An MS diagnosis might feel scary and overwhelming, but remember, you're not alone. Find out how other people have come to terms with their diagnosis.
Receiving an MS diagnosis in lockdown ended my RAF dream
Adelle was diagnosed with relapsing-remitting Multiple Sclerosis in May 2020, she was aged just 17 at the time of the diagnosis.
How I coped being pregnant and diagnosed with MS during lockdown
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.
Phoebe talks to us about being diagnosed with MS during lockdown.
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?’
Could you be an MSTV reporter?
We are looking for young people with a connection to MS to join our team of MSTV reporters.
My search for MS support while studying for a PhD
Laura is studying a PhD in Cancer Genomics and was diagnosed with MS in September 2020 following multiple hospital admissions. Here, Laura talks about how this affected her mental health and what more could be done to support other students going through the same thing.
Talking to your kids about MS
Talking to your kids about MS can be daunting. In this blog Chris Wallace and his family tell how they have dealt with this together.