Myalgic Encephalomyelitis

May is Myalgic Encephalomyelitis awareness month. Also known as Chronic Fatigue Syndrome, this disease is characterized by exhaustion after exertion. The exertion can be physical -taking a shower; emotional – worrying or obsessing; or mental- filling out forms.

The best source of information about ME/cfs, as we call it, is the Bateman Horne Center. They offer resources for patients, caregivers, and the medical field.

Unfortunately, not much has changed since my diagnosis in 2014. Medical professionals continue, for the most part, to know little about this disease. It’s frustrating from the part of a sufferer, and discourages me from seeking help.

I’m sure I’m not alone.

Shoo, Pity!

A kidney stone, coupled with an infection has set me back five days – two trying to soldier through the pain, and three pursuing medical answers. Anyway, I’m on the mend, tired already of this foray into self-pity.

Tomorrow, I keep telling myself, is a new day.

(Image my own)

Impossibility of Morning

Shards of light cut around the edges of blinds
puncture the bubble of sleep, my eyes
resist opening, consciousness absent
from body, lying corpse-like
under a mound of blankets –
the furnace failing in the night.

Incessant chirping accosts my ears
not yet ready to respond to birdsong,
brain encased in a cement-block fog,
the mournful coos of a dove more fitting
for this somnambulist state.

Mouth, cotton dry, dreams of that first
honey-sweet sip of hot tea, smells coffee
brewing, the warm, encouraging aroma
of toast, weakly considers the possibility
of moving, but body still bears the weight
of death – refusing to respond.

Minutes will stretch to hours –
these mornings when illness wrestles
me into submission, the harshness
of its reality wrapping me mummy-like,
imprisoned in immobility – sentenced
without crime, trial or jury.

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(Today’s prompt challenges us to use all the senses.)