible symptoms of PSP also makes it difficult to diagnose correctly and can mean it takes a while to get a definitive diagnosis. Your doctor will try to rule out other conditions that can cause similar symptoms, such as Parkinson's disease. Instead, the diagnosis is based on the pattern of your symptoms. The rate at which the symptoms progress can vary widely from person to person. slowness of thought and some memory problems.

an inability to control eye and eyelid movement, including focusing on specific objects or looking up or down at something.changes in behaviour, such as irritability or apathy (lack of interest).problems with balance and mobility, including frequent falls.Some of the main symptoms of PSP include: The symptoms of PSP usually get gradually worse over time.Īt first, they can be similar to some other conditions, which makes it difficult to diagnose early on. The condition has been linked to changes in certain genes, but these genetic faults aren't inherited and the risk to other family members, including the children or siblings of someone with PSP, is very low. This means the condition can have a wide range of symptoms. The amount of abnormal tau in the brain can vary among people with PSP, as can the location of these clumps.

In people with PSP, it isn't broken down properly and forms harmful clumps in brain cells. Tau occurs naturally in the brain and is usually broken down before it reaches high levels. 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. Most cases of PSP develop in people who are over the age of 60. The PSP Association estimates there are around 4,000 people with PSP living in the UK.īut it's thought the true figure could be much higher as many cases may be misdiagnosed. It's caused by increasing numbers of brain cells becoming damaged over time. Progressive supranuclear palsy (PSP) is a rare neurological condition that can cause problems with balance, movement, vision, speech and swallowing.