Friday, June 3, 2011

Rivka Solomon Acts Up for ME/CFS from Her bed

June 2, 2011 by Paula Kamen, msmagazine.com:

Rivka Solomon, the daughter of 1960s activists, has long been a rabble rouser. Her 2002 edited anthology, That Takes Ovaries!, now in its sixth printing, still inspires action with its essays by women telling their true stories of “being bold and brazen, outrageous or courageous”–from rallying against sexual harassment to chewing out a burglar in the act. That book (and play of the same name) has spurred its own international movement, serving as a blueprint for at least 600 open-mike speak-outs and performances in which girls and women celebrate their own “ovarian acts.”

But the amazing part is that she has done much of this from bed.
In 1990, while she was a graduate student studying international relations, she got sick, as she describes it, with an unknown illness from hell that took away all my physical energy and my brainpower. … The brain fog that accompanied–and still accompanies–the illness was scary. When I was halfway through a sentence, I’d forget what I was talking about. I forgot my own phone number. The exhaustion is so extreme, it is difficult to engage in routine tasks, like taking a simple shower. I crawled into bed and stayed in or near it for much of the next 20 years, and I’m still there now, to this day.

Solomon, now 48, who lives in the Boston area, was diagnosed with chronic fatigue syndrome (CFS), or what is officially termed ME/CFS, myalgic encephalomyelitis/chronic fatigue syndrome.

ME/CFS now has no treatment or cure, and typically creates extremely disability for the estimated one million sufferers in this country and 17 million worldwide. Adding to that suffering is the public stigma that it is all in their heads. As a result, the U.S. government has been resistant to fund research into the disease, with only an estimated $6 million allotted to it yearly.

So, following her own example of grassroots organizing, Solomon has been spearheading historic protests in the U.S. to raise awareness of the problem. She began last year with a one-woman protest in front of the Department of Health and Human Services (HHS) and Red Cross headquarters in Washington, D.C. She didn’t leave her bed to make her next protest video, a comedic one “where me and my family are demanding–via singing–’clinical trials now!’ for ME/CFS.’”

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