Recovering
from Chronic Fatigue Syndrome:
A
Guide to Self-Empowerment
By William Collinge,
Ph.D.
Table of Contents
Audio CD Program
Chapter 12. Using
Your Illness as a Teacher
"I feel that I have discovered
and recovered a part of my self that had been lost."
-Blanche
People with CFS often
find that the syndrome directly challenges all that their lives have stood
for. Many have found that to make it through this existential crisis, they
have had to find a way to fit this illness into the overall fabric of a
meaningful life. In this chapter we will explore how former patients successfully
dealt with this aspect of CFS, and how in many ways their lives were deepened
and enriched through this experience.
In his book Man's
Search for Meaning, psychiatrist Viktor Frankl described how people
living in tremendous adversity fared better if they were able to find meaning
or purpose in their circumstances.1 Frankl was talking about prisoners
of Nazi concentration camps in World War II. Yet we now know that his observations
also apply to the adversity of a chronic or life-threatening illness. There
is a growing consensus that patients who maintain a sense of meaning or
purpose have better medical outcomes than those who do not.
The invitation
I would like to offer you in this final chapter is to see illness as a
catalyst for personal growth and expansion. In short, you can use your
illness as a teacher. If you do, then it is not just a cruel, random act
of nature, and you are not simply a helpless victim. You redefine your
passage through this illness as a journey of discovery, and you have resources
with which you can confront the challenge and achieve mastery over it.
Research in health psychology has shown us that people who take such a
"challenge" perspective are hardier and recover more quickly from illness.2
How Can Illness Be Beneficial?
Psychologists
have long been interested in what they call the secondary gains, or benefits,
of illness. There are two ways in which illness can be beneficial. One
is when it serves to rescue or remove us from unacceptable or unwanted
circumstances. The other is when it brings us unexpected insights or discoveries
which enrich our lives and advance our growth.
Usually discussions
about this subject focus on the role illness serves in helping the person
avoid unwanted circumstances. Consider, for example, the child who creates
a stomachache on the morning that he doesn't want to go to school, and
the stomachache disappears shortly after Mother gives her permission to
stay home.
In this case,
the illness was created by the person to manipulate a situation and achieve
certain benefits. However, one of the most painful things a person with
CFS can hear is the suggestion that they created the illness for some gain.
Granted, there are many cases where CFS has forced people to make lifestyle
changes that turned out to be very desirable, such as quitting a high stress
job or leaving a destructive relationship. Yet this illness is far too
complex to be something that can be created for such a purpose.
It is certainly
worthwhile to examine whether the illness is bringing relief from some
otherwise unacceptable circumstance. If this is the case, then you may
not be pursuing your recovery program with full commitment.
Our focus here,
however, is on the other kind of benefit-one which, for many patients,
has been totally unexpected yet greatly appreciated. CFS has served as
a teacher and an opportunity for personal growth. As you have no doubt
found, this disease can force you to re-evaluate your values, purposes,
and whole way of life. Various people have described this illness as a
wake-up call or a two-by-four over the head. Perhaps a more sophisticated
term is to call it a "pattern-interrupt." This is a term used by hypnotherapists
to describe something that interrupts or changes old, unconscious patterns
of living or acting, and makes room for something new and better to happen.
Below is an exercise
that you can use to discover what CFS may be able to teach you.
EXERCISE: DIALOGUE WITH ILLNESS
In this exercise
you will be having a dialogue not with your inner child, but with your
illness. To be more precise, the dialogue is between your wise, adult self,
and an inner voice that represents the illness. Set out two chairs or two
cushions on the floor. Let one seat represent your wise, adult self while
the other represents the illness.
In this process
you will be physically moving back and forth between the two seats. You
begin with a few minutes of silence to prepare your adult self to be completely
focused on the process.
When you feel
completely present, begin asking the questions below. Each time you ask
a question, you move to the other seat to respond as the illness. It is
important to actually move in order for the process to work.
When you ask
the questions, do so with an objective, casual attitude. You are simply
seeking objective information, much like a journalist might do. This is
not a confrontation or a healing process. If you have a disdainful attitude
toward the illness, its voice will not be as clear and it will not be as
forthcoming with information. Remember, all you want from this is information.
In giving your
voice over to the illness, it is important that you take your time to relax,
close your eyes, and go inside to find an intuitive sense of what the illness
might say. When you respond, try to imagine that you are the illness talking.
