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September 1st
Every social
phobic painfully experiences the chasm between his or her inner vision
and its ultimate expression.
Isaac
Bashevis Singer
I am increasingly becoming
more depressed concerning my inability to communicate. Social
interaction has of course always been a problem but now it is more
keenly felt. I even have difficulties integrating in on-line news groups and
have abandoned so many after simply not knowing how to fit in or by
simply saying the wrong things. Often people take what I say the wrong
way. Even though of course I should be mindful that perhaps that is
their fault rather than mine. A while ago I joined an on-line anxiety forum and
left a message including a link to my website, which I worried would be
perceived as spamming. Well
there where many problems with this group which I had intended to
explain here in some detail but could not do so without the risk of
identifying the group and this I did not wish to do as of course the
problems which arose may be entirely in my imagination and anyway it is
not fair to cause upset about what is really a trivial matter should
anyone from the group read this blog. Suffice it to say there was a
misunderstanding and one that I do not know how to rectify or even if it
is now appropriate to do so or if there was any real problem in the first place.
It was one of those
situations where I tried to do the right thing but went about it the
wrong way and I have no idea what would have been the correct way.
However of course I have to keep in mind that in any social encounter
what is correct is a matter of perspective and oftentimes someone can be
hurt, offend, enraged or whatever for no logical reason simply because
their perspective is distorted or different from ones own. However because I experience a lot of
problems with any social interaction I tend to blame myself rather than
consider the problem may either be the fault of the other person or
simply a misunderstanding or is the result
of faults on both sides. The matter anyway was minor, trivial. The point
is that I don't know how to get past it.
The nature of the
difficulty is not important, suffice it to say there was a
misunderstanding, at least I perceived it this way. To cut a long story
short I have the feeling whether real or imagined that I inadvertently
messed up this particular social interaction.
As I have already said all of this may simply be my imagination, I write this only from my
perspective in order to convey the difficulty that I experience with social
interaction and not to have a dig at someone. I rather think in
hindsight that I was too sensitive and perhaps if I had written to try
and sort this out, if indeed there was anything to sort out it would
have helped. However I simply did not know what to do, how to put this
right or even if there was anything to put right. Again this could all
be my imagination but I sensed that I was seen as being pushy promoting
my website ,when all I was trying to do was to invite them to contribute to my website either art,
crafts, writings or their personal experiences with OCD and other
anxiety disorders. Now I feel
depressed by the whole business of on-line forums.
I would like to continue to post with
this particular group but don't know how to go about doing this or how
to mend any offence that I inadvertently made or even if after all this
time, it is appropriate to try to do so. I would even
imagine that if I did try to rectify the problem that the person
concerned has entirely forgotten this issue if indeed he considered it
an issue. It is ridiculous I know and perhaps this matter is best just
left alone but from time to time this incident and others like it haunt
me. This was by no means the first, there have been many similar
incidents, misunderstandings either real or perceived by my mind as
real, but that is the nature of OCD. It takes advantage of every
activity within every facet of your entire existence, it even
manipulates the detrimental effects of other conditions, such as in this
instance my problem relating to others due to my social ineptness borne
from the possibility that in addition to OCD I may well have AS. I have
no idea how to relate to other people in any social situation
particularly a relatively new one such as on-line forums and chat rooms,
I gave up on chat rooms years ago. I guess it is a matter of observing
how others behave in forums to establish the necessary etiquette, for
indeed this will never come naturally.
Often also with e-mail
there are similar problems, if it is a casual exchange I never know when
my reply has concluded communications. I do not know after a discussion
by e-mail if it is appropriate to reply or if the conversation has
concluded. Sometimes I have no idea what the other person wants, it
seems I am expected to read between the lines. The result has been some
near disasters such as nearly publishing an e-mail sent in by a sufferer
which I wrongly assumed was written for me to publish rather than an
e-mail seeking advice, advice which I hasten to add I do not feel
qualified to give. Fortunately because of my OCD checking compulsion I
asked prior to publication. I felt dreadful and couldn't apologise
enough, gave the advice I assumed this person wanted. But I never heard
from him again and as a consequence I felt dreadful. And such
experiences increase my anxieties concerning social interaction. It also
increases feelings of guilt for real or imaged hurts I may have
inadvertently caused.
To cut along story short I don’t fit in anywhere and my confidence is
now at an all time low and the motivation and inclination to make more
of an effort has diminished. I feel of late as though I am isolated from
others unable to relate to anyone. Not even able to hold a brief
coherent conversation except with my son, husband and a befriender (a
volunteer from a charity set up to provide people isolated by mental
health or other problems with a once a week opportunity to talk with
someone other than family members) and even in these instances there are many
times when I simply fail to express myself, or I get irritated even
angry as a result. Sometimes I have no idea what another person expects
from me. My befriender gets really intense sometimes concerning personal
issues or subjects of which she holds strong views, she just sits and
stare with intensity. I know she is waiting for a response but I have no
idea what she wants from me, is she looking for confirmation , a
discussion, advice what ! I usually end up getting irritated although
she appears not to notice - at least I hope not.
My doctor thinks that my inability to communicate may be the result of
OCD, because my mind is always preoccupied with intrusive thoughts and
so on I fail to focus on conversations. Yes indeed at times this may
indeed be the case. However there is something else, an inability to
converse, to make small talk, to connect with other people, to relate to
them or express my feelings and so on... Something that was present long
before my OCD became full blown, a difficulty which left me a social
outcast at school with few friends. A social awkwardness that lost me a
job and made associations with my fellow workers and indeed other
associations throughout my entire life extremely difficult and which is
becoming alarming much worse as I grow older. Well I have described my
social interaction hang-ups in my
articles about AS . Yes I continue to give strong consideration that
I may have AS in addition to OCD.
I would very much like to hear from other with similar problems.
Nowadays
social phobics lead lives of silent desperation.
James
Thurber
September 6th
Indifference
is the essence of inhumanity.
George
Bernard Shaw
Today I went to the
opticians, it was not my regular biannual appointment - at least it was
earlier. I have been concerned about an occurrence the previous week
with a distortion in my vision. It began with a blurring of vision right
in the centre of my focus. Both occasions occurred right here whilst
typing. It was a real scare the first time, after a few minutes the
distortion became larger, I was panic stricken. Well naturally what
hypochondriac would not be, was I going blind, did I have something wrong
with my brain the usual brain tumour fear naturally presented. By
coincidence I was on my way to the doctor to leave a sample for tests
about another matter which has not particularly worried me but for which
I need some help. Talk about this if appropriate another time. Suffice
it to say I was pretty stressed out about that, for people with
contamination OCD this sort of thing is an ordeal and I had put it off
for days. Now just an half hour before going to drop this off at my
doctors surgery there occurs a distortion in my vision. This panic replaces the
previous anxiety; sometimes a greater fear overwrites so to speak a
lesser fear. I was now less concerned about handing in my sample, now
overwhelmed by panic and indecision of another kind. On the way the blob
of distortion moved to the periphery of my vision but did not go away.
I could not decide whether
to ask for an immediate appointment. Still unresolved standing behind
another patient in the queue I felt overwhelmed with fear and indecision. The
women in the queue before me was indecisive about an appointment and fussed and
hesitated, I became angry impatient. My anxiety now was should I ask if
there was a doctor who could see me now... but was this an emergency...?
The doctor was sure to ask how long this had been going on, I worried
that if I answered that only about ten minutes has a lapsed that this would make
me look like a worrier, an hypochondriac which of course I am. In the
end I decided to return home and see what happens. I could, I consoled
myself, get an appointment with an optician, perhaps see if I can get an
immediate appointment.
