Writer. Mother. Living with trigeminal neuralgia, polycystic ovaries and a rare eye disease.
October 7th 2021 is Trigeminal Neuralgia Awareness Day 2021; the world is lighting up in teal and I have amassed 50 thousand readers.
Read more Trigeminal Neuralgia Awareness Day 2021: 50,000 Readers, Teal Lights and I’m Turning 30!
I'm not inspirational. I'm just sharing my journey.
My eye disease is rare, so there's not a lot of data about it. It's mainly reported by young, white females.. and not a lot of those! So I don't know what's going to happen with my eyesight. I manage well, but my vision still affects me on a day to day basis.
Read more How My Rare Eye Disease AZOOR Affects My Daily Life: The Vision Diaries
One day, I will wake up again and the pain will hit me literally square in the face and I am right back to where I started.
Read more Why I Couldn’t Enjoy Remission From Trigeminal Neuralgia
Losing my hair is just one more annoying thing that I'm dealing with that I don't want to. I thought I would put together a few tips for those currently in the same position as me.
If you are in a trigeminal neuralgia flare up, or attack, that is not managed by your medication at home and you feel like you cannot cope, you might find yourself considering attending A&E.
Read more The Trigeminal Neuralgia A&E Guide UK: What To Do In An Emergency
I am often asked what I can actually see, because I have a rare eye disease called AZOOR - acute zonal occult outer retinopathy.
Read more What Can I See? Living With AZOOR: The Vision Diaries
It's challenging enough to bring a newborn baby home from the hospital, especially when it's your first child. Throw into the mix that my little girl was born prematurely, that we were supposed to move house the week she was born and, finally, that I live with trigeminal neuralgia - and what you get is the toughest few months of my life!
