“The paints dance across the page, running into each other in ways you hadn’t planned but looking all the more beautiful for it. It’s like an analogy for life really. No matter what way you plan, life will do its own thing but that doesn’t mean it’ll be any less beautiful and worthwhile My MSContinue reading “The Art of MS – symptoms under the spotlight”
Tag Archives: MS
Everything from a list of neuro rehab services to self-help tips to help you manage your chronic illness
Outshining the pain
You are the first thing I think of in the morning because you are the thing that wakes me in the middle of the night. Pushing through that gap between dusk and dawn. Spotting a weakness in my armour you steal your way in so I always start my day thinking of you, rushing toContinue reading “Outshining the pain”
Fashion is my armour
In an upcoming MS & Me blog for MS Ireland, I talk about what fashion means to me and my identity. You can read the full blog post here. As any of us with a disability know, the fashion and retail industry are paved with issues, from a total lack of accessible clothing to notContinue reading “Fashion is my armour”
You’ve got the power
Every muscle in my body was screaming. Every little negative voice had creeped in. “I can’t do this,” I cried to Niall, my fiancée, as we struggled up the last hill of the 2015 Dublin half marathon. “Yes you can,” he shouted, reminding me of all I’d been through in the last few months –Continue reading “You’ve got the power”
I was being acknowledged at last but it was so bittersweet.
There she goes… The tightly-bound threads are loosening, unravelling. I’m unravelling. Little by little I’m making less sense of this disease and more sense of the scale of its destruction. I’m angry, sad and hurt. It hurts to look back and think of just how much it’s robbed from me, to watch my ghost laceContinue reading “The haunting”
Why am I not equal?
I’ve learnt that my biggest issue with using a wheelchair is not that I see myself as disabled, it’s that the outside world is designed in such an inaccessible way that it highlights my disability and sets up barriers for inclusion at every turn. Simply put, by using a wheelchair, you are not considered or treated as equal by society.
Kiss Goodbye to MS
To the people with MS who are reading this, I want you to know you are not alone. Together, side by side, we stand united in our battle against this cruel disease
Diary of a disabled bride
As you’ll know, I got married last July. We had an absolutely amazing day but during the months leading up to the wedding I really struggled. There was nothing out there for brides or grooms with disabilities, nowhere to turn to – and at times it became a very lonely road (see article I wroteContinue reading “Diary of a disabled bride”