With appointments even
immediate same day there is the anxiety about getting a headache and
having to cancel because the pain is too bad to go. So again I
hesitated. In fact to tell the truth anxiety about telephoning, getting
an appointment and travelling to the city was more than I could cope
with. So I decided to wait a while to see what happens . Within about an
hour this distortion resolved but my vision was not quite right and it
was difficult to read because of the line converging problem that used
to occur frequently in the past when I had to have a tinted plastic
sheet to cover over a page of text to make reading easier. It was never
explained to me what this phenomenon was except to say there was nothing
wrong with my eyes. Later I have found out this occurs with people who
are dyslexic and this may also be problem with people who have ADD or
are on the autism spectrum. I am not dyslexic unless being unable to
spell counts but I may be on the autism spectrum. Suffice to say the
condition is not serious, a threat to either my life or my eyesight.
I had a slight headache previous to this occurrence and afterwards a more
pronounced headache presented. I decided to leave it for a while as
the condition whatever if was had appeared to right itself.
Two days later the same
thing happened again whilst I was working here on my website blog with
the exact same format as on the previous occasion. I begin to blame the
compter and became anxious that I was not going to be able to continue
with my activities here on my website or else where, so typical of my
catastrophizing tendencies. But this was the milder concern
anxieties, about dreadful eyes disease or brain disorder predominated.
Than it occurred to me
that it might be a migraine aura. I have never had an aura with migraine
. An aura is a visual disturbance some sufferers of migraine experience
prior to an attack, but an aura can also occur without an attack flowing.
I looked up the symptoms on the web to see if my symptoms fit. I know
this is not a good idea for anyone, particularly for an hypochondriac who
is more likely than not to find all sorts of terrifying conditions with
similar symptoms upon which to ruminate with the result of feeling much worse
instead of feeling better. Fortunately this time this
did not happen. Nevertheless I was not happy and neither should I be of
course. Even if you are an hypochondriac it is imperative that any
symptoms which arise should be seen by a doctor at least in the first
instance. I rang the optician for an appointment and had to wait ten
days for an opening.
I worried all that time, I
always do . Sometime a few days prior to such an appointment even one
with the GP I find it difficult to focus on other things because of this
preoccupation. Worry worry that is all my life is. Whenever I have to go
for an eye test I worry about brain tumours as these can be detected
during an eye test with the gizmo they shine into your eyes to examine
them. No I am not going to look up the name of this gizmo,
everyone who has had an eye test will know to what I refer. I am trying
to resist the urge to be so overly accurate in my descriptions, to
obsess about having everything just right and precise. It is a
compulsion a facet of my perfectionism, yes if I was a professional writer
writing for a magazine for example, than yes I would need to ascertain the correct
terminology, but I am not a professional writer so really such
attention to detail is not necessary or appropriate as this aspect of my
blog I wish to keep informal. Most people have no idea what this device
is called neither do I, I am neither an optician nor a physician and therefore not
expected to know. Sometimes so much time and energy can be wasted by
trying to find out such things which are inconsequential. This is an
aspect of OCD that I can at least try to ignore.
Also I just hate
appointments, I can't cope with any kind of social interaction, being
tongue-tied, finding it difficult to explain my situation, knowing that I appear awkward...
well you have read so much about this that really it is superfluous to
repeat it all here. If you have not read about my social interaction
problems you may do so
here
I often miss the previous
optician I had when I lived in the south east. She was very thorough and
often would give me a quick eye check in-between appointments such as my
pressure points when I was panicking that I had glaucoma, this she did
free of charge.
Here the person is less
personal, each time you go there is a different optician. This time the
optician was rather aloof, indifferent . He more or less confirmed
my suspicions that the anomaly in my vision may be the result of a
migraine aura. He sighed when I began to explain my problems with the
converging lines of writing. He made no comment whatsoever concerning
this problem which is bugging me now, as I write the lines appear as
though they are about to converge, it is very disconcerting indeed. I
sighed heavily in response. I have no idea if he heard me or even
realised that he had sighed. Perhaps I am over reacting as I
myself often sigh but I did feel uncomfortable. He proceed to test
my eyes, it is difficult to decide which sets of black spots look better
between a selection of two. He examined my eyes with the gizmo that
would detect the tumour if there was one -- at least I hope it does,
according to my understanding it is supposed to. Everything was fine. He
recommend a change of prescription, they always do, tried to persuade me
to have bifocals or varifoculs in
stead of two separate prescriptions for separate pairs of glasses. He
simply could not understand that I would not be able to cope with the
distortion of vision each time I looked down. He said that
few people actually look down , he obviously does not have OCD or AS
patients, not that I of course mentioned either, often people with these
condtions look down as they walk. For instance with OCD it is because of
anxiety about stepping into something awful such as dog mess or strange
stains on the pavement. But even years before I developed full-blown OCD a
had the trendy to walk head down.
They say that people with
autism have no
theory of mind.
Theory of mind - Wikipedia, the free encyclopedia
I maintain that
no one has any theory of mind. Try getting someone to understand that
this is not an option for you when most everyone else is okay with bifculs or varifoculs. The assistant who took the
photos of the retina tried yet again to get me to have bifocals or
varifocals. Again try getting people to understand that you cannot
afford £400 for the highest range of varifocals. Its just outrageous!
I perhaps should not say this because really I have no idea what another
person is thinking or what his or her motives are but sometime you get
the feeling the optician is more interested in selling you a product,
the more expensive the better rather than offering sensible advice about
your eyes and which kind of glasses are the most appropriate for you. My
previous optician understood the way I am sensitive to changes in vision
and knew that I would not cope with bifocals or varifocals
September 5th
What we
focus on, we empower and enlarge. Good multiplies when focused upon.
Negativity multiplies when focused upon. The choice is ours: Which do we
want more of?
Julia Cameron.
I am sitting here tonight
writing in my blog which is unusual as most of the time I work on my
compter in the mornings but tonight I simply cannot stand to be in the
same room while a certain rather gruesome TV programme is showing. The
programme in question is Silent Witness, a programme about pathologists
investigating crime. I can no longer cope with these rather explicitly
gruesome TV programmes. One glimpse of some decaying corpse can stick in
my mind for hours. Rather like a thought an image such as this will
return to my minds eye again and again and there is no way to rid myself
of it. It will be there superimposed upon whatever view, I see it now as
I am looking at the keyboard to type, as I look at the screen, look
across the room out of the window, anywhere, everywhere. This imagine is
there when I close my eyes. I did not get out of the room quick enough
not to catch a glimpse of a dead decomposed body being dragged from a
river, a child's I think. In the morning this intrusive imagine may be
gone I certainly hope so.
But for now it is there as I
write this, all the time this image is in my mind's eye and I only
caught a fleeting glimpse before looking away but it is amazing what your
eyes take in and your brain records or adds. I think ones brain tends to
add things it has not actually seen particularly in such circumstances
or even to exaggerate things it has not clearly seen. Intrusive images I believe
are a common phenomenon for the sufferer of OCD. Intrusive imagines like
intrusive thoughts can be upsetting. The intrusive image also like the
intrusive thought always concerns something awful or something that will
distress you even if it does not distress other people. I don't get an
intrusive image of a rose or a tiny lamb or a beautiful landscape. Yes
of course such images arise as they are doing now because I am writing
to you about a rose, a lamb and beautiful scenery but these imagines
will fade quickly but the intrusive distressing imagine may remain for
hours even days. Many years ago when I was younger sneaking into the
cinema to see an X rated film I had thereafter to endure several days
haunted by an intrusive image which is there now in my mind after all
this time. At the time of course I did not realise that this did not
occur to everyone who saw this film, which by present day standards might
now be considered tame, or that most people would not be particualry
distressed by it, at least not for a number of days. It really made me feel anxious for a long time
afterwards. Try as I might I could not rid my mind of this image. It is now less disturbing as the imagine is more vague
but it is there right now nonetheless. Often this problem is not so bad
as it once was but still I have to be mindful not to allow such images access to my mind.
I really cannot understand
the trend now for this kind of graphically realistic TV. Why some people
find it entertaining to watch such programmes I cannot imagine. My husband and son like
this programme, they also like the similar American CSI programmes which
are
slightly less gruesome. Why I ask myself. If I was to watch this
not only would I be stuck with a whole bunch of disturbing images but I
would feel my mood become even more depressed than it is now. These
programmes which I describe as dark are nothing else but depressing, what
is the entertainment value. What do people get out of watching them.