Respond as sincerely and honestly as you can.
Begin with the following questions:
1. What are you here to
teach me?
2. How well am I learning what I
need to learn from you?
3. How do I make it easy for you
to remain with me?
4. What will it take for you to
leave?
5. Is there anything else I should
know?
Spend as much time
as you need on each question until you feel satisfied that you understand
the answer. If you need to ask for clarification about a response, physically
move back and forth between the two seats so as not to blur the two voices
together. And each time an answer comes, be sure to thank the illness for
speaking to you and helping you understand it.
Always end the
dialogue in the adult seat, thanking the illness for being willing to share
its secrets with you.
The answers are
coming from your subconscious, which is intimately in touch with events
in your body. Use the questions as a point of departure to pursue anything
else the illness might be teaching you. This is a device you may use regularly,
perhaps each day, to monitor your progress.
The balance of
this chapter offers the insights of several former or current patients,
in what CFS has taught them about living. Though it may sound hard to believe
at first, there is a consensus here: The lessons learned are of such great
value that they were well worth the price.
Your Relationship with Yourself
CFS forces you
to change your relationship with yourself. One of the most common discoveries
is that we can actually pay attention and listen to ourselves much more
deeply than ever before. Some experience this as listening to inner guidance.
Others describe it as listening to the body, as trusting yourself, or as
accepting yourself. Consider Tina's story:
"Getting sick
was the best thing that ever happened to me. It was what it took for me
to really. . . make major changes. I don't think I would have done it otherwise.
My body just had to stop me. I wasn't paying enough attention to my life,
my stress, my job, and my unhappiness to do anything about it, until I
got so sick that I literally could not do anything and had to stop. After
that, everything changed.
"I've learned
that I always lose when I don't listen to myself, when I don't trust myself.
I just have to do things from my heart or my intuition. Otherwise things
just go wrong.
"There were signs
all along when I was getting sick and would spend four or five days in
bed. But I never trusted myself, I would always push myself. Part of me
was telling me that something was wrong, that I had to stop and do something,
but I didn't listen."
A similar experience
is reported by Christy, who states: "I am actually grateful that I got
sick, for what I have learned has been that valuable to me. It taught me
to slow down and listen to myself. It also taught me that I will never
work for money again, only for something I like to do. Money will come,
but my job will never run my life again. I will do things that bring me
joy."
A variation on
this theme is offered by Debbie, who discovered that trusting herself was
paramount in coping with CFS:
"What has helped
the most has been knowing that what I really feel and sense is true, that
I don't have to doubt myself, that what I feel is true for me I can trust.
I trust my own thoughts and perceptions. I don't have to live for someone
else, not to please twenty million other people, which never worked. I
can live my own life for me.
"The hardest
thing in coping with this illness was the self-doubt, doubting myself and
what I really feel-feeling sick and having other people telling me that
maybe I'm making it up.
"What l have learned is that I am
me, l can trust me, and I like myself."
Ginger's work
with this lesson includes listening to her body as a source of wisdom.
We have discussed earlier how symptoms are actually an intelligent effort
to restore balance on the part of the body:
"While the initial
lesson was learning patience, what I am learning now is to trust my own
instincts, my own reasoning and thoughts and insights. I am learning to
trust my body's responses to the environment, to irritants, pollutants.
I have learned to trust my gut reactions to things rather than the mental
processes.”
In all of these
cases there was a turning inward, and a receptivity toward what was being
heard or felt. The relationship with the self became one of being interested
in, and trusting, one's own inner experience of life more than before.
Another aspect
of this transformation is the obvious shift in attitudes toward self-care.
A high degree of vigilance needs to be developed which involves paying
attention to your needs on a moment-to-moment basis. Maintaining your sense
of balance or integrity becomes a real priority in daily living.
Mike describes
his experience as follows: "I take care of myself much better than I ever
used to, as far as what I eat and how much sleep I get. Even though I consider
myself well, I still have not increased my office hours. I still take two-hour
lunches and a day off during the week. I just figure that there are more
important things in life than money-such as my family, my health, and my
wife."
For Kris, developing
a new attitude toward self-care has also been an important outcome. "I
have learned that I can influence my health, and I do so very willingly.
In the long term, I can affect positively any illness I have. Begrudgingly,
I can say I am grateful this illness came now because I needed to learn
these lessons. I've had chances in the past and I haven't acted on them.
