What are the symptoms of hereditary spastic paraplegia?
People with hereditary spastic paraplegia may experience:
- Stiffness in the legs
- Weakness in the legs
- Difficulty walking or balancing
- Muscle spasms
- Pain or discomfort in the legs
What causes hereditary spastic paraplegia?
This condition is caused by changes in certain genes that can be passed down in families. These genetic changes affect how the nervous system controls movement.
How common is hereditary spastic paraplegia?
Hereditary spastic paraplegia is quite rare. It is estimated to affect about 1 in 50,000 people.
Who is more likely to get hereditary spastic paraplegia?
Hereditary spastic paraplegia can affect anyone, but it is more often found in families with a history of the condition. It can start at different ages, from childhood to adulthood.
How can I treat hereditary spastic paraplegia?
While there is no cure for hereditary spastic paraplegia, treatment focuses on improving movement and quality of life. Treatments may include:
- Physical therapy to strengthen muscles and improve walking
- Occupational therapy to help with daily activities
- Medication to manage muscle stiffness and pain
Powered by pharmacies
With over 1,700 pharmacy partners across the UK, you can get the help you need, wherever you are based.
Our website and mobile app make it easy and convenient to manage your health needs and book services at a pharmacy nearby.
How to live with hereditary spastic paraplegia?
Living with hereditary spastic paraplegia can be challenging. It is important for people with this condition to:
- Stay physically active within their limits
- Seek support from healthcare professionals
- Reach out to support groups or communities for encouragement
Final thoughts
Hereditary spastic paraplegia is a rare condition that affects movement, but with the right support and treatment, many people can manage their symptoms. If you have concerns about this condition, it’s important to speak to your GP or healthcare provider.