What Works for
Managing CFIDS and Fibromyalgia
8:
Minimizing Relapses
By Bruce Campbell
Relapses, sometimes
called setbacks or flares, are an inevitable and often demoralizing part
of chronic illness. This final article in the series presents coping
strategies used by participants in our self-help
course to reduce the frequency and severity of setbacks.
We will look first
at techniques people use to prevent relapses, then at strategies for
limiting their impact.
Preventing
Relapses
Students describe
using ten strategies for preventing relapses.
1) Making Mental
Adjustments
Many of the coping
techniques in this section involve new habits and behaviors, but their
foundation seems to lie in having new expectations for oneself based on
acceptance of the limits imposed by illness.
“It has been
important for me to accept my new life with CFS, move on, and realize
I will not return to my former self. I've needed to redefine
expectations of myself based on the new me. Lowering my standards and
trying to break free from perfectionism has been a large part of
this.”
“I’ve
decided it's all right to take care of myself for a change, just like
I would take care of someone else.”
“I have
accepted that I will probably never fully recover and in acknowledging
that I am discovering better ways to co-habitat with the illnesses.”
2) Pacing
Pacing is a favorite
strategy for bringing stability to life and preventing setbacks. As
shown in the following quotes, pacing involves a variety of strategies,
such as reducing activity, shifting among different activities, having
short activity periods and living according to a schedule.
“I've cut
back my activity level substantially overall, and when I feel tired I
cut it back even more.”
“I do
stressful things like taxes in small bites. Just letting them pile up
just adds more stress.”
“Allowing
myself plenty of time between activities scheduled for the day and
scheduling the correct number of activities daily are two ways I
prevent relapses.”
“What helps
me is to have a balance of physical and mental activities,
interspersed with frequent rests. I have recently introduced a
checklist system to remind me about activities that are good for me
such as walking, exercises, relaxing and hobbies.”
“It
definitely helps me to make a list of weekly and daily activities so
that I can prioritize them. I know how much physical activity I can
handle in a day, so I remember this and make my list accordingly. I
always allow at least an hour's rest in the afternoon so this is a
given on my daily list.”
3) Rest
Rest can be used on
a regular basis to prevent relapses. Extra rest can help avoid setbacks
when there are special events or a secondary illness.
“I think my
two daily fifteen-minute rests were the most important thing I did to
aid my recovery.”
“I can never
get enough rest! The more I'm able to incorporate quality rest, even
little bits and pieces, into my day, the better off I am.”
“I plan ahead
for events requiring extra energy, such as appointments, shopping,
socializing and holidays. I rest beforehand, during (if possible) and
after.”
“Two of my
rules are to take extra rests before special events and to take extra
care when recovering from secondary illness.”
4) Control
Stress
CFIDS and
fibromyalgia are very stress-sensitive, so minimizing stress can prevent
relapses.
“I attempt to
avoid all situations that will produce stress because stress
inevitably triggers relapses. This includes avoiding contact with
people who naturally trigger stress in me.”
“I try very
hard to eliminate stress because I seem to react so strongly to even
small stress levels now. Eliminating or drastically reducing stress
seems to be a necessary thing for me right now.”
“Stress of
any sort is really tough on me. I minimize stress by avoiding some
situations and by decreasing my stress response to those situations I
can't prevent.”
5) Honor the
Body’s Signals
There is a strong
temptation to respond to the onset of symptoms by “pushing through.”
As suggested in the following quotes, listening to the body’s signals
at such times can prevent symptoms.
“I have
become more aware of the warning signals that my body sends me when I
am doing too much and I am learning to stop as soon as symptoms appear
- even if it’s just lying down for a few minutes.”
“I've learned
the signs of going too far and have a good idea of how and when to
back off to prevent a big relapse. I consider that a huge improvement
compared to how I started out.”
6) Take Care of
Secondary Illnesses
Having other health
problems besides CFIDS and fibromyalgia can make symptoms worse.
Treating other conditions and acknowledging that they intensify symptoms
can be helpful.
“I've learned
that I have to lower my expectations and level of activity when I have
extra illness, so as not to make this unavoidable relapse worse and
last longer.”
“I realized
through the course that I have about four or five different health
problems. I need to get treatment for the others, as well as taking
care of my CFIDS.”
7) Be
Assertive
Standing up for
oneself can help you meet your needs, reduce stress and thereby prevent
relapses.
