RETURN TO TABLE OF CONTENTS
By Ingebjorg Midsem Dahl
Authorís note: In England and
Scandinavia, the coping technique of pacing is taught to patients, while in
America, I feel the concept is often unused or misunderstood. Having used pacing
myself for years, Iíve been very pleased with how it has helped me and would
like to share what I have learned with other young people.
You wake up one morning, knowing it will be a good day. Remembering all the things you
were too ill
to do last week, you begin at the top of the list. Before evening, you are close to collapse, and you
spend the next two days in bed. On your next good day, the story repeats.
Does this sound familiar? Many persons with CFIDS (PWCs) push themselves all the time
to walk a little
farther or get just a little more done. Many of us do it in a desperate attempt to keep up with our friends,
but we just end up falling further behind them. We all know this frustrating roller coaster. However,
we have a technique called pacing that can flatten out the roller coaster. Pacing is not a cure, and it
isnít easy, but chances are it will improve your quality of life considerably.
Pacing is based on several principals:
- Listening to your body.
- Alternating rest and activity.
- Doing one thing at a time.
- Choosing low-energy activities.
- Using energy-saving devices.
Listening to your body
Most of us are familiar with the "I need to lie down
and other near-collapse sensations. If you think back, this feeling usually will have been precipitated
by at least one warning sign Ė for instance, an increase in symptoms. The trick is to stop your activity
at the first warning sign. Then after a period of rest you will be able to do something else. Looking
at symptoms as warning signs and not just a nuisance may seem weird at first, but when you get used to
it, it becomes a reflex and helps you keep your symptoms at a minimum level.
One Danish PWC described it this way: "My back begins to hurt after awhile when I sit
on a straight-backed
chair. Before, I would sit until the pain was so severe I had to lie down, and it would take a long time
before the pain went away. Now I lie down immediately when the pain begins. I have less pain, and I donít
have to rest for as long."
In the beginning, you may be unsure about how long you can perform an activity. The
first step is to
choose an activity you want to assess. I will use listening to music, as that is something most of us
can do. Now pick a time or level of activity. Will 15 minutes be too much, or could you manage 30? Say
we decide 15 minutes is enough, so after 15 minutes of listening to music, how do you feel? If you feel
fine, try the same amount of time tomorrow and reassess. If you feel worse, 15 minutes was too much. Try
just 10 minutes tomorrow. When you have found out how long you can listen to music without feeling worse
and have managed to do that every day for at least a week, you can try increasing the time. Try five minutes
more one day. If you feel worse, go back to your previous level, but if you feel fine, do it again tomorrow.
Donít increase the activity further until you can do it every day without getting worse. And donít go
beyond the time you set. That will just give you a relapse.
This method can be used for any activity. Write down how long you stay at each activity
every day and
how you feel afterward. This makes it easy to monitor progress. Donít forget that listening to your body
also involves willingness to cut down on activities when you feel worse. Itís better to cancel a bad day
and feel fine again the next than to have many bad days in a row.
Alternating activity and rest
When your body tells you to stop, you must
rest. Resting means
lying down with your eyes closed in a quiet place. Watching TV, reading and listening to music are activities.
Now as a young person, you might find resting boring. This is where alternating activity and rest becomes
important. Letís assume that you can mange an hour of activity every day. If you do that hour all at once,
you will be bored stiff for the next 10 hours, probably being really exhausted from the activity. Itís
much smarter to do 15 minutes of letter writing, 30 to 60 minutes of resting, 15 minutes of listening
to music, rest again, etc. This also gives you the opportunity to assess your energy level on an hour-to-hour
If you are severely ill, your activity periods will be short (perhaps five minutes)
and the rest periods
in between much longer. As you improve, the activity periods will get longer and the rest periods shorter.
Donít make the rest periods too short, and donít begin an activity before you feel up to it. Again, breaking
your limits is bound to catch up with you.
