Amyotrophic lateral sclerosis

ALS

What is amyotrophic lateral sclerosis (ALS)?

ALS is the most common form of motor neurone disease. It affects how messages are sent from the brain along the nerves to the muscles.

Without signals from the brain, the muscles gradually weaken and waste away.

The condition worsens over time and, eventually, the muscles stop working. At present, there is no cure.

What causes ALS?

ALS is caused by the gradual degeneration of motor neurones, which run from the brain and spinal cord and control body movement.

The exact cause is not fully understood, but genetic mutations have been identified in some cases. ALS has also been linked to smoking and exposure to certain toxins.

What are the symptoms of ALS?

Symptoms of ALS can begin with any of the following:

    • Stiffness and weakness in the limbs, causing falls and trouble gripping things
    • Twitches and muscle spasms
    • Cramping and muscle pain

    As the condition progresses, a person may:

    • Have difficulty swallowing, speaking and breathing
    • Lose the ability to walk and eventually move
    • Experience mood and personality disturbance

    The time it takes the condition to progress will vary.

Are you affected by ALS?

If you’re affected by ALS The Brain Charity can support you.

We are the only charity in the UK to be here for every one of more than 600 different neurological conditions in existence. Individually, many are rare, but combined they affect 1 in 6 people.

We provide practical help on all aspects of living with ALS, emotional support such as counselling, phone befriending and group therapy and social activities to people with ALS from all over the UK from our centre in Liverpool.

Looking to talk to someone?

Woman smiling, making eye contact and holding the hand of another woman to comfort her

Phone us

Contact The Brain Charity now

Our friendly Information & Advice Officers are here to help. We endeavour to respond to all enquiries within 10 working days.

0151 298 2999

Looking to talk to someone?

  • Please tell us which neurological condition you are affected by and what you need support with.

Caring for someone with ALS

We support carers, friends and family too

Are you a carer or relative of someone with ALS? It’s just as important for you to look after your own physical and mental wellbeing too.

The Brain Charity provides free support for carers, friends and family of people with any form of neurological condition, including ALS, from anywhere in the UK.

We also run additional carers advocacy service for all carers in Liverpool, regardless of which type of condition the person they care for has.

You don’t need to be a formal or registered carer

We can help you even if you don’t view yourself as a formal carer or claim Carer’s Allowance.

Find out some of the ways we support carers below.

Other resources

Support groups

Motor Neurone Disease Association

The MNDA has nationwide support groups searchable by area.

Click here to search for available support by postcode.

UK MND Clinical Studies Group

The UK MND Clinical Studies Group provides patient resources on various aspects of MND.

They also offer the opportunity for patients and their families to get involved with research studies and patient focus groups.

Support groups at The Brain Charity

Are you interested in setting up an ALS support group, or do you already run one?

Email activities@thebraincharity.org.uk to let us know.

Alternatively, check out our list of related support groups here.

Other charities

The Motor Neurone Disease Association

Find further information and support about living with ALS.

Website: www.mndassociation.org

Phone: 0808 802 6262

Email: mndconnect@mndassociation.org

My Name5 Doddie Foundation

A foundation set up to fundraise and raise awareness of MND.

Website: www.myname5doddie.co.uk

Email: info@myname5doddie.co.uk