For all my friends, here and there, across the world. Thank you. Thank you
for your offers for help, for your encouraging words, your friendship, and
concern.
I know it's sounds a bit funny, but you know what is the strongest feeling
right now? Disappointment. I have told thousands of you, my friends, how much I
love my country, how grateful and proud I am to be a Finn. How privileged we
are, to be born in Finland. And especially, how well we are treated in our
public healthcare. And suddenly... I would still want to be proud to be a Finn. I love my
country, I love the nature, I love the honesty, the incorruptible integrity.
But it hurts to notice how this bureaucratic system can swallow thousands of
patients, and nobody cares. No, that's not true (maybe it is), but what I mean is, nobody
takes responsibility of the decisions Finnish bureaucratic system is so capable
of spit out every few seconds.
I'll tell you shortly what's happening here in Finland now. The M.D. taking
care of me and hundreds of other patients has been told by officials now that
he cannot have a private clinic anymore. Because it might be harmful. I mean.
Seriously? Not one single facts are given to proof that argument. Not one. Not
a single one. It just might possibly be harmful. End of story.
So, let's restrict the rights and punish also couple of thousand patients on
the way. No biggie.
You might or might not have heard about chronic fatigue syndrome (CFS/ME) at
some point in your life. It's a highly-disputed illness, some think it's
completely fake, some that it's a real thing. You know, most illnesses were
considered as rubbish at some point, and only after there has been a way to measure
or proof it exists, it exists in the minds of doctors - even if the patients
are aware of the fact way, way earlier.
This is now the case with CFS. I have several other rare illnesses too, that
doctors accept, and they believe that I am truly and honestly disabled and
chronically ill, and I have medical care for these illnesses. However, with the
CFS... Well. Here in Finland we are fallen badly behind in the medical
development and knowledge, and doctors tend to think CFS means that you are
nuts, faking, and lazy. There are no official treatments, no coherent
agreement, nothing. We have one doctor trying to fight for us, who has over the
years seen many patients and trying to help, participating to the international
research about the treatment of CFS. He has used medication and medical treatments
that are widely used internationally, harmless, with no proved or shown side
effects for patients. The problem now here in Finland seem to be, that
international research is not considered to be trustworthy here. So we have
quite a problem, a vicious circle, as there are patients having real symptoms,
and doctors not believing them because the symptoms cannot be proved with the
current measurements - as the specific tests are only now being found in
international research - and there is no official coherent consensus how to
treat patients either.
So, while this doctor was abroad last week, in the EU conference (as the
official, selected representative of Finland) trying to find consensus with the
doctors all over Europe, about the coherent medical care for CFS patients in
the European Union, our lovely officials decide that wow, by the way, we don't
like this. And announce that they take his rights to have a private reception
away. They don't care that patients are left without help, just like that. Most
of them won't get any help from public healthcare, as they are, after all, only
pretending to be sick, or, as the officials say: "in need on psychiatric
treatments". Oh, how wonderful, thank you.
The problem is, some of us patients have a medication that literally keeps
us living. Including me. I have, with the help of this one M.D., a medication
that ensures my body to accept the vital myasthenia gravis medicine without
which I'd have a myasthenical crisis in half an hour. Without this extra
medicine, I'll have a colinergic crisis in half an hour too. With both
medicines balancing my body, I'm just fine. So, I have a real crisis now. I
have contacted all the bureaucrats imaginable, and then some more, just to be
sure, and all of them agree on one thing. I cannot be punished like this, I'm
just a patient, and public healthcare system should take now full
responsibility of my care. And guess what happened? Public healthcare proudly
presents: they cannot help me, as the treatment is experimental and not
medically justified - without actually not even trying to find
out, what might be the justification or medical reasoning behind it.
So, I am, now in square A again. Let's do this all over again, from the beginning. As I am not
giving up. I won't lose hope. I want still to be proud if this country, not having to look for help from abroad. I want to still believe in justice, in kindness, in life. What I want is my life, that is now in danger because of some petty, small minded officials, because of money and because of jealousy. I want to live. I'm not that old you know, thirtysomething. I just won't accept I'd either die or continue my life in hospital tubes.
When I was crying for the first time because
of this (after some more really, really bad news, as I just have not the energy to tell you the whole dirty story), this one started to play on
my Spotify... So, even if I've quoted it before, I'll do it again. The Sunrise
Avenue, and Nothing Is Over. I want to believe that there's still time, that I'm not broken, that I'm brave. That nothing is over.
"Nothing Is Over"
Don’t turn away
There’s still time
A tiny moment
Don’t let go today
We can still shine
We are not broken
Scares to see that we are
A step a way
The one to take us
one way wrong way
Say nothing is over
Though everything’s crazy
Be brave and trust me
It’s not a game over
We gotta try harder
You gotta stay with me
There’s nothing we can’t reach
Cause nothing is over
I won’t turn away
Cause I can’t hide
The pain would find me
Don’t send me away
I’m on your side
That’s where I want to be
It seems to me that we are
Just like the rest
We could use a word of guidance
I hate to see that we are
One step away
The one to take us
One way wrong way
Say nothing is over
Though everything’s crazy
Be brave and trust me
It’s not a game over
We gotta try harder
You gotta stay with me
There’s nothing we can’t reach
Cause nothing is over
Say nothing is over
Though everything’s crazy
Be brave and trust me
It’s not a game over
We gotta try harder
You gotta stay with me
There’s nothing we can’t reach
Cause nothing is over
Nothing is over
There’s still time
A tiny moment
Don’t let go today
We can still shine
We are not broken
Scares to see that we are
A step a way
The one to take us
one way wrong way
Say nothing is over
Though everything’s crazy
Be brave and trust me
It’s not a game over
We gotta try harder
You gotta stay with me
There’s nothing we can’t reach
Cause nothing is over
I won’t turn away
Cause I can’t hide
The pain would find me
Don’t send me away
I’m on your side
That’s where I want to be
It seems to me that we are
Just like the rest
We could use a word of guidance
I hate to see that we are
One step away
The one to take us
One way wrong way
Say nothing is over
Though everything’s crazy
Be brave and trust me
It’s not a game over
We gotta try harder
You gotta stay with me
There’s nothing we can’t reach
Cause nothing is over
Say nothing is over
Though everything’s crazy
Be brave and trust me
It’s not a game over
We gotta try harder
You gotta stay with me
There’s nothing we can’t reach
Cause nothing is over
Nothing is over
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