Childhood MS
This week, Sarah tells us her paediatric MS story. She is a child, she has MS and she has the support of her parents as they all deal with the challenges of this condition.
This week, Sarah tells us her paediatric MS story. She is a child, she has MS and she has the support of her parents as they all deal with the challenges of this condition.
This week Trevis Gleason deals with familiar, often unwelcome, phrases people with MS hear very often.
This New Year, the MS and Me team will bring you more of the things you love as well as a few things you didn’t know you wanted.
At the start of New Year 2019, Declan Groeger shares with us his plans for the year ahead. Read on for a plan of action we can all adapt to our own resolutions.
In the throes of the Christmas Season, Niall McGahon delves in his experience of MS and shares with us how he deals with the uncertainty by keeping things in the moment, in the day. Read on to calm….
This week Grace Kavanagh writes about what the International Day of People With Disabilities means to her and what we as individuals understand about living with a disability.
This week Aoife Kirwan writes about the upcoming event for Young People with MS on 29th November 2018 (6pm-8pm) in the Davenport Hotel, Dublin. Register for the event here
Monday, November 19th is International Men’s Day, a celebration of the positive value men bring to the world, their families and their communities. Today Keith Byrne shares his experience and talks about ‘manning up to MS’.
This week Willeke Van Eeckhoutte shares with us the value of writing about living with MS. She’s an award-winning, irrepressible blogger and we are delighted to have her continued contribution to the MS and Me team.
Six of our MS & Me bloggers attended the National Conference last month. They tell us why they’ll be back again next year.
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