Jenna talks about her MS diagnosis, pregnancy and the challenge of choosing a new disease modifying drug after giving birth to her son.

Annie's MS diagnosis came shortly before she found out she was pregnant. In this blog she talks about her diagnosis and how she coped during pregnancy.

John Peters tells us how his working life changed during lockdown and how he’ll be quite happy not to go back to ‘normal’.

The pandemic has meant huge changes to MS services. We talk to MS Lead Nurse, Mavis Ayer, about her experiences over the last 12 months.

Comedian, Jeanette and Poet, Lytisha, talk about how creating their own podcast, about life with MS, led to lots of laughs, feelings of empowerment and a sense of community during lockdown.

Adelle was diagnosed with relapsing-remitting Multiple Sclerosis in May 2020, she was aged just 17 at the time of the diagnosis.

We chatted to Jadie Codd, who finally received her diagnosis of MS following years of symptoms, on how she dealt with this, two young children and being pregnant with her third child during a pandemic.

Jess’s husband Neil lives with Advanced MS. During lockdown she noticed a decline in his arm movement. Here she tells us how she managed to hook up a hydration station for him.

When the neurologist said the words ‘multiple sclerosis’, my immediate three questions were ‘Am I going to die?’, ‘Am I going to be disabled?’, ‘Can I have children?’