This website uses cookies for anonymised analytics and for account authentication. See our privacy and cookies policies for more information.





The voice of Scotland’s vibrant voluntary sector

Published by Scottish Council for Voluntary Organisations

TFN is published by the Scottish Council for Voluntary Organisations, Mansfield Traquair Centre, 15 Mansfield Place, Edinburgh, EH3 6BB. The Scottish Council for Voluntary Organisations (SCVO) is a Scottish Charitable Incorporated Organisation. Registration number SC003558.

MS sufferers help to revamp charity website

This news post is almost 6 years old
 

More than 150 people with the condition have helped to create a new MS Society website

Over a thousand people living with a crippling condition have helped develop a charity’s new website.

The MS Society recruited a panel of 150 people from the MS community to share views on the new site, which goes live today (Thursday 3 May).

The panel provided feedback on everything from design and content, to ease-of-use. A further 1,000 people gave feedback online, and more than 800 visited the beta homepage.

Michelle Mitchell, chief executive of the MS Society, said: “We’re committed to improving the lives of our community in every way possible, and hear more and more how valuable digital tools are.

“We know that our content on the website is a particularly important source of support. It isn’t just a way to get reliable information about an unpredictable condition, it’s a way to bring people together and share experiences.”

The new website marks the start of the MS Society’s digital transformation, which aims to use digital technologies to achieve a better impact for people living with and affected by MS.

Members of the MS community have been involved throughout the site’s development. This included an exclusive two week testing period where they could review the site before anyone else saw it.

Rebecca is a photographer who was diagnosed with MS in 2015. She was involved in developing the website right from the start.

She said: “It’s been a real privilege to be given this opportunity and a bit of an eye opener. There’s so much to consider and it’s not just about how it looks, although that is still important. The most important thing for me is the personal element of the website – the forums and the stories.

“If you’re living with a chronic condition like MS, especially as people don’t really understand it, there are times you can feel very isolated. Particularly if you’ve just been diagnosed or are experiencing a relapse. Knowing there are people out there who know some of what you’re going through is more valuable than you can imagine.”

The new website is live now.