MS & Me

'Among symptoms such as difficulties with cognition, decreasing mobility, fatigue, bowel and urinary issues- my symptoms are in all parts of my body- pain is always a major factor'

This week Mary Devereux shares with us her story of day to day living with MS and pain.

This week Robert Joyce shares his hopes for the 2020 MS READaTHON

This week Joan Jordan shares with us why she is involved in clinical trials, research and EUPATI

Joan Jordan was diagnosed with MS 10 years ago, in her latest blog Joan shares with us how she looks at her MS differently after all these years.

Mourning the loss of one’s health at 33 is a strange preoccupation, especially in the midst of a pandemic. It has made me reflect on my own journey and how lucky I am that I was diagnosed last year before the world shut down. Looking back, I had had symptoms for years.

This week Mary Devereux shares her experience living with multiple sclerosis, after being diagnosed later in life.

Katie St Lawrence was 22 years old when she was diagnosed with MS. In her latest MS & Me blog she shares her story.

This week Fergal Hughes talks about his own experience of brain fog.

'Nerve pain in the face is the most misunderstood symptom' Willeke

This week Willeke Van Eeckhoutte shares how Trigeminal Neuralgia (TN) affects her day to day life.