7th November 2005
Dear Dr Stuttaford,
Thank you very much for asking me about the side effects of all the drugs
I have been given for paranoid schizophrenia. It is with a strange pleasure
that I can tell the horrible truth about what the NHS put me through from
1994-2004. Many before me, I believe, have endured or succumbed to the type
of misery I describe attached. My experience in the last 18 months gives me
hope that less will suffer in the future like I did during those years, though
I must say I am mindful of the possibility that test animals have suffered
greatly from psychiatric drugs.
I feel I should say that my psychiatrist says there is an illness called “post-psychotic
depression”. It would be unsurprising if somebody felt low after coming out
of a psychotic episode. However based on my experience alone I would have
to question if there really is such a thing as clinical post-psychotic depression
rather than clinical depression caused purely as a side effect of the drugs
forced into the patient by the NHS.
Why do I say this? Well you see on the one occasion when made to take an antipsychotic
which did not list depression as a side effect and, whilst still in hospital
having that changed to another drug which also did not list depression as
a side effect, I found I was released from hospital not suffering from depression!
I do not believe my experience is unique and therefore I am forced to suspect
that since the introduction of chlorpromazine, a drug derived I am told from
an insecticide, many patients diagnosed with schizophrenia have been tortured
to the point of taking their own lives, not because of their illness, but
because of the treatment they received for it. Having not given up the ghost,
a ghost I have a duty to, I feel I am a very good witness as almost without
exception I enjoyed the illness I have been diagnosed with.
When I was ill I indulged in the delusion that I was a member of the British
special forces, the Special Boat Service in fact. The only truth in this delusion
was that I had been in the Naval section of the school CCF and stroked the
school 1st VIII to victory over the GB National lightweight VIII in a practice
sprint at Henley Royal Regatta one year. This delusion actually helped me
to keep going as it enabled me to think that the torture was part of my training!
Others may not, I feel sure, have been lucky enough to have had such a protection
mechanism. It seems to me that there are people buried all over the country
and indeed the world who were driven to suicide not by their illness but by
the treatment for it. I believe this to be a national and international scandal.
Might I illustrate the extent of this scandal by telling you of two ladies
I met in hospital? I feel the GMC and Police are desensitised to the appeals
of psychiatric patients though I suspect neither of the two I refer to called
them like I did on many occasions. They were both lovely people and grew up
together on the same street where they played together as children.
One day, on the ward, one of them asked to be on one-to-one. Diagnoses can
be wrong, but I had seen the same look in her face as I had when I was suffering
the effects of, e.g. Depixol. She was refused one-to-one treatment. Does not
the fact that she asked say something? Later the psychiatrist called all the
patients on the ward into the smoking room and explained that she had just
hanged herself in her room and that it was “nobody’s fault”. Just what happens
at these inquests when it is “nobody’s fault”. Has any coroner ever said “The
deceased was driven to suicide by drugs they found totally intolerable to
take”? I don’t think so. I feel the psychiatrist was responsible for her death.
But what is the point of complaining, except to The Times’ medical doctor?
You see I hardly suspect he’s any worse than any other psychiatrist, though
at least Professor Liddle read my book and told me something I should have
been told the very first time I was sectioned, 11 years ago, namely the recovery
statistic. Before that nobody had ever told me anyone did recover (to the
point of requiring no medication). In fact, and I don’t like to say this,
but one psychiatrist I was treated by did not have a perfect grasp of English
and what sort of prospect of good treatment did that entail?
Is it any surprise that her friend since childhood took a fatal overdose a
year later? No doubt, I feel, the coroner smoothed over that just like he
had done with the death of any other psychiatric patient.
Yours sincerely
Dr Clive H.Travis
P.S.Thanks for your interest in my book. I shall send you a copy when it is
published.
P.P.S. Please be under no illusions as to how extremely hard I had to be to
survive this treatment below. But then how hard does somebody have to be to
commit suicide?
List of adverse reactions, though not comprehensive
September-November 1994
Chlorpromazine. Suicidal clinical depression. Inability to concentrate.
Nasty akathisia. Painful retroejaculation. Loss of appetite. Numbness in the
arms on waking. I was left in no doubt that this drug had driven many to suicide.
All the side-effects, including the depression went when I myself stopped
the treatment.
January- February 1996
Clopixol. Suicidal clinical depression. Inability to concentrate. Inability
to have sex. Loss of appetite. Numbness in the arms on waking. Strange effects
to the muscles around my eyes related, I believe, to ocular gyric crisis.
I was left in no doubt that this drug had driven many to suicide.
February-August 1996
My memory of this time (when I was out of hospital) is of three drugs though
I am not sure if they are actually just one or two drugs. They were Thioridazine,
Droperidol and Melleril. I recall no distinction between them
only endless months of nasty restlessness (akathisia), inability to concentrate
or have sex and suicidal clinical depression with loss of appetite. I also
recall numbness in my arms on waking. I was left in no doubt that these drugs
had driven many to suicide. I find it hard to believe I took them all voluntarily.
All the side-effects, including the depression went when I myself stopped
the treatment.
January- February 1999
Clopixol. An absolutely terrifying experience to have this drug forced
into me again. I begged and begged not to be given the injection knowing what
it was going to do to me. I was prescribed Olanzapine at the same time but
spat the drug out secretly every time for a whole month. As well as the same
side-effects as before I found that the Clopixol made me speechless by, I
think, paralysing my vocal cords. This side effect was cured in minutes by
Procyclidin. All side-effects went after I absconded and the injection wore
off. Again I was left in no doubt that this drug had driven many to suicide.
