gapingvoid

You’ve probably never heard of ME/CFS, which is why it needs a cube grenade. Here’s a brief introduction, in handy FAQ format. What the heck is ME/CFS? A disease. The “ME” part stands for myalgic encephalomyelitis. The “CFS” part stands for chronic fatigue syndrome. Oh, chronic fatigue syndrome! Yeah, I’ve heard of that. I don’t get what the big deal is, though. I get tired too. ME/CFS isn’t just being tired. Symptoms vary from person to person, but commonly include:

• Chronic, debilitating pain
• Post-exertional malaise—symptoms get worse after physical or mental exertion and require an extended recovery period
• Flu-like symptoms, such as joint and muscle pain
• Cognitive impairment, including problems with short-term memory
• Crushing fatigue, which is not relieved by rest
• Greater susceptibility to fatal cancers and heart failure
• Other common symptoms include cardiac arrhythmias, chemical sensitivities, food sensitivities, blurry vision, eye pain, irritable bowel syndrome, and a host of other conditions that are nasty in their own right

A friend of mine says she has this thing, but every time I see her, she seems fine. I think she’s just a hypochondriac. Probably not. It’s typical for sufferers to have good days and bad days (though a “good day” can still be pretty bad from a healthy person’s perspective). If you see someone with ME/CFS out and about, you’ve probably caught them on a good day. You don’t see them lying flat on their back for the rest of the week, in the privacy of their own home, recovering from their trip to the grocery store. Is there a cure? No. Any hope for a cure sometime soon? Hard to say. The Whittemore Peterson Institute for Neuro-Immune Disease recently found a link between this disease and a retrovirus called XMRV. However, it’s not yet known whether XMRV causes ME/CFS in the same way HIV causes AIDS, or whether it’s an opportunistic infection. More research is needed. Problem is, the disease still gets almost no real funding, largely due to the perception that it’s not a real thing. Much of the money it does get has gone toward questionable psychological research. WPI doesn’t receive ANY federal funding yet. That’s messed up. Yep. A cube grenade could really help the cause. A cube grenade would be a direct and powerful way to show:

• It isn’t just being tired.
• It isn’t imaginary.
• Just because sufferers often look fine doesn’t mean they feel good.
• Bad things do happen to good people. If you blame the victim because it makes you feel better, you’re part of the problem.

Change the culture surrounding ME/CFS, and you change sufferers’ lives. In the long term, it encourages funding. More immediately, it increases the likelihood that sufferers will meet with heartfelt sympathy from the people closest to them rather than skepticism and cruel rejection.

[Note: this is one of the Cube Grenade entries. Share your story for a chance to win a commissioned piece of art.]