The symptoms of MS vary widely from person to person and can affect any part of the body.
The main symptoms include:
Depending on the type of MS you have, your symptoms may come and go in phases or get steadily worse over time (progress).
See a GP if you're worried you might have early signs of MS.
The early symptoms often have many other causes, so they're not necessarily a sign of MS.
Let your GP know about the specific pattern of symptoms you're experiencing.
If they think you could have MS, you'll be referred to a specialist in conditions of the nervous system (a neurologist), who may suggest tests such as an MRI scan to check for features of MS.
MS starts in 1 of 2 general ways: with individual relapses (attacks or exacerbations) or with gradual progression.
More than 8 out of every 10 people with MS are diagnosed with the relapsing remitting type.
Someone with relapsing remitting MS will have episodes of new or worsening symptoms, known as relapses.
These typically worsen over a few days, last for days to weeks to months, then slowly improve over a similar time period.
Relapses often occur without warning, but are sometimes associated with a period of illness or stress.
The symptoms of a relapse may disappear altogether, with or without treatment, although some symptoms often persist, with repeated attacks happening over several years.
Periods between attacks are known as periods of remission. These can last for years at a time.
After many years (usually decades), many, but not all, people with relapsing remitting MS go on to develop secondary progressive MS.
In this type of MS, symptoms gradually worsen over time without obvious attacks. Some people continue to have infrequent relapses during this stage.
Around half of people with relapsing remitting MS will develop secondary progressive MS within 15 to 20 years, and the risk of this happening increases the longer you have the condition.
Just over 1 in 10 people with the condition start their MS with a gradual worsening of symptoms.
In primary progressive MS, symptoms gradually worsen and accumulate over several years, and there are no periods of remission, though people often have periods where their condition appears to stabilise.
MS is an autoimmune condition. This is when something goes wrong with the immune system and it mistakenly attacks a healthy part of the body – in this case, the brain or spinal cord of the nervous system.
In MS, the immune system attacks the layer that surrounds and protects the nerves called the myelin sheath.
This damages and scars the sheath, and potentially the underlying nerves, meaning that messages travelling along the nerves become slowed or disrupted.
Exactly what causes the immune system to act in this way is unclear, but most experts think a combination of genetic and environmental factors is involved.
There's currently no cure for MS, but a number of treatments can help control the condition.
The treatment you need will depend on the specific symptoms and difficulties you have.
It may include:
Disease-modifying therapies may also help to slow or reduce the overall worsening of disability in people with a type of MS called relapsing remitting MS, and in those with a type called secondary progressive MS who have relapses.
Unfortunately, there's currently no treatment that can slow the progress of a type of MS called primary progressive MS, or secondary progressive MS in the absence of relapses.
Many therapies aiming to treat progressive MS are currently being researched.
If you have been diagnosed with MS, it's important to take care of your general health.
MS can be a challenging condition to live with, but new treatments over the past 20 years have considerably improved the quality of life of people with the condition.
MS itself is rarely fatal, but complications may arise from severe MS, such as chest or bladder infections, or swallowing difficulties.
The average life expectancy for people with MS is around 5 to 10 years lower than average, and this gap appears to be getting smaller all the time.
There are 2 main MS charities in the UK:
These organisations offer useful advice, publications, news items about ongoing research, blogs and chatrooms.
They can be very useful if you, or someone you know, has just been diagnosed with MS.
There's also the shift.ms website, an online community for younger people affected by MS.