May-June 1999
Depixol. Oh my God. Truly a drug of death. Wholly unbearable restlessness
and inability to concentrate. Desperate, desperate clinical depression. Not
only did my appetite go but I suffered the most impressive inability to recognise
food items for what they were. A plate of food seemed, I assure you, more
like a plate of greasy bicycle chains, rusty razor blades and nuts and bolts!
How could anybody imagine the level of injustice I felt! I thought: Why oh
why are none of the nurses on their hands and knees in front of me begging
me to hold on and not bite a fatal hole in my wrist? Because they do not realise
what they have done to me with the injection the psychiatrist ORDERED them
to give me. I begged out aloud to God to help me but all he did was give me
the strength to somehow carry on. I KNEW HE HAD GIVEN OTHERS THE STRENGTH
TO KILL THEMSELVES. I was left in no doubt that this drug had driven very
many to suicide.
June-July 1999
Piportil. The nurse who gave me this injection told me it was a “nice”
drug and that the managers had discouraged them from prescribing it for reasons
of cost. I carried on feeling the same as I had on the Depixol. Hooray! The
section finished and was not renewed. I could refuse the next injection. Thank
God for that! ! I was left in no doubt that this drug had driven many to suicide.
All the side-effects, including the depression went when I myself stopped
the treatment.
September 2000-January 2001
Piportil again! “Why are they doing this to me!” Please just try to
imagine the level of injustice I felt! Again I was left in no doubt that this
drug had driven many to suicide. All the side-effects, including the depression
went when I myself stopped the treatment.
October-November 2001
Seroquel. I could not believe this! At last I was given a drug which
did not make my life a complete suicidal misery. In fact it raised my spirits
and I read 3 books! Only side effect I recall being rather severe constipation
treated I cannot recall how well by Senokot. But trouble was ahead. After
I had been on it some 3 weeks I started to get abdominal pain. Please let
me explain how the nurses tell you not to complain of side effects as they
want you to get out as soon as possible. It is the most horrible Catch 22
situation. So you have to put up with them rather than tell the psychiatrist
as he might want to keep you longer whilst he tries something else. So the
situation is terrifying and extremely lonely. You just have to put up with
it and hold on until you can either gain release, abscond, or escape. I both
absconded and actually escaped on occasions. Nothing in the world mattered
more to me than getting away from the people doing this to me. I told a patient
about my stomach pain and he mentioned irritable bowel syndrome. The pain
got worse over a couple of days and then I started vomiting one minute and
literally the next minute suffering diarrhoea. As usual I did not tell the
staff as I felt they might soon release me. I noted nobody else had a stomach
upset and that no bug was going around. In the end I was in so much pain in
my gut (which had completely evacuated through each end) that I could cover
it up no longer and collapsed in agony on the shiny ward floor. An A&E doctor
came and injected me to stop me vomiting and gave me some Boscopan. After
days of this I decided to secretly spit out the Seroquel and surprise surprise
I got back to normal! Except the drug left my upper lip paralysed and I could
not speak properly for months. It gave me a stiff upper lip! Unbelievably
the psychiatrist had gone on holiday before all this happened having phoned
my mother to tell her he was going to put me on Clozaril (without even discussing
it with me). Because they had put me on Clozaril there seemed no harm telling
the doctor about the irritable bowel syndrome and she said “It could not be
that, you have to have that 6 months”. So I replied “What would it be after
5 months 30 days, 23 hours and 59 minutes? A teddy bears’ picnic?” The Clozaril
made me terribly tired. I had itchy rashes and huge swellings all over my
body and would wake up with my arms entirely numb and my head in a sodden
pool of saliva about 2 feet across. But like the Seroquel, at least before
the IBS, it did not make me suicidal. Hooray!
October 2002-January 2003
Risperdal Consta. Hooray, I thought. No side effects atall. I was deluding
myself as there is no clinical effect from this drug until weeks after the
injection. This is why they start you with oral medication too. But I was
secretly spitting that out. Once it cut in it was the same old horrible story
of akathisia, clinical depression, loss of appetite and on this occasion insomnia.
All very horrible again. ! I was left in no doubt that this drug had driven
many to suicide, though not as many as the others simply because it is a newer
drug.
December 2003-April 2004
Risperdal Consta I can’t believe I let them give me this again. But
then I can’t believe what they did to me above and how they have killed so
many people with such horrible side-effects. I have no doubt the coroner has
been deluding himself (with help from the equally deluded psychiatrist) for
some 50 years or so since Chlorpromazine came in.
May 2004-November 2005!
That’s 18 months!
Olanzapine
Relatively mild ongoing depression, perhaps even post-psychotic, or due to
my habit of going to the pub every night at 10pm, the fact that my needlessly
lost flat in Barnes rocketed in value by £100,000 after it was sold due to
my illness and the 5 and a half year and ongoing employment tribunal case
I am involved in. I feel this mild depression is not Olanzapine as it does
not list depression as a side-effect. Hands sometimes go numb when I lie on
my bed to relax though perhaps this is due to my cigar smoking. Apart from
those two effects, which could well be nothing to do with the drug, nothing:
A MIRACLE!!! Thanks be to God! And thank God that, though restlessness is
listed as a side-effect, it does not make me restless! 2 Years since last
sectioned on December 2nd.
