After finding out that he had multiple sclerosis by accident, Daniel’s life changed entirely. In this blog, he tells us about how the unexpected news led him to become a doctor.

Multi-award winning health and disability advocate Trishna Bharadia blogs about her experiences of MS as someone from the South Asian community.

Great North Run fundraiser, Connor Peebles writes a letter to multiple sclerosis. Connor's sister Patsy was diagnosed with MS at the age of 14.

Fundraiser, Lis talks about her 5,000 mile British coastal cycling challenge and why the support of the MS Trust was invaluable following a diagnosis of RRMS in 2013.

Siblings Patsy and Connor talk about Patsy's diagnosis with MS at the age of 14 and why Connor is taking part in the Great North Run in support of the MS Trust.

MS has many symptoms that may often appear to be 'hidden' or 'invisible'. In his blog Ian explains how these symptoms impact him on a daily basis.

Helena was inspired to take up running after her MS diagnosis. She has now run the ASICS 10k 5 times and is running for the 6th time this July.

The British Medical Association (BMA) recently voted to change its opposition to assisted dying and has taken a neutral stance. In this blog Ian Daly, who has primary progressive MS, discusses why he welcomes this shift in position.

Beccy Huxtable from The Scott Mills Show on BBC Radio 1 talks about how she turned to the MS Trust for help and support when diagnosed with MS in 2012.