Mostly, I
manage not to think about the future. The present is enough to be dealing with
so, although I do look forward with a kind of dread, most of the time I am so
caught up with dealing with what is happening now that I succeed in pushing
thoughts of the future to the margins.
That is,
until I start a new medication or course of treatment. At these times I find it
hard to stop myself imagining what it would be like to be better. I am aware
that this is not a useful activity, but it is difficult to avoid.
I did it
last year before I began the Perrin treatment. I tried not to, but the
therapist told me that he thought I would make a complete recovery in twelve to
eighteen months. I didn't take this claim at face value, but did begin to
expect something, some improvement,
some more energy.
Naturally,
when it didn't happen, I was disillusioned, brought low. I felt stupid for
letting myself hope, for believing - even for a short time - the therapist's
confidence in a recovery.
And now it
is happening again. I am in the process of having tests and then hopefully
getting treatment from the Breakspear clinic in the UK . I am particularly interested in
trying anti-viral treatments, which some people have had success with in the
past, and which I know Breakspear do offer.
Having to
rest so regularly, I have too much free time to think, and so my mind wanders.
And naturally it wanders from time to time to thoughts of a fuller life, what I
would do if I could, the dangerous territory of imagining being better, or
close to.
I begin to
think about full time work, about saving for a house of my own, about
travelling, getting a girlfriend. I start imagining a scenario where I am a
more or less fully functioning member of society, with realistic ambitions and
not such a compromised existence. I do try to squash these thoughts, but I
can't keep them out forever.
And I think
what I most dream about is less about a fuller life - which actually seems
almost impossible to believe in after fifteen years with this - and more about
losing this aforementioned dread of the future.
Because
without some kind of significant improvement I really don't like the picture of
my future that I see. In my early forties now, I am experiencing the first
symptoms of aging, without really having experienced my youth. My late twenties
and thirties were devoured by CFS/ME, and although I have regained a limited
amount of functioning, and do have at least half a life now, I can never get
those years back. I could probably handle my mid-life crisis better if I had
actually had a full first half of my life.
And so the
idea of getting into my late forties and fifties and still having to deal with
this, is terrifying. Still struggling with finances, with no pension, pushing
myself so I can work enough to pay rent, all the while getting older and with
the normal reduction in health and energy that aging brings. And I don't have
any energy to lose. At forty-one I am just about coping, I can't imagine how I
could when the years start taking their toll.
The thought
is so terrifying that normally I don't actually address it head on, though it
still hovers there at the back of my mind. So an improvement would mean a
fuller life, it would open up possibilities that are closed to me now. But it
would also give me back some kind of positivity about what is to come, and
might give me some hope that I still have a life left to live that is worth
something, rather than what I am doing now, which is mainly just surviving.
Yet hope
can be dangerous too. I have been through this quite a few times now. Starting
a new course of treatment, I begin to believe in the possibility of recovery.
And when it doesn't happen, as it invariably doesn't, picking myself up again
after hope has been smashed, is tough.
Without
hope it is impossible to go on. Yet with a chronic illness for which there are
no real reliable treatments, you have to manage this hope. Maintain scepticism,
never let yourself get carried away imagining a better future, while also
trying to avoid getting too overwhelmed by thoughts of never getting better.
It is a
delicate balancing act, balancing hope and dread, and not one that is always
easy.
Another very relatable post from you, I sometimes get too carried away with dreams for the future and often use the words 'when I'm better' but I have to remid myself to be realistic and not get too ahead of myself. It's important to have hope because without it we have given in, but I agree it can also be dangerous. I hope your new treatment has some benefits, let us know how you find it.
ReplyDeleteYes, it is a dilemma. You have to have hope to go on, to be able to get up in the morning, to stop you falling into a pit of despair. But also you need to control it, because there is nothing worse than having your hopes dashed, after you had started to believe that improvement was on the cards. I suppose realism is what is needed, though that is easier said than done.
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