Before lockdown Lacey visited her dad every other weekend, but Covid restrictions have meant she’s not been able to visit her dad in his care home and give him a hug since March 2020.

Laura, a Community Staff Nurse who was diagnosed with MS 11 years ago, shares her experience of receiving the Covid-19 Pfizer-BioNTech vaccine.

Helena and Marissa, two members of MS Trust team who live with MS, chat about how they are coping with self-isolation, and the things that are helping them get through this very strange time.

Feelings lonely can be hard to deal with. But thanks to the wonders of modern technology, there are plenty of ways you can stay connected to your friends, family and local community.

Consultant neuropsychologist Jo Johnson answers your questions on MS and mental health.

Blogger Carla King reasons why people with MS may already have the skills to cope with the Covid-19 lockdown.

Advice and information for people with multiple sclerosis on coronavirus Covid-19.

A round-up of coronavirus and multiple sclerosis research.

Professor Helen Tremlett, looks at epidemiology (a study of disease in people) and the natural history of multiple sclerosis (MS).