Multiple sclerosis 

Introduction 

Multiple sclerosis (MS)

Multiple sclerosis is one of the most common neurological conditions among young adults. An MS specialist nurse explains how to recognise early symptoms and where to get help.

MS Charities

There are two main MS charities in the UK:

Both organisations offer useful advice, publications, news items about ongoing research, blogs and chatrooms.

It is highly recommended that you visit both these websites if you, or someone you know, has just been diagnosed with MS.

There is also the shift.ms website which is an online community for younger people affected by MS.

 

Are you affected by multiple sclerosis?

The University of Warwick is doing research on how people affected by MS use the internet to seek other people's experiences and share their own. Taking part in this research would involve a single telephone interview lasting about an hour. For more information visit the Internet Patient Experiences website or contact the researchers directly at: ipex@warwick.ac.uk

Have you had your flu jab?

If you have multiple sclerosis you should have a flu jab every year. Find out why and how

Multiple sclerosis (MS) is a disease affecting nerves in the brain and spinal cord, causing problems with muscle movement, balance and vision.

Each nerve fibre in the brain and spinal cord is surrounded by a layer of protein called myelin, which protects the nerve and helps electrical signals from the brain travel to the rest of the body. In MS, the myelin becomes damaged.

This disrupts the transfer of these nerve signals, causing a wide range of potential symptoms, such as:

  • loss of vision – usually only in one eye
  • spasticity – muscle stiffness that can lead to uncontrolled muscle movements
  • ataxia – difficulties with balance and co-ordination
  • fatigue – feeling very tired during the day

Read more about the symptoms of multiple sclerosis.

Types of multiple sclerosis

Around 8 out of 10 people with MS will have the relapsing remitting type of MS.

Someone with relapsing remitting MS will have periods of time where symptoms are mild or disappear altogether. This is known as remission and can last for days, weeks or sometimes months.

Remission will be followed by a sudden flare-up of symptoms, known as a relapse. Relapses can last from a few weeks to few months.

Usually after around 10 years, around half of people with relapsing remitting MS will go on to develop secondary progressive MS.

In secondary progressive MS, symptoms gradually worsen and there are fewer or no periods of remission.

The least common form of MS is primary progressive MS. In this type, symptoms gradually get worse over time and there are no periods of remission.

Treatment

There is currently no cure for MS but there are a number of treatments that can help.

Relapsing remitting MS and secondary progressive MS can be treated with disease-modifying drugs. These are designed to slow the progression of the disease and reduce the number of relapses. But they are not suitable for all people with MS.

For example at the moment, there is no treatment that can slow the progress of primary progressive MS.

There are also a wide range of treatments, including steroid injections and physiotherapy, that can help relieve symptoms and make day-to-day living easier.

Read more about the treatment of multiple sclerosis.

Causes

MS is known as an autoimmune condition. This is where something goes wrong with the immune system (the body’s defence against infection) and it mistakenly attacks healthy body tissue – in this case, the myelin covering of nerves.

This can cause multiple sections of the brain and spinal column to become damaged and hardened (sclerosis), which can disrupt the nerve signals passing through these areas.

Exactly what causes the immune system to act in this way is unclear, but most experts think a combination of genetic and environmental factors are involved.

Read more about the possible risk factors and causes of multiple sclerosis.

Who is affected

It is estimated that there are currently around 100,000 people with MS in the United Kingdom.

Symptoms usually first develop between the ages of 15 and 45, with the average age of diagnosis being about 30.

For reasons that are unclear, MS is twice as common in women than men, and more common in white people than black and Asian people

Outlook

MS can be a challenging and frustrating condition to live with but new treatments over the past 20 years have considerably improved the quality of life of people with the disease.

MS is not fatal, but some complications which can arise from more severe MS, such as pneumonia, can be.

As a result, the average life expectancy for people with MS is around 10 years lower than the population at large.




Last reviewed: 14/02/2012

Next review due: 14/02/2014

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inyanga said on 23 March 2013

There is a problem with the rating system. I was about to award five stars and started to click on the first star. The computer immediately registered "unhelpful" and would not allow me to input any more stars or retrace my steps to correct this.I then had to register in order to record my rating.Obviously , if registering is a prerequisite of voting then I would understand but I wonder if you get a true reflection of opinions that way? Perhaps an explanation of how to enter the rating would be helpful.

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Templeknight7 said on 22 May 2011

I would disagree with your statement that MS is not a terminal disease as would the 20% of people with MS who " have a considerably shortened life"
The reason for the general misconception about the teminal nature of MS is found in the fact that :-"Routine mortality statistics are usually based on identifying a single cause for each death. This is the 'underlying cause of death', defined by the World Health Organisation (WHO) as:

a) the disease or injury which initiated the train of events directly leading to death or
b) the circumstances of the accident or violence which produced the fatal injury

So the disease which initiated the train which directly leads to death is recorded as a respiratory problem (usually aspiration pneumonia ) or a urinary tract infection. As both of these are actuallt secondary to MS it makes more sense for cause of death to be recorded was an event secondary to multiple sclerosis which should be recorded as the primary cause. This would make life a lot easier for MS patients trying desperately to meet continuing healthcare criteria for the purpose of ecieving funded care.

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