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Targeting innate immune mechanisms to promote myelin regeneration in MS

This week Mary Devereux shares her thoughts on how MS, the Leaving Cert and Covid-19 are alike!

This week Joan Jordan talks about World MS Day, a blackbird and the soundings poetry book!

My name is Paul Dawson and I am 52 years of age living in Portnoo, Co. Donegal. I have had MS since 1993, however in the last 10years there has been a marked progression in my condition to the point I am now permanently confined to a wheelchair. Initially, I was quite hesitant to contact the MS society as I am a private individual at heart. Since taking the first steps I have discovered just how much support and help the Donegal MS society can provide to people like myself.

MS is different for each person who lives with it. The manner in which MS impacts a person and the severity of that impact is unique to each individual. Here, Sadhbh O Neill tells us about the journey that she has taken with her partner Sam, who lives with MS.

Researchers in the University of Reading are interested in hearing what people with MS have to say about the supports they would like to made available to them to support them with mental health difficulties.

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