When MS Comes Later in Life
This week Mary Devereux shares her experience living with multiple sclerosis, after being diagnosed later in life.
MS & Me
When MS Diagnosis Comes Early in Life
Katie St Lawrence was 22 years old when she was diagnosed with MS. In her latest MS & Me blog she shares her story.
Trigeminal Neuralgia Pain and MS
'Nerve pain in the face is the most misunderstood symptom' Willeke
This week Willeke Van Eeckhoutte shares how Trigeminal Neuralgia (TN) affects her day to day life.
Sun, Sea, Sand & MS
This week Ciara O' Meara shares her top travel tips and advice when travelling with MS.
Partial Capacity Benefit (PCB)
'Researching benefits is no one's idea of fun. It is really difficult to admit you need help and support. The amount of information and forms you need to fill in for any benefit can be a huge barrier - especially when you’re not even sure you qualify' Grace Kavanagh
Me, MS and Fatherhood
This week to mark Father's Day, Fergal Hughes takes us on a personal journey of life with MS and Fatherhood.
There is Only Love
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.
My life with MS, Paul Dawson
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.