Photo: Man pushing his wife in wheelchair

Support for carers

Most people with MS will need support from family and friends at some point. And it's only natural that many carers see themselves first as partners, sons, daughters or friends.

But using the formal term 'carer' can help you get extra support and do the best for you and the person you care for. We're here to help you find out how.

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Caring for my mum

Zena looks after her mum Nikki who has MS. In 2016 she won our Carer of the Year Award.

Watch this video to learn a bit about their journey together and how they keep smiling. There is an audio described version of this video.

We all need support sometimes. Our online community has a dedicated space for carers.

Connect with people online
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In this section

Photo: couple sat in the garden drinking tea

Getting help and support
Caring for someone with MS can take its toll both physically and emotionally. Help is out there.
Find out about getting help

Financial help
This page covers some of the financial help and support available to carers around the UK.
Read about carer grants and credits
Photo: couple at home with baby

Carers' rights at work
There are currently over three million working carers in the UK. Work is important for well-being, income and to keep social contacts.
Read more carers' rights at work

Taking care of yourself
If you spend a lot of your time caring for someone else, it can be all too easy to neglect yourself.
Find more out about looking after yourself
Photo: Mum with MS is sat in wheelchair exchanging smiles with her young son as he helps by putting her shoes on

Young carer support
If you're under 18 and have a family member with MS, you may be giving them extra help and support.
Read about young carer support

Planning and end of life care
Everyone with MS has the right to make choices about the care they receive now, as well as in the future.
Read about planning and end of life care

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Improving my wellbeing and living with purpose

Despite all the challenges of MS I've been determined to stay positive.

Read Katy's story
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My experience of pregnancy and MS

I’ve always wanted kids. Being diagnosed with MS in 2014, and then getting married, made me think more about it.

Nicola talks about her hopes and fears before and during her pregnancy.
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Having people to talk to made all the difference

When I was first diagnosed I felt like I’d lost a lot. Finding people to talk to motivated me and helped me find myself again.

Read Juanita's story
Members of a local group smiling

Find support near you

From support groups to information events, there's lots of ways to connect with people who understand what life's like with MS.

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