This Lupus Life

I am the dancer and Lupus is my music. I want to make it look beautiful

Who Am I?

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I am a daughter.

A sister.

A middle child.

An adult.

A woman.

A relatively petite lady.

A twenty six year old.

A single white female.

A mature-aged university student.

A literacy tutor.

A pre-service teacher.

An education support assistant.

A small business owner.

A yoga practitioner.

A Lupus sufferer.

A partially disabled youth.

A healthy-eating advocate.

A Raw Food advocate.

A migraine sufferer.

A kidney stone sufferer.

A positive thinker.

A philologist.

A spiritualist.

An art enthusiast.

An artist.

An amateur musician.

A designer and a decorator.

A singer

A writer.

A renter.

A car owner.

A cat owner.

A credit card holder.

A resident of Perth.

A Western Australian.

An Australian.

A resident of a first world country.

Who are you?


Author: Chevron Spots

I am in my mid twenties and fighting my battles to discover who I am and where I fit in to this zany, beautiful world. I was diagnosed with Lupus in in 2008. This takes up most of my focus, as I want to share the experience of trying to live with and rise above chronic invisible illness, so to speak. I would like to stress very much the information regarding medications, medical procedures and illnesses are discussed from my point of view, and with my understanding, colloquialisms and metaphors. I do not attempt to be legally and precisely accurate for the general population, rather I try to be emotionally and descriptively true to my experiences. I hope I can help in understanding others with chronic illness by providing one more personal recount of just how spontaneous and difficult these lives really are. One day I hope to visit every continent, climb some pretty high mountains, sleep in an ice cavern, marry a wonderfully understanding man, have children and teach more children. Mostly, I just want a simple life, you know the house with a husband and kids. Oh, and no pain.

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