That's one way I've benefited."
As I discussed
in Chapter 11, one challenge with which many patients struggle is their
own inner resistance to change. Even though we know what is good for us
and what would promote recovery, it is still hard to follow through with
changes to old habits. Kris describes what it was like for her: "I've learned
to laugh at myself, at how stubborn I am. Because I REALLY AM STUBBORN.
And there's a little girl inside me who really doesn't want to change.
So we have a good laugh every now and then."
SELF-ACCEPTANCE
Tremendous strides
in self-acceptance are very common for people who have been through CFS.
The syndrome forces people to acknowledge and accept their vulnerability
and their limitations. In the process of doing so, there very often is
an overall shift toward greater self-acceptance. As Debbie states, "I feel
now that whoever I am and whatever state I am in, I'm okay, I love myself."
Self-acceptance
also involves acceptance of aspects of your self that were previously denied
or discounted, such as your wants and needs. Debbie had previously taken
an
attitude of self-denial, self-sacrifice, always putting others' wants and
needs before hers. This would happen not only in family life but with friends
as well. Her belief now is that "My wants and needs are valid, and I say
what they are. I may not always get it right now, but I no longer wait
for someone else to give me permission or encouragement to have what I
want or need."
REDISCOVERING YOURSELF
Much of the suffering
brought by CFS is on the mental or emotional level, as a result of having
to cope with the limitations on our ability to do things. It stands to
reason that to the degree that you define yourself by your actions, you
will suffer more.
Yet many are
learning that as this self-image as a "doer" changes, life goes on. They
discover that there are dimensions of life other than external accomplishments.
They learn that they are valued by others, and can value themselves, simply
for being who they are. Consider fur example Gail's perspective:
"The big revelation
for me was that I am not what I do. I discovered that it didn't matter
to my husband whether I could do anything or not. Even though I wasn't
doing a thing for anybody, there were still people around that loved me.
That was a new awakening for me, and that's really what brought me out
of the depression. I felt like I was a big zero, but other people were
seeing something in me that I couldn't see.”
"I began to think
that maybe there was something left, maybe I had something within me that
I could give. If people could see something in me deeper than my everyday
roles, there must be something there and I needed to look for it."
We are not the
roles we take on. We are not our careers. We are not our actions. We are
much greater and deeper than those external identities. CFS has forced
many people to rediscover who they are, and to become very clear about
the fact that they are not what they do.
According to
Gail, "I became aware that I had always been the rescuer, taking the responsibility
for everyone in the world on my shoulders. And I realized that I cannot
survive that way. It became evident to me that I needed to learn new skills,
such as how to just be 'simple,' how to be present, how to live in this
moment."
DISCOVERING YOUR DEEPER VALUES
Related to the
lessons about being versus doing is a more general re-examination of values
about living. This, naturally, brings different insights for different
people. Bernice offers us the following reflections:
"It's made me
more compassionate, more understanding. It's made me slow down and smell
the flowers, and get off the rat race and start looking at what's real
important in life. I think had I not gotten ill, I wouldn't be spending
as much time with my children. I'd be at work, and I wouldn't have learned
meditation."
For Kris it was
a simple message about living in the moment: "I've learned to pay more
attention to the present, and worry less about the past and future."
Debbie reports
shifts in several values: "I am now happy, and I don't even think I knew
what it was to be happy before . . . I’ve come to believe that what's most
important is the quality of relationships-honesty, truthfulness, communication.
I say exactly what I feel and what I want. Some people think I'm selfish,
but I'm just being honest."
And Gini reveals
a deeper reverence for life: "I've learned to cherish life a lot more than
I did before, with a lot less taking for granted. I cherish my husband
more too, our intimacy and our everyday life."
DISCOVERING INNER STRENGTH
After recovery,
people have often reported a new calmness, greater feeling of inner strength,
or new confidence in inner resources. Perhaps these changes come from having
plumbed the depths of despair and making the journey back to balance. Linda
offers her observation:
"If you survive
something like Chronic Fatigue Syndrome and don't commit suicide, you have
a greater inner strength than you ever had. It was like a trial by fire.
That's what I experienced.
"For me, that
inner strength came from seeing that life goes on and I didn't need to
do a whole lot to survive. Now that I have the energy to do anything I
want, I don't have to do all the mundane things that I thought I had to
do."