They are so negative. Even if you do not have OCD and are not subjected
to the torment of intrusive images or you are not a sufferer of
depression or you are less sensitive, what do you gain from such programmes?
How is there any entertainment
value. Is it interesting to you, fascinating or what? I fail to see anything of
any value, anything to in anyway enhance your life or make you feel
better. Isn't there enough real suffering and misery in the world without
watching
it on TV in this factious yet realistic guise, Don't you get sick of violence and suffering in
the world as it is, I know I do.
Today evil
spirits are seen as negativity which floats around the Earth in large
quantities.
Scott
Cunningham.
September 7th
Concerning the autism and OCD connection which I have discussed here on
my blog and website now for months. I have recently received some interesting information which
confirms my supposition that there is a connection between OCD and
milder forms of autism such as high functioning autism HFA and Asperger
syndrome AS. Those of you who regularly read my blog will know that in
the last year or so I have given serious consideration that in addition
to OCD I may have AS or be somewhere on the autism spectrum or at the
very least have autistic traits. Up until recently I have not been able
to find much information to either confirm or refute this possibility
and with a less than positive attitude on behalf of some mental health
professions that I have shared my idea with I have begun to feel that
this idea was simply a notion which had no bases in reality and perhaps
it was some kind of obsessive thinking, a bee in my bonnet as my mother
used to say.
After writing two articles
concerning why I think that I may have AS, and after over a year
obsessing about the appropriateness of including them here on my
website, I decided to make enquires with a researcher currently
conducting research into OCD to ask for an opinion as to whether or not
the characteristics I described in these articles where indicative of AS
and if my idea that there was a connection between OCD and autism was
valid, and if it was possible for OCD and AS or other autism spectrum
disorder ASD to coexist in the same individual. Yes I do realise that
OCD can present in a person with autism but as a secondary condition, as
traits or if the symptoms where severe as a separate diagnosis to
autism, but with autism being the primary condition. What I am saying
here is that I believe that autism can exist with OCD in a milder form
but as a secondary condition whilst OCD is the primary condition. Or
even a dual diagnosis of OCD and and an ASD. I know it sounds like hair
splitting but with conditions such as autism and OCD these
considerations need to be precise.
Also I think there is a more
significantly complex connection and not simply that these conditions
coexist in one way or another in the same individual. For instance autism
and OCD often present in the same families, for example a child with
autism, and of course adults, will have a person with OCD as a first
degree relative, a parent, sibling or offspring ( I think that there is so much emphasis
on childhood autism that in general people may be led to believe that
the condition does not exist in adulthood... if only ...children grow up
don’t they...).
I quite expected my request and my ideas to be dismissed however quite
the contrary happened as within twenty four hours I received a reply
confirming that my conjecture concerning the possible connection between
OCD and Autism was indeed a valid consideration and yes indeed it was
quite possible for the two conditions to exist co morbidly. The
researcher told me that AS and OCD can and indeed often do coexist in
the same individual and that this is widely accepted.
I was particularly
surprised that not only is it widely accepted that these condtions
coexist but that they in fact often do so. This confirmed my
assumptions about the frequency of this occurrence, as after many
associations with fellow OCD sufferers both on-line and in real-time who
exhibited at least significant traits of autism I suspected as much.
However it was nice to have my ideas confirmed as a real possibility.
The same researcher also said that the symptoms I indicated in the
shorter version of the two articles which he read may be indicative that
I may have AS although for a formal diagnosis and a definite
confirmation I would need an assessment by an experienced clinician.
Nonetheless his opinion has helped me to validate my assumptions and
despite the less than positive prognosis associated with the co
morbidity of OCD and AS I felt enormous relief. I think it is vital to
know precisely the conditions from which one sufferers as of course each
condition effects the other or others as all co morbid conditions
interact and produce additional complications and complexities.
The researcher cited the article, An Autistic Dimension: A
Proposed subtype of OCD by by Suzanne Bejerot which can be obtained here
:
Obsessive-Compulsive Disorder - Studies from Karolinska Institute yield
new ...
In addition to the above
source you may also obtain a copy
from the National Autistic Society NAS, here is the link.
The National Autistic Society - Autism Data article
According to the
information provided on the page linked above
you will need to enquire
at the NAS information centre, link below.
The
National Autistic Society - NAS Information Centre
How to order is rather
vague so I made enquires.
To order you will need to
send an e-mail explaining your requirement to
info@nas.org.uk
quoting the
reference details included in the first link and you will receive a
reply with an attached photocopy declaration which you are required to
complete and return with a payment of £3
Complicated I know.
This article confirms for
me my notion that there is indeed a connection between OCD and some
types of Autism. I quote from the opening paragraph:
“ This article focuses on the possibility that autism spectrum
disorder (ASD: Asperger syndrome, autism and atypical autism) in its
milder forms may be clinically important among a substantial proportion
of patients with obsessive-compulsive disorder (OCD), and discusses OCD
subtypes based on this proposition. The hypothesis derives from
extensive clinical experience of OCD and ASD, and literature searches on
MEDLINE. Neuropsychological deficits are more common in OCD than in
panic disorder and depression. Moreover, obsessive-compulsive and
schizotypal personality disorders are over-represented in OCD. These may
constitute mis-perceived clinical manifestations of ASD. Furthermore,
repetitive behaviours and hoarding are common in Asperger syndrome.
It appears that for OCD
,there are clearly recognised subtypes and that each set of subtypes has
its own distinctive presentations of OCD. However there is at present no
consensus concerning the definition, categorisation or validation of
these subtypes. For example one of the more obvious and recognised subtypes is OCD
with tic disorder. This type of OCD is very distinct. OCD with tics
presents mainly with the following OCD symptoms : symmetry, ordering
touch rubbing counting and hoarding.
It is important that these
subtypes are taken into consideration as different treatment may be
required. For instance there is a type of OCD where a patient has no
insight. The result here is obvious that therapy for such a patient will
be less successful due to lack of motivation. OCD and tics is obviously
a distinct form of OCD.
The article referred to above proposes the existence of a
possible sub type of OCD which presents comorbidly with an ASD or
significant traits of autism. The paper also cites a genetic study
connecting treatment resistant OCD with AS and other forms of Autism as comorbid
(coexisting) condtions:
"It is suggested that the comorbidity results in a more severe and
treatment resistant form of OCD. OCD with comorbid ASD should be
recognized as a valid OCD subtype, analogous to OCD with comorbid tics.
An odd personality, with paranoid, schizotypal,avoidant or
obsessive-compulsive traits, may indicate these autistic dimensions in
OCD patients."
Now I am not a mental
health professional, the above is my very basic interpretation and
summary of a very complex article and therefore my interpretations may
not be accurate. If you are seriously interested and feel this
relates to you, you are advised if at all possible to read the
article which sadly it appears will require a fee. However if your
interest is less keen it is only a short article of consisting of six
pages of actual information, which you may feel is rather expensive.
I found the article
informative as of course this effects me personally. Reading this
article has helped to validate something that I have been considering
for a long time. it is not an easy read, it is an article meant for
professionals.
Basically according to my
understanding the article discusses the possibilty that there exists a
subtype of OCD which presents with a coexisting ASD or significant
autistic traits. OCD comorbid/coexisting with an ASD is often more
severe and intractable. Different treatment approaches may be necessary.
It is of course better to
read the article as my explanation may not be entirely accurate.
September 9th
I have had a really
difficult time with updating my blog. Mainly due to feeling so ill,
tired and weary as a result of my fibromyalgia symptoms which include a
dramatic increase in aches and pains which become worse with any
exertion even too much typing. Although I suspect that anxiety and
frustration because of the difficulties which present with typing
and writing as a result of my inabilities in this area and my OCD checking
and ruminating compulsions. Moreover anxiety about the previous entry
has caused delays as I am not sure about how easily obtainable this
article is and how well or otherwise I have interpreted it in my brief
summary. It was a very enlightening article which has validated so many
of my considerations concerning OCD and autism that I am keen to share
this with you and feel very frustrated about the complexities of
obtaining this article.
