Caroline's Story
Hello, my name is Caroline Brennan and I was diagnosed with MS in May 2014. I experienced prolonged symptoms both before and after my diagnosis and got no relief from disease modifying drugs- just a selection of side-effects.
Hello, my name is Caroline Brennan and I was diagnosed with MS in May 2014. I experienced prolonged symptoms both before and after my diagnosis and got no relief from disease modifying drugs- just a selection of side-effects.
Saturday May 12th saw the Wexford South Branch leading the way to celebrate World MS Day. The Branch welcomed President Michael D. Higgins and his wife Sabina to a physiotherapy clinic where people who are living with MS, their friends, families and supporters are successfully running a professionally led programme in collaboration with a group of physiotherapists located at Clonard Medical Centre
This week in a blog about MS and Hope, Emma Rogan explores her understanding of the word ‘hope’ when it comes to living with MS.
Campaign by 17 National Charities calls on new Taoiseach to address “unfinished business” in health by tackling silent crisis in neurorehabilitation
The Southern Region held several successful events to celebrate World MS Day. Without the generosity of local sponsors, and help of local people and branches such events would not be possible. From the sponsorship of venues, tea’s/ coffee’s & pastries, raffle prizes, to free live music, excellent staff and of course everyone with MS, their families and friends who themselves endeavor to support the society and mark World MS Day events.
Ireland’s 360,000 Family Carers given opportunity to be recognised for their contribution to our society’s wellbeing.
This week Niamh McCarron lets us in on challenges she confronts, the bridges she has crossed and the fears that sometimes haunt all our nights.
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