Given the lack of scientific evidence, and the continued
confusion over the causes (and therefore possible cures) for CFS/ME, there is a
myriad of different approaches to CFS/ME management out there.
It seems that some of these approaches take great pride
in discounting other approaches, but the reality is that nobody knows what
causes CFS/ME, its symptoms are broad and varied, and each person’s experience
appears to differ. Until science has caught up with this illness, I honestly
don’t think we are in a position to discredit any source of potential relief,
and whilst there appears to be some bogus claims out there, I think it’s
important to analyse and weigh things up before you turn your shoulder to them.
In saying this, if you search online for CFS/ME
treatment, you will literally be bombarded with a million and one different
treatment options and claims. It is very easy to become disillusioned and
overwhelmed by this. It’s also very easy to become caught in the trap of
shelling out literally thousands and thousands of dollars on that treatment
that promises to take away your suffering.
I know, because I fell into that trap.
Ultimately however, I am able to share – with the grace
of hindsight – the two best steps that I took in my recovery thus far. I cannot
and will not say that they solely have led me this far in my recovery – nor can
I say that they will definitely assist you in your own recovery. In all
honesty, the level of recovery I have experienced to this point seems to have
just ‘happened’. And strangely enough, the two most helpful treatments are
those that I kind of ‘fell’ into, not really knowing what it meant for me and
the management/recovery from my CFS/ME symptoms.
My #1 DifferenceM@ker –
Therapy.
Before you think any further, I am 100% adamant and science shows that CFS/ME
is NOT A PSYCHOLOGICAL ILLNESS. That’s not what made the difference. But a
chronic illness seeps its way into every facet of your life, and it doesn’t
take long to be lost in the darkness and depths of anxiety, depression, and
suffering. I find it almost comical now, that my original reason for seeking
psychological services, was for assessment to see if I was ‘crazy’ and if I was
somehow making this all up in my head. I didn’t want to believe it, and I’d
surely read plenty of information that said it was not a psychological illness,
but the stigma and the reactions of people in my environment were contradicting
this very heavily. And I came to a point that I just needed to know. It’s
better to know your devil – whatever it may be. Here’s what I have gained
through engaging in therapy:
1. Validation. Finally, amidst all of my confusion, all
of my pain and suffering and fear, and with all of the controversy and at times
downright ignorance of other people in my life towards my situation, somebody
was able to stand by me and say “You are not crazy. This is real. And you are
suffering, and it’s ok.”
2. An Unconditional ‘Friend’. I use the word friend cautiously in this
sense as your therapist is not your friend in a usual sense, but I think it is
truly the best word to describe what can be obtained in the right therapeutic
relationship. In a time when I felt very isolated, very alone, and like the
world was against me, this one person was standing there – a foundation that I
could lean on in confidence that they would not turn their back on me. I can’t
even put into words what that meant for me, and what that provided me with. In
some of my saddest and darkest moments, that unwavering support was what kept
the embers burning – because it offered me hope.
3. Courage to Make a Change. I’m changing my life. It
has had to change. I can’t perform my old work anymore – and to be completely
honest – I’ve changed a lot since I became ill. I can’t live the way I used to,
because my health no longer allows me to abuse and take my life for granted. In
truth, I’m not sorry about that. Not now (although it has take a lot of work to
get to that point). You see, I feel like an entirely different person; my heart
has changed and so have my passions. Being able to sort through all of the
‘stuff’ – the emotions, the cognitions, the limiting beliefs, whatever else can
be lurking in the depths of your psyche – has granted me the grace to find out
more about who I am, what I want, and where I want to be. And this, along with
the support provided, has given me the courage to take steps that I was always
too scared to take, even if I somehow knew deep down I wanted to or should.
4. A Non-Biased Sounding Board. No personal motives, no
connection to the people or places involved. No gain or loss from the results.
A person whose pure purpose is to help YOU make the decisions and take the
actions that will create a better life for YOU. Don’t underestimate its power.
5. Gratitude. I know, it sounds completely ridiculous.
How could someone possibly be grateful for a chronic illness that almost
destroyed them physically, mentally, spiritually and emotionally? In my own
experience, it really has happened though. I didn’t have a ‘perfect’ life prior
to my illness. Sure it took a while (and numerous occasions where I felt like I
was being plagued by some form of mental illness), but eventually I was able to
cope a little more with the grief of having lost all I had and to actually say
“Well, why was it so wonderful? What was it that made it so great that I miss
it so much, and how can I recreate those bits that I love?”. [You may insert
the lightbulb moment here]. Ping! Light flicks on! Life wasn’t all that grand and
amazing – the pain is at having lost what I DID have – fair call. But then I
realized, that starting from scratch didn’t necessarily have to be a bad thing
either. Sure it’s not easy, and sometimes I just wish none of this ever
happened, but I was also presented with an opportunity to assess my life and
decide what I liked and what I didn’t like about it. I could find a way to
reestablish what I did like, and work on ways to improve or change what I
didn’t like. Perhaps its total measure will be of greater value than the total
measure of suffering I’ll have endured when I come out of the other end of this
illness.
You might say that you could achieve all of this on your
own – and you may very well be right. For me, I don’t think I could have gotten
as far as I have alone. At least not to the extent I have managed thus far.
Each to their own. But I maintain that, for me personally, the decision to seek
and continue therapy has been a very strong player on my team. Perhaps the
strongest. The fact that it has not directly made me physically better is of
little consideration. The fact that it has given me the emotional support to
cope is its true value. And that leaks into other areas of your life aswell.
Hang tight for My #2 DifferenceM@ker, coming soon.
Oh my gosh reading this post is like reading my own mind. So many of your points I totally relate to and are the same thoughts that I've been having/struggling with, It helps so much to read how someone in a very similar situation to me is dealing with these issues, not to mention that there is actually someone else with the same issues (not that I'm glad that you're sick but it's nice to know I'm not alone if you know what I mean). Can I ask what kind of therapist you saw? I don't know very much about the therapy world! Such a great post, thank you for finding my blog as it has led me to yours which I can tell from just this post is going to be very valuable for me. Looking forward to exploring your blog and reading more.
ReplyDeleteThank you so much for checking out my blog! I'm so glad that my post has rung true for you and I hope it helps you in some way in your journey to wellness :) As I was having some issues with sending a response here in my blog, I did send you an email with the information you were asking about, but I wanted to answer here aswell, just in case someone else wanted to see it. The type of therapist I see is a Clinical Psychologist who specialises in chronic illness. I was able to locate them by searching Google for "Psychologist chronic illness" in my area. Best of luck in your searches!
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