I think that for those of
us who have an ASD in addtion to OCD the prognosis is less favourable,
nevertheless if we do not recognise this possibilty we can waste time
with treatments that are not effective, became depressed because we do
not understand why for us treatments that help others seem less
successful. Moreover we can feel guilty, inadequate and a failure unless
we understand that perhaps there are other factors involved such as an
ASD which may be the reason why our OCD is more severe, less easy to
treat. I do not believe that anyone is untreatable and I think that with
the right therapy we can learn to live better lives, to be more
functional and able to cope with our symptoms even it we cannot be
cured. In all honesty I think that no one with full blown OCD can be
entirely cured inasmuch that he will never have an OCD thought or
behaviour ever again. But there are degrees of success and an
understanding of the nature of the different types of OCD are important to
recognise in order to provide the best and most appropriate therapy. I
am going to discuss this in more dept in the future and I am in the
process of preparing an article on the importance of recognising co
morbid conditions and the different subtypes of OCD.
September 10th
In the forthcoming October
edition of Details magazine there is an excellent article about OCD. The
article focuses on both the
Obsessive
Compulsive Foundation's annual conference and the disorder itself, with
anecdotes from sufferers and explanation of current treatment.
Well worth getting a copy
if available, not sure if its published outside the USA.
Here is a link to the
article on-line
This Story Has Been Rewritten 43 Times: DETAILS Article
on men.style.com
September 11th
Well to date I have not
uploaded to my blog any of the above September entries. I have read them
again and again, checked and rechecked added extras to clarify, deleted
material that I fear might be harmful or misunderstood or which I have
had some anxiety or other concerning. Of course if you are now reading
this I have somehow managed to click that publish button, but it has
been a nightmare of doubt, anxiety, frustration and exhaustion. I feel
so depressed by this problem which is becoming increasingly more severe.
This evening when the rest of my family are again watching one of those
grim pathology TV dramas whilst trying to record another even more
gruesome rendition which I have talked about
earlier I really did not feel as though I wanted to come up
here to work on my computer, which I usually do to avoid being in the
same room whilst these programmes are showing. I just could not face
coming here and checking again. I had thought to upload these entries
this evening but will have to now wait until tomorrow as there is not
really the time... well to be honest yet again I simply can't face it
unsure still about these entries which if I check them any more I will
soon be able to recite them from memory.
Unless you have OCD you have no
idea what it is like, how inhibiting it is, incapacitating to the
extreme. I have much I wish to write and discuss but this is hampered
and delayed as a result of this checking compulsion. There is
incidentally an account of a journalist in the above Details magazine article
with this same problem who had to give up his job for a while as a
result of checking and his perfectionism.
I really have to get past
this somehow but quite how I do so I don't know. There is little to
validate my concerns although of course anyone can do harm in the sense
of saying the wrong thing and causing offence but to really cause real
significant harm
by anything I write is unlikely and I know this on some level. In any
case it is the more subtitle harm such as the first entry about the
forums. I am a member of so many forums it would be impossible for
anyone to identify themselves but I have obsessed and worried and have the strong
compulsion to delete the entire entry. Which I have not written in order
to gossip but simply to describe the nature of my social ineptitude
which is difficult to do in any real sense without referring to other
people and to social situations.
I was hoping to sign up
for another blog separate from this website in addition to this blog
where I hope discuss a verity of issues about which I have strong
feelings and which I am reluctant to discuss here too often because of
the fear of making this website too negative, as my intention for
creating this website was to add some positivity to offset the
negativity which is naturally an ever present fact for sufferers of the
disorders featured on this website. But other than the introduction I
cannot write one entry, feel anxious to do so because of all the
checking and obsessing. What to do... I have no idea. The problem with
checking for errors is valid to some extent as I make many errors. This
I believe is due to ADD , this has become worse and now not only do I
miss out words or not notice that the spell checker has put in a word
that I had not intended and I fail to notice but now I am missing out
whole phrases. These mistake validate my compulsion to check.
Well writing all this is
hardly going to help as I might end up adding another few days to the
already significant delay as I check all the above umpteen thousand times.... What a life...
September12th
Well today I hope now to
take the plunge and upload the above entries. Odd how the last one was
checked only three times. I probably will check it again a few times
though after publication as I do from time to time to correct mistakes
which have slipped through the net. I guess I have got to the stage where
I am exhausted and just want to upload and try to forget about it until
next time. Sad that in the end rather than determination it is only
exhaustion that finally allows me to click the publish button.
September 14th
Climb
the mountains and get their good tidings. Nature's peace will flow into
you as sunshine flows into trees. The winds will blow their own
freshness into you, and the storms their energy, while cares will drop
off like autumn leaves.
John
Muir
Well we did not climb any
mountains although we ascended one as we made our way along the narrow
winding and very precarious road, the Hard knot pass in the Lake
District.
It is rather scary but
with care it is unlikely to present serious hazards but of course that
could be said for driving anywhere could it not, but with care few
people would come to harm on this very narrow single track road.
Today was one of those
extremely rare days when I am not forever looking for a toilet or
anxious about a tension headace and if it is about to become a migraine
or I am overly tired and
unmotivated inhibited my aches and pains, although of course these aches
and pains never go away, some days are easier. Easier but sadly never
easy. These days are though the
exception but I have to make the best of them, we even went for a short
walk near the ruins of an old Roman Fort situated along the hard knot
pass which a short distance away has a splendid view over the valley.
Some of the most spectacular scenery can be viewed along this pass and
it is well worth the effort and any trepidation those of us of a nervous
disposition may feel.
Down in the valley is a
field of about three hundred sheep, the cute little Herwick sheep only
found in the Lake district.
We had passed other sheep
on the ascent of the pass, the cutest little brown sheep which are also
I believe Herdwick sheep.
We stopped at a pub as we
arrived in the valley for coffee and a snack. There was local mutton on
the menu, it amazes me how people can see these adorable creatures than
go and sit down to a pub meal a few miles distant and eat mutton. It was
one of those sad moments of the day as despite the beauty of nature and
the adorable sheep, which harm no one and are an utter delight, is the
reality of their ultimate fate which is never far from my thoughts.
A ride through more superb
scenery, most probably among the best in the country, past Lake Lowes
water and Derwent water we stop off now and again to admire the views,
at least where we are able.
Often there are few
stopping places except along the mountain passes. At the stopping places, if
there are any, there is often a car park fee of over £1 an hour, it is
very expensive if one was to go hiking for the day. But I will save that
complaint for another time perhaps, suffice it to say that these days
there is a charge to do anything and such charges are unreasonable and
it is getting increasing more expensive to even go for a day out in to the
country.
But I don't wish to get
too bogged down in negativity today as this day with one or two exceptions
was one of the best days out I have had this summer. It is a fact
that one does feel better in such places, whether it is the spectacular
beauty or the elevation it is hard to tell. If you can reach the summit
of a hill or mountain you may feel a lift in your mood, if you are
fit by climbing or for me now less fit by car, although the summit of
course is not accessible by road but certainly you can reach some high
places affording splendid views. When I was younger my husband, son and I
climbed several of these mountains here into the lake district and other
parts of the UK including Snowdon in Wales. I do long to be able to do so
now but sometimes you have to accept your limitations and enjoy
whatever you are able and being out in the fresh air, out in nature is a
tonic even for a long suffering ole misery such as myself.
