When a member of your family is diagnosed with MS, there will be a lot of changes in the family. Being a young carer is more common than you may realise and there are probably about 175,000 young carers in the UK. They are all looking after a member of their family with a range of illnesses including Multiple Sclerosis. Whether you are looking after the family member on your own or you have another family member to help you it is important that you remember to ask for help when you need it.
Are you or do you know a young carer who is coping with life with MS in the family? Perhaps they would like some advice but are shy to ask.
The MS Society has produced a Booklet ‘MS in your Life - a Guide for Young Carers”. You can obtain this book by contacting our Welfare Officers and they will arrange for you to receive one.
A Chance to Talk – this is a young people message board where you can talk to other young carers coping with MS in the family. Log into to www.mssociety.org.uk and click on ‘A Chance to Talk’. PLEASE NOTE: Whatever website you go on, please get parental permission and let them know you are going to look at them for support.
Annie & Dan talk about MS – this is a new DVD aimed at children under 10 years old, although it is suitable for any age. It features two puppets discussing MS and what is means. If you would like a copy, please ask your parents to contact our Welfare Officer and they will arrange for you to receive one.
Some of the common tasks that young carers perform are:
- Housework

- Household shopping
- Looking after brothers and sisters
- Supporting other members of the family
- Helping the person with MS get washed and dressed
- Simply being there to listen to a person with MS
- Preparing meals for the family
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