“Communicating
clearly when I need medicine, rest, or quiet time and taking time for
these things when I need them help me to prevent a relapse.”
“It is
extremely important for me to communicate my needs and limits to
others. I find that my true friends will accept this and often will
remind me about resting or stopping what we are doing.”
“I’ve come
to accept that it is okay to say "no". I can avoid people
and situations that upset me.”
“I’m OK if
I stick to my routine. But if I go off it very much, I pay for it. One
new rule I have developed for myself is no overnight guests.”
8) Solitude
Time alone can
reduce stress and allow for recharging of batteries.
“Solitude
helps me balance everything out. I have found it to be as necessary
and fulfilling as resting . I get to know myself, tune into how I'm
doing, and listen to what my body is telling me I need at that
time.”
9) Making Time
for Pleasure
Chronic illness
often means pain and frustration. Having pleasurable activities helps to
reduce frustration and thereby makes it easier to live within limits.
“I try to do
plenty of fun things, in small bites, to keep the endorphins
flowing.”
“I must make
time for fun or pleasurable activities. This is crucial to my feeling
good. Nurturing my creative side, for this brings me great pleasure
and validation within myself. Enjoy the beauty of nature, for there is
so much around me.”
10) Identifying
Relapse Causes
Last, relapses can
be prevented by identifying and avoiding their causes.
“I’ve
identified three main causes of my relapses: not pacing myself,
secondary illnesses and stress.”
“I’ve tried
to identify precipitating factors and them eliminate them by using
problem solving, communication, assertiveness, relaxation techniques,
movement/exercise, tending to my asthma and allergies, making myself
as comfortable as possible.”
Limiting Severity
of Setbacks
Students in our
groups report using the following five strategies for reducing the
severity and duration of setbacks.
1) Take Extra
Rest
The most common
strategy for overcoming setbacks is to take extra rest, continuing it
until the flare subsides.
“When
relapses occur, for whatever reason, I tell myself just to go with
what my body is telling me to do...rest! If I have some things planned
for that day, I try to tell myself that it will wait for another
time.”
“One of my
rules for living with CFIDS is: if all else fails, go to bed. This
rule gives me permission to acknowledge that at times I am powerless
over the disease and the smartest thing I can do is to give in to
it.”
2) Act
Immediately
You may be able to
reduce the impact of relapses by taking action as soon as symptoms
begin.
“I can
curtail the severity of flare-ups by reacting immediately. As soon as
I begin to feel edgy, nauseous or tired or have muscle pain (all
indicators that a relapse is imminent), I stop whatever I'm doing, go
to my bedroom, draw the blinds and lie down. That action alone makes
me begin to feel better. Then I practice deep breathing to clear my
mind. This relaxation period can take from 45 minutes to over two
hours. Usually, I arise refreshed and energetic, and can resume all
normal activities.”
3) Postpone,
Delegate or Eliminate Tasks
Reducing activity by
postponing tasks, asking for help or even letting go of something as
unnecessary can help speed the end of a setback.
“Asking for
help if I can not do it all or just letting go of the less important
things that I am unable to do at the time helps me reduce stress and
my setbacks.”
“On relapse
occasions I am not so hesitant, as I once was, to ask for help with
either daily chores or whatever comes my way. I know my family wants
to help me and it makes them feel good that they give me a hand.”
4) Seek
Consolation and Support
Students report
being helped by saying consoling words to themselves and by making
contact with other people.
“If I find
myself in a flare-up I tell myself ‘this will pass’. That helps me
relax and quiets the inner voices that say I’ll never get better.”
“When I’m
in a crash, I try to reach out for support. It's much harder to be
alone when I'm crashed, so I find a friendly voice on the phone for
comfort. Also, I try to remember that things always return to some
level of tolerable, and that there is always the possibility for
positive change.”
“I have found
it very useful to talk with another person when I’m in the middle of
a crash, and often it doesn't matter what we talk about. Just feeling
connected to something beyond myself helps lift my spirits.”
5) Prepare
Having things handy
and in place can help reduce the anxiety of a crash and make it easier
to weather it.
“One thing
that has helped me is to plan for a flare-up. I try to keep
‘extra’ of everything in the house, including food that my family
can cook. Also, I changed my room around and added a book case next to
my bed with things I can use if I'm stuck in bed. I have our family
finances, my writing and my books. It gives me a lot of peace of mind
knowing I'm ready when one hits.”
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