September 15th
My neck aches something
awful today, the problem I have with my neck seems always to
present itself on Saturdays the day when I am able to concentrate on
working on my website. At least the more severe manifestation of this
chronic problem. Usually when this happens I pace myself, take it easy,
but today I am so fed up with the continual perversity of life that I
am just going to throw caution to the wind and continue and
work through the pain and see what happens. My life is so restricted day
after day with one or another of the conditions from which I suffer, it is
becoming an increasing misery and a frustration of continual struggle
with so many obstacles and hindrances . There is never a good day, if it
is not one thing than it is another. You know you get little or no
understanding from anyone... empathy... well this is a misconception, no
one has any empathy for something they have never experienced, so it is
perhaps unreasonable to expect any but just now and again a of word of
sympathy wouldn't come a miss.
There is supposedly four percent of the
population have CDH ( chronic daily headache) yet I have met but one
other. One can feel so alone . I am told that CDH
is all the result of anxiety and depression. I don't agree I think a
more accurate diagnosis is Fibromyalgia but like the AS that diagnosis
it seems is elusive. I guess unlike the AS I have had a diagnosis of
sorts, a few blood tests which have ruled out other condtions. And
thereafter the doctor simply said the symptoms are caused by anxiety.
Yes apparently anxiety and depression can cause a number of similar
symptoms such as headaches and aches and pains.
Aches and pains linked to depression, anxiety
However my symptoms are
far more numerous and are as follows:
Chronic aches and pains in muscles and joints
fatigue
Chronic daily headaches
migraine
Sleep problems which include: waking from sleep unable to breathe
or choking; difficulty staying asleep; waking not feeling refreshed
with a marked increase in aches and pains.
Irritable bladder
IBS ( irritable bowel syndrome)
Episodes which are stroke like in nature and include: weakness,
numbness and sensations of tingling in limbs usually down the right
side but spreads sometimes to include part of the left side also.
These episodes occur mostly upon waking but occur at also at other
times. It has been suggested that these episodes may be a result of
anxiety or a symptom of migraine although they mostly present when I
do not have a migraine. I am concerned about this particular
problem and the one below which may be related to this and intend to
ask for a more definite diagnosis.
Important: The above stroke like symptoms of course need to be
checked out immediately with an hour by anyone experiencing
similar symptoms for the first time, as of course these symptoms are
similar to that of a stroke.
Weakness in limbs mainly legs
Pain in the extremities of fingers and toes.
Brian fog
It is my opinion that some of the above symptoms may be far
better diagnosed as Fibromyalgia, although my level of pain is perhaps
not as severe as that described in the following website .
UKFibromyalgia
Just my opinion of course
I feel strongly about this but I am not as arrogant to consider that I
am right. I am not a doctor . I recognise it is not easy for doctors to
come to a decision about this sort of condtion, which cannot be diagnosed
by blood tests and other diagnostic means except by the elimination of
other serious conditions. So the doctor has to make a decision and like
everyone else in such matters he or she have the right to his or her
opinion. I either accept it and diagnose myself or go elsewhere and
really I am very satisfied with my doctor and the others I have
consulted at this practice. So for the time being I have to let this go.
But who knows things may change, there may eventually be more conclusive
tests to ascertain Fibromyalgia and its related condtion CFS/ME.
I am depressed though by
this as I am about the AS assessment. But quite frankly if I am not
depressed over one issue than it is another. I can't see a way out of
depression.
Does it matter ... ? Yes it
matters to me. I know there is no cure for fibromyalgia, antidepressants
are prescribed for pain so some would think it doesn't not matter what
name you give it. But similar to the reasons I give why it matters that
I have an accurate
diagnosis for AS , it is important to have a
diagnosis for this assortment of complaints.
September 16th
Perfectionism is the voice of the oppressor,
the enemy of the people. It will keep you cramped and insane your whole
life.
Anne Lamott
Today while sizing my husband’s photos for inclusion on this website,
hopefully later this month or in October if I can stop obsessing about
them, I noticed that the beautiful
red rose photograph below was marred by the fact that the roses had
black spot, a common disease in roses as well as other garden plants. I
hesitated thinking that this somehow blighted the picture and I
considered removing it from the collection. But on reflection the roses
are so stunning that really the black spot did not matter for it really
did very little to detract from the splendour of these flowers. The
photo also looked a little blurry. Than the thought came to me that
there is little in existence either in the creations of nature or of
man, and that includes myself, that is perfect. This photo so clearly
demonstrates that something does not have to be perfect in order to be
beautiful, that imperfection and beauty can sit side my side.
Perfectionism is a tendency in people with OCD and related conditions that can become a
creativity stifling problem. For many people, in extreme cases, it can
become so inhibiting as to impede creativity altogether. Often I become
anxious about picking up a paintbrush to paint or to come and sit here
and write because of the fear that I will fail and that there will be
some imperfection that will result in considerable torment for me as it
will cause me to obsess until or if such imperfection is rectified.
Sometimes this never happens, in fact it never happens because
perfection is impossible, but sadly the perfectionists can never accept
this and often I complete a piece of writing or a painting putting my
brush down or clicking the publish button respectively, not with any
sense of satisfaction but simply as a result of exhaustion and
depression.
In fact often the more I strive for perfection the less I am
likely to achieve it.
Since my obsession with getting it just right introduced itself
concerning my website the quality of my writing has in fact deteriorated
as the more I check and check, rewrite, edit, obsess over and over the
more it is distanced from the original spontaneity of my first
rendition, and as a consequence finally when I can stand it no more the
finished piece is probably less perfect than the original, which in
reality perhaps needed just a couple of checks before finalising and
publishing .
The same is true of a painting, an overworked painting is never as
pleasing as it was in the first instance and the overworked painting is
in fact something that is always mentioned in art classes as something
to avoid. There is a point when you know your painting is finished, it
might not be perfect ... well it most likely won’t be, but if you
continue past this point of completion you tend to ruin the freshness
and spontaneity in the same way as you can do with the continuous
editing of any piece of writing. I am reaching that point here and now,
when perfectionism, and of course OCD, will if I am not careful, easily
spoil this piece of writing.
I can’t tell you which website it was, I only wish I could but there was
a commentary on a website about a collection of paintings which the
person who was writing the commentary said where less than perfect, and
although the figures in the paintings where not anatomically correct the
paintings where nonetheless very aesthetic and pleasing works of art. I
wish I could recall the website for the exact quotation as this comment
has helped me concerning my artwork. Now when obsessing about
perspective and other technicalities I try to recall this comment and
look at the painting from an aesthetic viewpoint, rather than fussing
over perspective and other issues. Yes I am still never satisfied,
nonetheless thinking about this comment has helped somewhat towards
accepting some of my artwork with more sense of satisfaction
notwithstanding some imperfection.
So I am too publish this picture of these beautiful roses black spots
aside taken in the gardens of Sledmere House
Sledmere House Yorkshire
September 17th
When the disease is known it is half cured.
Erasmus Colloquies
There is an
article in the Times which may be of interest to anyone with Aspergers
Syndrome and anorexia nervosa.
It is now thought that
brain mechanisms are the underlying cause of anorexia nervosa rather
then the whims of fashion or an awkward adolescent phase. And that these
mechanisms are genetic. It has also been postulated that anorexia
nervosa may be a female form of Aspergers syndrome
"What we now realise
is that we need to be looking at
underlying neural networks in the brain
– how patterns of information are
processed, how this affects both
behaviour and the way an individual
reacts to her environment, and why this
goes wrong. We need to consider those
aspects of how the brain functions that
increase the risk of someone falling
prey to an eating disorder. "
"We also discovered that this
distorted pattern of processing
information has a strong similarity to
autistic spectrums. It has even been
described as the female form of
Asperger’s. Traits that may appear
present in childhood, such as
obsessive-compulsive disorder or
overperfectionism, can often indicate a
vulnerability to developing an eating
disorder later in adolescence."
To read the complete
article click the link below.
Is anorexia the female Asperger’s? - Times Online
Also read the comments
section
I think as you may have
realised unless you are here for the first time that there is a
connection between OCD, ASD and anorexia nervosa although the last
condtion I have been hesitant to express such an opinion as I really do
not suffer from this disorder personally, although there was a time when
I became on the verge of becoming like my sister, anorexic.
