Gideon, who trained as an Orthodox rabbi while living with secondary progressive MS, talks about the Jewish celebration, Hanukkah (the Festival of Lights) and how he’s adapted to life with multiple sclerosis.

Emily was diagnosed with MS in 2010 when she was still physically, very active. However since being diagnosed, she now struggles with mobility issues and uses a wheelchair to get around. We chat to her about how she finds exercising helps with her MS

Nick, was diagnosed with relapsing remitting multiple sclerosis at the start of the first lockdown. In this story we talk to him about how he coped with his diagnosis and how running helps him with his MS.

Twenty-six-year-old Amy is newly diagnosed with multiple sclerosis. Here, she talks about how the diagnosis has made her appreciate life more as well as the importance of resting when you need to.

Cat was diagnosed with RRMS two years ago. Here, she shares how getting active and doing canicross with her cockapoo, Stanley, helps take her mind off things during tougher times.

Ever forget where you’ve put your keys? Struggle to find the word that’s on the tip of your tongue? You’re not alone. he MS Trust has launched a new, interactive web zone to provide everyday tips and tricks to help lift the ‘cog fog’.

A “life-changing” diagnosis of MS in 1999 inspired John Hambly to set up a new therapy centre to improve his own situation and bring support to others living with the condition

Sally talks about her use of scooters as mobility aids, reminding us that there are a number of options available to suit all levels of ability.

Multiple sclerosis (MS) is not considered a terminal condition and long-term studies suggest that MS only has a small impact on life expectancy.