LOOKING WITHIN:
THE VALUE OF INTROSPECTION
One of the most
rewarding experiences for me in leading self-help retreats has been in
witnessing tremendous breakthroughs of self-discovery. People who would
never have had anything to do with introspection or personal growth become
genuinely interested in themselves for the first time. Some who would never
have considered meditation discover how nourishing and healing it can be
simply to become quiet and look within.
I have seen the
discoveries that have been precipitated by CFS truly transform people's
lives. For example, consider the results of Gail's search:
"I really went
on a treasure hunt of the things that I could do to make my life better.
First of all I had to look inside and see what was wrong in the first place.
One thing was my 'controlling' nature. I had always thought that I could
control other people. I thought that if they failed it was my fault.
"I thought my
mother's death was my fault. I thought if I had done something better,
she wouldn't have died. If I had taken better care of her. . . Realizing
that it wasn't my fault or my responsibility that she died was a major
step. She had told me many times that she was ready to go, and I didn't
want to hear it. Also, realizing that death is not a failure was a real
big one for me.
From Sarah's
perspective, a great deal of suppressed emotion was unearthed: "I'm finding
out that I have been walking around with a lot of angry and frightened
feelings for a long time that I simply haven't dealt with."
This theme is
repeated by Bernice, who states:
"I'm realizing
that the purpose of this disease is for me to go within, learn a lot more
about myself, and make some incredible changes in order to survive emotionally.
I realize that I came from a very dysfunctional background, that there
is a lot of learned fear and guilt that seem to be blocking the natural
healing energy within me.
"The lesson boils
down to my drowning in negative thinking, self-doubt, self-hatred, and
guilt all my life. The illness has forced me to realize it, and that those
are the very things that are preventing me from getting well. The healing
energy's there-I mean, if I cut my finger it heals. It's there, but I was
blocking it."
SPIRITUALITY
Times of adversity
inevitably bring people more in touch with the spiritual dimensions of
life. One result can be a change in the frequency or quality of prayer,
as noted by Mike in Chapter 6. This is supported by Gini, who tells us,
"I would say overall my spirituality is more alive. We pray on a daily
basis. I get the feeling that I can cope with whatever comes, like there
is somebody there who is stronger than I am."
It may also mean
a wholesale reappraisal of one's spiritual values and belief system. This
was the case for Gail, who says: "I had to really look at my religious
side and what I believed in. I found that it didn't work for me anymore.
And so I started searching for other things of a spiritual nature. I found
that meditation did work for me, going inside to find answers, relaxing,
quieting my mind, to find my higher self."
Or it may be
of a simpler impact, as described by Debbie.. "I am healing myself by getting
in touch with my true spirit." In all of these cases, the patients agreed
that the illness brought them to a greater recognition of the place of
spirituality in their lives.
Lessons in Relating to Others
As reflected
in Debbie's comments above, having a more accepting relationship with yourself
will affect your relationships with others. I have often heard former patients
point to a deeper sense of empathy or compassion for others, learning the
meaning of forgiveness, and learning to set boundaries in relationships.
EMPATHY AND COMPASSION
The mystics have
taught for thousands of years that suffering is a universal and unavoidable
human experience. Yet for many of us in modern times, it takes a chronic
illness such as CFS to give an experience of the depths of suffering. This
will inevitably lead us to a greater ability to empathize with others who
are in deep suffering.
A good example
of this is offered by Mike, who states: "In my own profession (physician)
I believe everything patients tell me now. I have more empathy. After experiencing
CFS, I know what it's like to have a chronic illness, so I think I'm probably
much more compassionate than I ever was before, and that has been a real
help for me in my work."
For Gini the
effect was felt in terms of being accepting and nonjudgmental of others:
"I've grown in my acceptance of people. I am more patient, and I'm a much
less critical person than I used to be."
FORGIVENESS
Many spiritual
traditions have taught that forgiveness is healing for the soul. Yet very
often we are unaware of resentments we are carrying, which can create an
undercurrent of stressful responses in the body. Most likely you have had
your share of abuse at the hands of uninformed or insensitive health-care
providers, and it would not be unexpected that some resentment is there.
Yet forgiveness can be empowering. ft helps us let go of the past. It frees
up vital energy that may have been going into festering resentments that
will never he resolved.
