
Wordless Wednesday #1
I’m taking part in WEGO Health’s Health Activist Writer’s Month Challenge Day 3 #HAWMC – Wordless Wednesday #1 – Post a picture that symbolizes your condition and your experiences.
I’m taking part in WEGO Health’s Health Activist Writer’s Month Challenge Day 3 #HAWMC – Wordless Wednesday #1 – Post a picture that symbolizes your condition and your experiences.
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 have never have heard of it before you or a
I’m taking part in WEGO Health’s Health Activist Writer’s Month Challenge Day 1 #HAWMC – Why you write – tell us a little bit about why you write about your health online and what got you started. Why do I write? My thoughts about my reasons for writing changed several
As strange as it may sound, approaching my 23rd anniversary of being a sick person (I remember it well – the food poisoning, giardia or whatever it was that triggered the whole thing and led to me spending most of my 24th birthday puking), I think one of my best
There are many types of fatigue, some of which are unknown to those who have never experienced a chronic invisible illness. The first kind is the result of physical exertion, which generally leads to an almost pleasant tiredness, as it is often accompanied by the knowledge of a job well
From Jane: I apologize for the lapse in time between posts. On March 1st, 2013, my wife’s mother died. It was 18 years to the day of my father’s death in the antipodes, so many miles and years away. In the following week, my wife and I helped her stepfather
“Rain fell too, on the day they took you from me. It was not like this rain, which struck the dirty window and filled the barren room with its rhythm. That rain was different: flooding my thoughts, and driving me into a frenzy. I supposed that was why they took
When I was diagnosed with primary Sjogren’s Syndrome by Dr A-, some 12 years after I first became ill in 1990, I was relieved to have a name for the invisible illness that had wracked my life with its silent misery. However, there was one part of the diagnosis that
Hi, I’m Jane! I create blogs, fiction, art, and adaptive yoga as I seek peace and healing in this strange and sometimes beautiful world. I’ve been chronically ill and probably crazy for 30 years, but I try not to let it stop me!
Please visit the about page to learn more about me and my hopes for this community! If you’d like to support my work, please visit my tip jar at ko-fi.com/jane or my ongoing creative projects at patreon.com/janewaterman.
Blessings,
Jane