Adelle was diagnosed with relapsing-remitting Multiple Sclerosis in May 2020, she was aged just 17 at the time of the diagnosis.

We chatted to Jadie Codd, who finally received her diagnosis of MS following years of symptoms, on how she dealt with this, two young children and being pregnant with her third child during a pandemic.

Jess’s husband Neil lives with Advanced MS. During lockdown she noticed a decline in his arm movement. Here she tells us how she managed to hook up a hydration station for him.

When the neurologist said the words ‘multiple sclerosis’, my immediate three questions were ‘Am I going to die?’, ‘Am I going to be disabled?’, ‘Can I have children?’

As we approach another MS awareness week after what has been a very different last 12 months, Martin Baum reflects on the impact the coronavirus lockdown has had on him.

Struggling to find a mobility aid as stylish as him, Martin’s search brought him to a rollator that unlocked his independence.

Ian Daly writes about the day to day reality of living with PPMS.

Bladder problems are very common in people with multiple sclerosis, but what steps can you take to look after your bladder and give yourself the best chance of maintaining good bladder function? Here are some top tips from an MS specialist nurse, a dietitian and a physiotherapist.

Bowel problems like constipation, loose stools or diarrhoea are common in multiple sclerosis. How can you keep your bowel healthy and improve your bowel function? Here are some tips from an MS specialist nurse, a dietitian and a physiotherapist.