Choosing the right DMD can feel like a daunting task. In this honest account, Helena shares her MS and Tecfidera journey. Find out her take on the side effects and tips for taking it.

Brrrr! Ice, snow and wind can wreak havoc on MS symptoms. But fear not, Antoinette has some top tips to chase the chills away this winter.

Looking back over 2023, we've been delighted to have some amazing stories and personal experiences to share from our MS community. Here are some great reads from 2023 that you might have missed.

Antoinette was ready to ditch the online retailers this Christmas, in favour of shopping local. Hoping for an accessible journey, she boarded her mobility scooter and set off in search of undiscovered gems.

Pipe band drummer, Leoni, felt heartbreak when she had to stop her passion due to her MS worsening. She outlines how love, family time and building connections help her deal with her lifestyle change.

From falling leaves to cosy nights in, Chris’ love affair with the autumnal months is strong. Here he explores why he favours the colourful joys of autumn over the summer heat.

Recently retired nurse and crime writer, Chris, was diagnosed with relapsing remitting MS in 2020. He shares his journey of finding his identity after leaving the profession.

How accessible is Radio 2 in the Park for people with MS? Antoinette takes along her powered wheelchair to find out.

Cora’s MS bladder issues were causing chaos in her day-to-day life. Find out how intermittent catheters made things a lot easier for her.