This Lupus Life

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

The bare bones of me and Arthur-Itis

2 Comments

Everyone has heard of Arthur Itis. In the same way that when you come from the country everyone knows someones who knows your friend or cousin, on a basis more regular than you would probably guess you have met someone with Arthur too.

In fact, most people haven’t even taken a second to consider Arthur. Have you? There are a few Arthur’s out there so I will only tell you about mine because he is the only one I know well.
Rheum Atoid Arthur Itis is his full name. This particular Arthur has been a personal friend of mine for 5 years, since I was 18. Most people aren’t familiar with him until they are over the age of 30. I guess I am just lucky in that respect. I once knew a girl who has been with him most of her life. I think she was only 4 when she was diagnosed and most of her childhood was spent in braces and probably more pain than you can imagine.

For me Arthur is a tease and a nuisance reminder of what was at an age where I shouldn’t yet have a need to reminisce. As an active little girl, I have always been much more active than my friends. Running rings around everyone else simply because the energy and the joy was there to be burned.

Until one day I woke up and my hands were burning in a cold flame for some reason. The fingers couldn’t wriggle too good, not to mention the elbows and shoulders wouldn’t extend or move at all. I wasn’t sure what had happened, or what I had done, but I lay in bed for a while wriggling the joints around until I felt strong enough to get up.

….

Advertisements

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.

2 thoughts on “The bare bones of me and Arthur-Itis

  1. Pingback: Recovery: My Fit | This Lupus Life

  2. Pingback: Plaquenil, Toxicity and My Eyes | This Lupus Life

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s