Inspiring MS: Kayla Montgomery is the very best of MS
I’m 15 years older than you, Kayla Montgomery, and only a year into my MS diagnosis. All I […]
Falling apart with MS: ‘You’d bleed just to know you’re alive’
November was no bed of roses. After 33 years in this body, it is surreal when it stops […]
Coming out of the MS closet: The secret world of MS
To tell or not to tell? My approach has been open and honest, although that has drawbacks. Everyone […]
Seeing MS: The invisible disease
It is hard to explain to others the sensations that come with a neurological disease. I am healthy […]
Walking for MS: MS Walk + Fun Run 2014
My family surprised me today. Six of my female relatives – mother, sister, sister-in-law, cousin and aunties – […]
Delaying treatment: When to start MS medication?
This is a tough entry to write, one I have been avoiding. I found the decision a simple […]
Seeking income protection: Chronic disease rejection
I’m writing this blog as a record for myself. I want to be able to look back on […]
Joining a trial: Delaying multiple sclerosis?
So, I haven’t posted in a while. I’ve been feeling (relatively) fit and normal… and, well, that always […]
Failing to deal: Deing diagnosed with a chronic disease
This blog is intended as a record of my experience. In the spirit of honesty, I didn’t take […]