This Lupus Life

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

Featured Me

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In the midst of all my scattered thoughts and difficult end of semester preparations some very exciting things have come my way. I can confirm first and foremost that my semester is officially over and my study break of three months has begun.

I insert the suggestion of a happy dance here. You may not be able to see it but rest assured it is there!

2014-04-08 17.49.40

Now I would like to deliver the second piece of exciting news that has happened to me. Over the weekend my blog was listed as a feature blog on a prominent website and blog developing site. The interview and feature if you would like to see it is on My Boring Channel. I was very pleased and excited to go through this process, as Eric the host of My Boring Channel has created some very interesting and useful tutorials on how to develop and create your own blog or website and what to do with it once it is up and running.

This is a great tool for anyone looking to get started. I myself am in the process of upgrading and have found much inspiration from the tutorials Eric has posted. Last week I suggested I was upgrading and hinted to this very feature. If you didn’t notice then, then you may notice now that my Blog name has changed from Nitya Nata, which was sanskrit for Eternal Dancer. Whilst I do not believe that the name no longer suited me or my purpose, I did realise it did not exactly address the content of this blog, which is a direct correspondence on this life that I am living with Systemic Lupus Erythematosus (Lupus).

So I changed my name. And I bought a domain. I am now not only This Lupus Life, but I am Yes Big Girl Pants or what!

I have now begun to organise my posts.

Now for the big reveal…I am going to start the tremendous job of publishing all the thoughts that I have had over the course of the last six months and kept to myself due to lack of focus in concentration and in neurological function. You will hear about what I have been through, how it has made me feel, what I am doing now and how I plan to progress.

Are you ready? You better be!



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.

One thought on “Featured Me

  1. Pingback: My mind is all a flutter | This Lupus Life

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