In the darkness

August 8th is Severe ME Day and this year’s theme is home care. I’m going a but tangential here because I’m not exactly writing about the need for home care for daily living (which I certainly do need). Nonetheless, when I heard this year’s theme, it reminded me of my experience with professional in-home care visits I received from the hospital discharge order.

Severe ME Day 2015. #sufferingthesilence photo

Severe ME Day, 2015.
I wanted to mark my arm with “M.E.” like others have done, but decided not to because, thanks to M.E., I wouldn’t be able to wash it off for a long time. Taking a shower is a luxury that I have not been able to enjoy for months now.

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The Walk

It’s been a couple of weeks since I set my feet on the floor and motioned forward. When I did, I knew there would be consequences, but I never expected that would be the last time I would be walking for a while. I don’t know how long that ‘while’ would be. Days have been past. Weeks? Months? Years (I certainly hope not)?

A day at the hospital is surprisingly long and busy. You get woken up early in the morning by a phlebotomist for blood work. You fall back asleep, and it is time to take your vitals. Early morning flies by with nurses coming in and out introducing themselves after morning shift change, brining your morning medications, and asking you questions about your latest bowel movement, pain level, etc.; ordering breakfast and eating; and talking to your primary team doctors. Doctors discuss with you plans they have for you, and often times, you find out you need to talk to multiple doctors for specialist consults, all sort of therapists, nutritionist, social worker, financial team, and the list goes on. And all these people involved in your care come in one after another, and before you know it, your resident doctor is checking on you in the late afternoon before s/he passes the baton to the night cover doctor.

M.E. (myalgic encephalomyelitis) does not care about what you need to do, even if those are to make your health improve and help with M.E. symptoms, or very important life events that you absolutely don’t want to miss. It decides how much your body and mind can take before you must rest without consulting you, and often doesn’t tell you where that limit is. If you try to exert your will power and show who’s the boss, you quickly learn repercussions are not worth it and must obey M.E.’s will. Otherwise, it can leave you with heavy damage, sometimes irreparable.

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