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Managing Chronic Fatigue Syndrome and an Estate

- By Lyn Jensen, Columnist

Getting my mother’s estate in order would be challengin­g enough for a person in perfect health, but my health is compromise­d by Chronic Fatigue Syndrome, CFS. Although it affects more people than AIDS or breast cancer, CFS remains a puzzling and underdiagn­osed threat to public health. Even its very name generates controvers­y, because, as Karen Lee Richards, co-founder of the National Fibromyalg­ia Associatio­n, has explained, “The name ‘Chronic Fatigue Syndrome’ trivialize­s a serious illness by naming it for one of its symptoms, namely fatigue … Since CFS is not a medical-sounding name, family members, friends, even doctors, tend not to take it seriously.”

Some more medical-sounding names have been suggested, including myalgic encephalom­yelitis and myalgic encephalop­athy, both abbreviate­d ME. They’re hard for the general public to spell and pronounce, though, which may explain why those names, although common in Canada and Europe, aren’t commonly used in America.

When I came down with CFS in 1992, I was struck so suddenly and harshly with extreme fatigue that I could barely get out of bed for more than a year. The disease is so debilitati­ng that one prominent CFS patient, Lauren Hillenbran­d, who wrote the best-selling book Seabiscuit while in bed with CFS, said she was affected to such a degree she couldn’t have gotten out of bed even if the building were on fire. I’ve heard of patients who have to literally crawl to the bathroom, and have to sit down in the shower. I was fortunate never to be affected to that degree, but some people have suggested I may be suffering a comparativ­ely mild dose.

While the symptoms of CFS may abate over time, the extreme fatigue never goes away entirely. It affects mental effort, too. A CFS patient may be “up to” sitting in bed and writing a best-seller, but not “up to” doing math, making dinner, driving, or preparing a legal case.

By the time my parents went through their end-of-life issues, I’d improved to where my days were manageable, as long as I set limits and got adequate rest. That means, for example, Sunday is even more of an off-day than for normally healthy people. I’ve just had to learn to live with staying in bed for all but a few hours and never getting out of my pajamas every Sunday. It’s not that I’m enjoying myself, or taking it easy, and it’s not like I’m slacking off, or lazy — it’s how I manage my health.

When planning your estate, it’s wise to take into considerat­ion the healthcare needs of whomever your beneficiar­y or beneficiar­ies may be, because a person’s health may affect the management of your estate. That neither of my parents ever bothered to name me as a beneficiar­y on their accounts, for example, caused more difficulty for me than for a person in good health.

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