This post is part of the World Autoimmune Arthritis Day 2014 Blog Carnival. The theme of this year’s WAAD virtual conference is “A Day in the Life of an Autoimmune Arthritis Patient”. A link to the WAAD site follows this … Read More
I had big hopes for this year. I still do. However, the difference is those hopes have been modified from the impossible, unrealistic ones I had grasped for as I fled 2013, and have reformed as smaller, realistic, and somehow … Read More
I didn’t want to be here right now. After a year and a half of hell of dealing with a mental illness that wasn’t my own and dealing with the aftermath of that; of trying to get my abdominal pain … Read More
The main symptom of the disaster was the kitchen. For the past four weeks, supplies from the constantly aborted deck painting project mingled with dirty dishes, even though not much food was eaten. Food was a source of rough comfort … Read More
I have mentally begun this post for weeks, but a chronically ill life has a way of shaking loose any idea of control over one’s destiny. Anyone who has been ill for a while will understand what I mean when … Read More
I’m taking part in WEGO Health’s Health Activist Writer’s Month Challenge Day 2 #HAWMC – Introduce your condition(s) to other Health Activists. What are 5 things you want them to know about your condition/your activism? Sjogren’s Syndrome – Like me, you may … Read More
Day 20 – Write about alternative treatments/regimens/medicine. What do you support? What is crazy? Today’s prompt amuses me. Alternative treatments – what is crazy? What, indeed? I could wax lyrical about people in tin foil hats dancing naked under the … Read More
This is part of my contribution to Invisible Illness Week. What’s that you ask? Click on the graphic at the end of this entry to learn more! 1. The illness I live with is: A wily combination of things, but … Read More