Jenna, 29, was diagnosed with relapsing remitting MS in 2017, just two weeks before Christmas. After three years on one of the injectable disease modifying drugs, Jenna was forced to consider changing her treatment following a relapse shortly after the birth of her baby. Here Jenna talks about why she chose to switch to Mavenclad and how she’s found the treatment so far.

Will returns with another episode taking a peek behind the scenes of the MS Trust. This time he talks to MS Trust CEO, David Martin and Chair of Trustees, Caitlin Sorrell to find out more about how the MS Trust supports people with MS.

Take on the three highest peaks in England, Scotland and Wales.

Neuropathic pain in MS can be unpredictable and difficult to live with. In this episode, lead pain specialist nurse Katherine Dyer and mindfulness teacher Justin Standfield share practical strategies and calming techniques to help ease symptoms and give people with MS back a sense of control.

Dionne Trotman, who lives with MS, tells us about her search for the right exercise class to help with staying active.

Dan has a rapidly evolving severe case of relapsing MS. We spoke to him about why he chose to receive HSCT just 20 months after diagnosis.

Frances was diagnosed with MS in 2018. Four years on, Frances and her fiancé Alexis are planning their wedding after finding love at a local support group for people with multiple sclerosis.

Regan, 22, was diagnosed with multiple sclerosis when she was just 16. Whilst navigating school life and completing important exams, she started her treatment with Lemtrada – one of the strongest disease modifying drugs available for relapsing remitting MS. Here she sheds some light on her experience with the drug. She discusses what infusion clinics are like, the side effects she experienced and the ongoing monitoring after treatment.

If you are celebrating a wedding, anniversary, birthday, graduation, or retirement, you can add an extra meaningful touch to your day by supporting MS Trust.