Progressive Supranuclear Palsy (PSP)

Progressive supranuclear palsy (PSP) is a rare brain condition that affects movement, balance, and vision. It can lead to difficulties with everyday activities and can be quite challenging for those who live with it.

What is progressive supranuclear palsy (PSP)?

Progressive supranuclear palsy (PSP) is a type of neurodegenerative disease. This means it causes the brain to slowly lose its abilities over time. It mainly affects areas of the brain that control movement and balance.

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What are the symptoms of PSP?

The symptoms of PSP can vary, but common signs include:

  • Stiffness in the body and difficulty moving
  • Problems with balance and coordination
  • Changes in eye movement, such as trouble looking up or down
  • Speech difficulties, including slower speaking or slurred words
  • Difficulty swallowing

What causes PSP?

The exact cause of PSP is not fully understood. However, it is believed to be related to the build-up of a protein in the brain, which damages the brain cells. This leads to the symptoms experienced by people with the condition.

How common is PSP?

Progressive supranuclear palsy is rare, affecting about 5 in every 100,000 people each year. It can occur in both men and women, usually starting in middle age or later.

Who is more likely to get PSP?

There are certain factors that might increase the risk of developing PSP, including:

  • Being over the age of 60
  • Having a family history of neurological disorders

How can I treat PSP?

While there is currently no cure for PSP, there are ways to manage the symptoms. Treatment options may include:

  • Medication to help with stiffness and movements
  • Physical therapy to improve balance and mobility
  • Speech therapy to assist with communication and swallowing

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How to live with PSP?

Living with PSP can be challenging, but there are strategies to help manage daily life. It can be helpful to:

  • Stay active with gentle exercises to maintain strength and balance
  • Join support groups to connect with others facing similar challenges
  • Educate family and friends about the condition to encourage understanding and support

What support is available for people with PSP?

People with PSP can access various types of support, such as:

  • Healthcare professionals for ongoing medical care
  • Occupational therapists to help adapt environments for safety and comfort
  • Support groups or organisations that focus on PSP and related conditions

Final thoughts

PSP significantly impacts daily life and can lead to various challenges. If you or someone you know is concerned about symptoms, it is essential to speak to a GP or healthcare provider for advice and support.

Always consult a medical professional
This article is for informational purposes only and is not a substitute for medical advice. Always consult a healthcare professional before starting, stopping or changing any medication. If you have concerns about your medication or experience side effects, speak to your doctor or pharmacist immediately.

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