The Psychological impact of Fibromyalgia and Chronic Fatigue Syndrome: Coping strategies

-- End Ad Box --->Becoming chronically ill is very much like a
I suffered from Fibromyalgia and Chronic Fatiguebereavement. The losses and emotions involved
for 4 years before reaching a point where I amare very similar. Giving up works means not only
90% better than I was at the beginning of thethat you lose income but you also lose status,
illness.friendship and a purposeful role in life.
I will say from the outset that I believe this is oneFibromyalgia and Chronic Fatigue Syndrome
of the worst afflictions that can strike anyencompass the full range of human emotions and
person, at any age and at anytime.magnify the negative ones ten-fold.
Not only is it so debilitating that it now has theThis disease really is a monster. The usual
same disability rating assigned to heart diseaseresponse is to want to hide away from the world.
patients, but at the same time you have to dealHowever, confronting these emotions can be
with negative connotations that surround it.very important as part of your psychological
Even the name doesn’t sound credible,rehabilitation which should be addressed in
"Chronic Fatigue Syndrome", "what is that like aconjunction with the manual therapy discussed
bad hangover or something" people will say. At alater.
time when you need the most support in yourThis really is an area where a healthy mind can
life, often, people are turning their backs andassist a healthy body towards better recovery.
walking away or muttering under their breath. It isThe pain that comes with Fibromyalgia and
a frightful condition.Chronic Fatigue Syndrome can be frightening and
This will be a pivotal point in your life. You will findthis in itself can cause fear, loneliness, isolation,
that during the course of your illness you will findpanic and anxiety.
out who your real friends are, and who reallyFibromyalgia and Chronic Fatigue Syndrome can
cares.create a fear of rejection by others even when
There is no point disguising the reality which is,there is no evidence of this happening. I mean,
I’m afraid to say, that you will lose a lot ofwho wants to be around someone who is like
friends and colleagues along the way to thethis, we say to ourselves.
monster that is Fibromyalgia and CFS.Again this is a normal reaction, our self esteem is
It is NOT possible to explain this condition tobased on what others think of us, and usually that
people who have no experience of it either byis based on what we “do” or “how we
having suffered, or through having a particularplay” , or “what we say”, generally how
medical interest in the area. They WILL NOTwe interact with other people. As we take to
understand what, or to what extent, you are“doing less”, “playing” less and generally
suffering. Again, I’m afraid this is the norm.interacting “saying” less, then our self
Accept it as such and you will not then beesteem plummets along with our health.
personally offended by acts of prejudice. EasierWe are worried about the future; the dark
said than done I know. Let us examine a commonshadow of uncertainty is round every corner. Will
sequence of events which may ring a bell withI ever get better? What if I don’t? How
sufferers, to understand the prejudice from anlong is this going to go on? We ask these
outsider perspective.questions every day. We begin to experience life
You had a viral/ bacterial/ chemical exposure ofin a shadow land. Our hopes and dreams have
unknown etiology, the same as happens to millionsbeen shattered and the road ahead can be bleak
of people throughout America every day, and forand never ending.
some reason that no-one can explain to you, youAnger is very common emotion - Why me? -
have felt generally ill and exhausted with multipleWhy now? — What have I ever done to
symptoms and multi-systemic involvement everdeserve this? Unfortunately this anger alienates
since. Your doctor appears cynical andthose we love even more.
can’t give you an adequate diagnosis soYou will find supportive people, often, and
you may by now have been referred to aencouragingly the last people you would expect.
psychologist for analysis as a suspectedThose who are supportive are often people, or
depressive incident. “hmmm okay” you hearthose close to them, who have experienced
them mutter.serious illness and are living with it, or have come
Ask yourself this question.through it.
If you had no knowledge about Fibromyalgia andOr, those who have experienced Fibromyalgia and
CFS what would your reaction be to someoneChronic Fatigue Syndrome or have someone
else developing these symptoms?............ You see?close to them who has it. These are the people
Its human nature, it’s cruel isn’t it?you should aim to spend your limited energy
So how do we as sufferers cope and rationalizeresources building relationships with for the
what is happening.moment.
Knowledge is power. Educate yourself about yourDo not feel bitter towards people who you lose
condition.at this stage, hold on while you can then just let
Concentrate on yourself and try not to dwellthem go lightly, they are not your problem.
morbidly over the people that you have lostFibromyalgia and Chronic Fatigue Syndrome IS
already. Those that do not stand by you, andyour problem, and fighting it hard is your duty to
there will be some, are what we termyourself, to get your health back, for you and
fair-weather friends, usually activity based theyyour loved ones. You are going to need the
were your friends due to your common interestenergy you have left for this fight.
in a certain activity, be it sport/ work etc.I do advocate counseling and support groups. You
The activity has gone due to your illness,will need to find someone who has specific
therefore by association so does the friendship,knowledge about the emotional effects of
this is okay because we are going to get you toFibromyalgia and Chronic Fatigue, again a good
a stage where you can resume the activity, youdoctor should be able to put you on the right
can forgive those “acquaintances” if youpath, there are also Fibromyalgia and CFS support
wish and resume the activity with them, you willgroups based in most cities and towns across the
also be wiser and more aware of “the type”US.
of friendship you have with this person.Once you have found a good support group you
What goes around come around and what iswill also find good counseling.
going around is that you are going to get better!!However, the majority of cases will NOT need to
There is a small consolation that I allow myself,see a psychologist unless you are being referred
and this is the level of self-knowledge and wisdomfor Cognitive Behavioural Therapy, as your illness
that you will gain from this painful journey.is NOT depression, and therefore you should not
It’s a small consolation I know and I hearaccept anti-depressants, with the exception of
most of you screaming, “it’s wisdompossibly low dose amitriptyline if your symptoms
and knowledge I could well do without”, but it isinclude severe nervous pain and sleep disturbance.
there and when you do come out the other sideHowever I cannot personally vouch for this but
in the following weeks and months what youthere is enough evidence to suggest is a valid
have been through will make you ten times thetreatment.
person you were before.Mental and emotional preparation, knowledge of
You have plumbed the depths of pain and despairyour condition, and the correct course of
and in the future you will be scaling the heights. Iftreatment are all essential and work symbiotically
you come through this nothing in life will phaseto assist your recovery.
you again. You will value the simple things in life.In my next article I will explain new research
You will live every day. You will scoff at thewhich is allowing us to determine how genetic and
vanities and selfishness of our systems andbiomechanical anomalies, predispose certain
culture.individuals to attacks of Fibromyalgia and Chronic
Fibromyalgia and CFS will create emotional havocFatigue Syndrome.
for you and for your loved ones. This is normal.