Bernice offers
this observation: "One thing that I'm working on now is forgiveness. I'm
having to forgive my husband, my mother, my brother, and all the doctors
who for four years told me I needed to go to a psychiatrist. I'm working
on that a lot, because I don't need to hold that hate inside."
Various rituals
can be used to release resentment. An example is to write down a list of
all the resentments you are still carrying from the past, going as far
back as you can. Then burn the paper and release the resentments from your
life as you see them go up in smoke.
SETTlNG BOUNDARIES
One of the more
crucial changes of lifestyle in the recovery from CFS is in setting boundaries.
As we shall see below, this issue is played out in many ways. Several aspects
of this are summarized in Bernice's statement that, "I've had to set limits
and boundaries. My kids have to know what those boundaries are, my friends
have to know that I'm ill and I can't make plans beyond today. I've had
to educate the people that are around me about my limitations."
It is an issue
that comes up within the home as well as with outside relationships. But
perhaps the most difficult place to set new boundaries is with family members,
where roles have been established for a long time.
Tina offers us
an example which would be a stiff test for most anyone, even without CFS:
"My daughter
(age seventeen) was very angry with me for not being able to manage things.
Even now, it makes her angry, because when I start getting symptoms I start
taking care of myself again, putting myself first again. This always affects
other people because they want my energy. My daughter had a tantrum, and
I simply chose not to respond.
"A few days later
she came to me and we had a beautiful talk because I had stood my ground,
and she finally accepted it. Standing my ground was good for her in that
she realized that I wouldn't always be there for her. That was difficult
for her at first because she had always counted on it. She realizes now
that she has to be responsible. The breakthrough is not so much that she
has more respect for me as that she realizes she isn't always going to
get what she wants from someone else."
We could assume
that this step toward emancipation for Tina's daughter would have come
sooner or later anyway. Yet it was precipitated by Tina's having to set
limits in order to care for herself. It reminds us that people, and perhaps
children especially, are often more resilient than we give them credit
for.
Another area
of boundary-setting is in what I call "toxic" relationships. Debbie found
that avoiding such contacts was a necessity for her in maintaining her
balance. She states:
"I simply try
to avoid anyone who is not an uplift for me. My brother and sister, and
my in-laws don't understand or accept CFS. So I just don't relate to them.
It's too stressful.
"Also my best
friend has marital problems, and I haven't spoken to her for months. It's
just too much when she wants to talk about her problems, and that's all
she wants to talk about. As much as I love her, and she knows this, I avoid
her because she's not good for me to be around now. I tell people why I'm
avoiding them, and they accept it." This was a gutsy position for Debbie
to take, but like Tina, she chose to stick with her boundaries and communicate
honestly about them.
Another perspective
is offered by Sarah, who was an activist for several years in the CFS patient
advocacy movement. After being heavily involved in the information and
referral network, as well as support groups, she reached a point where
she had to let it all go in order for her healing to progress.
"For almost two
years I didn't want to be involved on any level with anyone who had CFS.
I was well and it was upsetting for me to be around them, so I kept myself
pretty isolated from it. That was all part of my healing process. I needed
some distance from it.
"I've been back
working with the CFS people this year, but I'm coming back because I believe
it's important to stay active in the movement. It's true that I am sad
when I see people so ill, but it doesn't pull on me like it used to. I've
got my boundaries now, and I can leave it behind."
For many, the
lesson of boundaries is that old patterns of accommodation do not work.
As Debbie tells us, "I've learned to say no. Not that I'm a bitch, but
I used to be a doormat. Now I can say no when I need to-to my mother and
my family members, even my best friends." New ways of relating are needed,
based on honest communication about needs, energy levels, and willingness
or unwillingness to give to others. Many patients have discovered that
they must care for themselves first, even though this goes against their
old training to always defer to others.
Perhaps it is
good to reflect on this compelling insight about how your body keeps itself
alive: Your heart pumps blood to itself first.
Couplehood
The effects of
CFS on couples have ranged from devastation to transformation. Some relationships
do not survive intact, while others seem to flourish. Any couple experiencing
a chronic illness undergoes a test of commitment to the relationship. For
some the test is an easy one, while others are unable to sustain the stress.
For those who do hang in, the rewards are that the relationship is strengthened
for having been through the adversity together.
