A Little Taste of Nature

I've had a bad day for chronic fatigue, so I decided to go on a walk with my camera to capture the beautiful autumn colours to try and see if the outside would help energise me as it sometimes does. It didn't, I had to get the bus back and I've been napping since, but [...]

Tips for being a student with lupus

I feel really lucky that four months after my diagnosis I was able to begin my masters degree in a foreign country - not everyone gets that pleasure. Often lupus forces people to quit school or university, with hope of maybe returning when things are a little better. I, however, am a stubborn individual, so [...]

The perks of having lupus

Okay, so it's not great having an incurable, life threatening, life changing disease that can control your life and ambitions, affect your relationships and can make day to day life a struggle. It actually sucks. It's even worse when you feel like people don't understand, which is a top complaint from anyone living with a chronic [...]

Life with Lupus (as told by pictures off the internet)

I decided to write a Buzzfeed style article about having lupus. They are pretty great at creating funny but insightful posts about living with different illnesses, both physical and mental. They've covered chronic illnesses a lot, and it's great being able to see people sharing the same pains also able to share the same humour. [...]

First Impressions of Lupus

It's been just over 2 months since I received my lupus diagnosis and started on all the treatment and medication that entails. I've discussed things with friends and family, I've already seen a multitude of doctors, and god knows how many blood tests I've had (I think I'm finally getting used to them - have only fainted [...]