The question of the fundamental cause of ME/CFS is an intriguing one. It's one that I
find fascinating, mostly because it effects me personally, but also as it is
something that medicine largely seems to have no answer for. It's like a
puzzle, an intellectual challenge. I am only surprised that more scientists
haven't shown more of an interest in working out the enigma.
From what we know, and from our experience, the immune system certainly
seems to be implicated, but in my own case my symptoms appear to be more
closely tied to dysautonomia. Dysautonomia is simply a malfunction of the
autonomic nervous system, and something that most people with ME/CFS have, in
one form or another.
The next question, of course, is What is the autonomic nervous system?
The autonomic nervous system (ANS) is the system in our bodies that controls anything
that is not conscious on our part. This includes heart rate, blood pressure,
digestion, saliva production, breathing, sweating and temperature control. It's
what happens automatically when we're doing something else. It's supposed to
run like clockwork.
Most people with ME will recognise the above list, as they are all areas
people suffer with. Personally I have problems - like most PWME - with regulation
of blood pressure, I can't stand for long periods and feel drained if I have
to, and being upright at all can be tiring.
I don't really sweat, even in my sauna at 50 degrees Celsius, I have had
problems regulating temperature, I have low saliva production, some digestion
problems, sometimes a tight chest, and a heart that occasionally pounds or
beats too fast. This is all related to the autonomic nervous system.
I recently discovered the website of a group called Dysautonomia International, which represents people from a wide range of conditions that all
suffer from elements of this problem with the nervous system. It makes
reference to POTS (Postural Orthostatic Tachycardia Syndrome), which a lot of
people with CFS/ME experience, as a
difficulty staying upright or standing, and a tendency to faint.
There is a certain amount of research being done on this area among scientists,
and I know that in Breakspear, the clinic just outside London
They do what they call an Baseline Autonomic Index. To do this they
attach sensors to the chest, stomach and heart, and clips on the fingers to
measure the blood gases, and also put a band around the chest. And they measure
heart rate and pulse, as well as the levels of oxygen (O2) and carbon dioxide
(CO2) in the blood, blood pressure and breaths per minute.
Also part of the test is a challenge to the central nervous system. In
my case the doctor asked me to take six very deep breaths, one after another.
Even though I was lying down I felt quite light headed quite quickly. This, he
said, was due to a lack of CO2, which he could measure from the sensors. To
counter this he gave me a rebreathing mask, which I have written about before.
The mask is worn basically to correct the lack of CO2 in the body. This
in turn is supposed to help the levels of O2, which are necessary for producing
energy in each cell in the body.
Another one of the therapies that I have been looking at recently is
called Somatic Experience therapy. A friend of mine - also with ME - has had good results from it, she says. It
aims to engage the parasympathetic nervous system (PNS) - the so-called
"Rest and digest" part of the nervous system - and to turn down the
sympathetic nervous system (SNS) which manages the "fight or flight"
impulse. The difference can be seen here. The SNS is for emergency situations, though what happens in CFS sometimes, is
that people get stuck in the "fight or flight" mode long term, thus
causing many of the symptoms common to dysautonomia and also to ME.
It is something
I may try in the future. Another thing on my list is H.O.T. This stands for
Home Orthostatic Training. It was developed, as far as I know, by Professor
Julia Newton, in Newcastle
University
The training is
quite simple. The patient stands against a wall, with their feet 15cm from the
bottom of the wall, and their head leaning against the wall. This creates a
kind of tilt. The idea is to do this for thirty minutes, though the vast
majority of people with ME will have to build up to this period of time slowly.
I can imagine starting at 30 seconds, and increasing from there.
It is important
to say that for people with ME/CFS - and especially for those who are more
effected - this may not be possible, and may induce a faint, so should only be
done with caution and probably with someone else there. They also advise that
you discuss this with your doctor, and also have cushions around you in case
you do pass out.
The general idea
of HOT is to retrain the body to tolerate being upright, standing, maintaining
blood pressure. I have actually been in touch with Professor Newton, I emailed
her and she kindly responded within a few days. She says that for those who can
tolerate the therapy, they have got good results with improvement in energy and
greater tolerance of being upright. There is info on a preliminary study here.
Again we can see
that it is about retraining or resetting the autonomic nervous system. It is
about correcting what has gone out of balance, getting the ANS to behave as it
should.
This is the key, I think, resetting
the autonomic nervous system. This is what these therapies do, and what I feel I really need.
It makes me think of my laptop, which at times begins to malfunction. Processes
like opening a file or playing a video, that are normally almost instantaneous,
become slow and sluggish. The connection to the internet drops, or it refuses
to sleep when I close the top, or it doesn't recognise my printer when I
connect it.
Whenever this happens, my first instinct is, naturally, to reboot it.
Turn it off and turn it on again. Invariably, this simple action improves or
resolves the problem. More often than not my laptop is working perfectly again
after a chance to reset itself and start again, its central nervous system now
in synch.
And that's what I wish someone could do for me, I feel that I need to be
rebooted. I need to be switched off, and then switched back on again, to be
able to reset. I feel profoundly out of synch, out of rhythm, unbalanced. I am
sleepy during the day and sometimes can't sleep at night, my energy runs out
way way before it should do, I can stand for a few minutes but then feel the
blood draining from my head and brain, and lose basic functionality. I am stuck
in this malfunctioning rhythm where things just don't quite work as they
should, and where everything is slow and sluggish and out of phase.
And all of these approaches, the rebreathing mask, SE therapy and HOT -
as well, no doubt, as many others - seek to help this rebooting process. They
may or may not work for me, though I intend to try them all, but somewhere here
I am convinced is a key to what has gone so wrong with my autonomic nervous
system.
There is a running joke from the British Channel 4 sit-com, The IT
