September Feels Like

My ongoing journey with chronic illness has been particularly painful and difficult lately. It has become clear that I'm not able to work even a part time job at this point in time, I don't not know when or if that will ever change, which is very upsetting. Besides short daily walks, I rarely make … Continue reading September Feels Like

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How to Support Your Sick and Disabled Friends Beyond Prayers for Healing: An Open Letter to My Christian Friends.

 I’ve been diagnosed with fibromyalgia and chronic fatigue for almost a year and a half. I deal with widespread chronic pain, perpetual exhaustion, executive dysfunction, and a handful of other delightful symptoms. I have good days where I can function reasonably well and present as able-bodied and healthy, and I have bad days where I … Continue reading How to Support Your Sick and Disabled Friends Beyond Prayers for Healing: An Open Letter to My Christian Friends.

Tattoos and the Art of Process

This February and March mark the first anniversary of my chronic illness diagnosis (the anniversary spans a couple months because as some of you might know the diagnosis process for many chronic illnesses is long and weird--arguably I haven't actually completed it yet). The onset of my illness and the many subsequent life adjustments that I've … Continue reading Tattoos and the Art of Process

The Heartbreaking Beauty of Shared Burden

I've been trying to marvel at humans a little more lately. There is so much in the world to make me despair of truth and goodness. Maybe becoming more aware of the intense pain and brokenness of humankind is a side-effect of growing up, but it's also incredibly heavy and discouraging. When it all feels … Continue reading The Heartbreaking Beauty of Shared Burden