For example,
Mike and his wife come from a religious back-ground with a strong family
orientation. Through the struggle with CFS, they used some marital counseling
to improve their communication skills and ventilate feelings. In retrospect,
Mike stated "I think our relationship is much better than if I hadn't gone
through this. It's been a big blessing in disguise."
A similar experience
is reported by Gini, who states: "I believe it has strengthened our relationship.
He completely revamped his work situation to take care of me, and the result
was a lot more intimacy. He now says, 'What I have with you is five hundred
times more than I thought I would have in my life.'"
But others had
a rockier road before things smoothed out. Gail describes her experience
as follows:
"We fought when
I was first ill. When I didn't know what was wrong with me, I was angry
so I took it out on him. I made his life miserable. I threw him out a couple
times. I thought if he can't deal with this, I can't deal with it either.
"I was always
angry because I felt I had the responsibility to do everything. Now it's
different because I don't feel I have that responsibility.
"Our relationship
is now better than it ever was. We communicate a lot more. There's less
pushing for things to be done. My husband has learned a lot of patience.
The illness helped me to see him differently, too. When I found that I
didn't have to be the 'doer' all the time, and I allowed him to do things,
then I started seeing him in a different light.
"We're a lot
closer. He has said our marriage is one hundred percent better than it
was before. He learned that he could lose it, and it frightened him. He'd
never really thought about that."
On Being a Spouse
Being the spouse
of a person with CFS can have its own lessons, no less valuable. For Dick,
Bernice's husband, there was a period of painful soul-searching over several
years. "It got me in touch with what helping one another is really all
about," he says, "and that made me a lot deeper. I had to turn within to
answer a challenge as severe as this. There was no other way. And that
deepened our relationship.
"Either I had
to accept it and dedicate myself toward solving it, or give up. There are
a lot of people who give up~ I'll tell you what: I don't blame them. This
is the toughest thing I've ever had to deal with, and I don't even have
the disease."
Dick summarizes
his learning by saying, "It allowed me to deal with the real core issues.
I think we're basically here to learn about relationships, and learn about
loving one another."
Deidra, Mike's
wife, had a similar experience. The most difficult part of CFS for her
was handling Mike's personality changes, and especially coping with his
paranoia. "I learned the importance of patience, and having the willingness
to endure to the end. I learned tolerance.
"My religious
faith was very important. I developed a lot of faith that this was temporary,
and that I could live through it. It was clear to me that the situation
could either tear our relationship apart or strengthen it."
Now that her
husband is well (and jogging four or five miles several times a week),
she expresses gratitude that their marriage has continued at a deeper level
after CFS.
Acceptance of "What Is"
One of the ways
that we add to our suffering is in our nonacceptance of what is true now.
Our denial of the truth of our circumstances postpones our acceptance of,
and our working with, the present. Energy is consumed by our struggle to
hold on to the past, which is impossible and prevents us from living fully
now.
One consequence
of this for many people with CFS is depression. I refer here to the depression
that can arise as a result of our appraisal of our circumstances, not as
a result of the chemical changes from the disease process. The antidote
to this kind of depression is acceptance of what is true now, and letting
go of our fixed ideas from the past about how things should be. This is
illustrated beautifully by Debbie, who states:
"I don't get
depressed anymore. I used to, but I've learned acceptance. I accept that
I could be sick the rest of my life, and I have to just appreciate every
day, every moment. And I accept that a miracle could happen and I could
recover any day."
Another example
is offered by Bernice, who comes from a history of high achievement in
many areas of her life. "I have had to realize the fact that I cannot do
what I was doing before, owning my own business, running, and being an
active mother. I'm having to release that and be okay with what is so now,
which is very difficult.
"But I have surrendered
to the belief that it's my journey, and that I will come out of it a better
person. I try not to dwell on the past and who I was then. I just know
that I am becoming someone new."
Bernice and Debbie
are among the more severe, long-term cases I have known, each lasting several
years. They could easily have caved in to despair, seeing that their lives
are not going according to their dreams. Yet they have courageously chosen
another path.
Using CFS as
a teacher gives you the opportunity to make this a time of growth and self-discovery.
You may not have chosen this path of learning if given a choice, but you
will certainly benefit for the rest of your life from the lessons it brings
you, if you are open to them.
Audio CD Program
Available
Recovering from
CFS:
The Home Self-Empowerment
Program
For information about Dr. Collinge's
four-CD audio program of inspirational talks and guided self-healing
exercises that accompany this book, click here.
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