It is my opinion that if you suffer from OCD you are more likely to
become effected by an eating discover, or have a close relative with an
eating disorder, have AS in addtion to a your OCD or eating disorder or
at least have significant traits. Or if you are very unfortunate you may
have all of these conditions or a primary condtion with the others
existing as secondary condtions. Such as for example I have OCD as my
primary condtion and have significant traits most likely enough for a
formal diagnosis of AS as a secondary condition or even as a dual
diagnosis. A complicated mix of dysfunction leading to a very difficult
life.
I consider that there is a connection between all these conditions.
Perhaps which condition you have or which is primary, secondary or
merely traits may depend upon how these genes manifest
in each individual. But these condtions are there in most families with
one or more of these disorders presenting to some degree and I think
that most of us have at least two existing as a primary and secondary
conditions, as a duel diagnosis or as significant traits.
Note one of the comments from a person who has had anorexia nervosa, has
a father who has Aspergers and an older brother with OCD.
Also read the comments from a perosn who again has had an eating
disorder, a son with AS and who also, it seems recognises that there is
a link.
"It is interesting to
read this article as I had an eating disorder many years ago and this
link may help me understand why my son aged 6 has aspergers, as this is
a genetic condition and was passed onto him, and from the research it
may have been passed on from me to him. I do feel not enough help is out
there as people don't believe in this link. so it is nice to see that
people are begining to take notice"
I echo the comments of
both of these people. There is a connection between these conditions and finally it is being
realised.
I have OCD and most
likely AS but as you have read can't get an assessment to ascertain AS, my son has
a formal diagnosis of AS and traits of OCD, it is highly likely my mother
had AS and my late sister had anorexia nervosa and she most likely would
have qualified for a diagnosis of AS.
The case of my sister
also highlights the fact that anorexia nervosa is not confined to
teenage girls from well educated middle class backgrounds. My sister and I
are working class, our families where poor, are education was basic, both
of us leaving school at fifteen. Moreover my sister did not develop
anorexia nervosa until her late twenties from which she never recovered.
Lynda displayed symptoms of AS in her social ineptness, her shyness, her
inability to socialise. Particualry marked was her often outspokenness,
she seemed unable in many instances not to say exactly what she
thought, even about personal or private matters. Also marked was her
perfectionism and her tendency towards intense interests which where
often but not always of an obscure nature. The last of these was her
patchwork the perfectionism involved in this and her intense
preoccupation, I, in retrospect, consider may be due to at least the
presence of significant autistic traits. Sensory overload and
sensitivity also presented, noise being the most significant.
I think the more we
understand the interrelated nature of these conditions the better the medical profession will be able to treat them. You cannot treat any
condition in isolation.
Well it seems that today I
have finally to resign myself to the fact that I will not be able to
obtain a formal diagnosis for AS. My doctor made enquires at a hospital
in the area which until recently carried out assessments for adults to
ascertain an ASD. Unfortunately the psychiatrist had since gone to
practice elsewhere and has not the time for what is I assume the long
process of an assessment. The only other option which was recommended by
the psychiatrist is a private assessment centre which although is a
registered charity charges £1,500. The assessment my doctor was informed
would take a day which was cited to justify this rather high cost. Ummm
how many people earn that kind of money for a days work, not many I
would imagine. Although of course more than one person may be involved.
Nonetheless it seems rather exorbitant for a series of tests most of
which are carried out as questionnaires and which are available on the
internet. Aren't charities supposed to be set up for humane purposes,
nothing very humane about such a high charge. Perhaps health care would
not be so costly if practitioners did not demand such high fees.
Certainly a GP or a surgeon deserves a good wage but quite honestly when
it comes down to these less demanding tasks in health care such as this
type of assessment high fees are perhaps not so well deserved.
I told my doctor that I would not even contemplate requesting a referral
by the NHS that required such a fee even in the unlikelihood that such a
request was granted, I simply would feel awkward. The request would most
likely have to go before a Primary Care committee, the likelihood of it
being accepted is virtually zero. It seems to me now an impossible task
to get medical professionals to understand that there are many people
who need a formal diagnosis in order for them to understand the
conditions from which they suffer, to be in a position to conduct their
own research into the condition, find others who suffer with the same
condition and to get services and join support groups. I certainly am
not in a position to pay the fee myself and even if I was I would not do
so as I consider the cost outrageous.
So for now there is no way that I am likely to ever have an official
confirmation. The article and e-mail from the researcher mentioned in an
earlier entry has added weight to my consideration that it is indeed
quite likely to have OCD and AS as coexisting conditions or at least
significant autistic traits. Knowing this has helped to validate my
assumptions and has helped me to understand why my OCD is severe and
seemingly intractable.
From now on regardless of a formal diagnosis for AS I will consider
myself as a person with a primary diagnosis of OCD - formal assessment
and diagnosis for OCD took place the mid 1980s ,- with AS as a secondary
co morbid condition. To put it simply until I know otherwise I will
assume I have AS either as a secondary or even a duel diagnosis to my OCD.
I will continue to try and acquire a formal diagnosis for AS but have
now accepted that this is unlikely unless resent circumstances change.
Also during the consultation with my GP I decided as far as mental
health is concerned that I have come to the end of the road so to speak
. We discussed why I could not cope with CBT, and because of my social
interaction difficulties this was difficult to explain and after a lot
of incoherent waffling it suddenly came together in one simple sentence:
The reason why I can’t cope with CBT is that one has to be reasonably
functional to participate. At least to be able to fill in the automatic
thought forms and eventually with the guidance from the psychologist to
think of more rational ways of thinking and behaving. This requires you
to be able to organise your thoughts in order for the process of CBT to
be effective, This I can not do. Yes you might think that this would be
easy for me, after all I write so much here about my OCD. But this is
different in ways not easily defined. In fact this is my whole point,
oftentimes there are many thoughts which are not easily explained, or
put into so many words either spoken or written, and it can take time
for me to organise my thoughts and to focus upon how to express them.
Writing does not come easily at all, it is indeed a difficult task to
sit here and try to explain what is going on in my mind, than articulate
my thoughts in order to coherently express them. With CBT one is
required to record every thought that is of a negative nature, that
results in feelings of anxiety, stress and or depression. This is not
easy for me for I can’t always articulate them in such a way as they
occur in such rapid succession. Moreover I cannot be concise.
Such a task would simply be generating more anxiety and more thoughts
which I would never be able to express. Yes may be the psychologist
needed only a sample but I got the idea that every thought needed to be
recoded in this manner, and even if this was not the case I would still
feel overwhelmed as indecision and my inability to edit the thoughts to
decide which new thoughts should be included and which had already been
mentioned, which thoughts were of a similar nature and so on. I did try
for three weeks and indeed there were several charts of automatic
thoughts but these did not reflect my real torment, as the torment had
began to be centred on the task at hand which was trying to record these
thoughts. Moreover also mostly the thoughts which were older and which I
was more used to expressing were recorded, the simpler more easily
explained ones. Like the thoughts that precipitated the regular hand
washing rituals for instance. But even here there is difficulty and
oftentimes great complexity.
Here I must point out that after a while, except in new circumstances,
many of the thoughts are now automatic and it would take a while to
recall and clearly express the original precipitating thoughts in so
many words. For instance the thoughts that compel me to wash my hands
after opening the blinds. This compulsion has been with me a number of
years, it is one of many, too many to account for one by one or to
clearly articulate the precise thought. Concerning this compulsion the
thought behind it arises from fear of a drop of water from the radiator,
the fear here is legionnaires disease, which the cord for controlling
the opening and closing of the blind is near. At one time the radiators
where removed with a water spillage, a big panic in itself but since
than I have now to wash my hands when in contact with the blinds, the
cord ,the curtains and most certainly the radiators. However all this
complex thinking does not occur each time I carry out this compulsion,
there is just the compulsion and if it is not carried out there is
anxiety fear and dread . There are so many instances of these types of
entrenched thoughts which never actually present now in so many words
that trying to write each of these would be impossible. Besides many of
my thoughts are entwined, commingled, for instance religious OCD and contamination OCD
often go hand in hand, expressing these in such a way would be nightmare
of anxiety and in the limited time available, far to stressful for me to
consider.
