Emma Rogan writes about Pride. The MS community is a mix of humanity- straight, LGBTI, different ethnicities, cultures and experiences. For Emma, the power of the MS community, the value of being visible and the progress in patient empowerment is worth celebrating.
This week Rosie Farrell talks about grief and in particular, how she has dealt with depression. Read on for an enlightening piece on what can be a very challenging experience.
On Father's Day blogger Niall McGahon shares his thoughts on life with MS and with being a Dad to Seán (2 years old) and newborn Robyn.
Research shows online supports vital as majority of carers feel isolated in their role
This week Robert Joyce shares his thoughts on World MS Day and invisible symptoms.
My name is Maggie Green…
NEW Research shows that 44% of Irish people have poor understanding of the symptoms and nature of Multiple Sclerosis (MS)
With the Women’s Mini Marathon less than two weeks away, Christina McDonald reflects on the build up to race day and the goals she has set herself…
Short Story Evening to mark World MS Day
Local Authority and European Parliament Elections