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Young people
MS is most often diagnosed between the ages of 20 and 40 but children and teenagers can also develop it. Young people may also be caring for someone with MS. If you are a young person affected by MS you may find some of the resources on this page useful.
Please get in touch if you have any comments about this website or about how MS Society Scotland can better support you. Or maybe you would like to share your experiences with others - we would love to publish your stories on this page.
 Young people's page on the UK site
The UK site of the MS Society has lots of useful information for young people. You can also read people's personal stories.
Daniel's story
Daniel lives in East Lothian and was diagnosed with MS when he was fifteen.
He has recently written an essay for his forthcoming Higher English entitled 'The sound of the second hand on the clock' about his experiences with MS. It is very emotional, uplifting and inspirational.
You can read Daniel's story, and the stories of other teenagers with MS, on the Multiple Sclerosis Resource Centre website
Young carers
Under 18? Visit www.youngcarers.net for support and advice. There is a special section all about MS.
A young person's guide to MS
This booklet provides information to 10-15 year olds with a parent with MS. It was produced by the MS Trust. Read more on their website
Brochures for children and teenagers
Some nice, colourful publications from the american National MS Society
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For more information:
Information team
MS Society Scotland
Tel: 0131 335 4050
email
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