Tag Archives: post-exertional malaise

Alternatives to the alternative

pillsChronically ill skeptics will probably find themselves disappointed if they go looking for critical thinking about complementary and alternative medicine (CAM) on online support forums. This is a thesis I keep returning to because it cropped up again for me recently. I decided to leave one community because of a thread in their CAM subforum (not one in which I was involved). A link to a news story in which a child died due to its parents’ reliance on a popular CAM treatment was met with hostility, unwillingness to start another discussion about CAM, and the notion that “it’s a support forum.”

The original post was intended to help answer the question of “what’s the harm” of relying upon certain treatments. From this I infer that “support” only goes as far as saying yes to whatever treatments people decide upon, even if they are at best useless and at worst dangerous. I have a very different definition of support, which starts with understanding both sides of the issue. The person considering the treatment is sick, in pain, and has heard good things about it from people she considers reliable. The person offering the opposite view (as at the website I just linked to) wants to provide facts showing that there are dangers to these therapies. This isn’t done out of spite, but rather with the first person’s welfare at heart. This is a very good form of support. Should we only be providing the pros and never the cons? Does that sound supportive? Not to me.

Like what’stheharm.net, I am not an enemy of CAM on principle, especially because so many of us have these annoyingly intangible illnesses, where conventional medicine often just throws up its hands at a certain point and says “Good luck feeling better.” After five or so years of involvement with online chronic illness communities, I sometimes deviate from the skeptical motto that “anecdotes do not equal evidence.” Are there reliable randomized controlled trials (RCTs) about acupuncture’s use in easing the symptoms of ME/CFS? I’ll go out on a limb without searching and guess there aren’t many. But I’m just not inclined to leap on people who decide to give it a try, as long as they’re well informed about it. (My exception to this is homeopathy. This is nothing more than a sugar pill and should not be promoted by anyone. Now, if someone is completely informed on the subject, and is both willing and able to shell out money for an at-best placebo effect…well, I can’t understand that one, but I guess I support it too.)

The part I protest is where people reject what Western medicine has to offer. By all means, if you can afford it, go hog-wild with the echinacea and vitamin C, as long as you also get the flu vaccine. (With exceptions for people who have legitimate medical problems with it, of course.) Without a doubt, treat your child’s nausea with ginger root, as long as she also gets the chemotherapy she needs. I completely understand and identify with the frustration chronically ill people may develop towards Western medicine, but rejecting it outright isn’t the answer. If the recent science-based XMRV discoveries and new evidence-based studies eventually produce a cure for CFS, what are you going to do then?

If my position sounds wishy-washy, well, it is, to some extent. As I’ve said before, it’s too hard for me to ignore that desperation felt by people who may be sick and in pain for their entire lives, something that I don’t think is always taken into account by enemies of CAM, or even neutral skeptics. This is a really powerful force. This isn’t about fixing something with a vaccine or radiation: this is a lifetime of doctors saying “We don’t know.” People will seek alternative therapies, and it is supportive both to understand and respect why they are doing so, as well as to provide evidence for why they may not want to choose something they’re considering.

Here are a few examples of alternative therapies I have seen suggested for ME/CFS patients, and things I would suggest instead. Of course, these are only suggestions and anything I mention here should certainly be researched by you and discussed with your doctor. Don’t do or stop anything on the basis of this post alone.

drinking-water-to-improve-your-complexion

“Alternative”: Homeopathy

Alternative: Water

I’m completely serious. Homeopathy is based on this idea that water retains the memory of molecules of stuff that was in it once but has now been diluted a whole mess of times so it doesn’t even contain that anymore. Instead of paying for this silliness, just drink more water. Especially when you’re constantly running fevers and have other chronic symptoms of infection, it’s very important to stay hydrated just as though you had an acute infection.

“Alternative”: Graded Exercise Therapy (GET)

Alternative: Find your own ways to exercise

GET is controversial. Some studies have supported it; however, studies tend to exclude severely affected patients. Also, not all studies include reporting of post-exertional malaise, a very common and very significant side effect of exercise for people with CFS. Finally, as it has to be done with a therapist, you’re much better off saving the money and constructing your own exercise program around your own skills and limitations. This post has some very good advice; I particularly like that it includes mental as well as physical exertion. Personally, when I’m feeling up to it, there’s one or two songs on iTunes that I am incapable of not dancing to when I play them, so I dance around like an idiot for a while with the curtains closed. Or I like to play air violin to Tchaikovsky’s violin concerto, which if you’re doing it right is a good 15 minute workout!

