'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 Joan Jordan shares with us why she is involved in clinical trials, research and EUPATI
COVID-19, immunity, vaccines & risks for people living with MS
Since the outbreak of the pandemic, MS Ireland has had to change and adapt to how we provide services throughout the country. We have moved some of our services online, where people living with MS can log in and take part from the comfort of their own home. Joan, avails of our services in North Dublin, below she outlines how she has found this whole new experience.
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.
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