My OCD is now so complicated that I cannot divided and separate the
different thoughts that entwine each other. Often two or more types of
OCD coalesce to form a very complex web of obsessions and compulsions,
thoughts and behaviours not easily expressed in a simple sentence or
two. For instance religious, superstitious and contamination OCD often
mingle and it is not easy to separate these thoughts or their resulting
compulsions.
Here is an example of the most common type of this kind of thought.
I need to change my cloths, (a contamination thought) and take yet
another shower, it might be the third or even the forth today. I am
tired and weary and really don’t want to take off my cloths, find clean
ones, a difficult feat at the best of times involving in itself many
thoughts and compulsions. I am really tempted to forgo this but there
is fear that I will spread contamination and cause harm and also there
is the fear of the fear. I am afraid of the feelings of anxiety, dread,
and even fear that will arise if I ignore this compulsion. I also fear
spreading contamination to other parts of my home because thereafter
they will become no-go areas or become in themselves reasons to wash and
shower when in contact with them. So there is fear of increasing the
problem if I forgo the shower and change of cloths. But than the
thought comes, an even more powerful thought that something bad might
happen to someone I care about, a kind of divine intervention, in a
karmic comeuppance way (a religious superstitious thought) if I don‘t
shower and change my cloths, such as a person I care about my come to
harm. This further compounds my fear. But I am exhausted so to try to avoid showering I may make a vow
as described in my
memoir
and
My Story
not to shower ( a religious
compulsion) . I vow not to take a shower, some times this thought is
unbidden, involuntary; sometimes however I do this to try and over write
the previous compulsion, in this case to shower. I hate doing this but
it all happens in the blinking of an eye. Thoughts arise before I can
prevent them or think them through as of course such thoughts instead of
easing the situation make it much worse. I really do not wish to go into
huge detail now about these vows as they are the cause of much
anxiety... no fear, anxiety is too mild a word sometimes.
Suffice it to say this results in a conflict of OCD thoughts and
behaviours which result in even more anxiety and misery than a straight
forward obsession or compulsion. There is also guilt for having sworn
the vow to try to counteract my contamination compulsion, so I than fear
that something bad might happen to a loved one just by having done this
for selfish reasons. The conflict now is between fear of contaminating
others by not washing and changing my cloths and keeping this ridiculous
vow. Ignoring one for the other brings no peace. If I do not wash
someone may be harmed or die because of contamination. But if I break the
vow, which I have made to overwrite the contamination compulsion,
than as a result I fear harm coming to loved ones because I have broken
the vow, even a stranger if the
clauses of the vow are directed that way.
I feel I am failing here to explain this, you can read all about this by
accessing the links above. The problem is now that I am dammed it I do
but conversely dammed if I do not. If I shower now I will break the vow
with perceived fearful consequences, remember that this is from an OCD
perspective, my OCD perspective which is unique to me. Each person's OCD
manifests differently even though it my be basically similar.
Although that type of problem is not as prevalent as it once was or at
least the thinking is more automatic there are others now even more
complex which are practically impossible to describe in so many words in
a concise way suitable for CBT or indeed to describe here now.
So for now CBT is not an option for me.
Now I am concerned here that my experiences described above may put
others off CBT. But the idea of this blog is to explain my difficulties
to help further an understanding of this condition, and if I did not
accurately describe my experiences my purpose in writing this blog would
be meaningless. CBT is considered the best treatment option for OCD and
it does help a lot of people to cope more effectively with their
condition. it is also useful for the treatment of depression which is
the result of negative thoughts or view of circumstances. My OCD is very
severe it has become entrenched over a very long time, it has been about
twenty years since I received any sustained therapy of any kind.
Moreover I have AS. In the recent entry above the idea is postulated that
there is a subtype of OCD with AS a duel diagnosis and this type of OCD
may be more severe.
Now I don’t think that there is anyone without hope and even the more
severe cases can improve with the right therapy and support. There are
other factors which prevented me from having CBT such as migraine and
CDH. It is not easy to talk with a therapist for an hour if you have a
headache, are sitting in a room with ether a florescent light or facing
a widow with a sunlight in your eyes or you have to ask for the key to
the toilet whilst waiting in the waiting room which if you have IBS and
need to use the toilet several times is embarrassing and very anxiety
provoking.
CBT has helped a lot of sufferers. However it is my opinion that
treatment fails because there is lack of support. Once the patient has
gained some ability to cope with his or her condition and has made
progress such, support as little as there is, is withdrawn. Therapy is also only for a scheduled and
limited period of time and thereafter the patient maybe discharged with
no follow up support. This has been my experience throughout my life. I
do understand that the NHS does not have finite resources but the fact
nonetheless remains, in my experience once the patient is left to his or
her own devices without
any support the condition soon returns and one finds oneself back at
square one.
Sometimes OCD is about perspective. Often sufferers, particularly those
of long standing, loose perspective . Initially and in relatively mild
cases or newly Diagnosed cases sometimes a little normal perspective from
another person can make all the difference. I am not talking about
enabling or reassurance I am talking about giving the person a normal
perspective. I found it so frustrating in times past when a CPN would
sit there and do nothing, not even provide a perspective when I related
certain scenarios concerning contamination.
Once having made progress it is very difficult for the OCD sufferer to
retain this progress. OCD is powerful, the mind is a powerful tormenter
when it is under the dictate of OCD, it is so easy to slip back into
ones old ways if left to ones own devices.
September 21st
When in
doubt, do the courageous things.
Jan Smuts
Well I am about to publish
another batch of entries, again another torment of obsessing and
checking. Concerning my perfectionism, my intense dislike of not having
everything just right, my tendency to make mistakes is of course a
dreadful torment. This tendency could be the result of ADD.
No matter how many times I correct something there are always mistakes,
letters missing, whole words, even several words missing and words spelt
incorrectly despite the word processor. Sometimes it makes a correction
and at the time I perceive this correction to be the word I intended,
but than after publishing I may need to check for one reason or anther
and there are so many mistakes and words which the spell checker has
corrected with entirely the wrong word. One such word might be for
instance, aberrant and abhorrent but sometimes things less
obvious .
And sometimes there is the
phenomenon of thinking that everything is reasonably to your satiation
at the time, but weeks later you look back with horror and wonder how on
earth you managed to feel comfortable about publishing this or that.
The mind is a source of
continual torment, it will torment you your entire life, turn a pleasure
into a misery, a good event into a feared event, satisfaction into
dissatisfaction - yes at one time this website was enormously
satisfying. There was some OCD checking but but no so much to be of
detriment, however it has gone from bad to worse and than some. There
are all sorts of things going on with my health that make it an
endurance test but I wish to persevere as my life would seem very empty
without this distraction. I feel it gives me some purpose, that at
the end of the day something I may have said will help fit together all
the pieces of the puzzle.
September 22nd
Autumn is a
second spring when every leaf's a flower. "
Albert
Camus
I don't know about a
second spring, I don't think we had the first one. We most certainly by-passed summer this year.
Today it is the last day
of summer according to the Celtic calendar, tomorrow is the autumn equinox.
Naturally the weather is not determined by such considerations for
indeed throughout this dreadful summer it has felt more like autumn
throughout. It
is as though we have not had a summer, after a unseasonably warm... no
hot April, during which most people expected a continuation and a long
hot summer it has been unseasonably cool and wet. And this went on to
become one of the worst summers I can recall in my entire life. For most
days the sky was heavy with cloud, with frequent and at times torrential
monsoon like rain. In many parts of the UK homes where floored ,many people
now live in temporary accommodation and it will take many months
for flood damage to be rectified.