Doing one thing at a time
My activity level these days is quite high, but
I canít concentrate
on something as simple as writing a postcard while Iím listening to music. It seems that doing two things
at a time takes up twice as much energy. You will feel worse much faster. Instead, one should listen to
music, rest, and then write the postcard. Your energy is precious; if you spread it out evenly over a
day, you will enjoy it much more.
Choosing low-energy activities
This part will be hard for many of you, especially
were very active before your illness. You may no longer be able to participate in competitive sports,
but some activities can be continued with a little bit of imagination. I learned roller-skating by rolling
slowly a few meters down the parking lot, resting on a fence, then rolling a little again. I did skiing,
skating and swimming that way, too. Of course, I couldnít do it very often, I didnít get very good at
it, and I envied the other kids who could go on for much longer than I could, but I got to try the stuff
without severe relapses. Today, at 18, I can look back on 14 years of illness and say I didnít lose my
childhood, it was just different than others.
You might not have the self-control to stop such an activity before a collapse. You
may need to find
new hobbies and interests. Try to look at this as an opportunity to learn new things. Choose carefully,
though. Some crafts may take you so long to prepare that you are exhausted after five minutes into the
actual work. Itís better to find something that can be taken up and put down when you need to. If the
activities you choose are low-energy enough, you still will be able to do them on a smaller scale if you
You might like to do something more serious than a mere pastime. With a language course
on tape, you
can learn as little as a sentence a day. If you have trouble reading, books on tape are available, and
you might even be able to get a "tape friend" instead of a pen pal. Watching TV and videos for much of
the day can be tempting, but my own experiences with these are that they are powerful stimulants. You
donít use your body, but your mind, eyes and ears are constantly at work. And computer games involve the
body, too. By contrast, books on tape stimulate only one sense.
Using energy-saving devices
This is a highly individualized area. Try having
session with someone who knows you well and go through what you do each day, what kind of symptoms you
get from it, and how those things could be done differently. Remember that some devices may have drawbacks.
For instance, a hands-free phone will save your arms, but then you can talk much longer, and talking uses
The wheelchair is undoubtedly the most hated and most loved of all energy-saving devices.
a lot of courage to get it and use it, but those who have taken the step usually donít regret it. The
wheelchair saves energy because you donít have to walk. But donít use that saved energy on pushing the
chair yourself. Your arms will get just as tired as your legs. You must also remember that the vibrations
from the chair may bother you at first, and sitting up in itself requires energy. A mall or a school is
just as noisy in a wheelchair as on foot.
When you get a wheelchair for the first time, try sitting in it at home at first. Then
try a 10-minute
"walk" outside and assess as described earlier under "Listen to your body." Using a wheelchair has to
be built up slowly like all other activities.
Pacing your schooling
The topic of coping with school is so big it deserves
itís own article,
but the general concepts of pacing apply here, too. Generally, you have three choices when you have CFIDS:
- Home tutoring or homeschooling.
- Part-time attendance.
- Full-time attendance.
Some places, it will be possible to combine home tutoring with part-time attendance.
This would be
useful when you have been home for awhile and part-time school seems possible. No matter what you choose,
build up slowly. Begin at a level you are absolutely sure you can manage. Your school will be much more
pleased if you manage to increase your level of schooling rather than get worse and miss lessons. In my
experience, only a few school-age PWCs are able to go to school full time. Donít attempt this if you have
been away for awhile. It is better to go part time to begin with and build it up.
I hope Iíve been able to give you a few ideas about coping with CFIDS. I have had good
progress has been slow. Reports from England suggest that improvement will come faster the shorter you
have been ill, but itís never too late to begin using these coping techniques. Just be patient. Donít
force the tempo, and please, donít expect miracles. If nothing else, pacing improves quality of life by
flattening the course of the roller coaster and making it easier to plan ahead.
Ingebjorg Midsem Dahl, 18, was born
in Norway and now lives in Denmark. She fell ill with acute-onset CFIDS in 1983,
when she was 4. Today, after many years of non-attendance and part-time
attendance in school, she is able to go to school full time and hopes to become