“Alternative”: Bikram (“hot”) yoga

Alternative: Easy yoga

Yoga is great for people with CFS. All you need are some beginner’s resources — I like this video — and you will learn breathing techniques and a range of exercises you can use depending on how good a day you’re having, and you can do as much or as little as you want. The idea behind hot or Bikram yoga is one that is very attractive in CAM and especially with quacks: removing toxins from the body. Another ME/CFS forum I took one look at and left supported the idea of chelation, which is most often touted as a treatment for autism. Besides the fact that there’s not much need to worry about “flushing toxins,” the high temperatures at which Bikram yoga is practiced should be an automatic warning sign for people with CFS and many other illnesses that affect thermoregulation. Take five, 10, 15 minutes a day to do some yoga poses in your bedroom, but forget about the sweat. And on that note…

“Alternative”: Master Cleanse (and the like)

Alternative: Limited juice fast

The Master Cleanse and other detoxification programs also appeal to this fear that we are ill because we are full of toxins. They are a fairly useless strain on the body; you would do much better to simply eat right and drink a lot of water. That said, short (three-day) juice fasts including snacks of crackers and brown rice, after a doctor’s consultation, can have a certain psychological benefit, like breaking bad eating habits. But in general, our bodies are too stressed out as it is with all the windmills our immune systems are tilting at, and deliberately upsetting the balance by fasting instead of eating healthily just isn’t a great idea.

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Wii Fits into CFS exercise plan

Wii FitWii Fit is an exercise game in which you stand on a specially designed balance board and perform activities from four categories: Yoga, Strength Training, Balance Games, and Aerobics. As you play, you unlock new games and exercises as well as more options for the current ones. The game also keeps track of your weight goals and allows you to keep an exercise journal, including activities aside from Wii Fit.

There is a wealth of information about all the various aspects of Wii Fit, not to mention opinions galore on its use as an exercise device or supplement. This review will focus on the details that I believe are of most interest to people with CFS and similar physical limitations.

The short version

While there is controversy about Wii Fit’s role in exercise routines, as someone with CFS I recommend it heartily. While it won’t remove the possibility of post-exertional malaise, the wide variety of activities makes it possible for a patient to enjoy a fun, diverting workout while precisely controlling its time and intensity, and design routines to help avoid the malaise. If a walk around the block isn’t going to work for you today, maybe you can still take five minutes to avoid a slew of soccer balls being kicked at your head. Prior knowledge of yoga and strength training, while not required, will improve your experience. As long as you can muster the ability to laugh at yourself and your poor little Mii when you crash and burn on that ski jump — because you recognize the exercise benefits you’re getting even when you fail — this game is an excellent addition to a CFS gamer’s library.

The long version

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Exercising, my demons

When I think of how often I used to skip going to the gym because I was “too tired,” I want to go back in time and slap myself sane. But really, I enjoyed working out — for the most part — and was especially regular about it when I was also fencing three times a week and competing on some weekends.

Now I’m afraid to exercise.

Yes, this sounds ridiculous. Not wanting to work out is one thing, but why be afraid of it? One of the hallmarks of CFS is “post-exertional malaise,” which means that feeling like crap after exercising is both a helpful diagnostic symptom and also not fun in any way. Some evidence suggests that even graded exercise therapy, or GET, in which severely affected patients very slowly increase their daily activity, may do more harm than good. So how do CFS types get the daily exercise we need when said exercise can land us in bed for a day or more?

It’s a cruel catch-22, as well as one of those mind vs. body frustrations that many of us nerfed people, especially the new ones, share. Exercise is one of those things I never did halfway. I’d jump into a new routine and be happily unable to move for a week, instead of easing into it like intelligent people do. While I wasn’t compulsive, I wasn’t content if I wasn’t at least a little sore, and preferably more, after every workout.

The second-to-last time I started a serious workout and moderate diet plan, it was in preparation for a two-week-long marine biology study trip to Baja California. I worked out like you would not believe, and not only did I not lose any fat, my bad cholesterol actually went up. This is how I eventually found out I had Graves’ disease.

The last time I started a serious workout and moderate diet plan, right after I got engaged and was faced with the prospect of modeling a fancy dress for 120 people, I trained smart but hard, lost 20 pounds in six weeks, and felt sick all the time, especially after workouts. This is how I eventually found out I had CFS.

You might get a little gym-phobic too.

Totally worth it, though.

Totally worth it, though.

In all seriousness, I’m still in the process of accepting my new standards for exercise, which currently go like this: “10 minutes a day of doing practically nothing so what’s the point?” I need to stop thinking of working out as a luxury that will make me look hot if I stick with it, and start thinking of that piddly 10 minutes as equally necessary for my health as the elephant tranquilizers I take to sleep.

Some months ago, Paul brought home Wii Fit, Nintendo’s hugely popular exercise game. As I started to get into it, I realized that there are aspects of this system that work particularly well for people with CFS and similar illnesses where exercise causes problems. And then I thought “I wonder if any chronically ill gamers might want to read about these kinds of topics.” So you may feel free to blame Shigeru Miyamoto for the existence of this blog (as well as the demise of gaming, if that’s your thing).

Next week, I’ll review Wii Fit’s potential as an exercise system specifically for people who are averse to activity due to post-exertional malaise. Here’s a little preview: I think it’s dandy.

Thanks to everyone who has been kind enough to visit and comment on the blog, here or elsewhere. You’ve all been very encouraging, whether you meant to or not. If you’re struggling with the same kind of problems with CFS (or other illnesses) and exercise, and it won’t cost you any spoons, please share your experiences!

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