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.

Findings from a research study investigating how common nerve or neuropathic pain is in early multiple sclerosis (MS).

Pins and needles, prickling or burning feelings? Find out what’s causing the strange sensations in your skin.

Fibromyalgia is a chronic neurological condition that can cause symptoms similar to multiple sclerosis (MS).

Many MS symptoms seem invisible to other people. Why is this, and what you could do to raise awareness?

In this episode, we talk to Erika from our fundraising team about what's happening at the MS Trust in the coming months.