Also of importance to many
people who visit this website and blog is the effect this dreary
miserable weather has had upon ones mood is not inconsiderable.
From my own experience trying to cope with a difficult life can at times
be compounded by depressing miserable gloomy weather. Waking each
morning to a cloud leaden sky is disheartening, particular when one
wakes each morning very dejected and anxious greeted by depressing and
frightening thoughts not to mention the diversity of co existing
conditions the most prominent of which is headache. For many with
an anxiety disorder, depression or mental health issue or indeed anyone
going through a traumatic time the dullness can make matters more
unbearable than would otherwise be the case. Yes I am labouring the
point here as for me and many others it is a significant issue and one
which determines ones mood . A bright warm and sunny day may not of course
rid you of your anxiety or depression but it sure makes you more likely
perhaps to cope, except of course during severe traumas and
circumstances, but in the main a pleasant summer's day is a boon to ones
ability to function.
I get every nervous over
medical appointments for many reasons not only because of the fears of
invasive treatment and hyphochondrical concerns but also due
to social interaction, making myself understood. And with sensory
overload, headaches and coping with the usual waiting room delays, which are
an understandable a part of any medical waiting room experience,
such necessities are a nightmare of dysfunction for people such as myself. However such
anxiety ridden experiences are enhanced by a dreary wet and cold day. In
simple terms you are more able to cope and feel more motivated when the
weather is pleasant.
Yes of course one has to
accept inclement miserable weather living in the type of climate we have
here in the UK, however after the respite of summer the gloom of winter
is less awful to bear, at least initially. However with the summer this
year it will feel as though we have had no respite and autumn and winter
will appear to be more protracted than would otherwise be the case if we
had had the summer that was predicted in April.
For many who suffer with
seasonal affective disorder SAD this summer has been a difficult time
and there has been no respite that suffers of this condtion have come to
expect during the summer months and which they rely upon to give them a
boost to face the depression of the coming shorter and mostly gloomier
days.
An interesting article on
this subject can be found in the Independent on-line website
"The summer is
traditionally a time of respite for those susceptible to SAD, but mental
health experts have warned that with sufferers reporting winter symptoms
throughout the season, the effect of the prolonged bad weather will make
the winter months even more of a struggle than usual."
Winter may herald SAD
epidemic for millions.
To read the rest of the
Article click the link below
Winter may herald SAD epidemic for millions - Independent Online
September 25th
I am rather behind with updates to the
main website but finally today I am about to click that all important
publish button with the usual amount of apprehension, trepidation and
doubt. Doubt of course being the precursor of the aforementioned emotions.
This month there are
more letters in the
self help section from
Annette.
There is a new
publication in the
Sufferers Stories section from Gary a suffer of AS and OCD,
this is an insightful autobiographic account concerning his childhood
experiences. There are also three very interesting e-mails which Gary
has given permission for me to include
Website
visitors' comments is a new section where I hope to include the comments of people visiting this website. Only with permission of the
author of course. So please anyone who writes to me don't worry your
comments will not be included without your permission. You will
probably in fact be asked a couple of times even after giving your
permission initially to ascertain that no mistakes are made. I appreciate your comments
so please do not hesitate to write.
Also if anyone wishes to
write about their experiences of or indeed anything pertaining to
any of the conditions included in this website your articles will
be most welcome. I think that the sharing of
experiences with one another is beneficial and supportive. Often
sufferers of the conditions included on his website may feel alone and
isolated and it can be of help simply to know that they do not suffer
alone. Also often it helps others to share our experiences or courses of
action which have helped us in the past or the present. It is also of
help to exchange information and ideas. Even accounts of our less than
positive perspectives can be of help to further increase an
understanding of these condtions and how they effect the individual.
Real understanding of these conditions can only come as a result of
sufferers sharing their thoughts and perspectives. No matter how many
text books a psychologist can read there is nothing more insightful than
the perspective of a person who has to endure the problems related to
such conditions and indeed as a result of multi- disorders.
September 27th.
The
oldest and strongest emotion of mankind is fear.
H.P. Lovecraft
Today on breakfast TV was a segment about unusual phobias such as the
fears of buttons, which I believe is a more complex condition than a
specific phobia concerning more
common fears such as arachnophobia, fear of spiders, and Ophidiophobia, a
fear of snakes. However this is not the point of my comments here today.
What shocked me the most was the way this segment was introduced with a
picture of a huge tarantula straight on the screen with no warning.
There are invariably warnings concerning strobe lightening and flash
photography because of the effects on people with epilepsy and of course
rightly so. However it doesn't appear to matter if someone with a severe
phobia of a spider is thrown into a panic by this unexpected
presentation which appeared long before any commentary of any kind. And
even if there had been some introductory comments it would not occur to
anyone that he or she would suddenly be confronted with an image of a
spider as you can't imagine that there could be such insensitivity.
After all when phobic societies explain phobias on the net or in
leaflets and so on they do not do so by displaying images
of one of the most common of phobias.
Yes I know that there
could of course in theory be a long, no infinite list of such
considerations and such would be
an absurdity, however with common place phobias I think that people
should be forewarned that they are about to see a huge photograph of a
spider, a snake or rodent, to name just three of the more common phobias
. After all what was the point, are we incapable now of simply listening
to commentary without the necessity of visual imagines plastered
everywhere
Moreover during the entire
interview with someone, not sure if she was a suffer or specialist as I
was too occupied by my tirade of angry comments aimed the producers of
this TV program,
there where two prominently displayed photographs of a spider and a
snake.
I thought this was grossly
insensitive particualry considering the subject of this segment. I do
not believe that people in general have empathy for fears or emotions
that they themselves have no experience, however this I think was
shocking insensitivity and this is in fact a fine example of the
lack of understanding there is in general by society for people who
suffer with these and other phobias.
Fear of spider and snakes
are not to be lightly dismissed. My mother feared snakes looking at a
picture of one induced fear. The apprehension concerning the possibility
of such an encounter in the countryside was significant despite
the fact that snakes are seen relatively rarely in the UK. Spiders are
of course something a number of people feel uncomfortable about and have a
aversion to. However full blown Arachaphobia can be a very disabling
condtion as of course a spider may present itself virtually anywhere. I
recall in the 1960s an article which both shocked and saddened me about
a man who lived alone who one day left his home and shot himself. He
lived in a thatched cottage, the kind of chocolate box cottage, the
idyll we all envision of country life. Yet his home was anything but
idyllic infested with spiders, as thatched roofs tend to be, he could
cope no longer and took his own life. Fear, phobic fear can become
that intense for some that in the intense throes of such fear death may
appear to be the only way out. Fear can overshadow our lives so
much so that more rational courses of action, such as in this case
moving, are not considered and in any case unless one is of a certain
financial position moving may be impossible or even delayed and the
person than feels trapped by what he may perceive as inexorable
circumstances with which he can cope no longer.
To suddenly be confronted
with the source of your fears in such an unexpected way can effect the
rest of your day or even weeks or months ahead. As I have said I
appreciate that not everyone's fears can be accommodated but surely it
is not asking too much that some consideration for the sensitivities of
people with these more obvious phobias should be taken into
consideration.

*
Disclaimer :
No responsibility is accepted for the content of external links
including blogs:
Concerning blogs : Although I have initially looked through the
recommended blogs in my blog roll I have not read every single entry and
have selected each on its overall merit: interesting regular entries .
However the comments and opinions of the respective blog owners do not
necessarily reflect my own opinions.
*
Contact
I will endeavour to reply to all e-mail, however please bear in mind
that I have a number of quite debilitating illnesses and there may be
times when there will be considerable delay. Also I will not
publish anyone's comments, as appears to be the procedure
with blogs, without permission of the author : If you would like me to
publish your comments please indicate clearly at the end of your e-mail.
All comments are welcome including polite constructive
criticism and difference of opinion. However I reserve the right not to
publish anything that I consider would be offensive or in any way of
detriment to anyone particularly those who sufferer with the illnesses
included on this web site.
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September 19th