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Extended
version
Note: I had
some considerable anxiety about publishing this longer
version as it is very repetitive and rambling. I am now
simply so exhausted by trying to edit it to make it more
acceptable and eliminate unnecessary repetition that I am
now unable to do so without causing both considerable delay
in publishing and an increase in my anxiety. Therefore I
have decided to publish it as it is notwithstanding these
failings which I may rectify when circumstances are more
favourable.
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Introduction
Aspergers syndrome: A personal
consideration .(Shorter version).
"Having a dash of autism," is how author Uta Frith
describes individuals with Asperger's Syndrome (AS)
Today this very morning I have had what can only be
described as a eureka moment; a moment or a series of
moments when suddenly all has been revealed and some of the
problems, frustrations and confusions of years has been cast
aside. No sadly it is not a positive event inasmuch as I
have overcome any of my difficulties, however I have gained
what can only be described as an enlightening moment
concerning the conditions from which I suffer, most
particularly my OCD and why I experience difficulties
communicating with other people. I need of course to get a
diagnosis or a confirmation from a doctor. I anticipate
difficulties here as it appears to me that in general with
this kind of condition, and this includes anxiety disorders,
that mental health professionals think the only thing that
matters is addressing the symptoms and that precise
diagnosis really is not important. In fact it was not
until I was as admitted to hospital that I formally received
the diagnosis of OCD despite having spent the previous 10
years from the time of it’s full blown manifestation
thinking that my problems, as bizarre as they are, where the
result of anxiety. Consequently much time and energy was
wasted reading material and so on which was totally
irrelevant to my condition with the added result of feeling
incredibly lonely and isolated as there appeared to be no
one similar to myself. And that is the result of not having
anything upon which to base my research. So yes it matters
to me and one of my favourite quotations sums it all up for
me: When the disease is known it is half cured, Erasmus
Colloquies. The “disease” in question is Aspergers
syndrome AS
In 2005 I wrote the above in my journal: I have never
posted this entry on my blog because at that time there were
still doubts but many of these doubts are being dispelled
the more and more I look into this possibility.
I am a sufferer of OCD and you can read my
memoir
concerning my life from the perspective of a sufferer of
this very incapacitating disorder, which has for me despite
much therapy remained intractable. When I wrote my memoir AS
was not a consideration, at least at that time I had not
heard of this condition. However by a strange quirk of fate
I had read Donna William’s autobiography Nobody
Nowhere, a autobiography of an high functioning autistic, in
order to get some idea how to write my memoir. At the time I
did identify with much of what Donna wrote about in her
autobiography, at least I could identify with many of the
symptoms of Donna’s autism albeit milder then those
typically described but until my son’s diagnosis I did not
consider the possibility further.
I now give a great deal of consideration that I may also
be on the autism spectrum as a duel diagnosis to my OCD, OCD
being the primary condition, by primary condition I mean the
condition that is of greatest detriment to your life . At
least that is how I define the term primary condition and
how I will use the term here and elsewhere in my writings on my website. I now consider that in addition to OCD I
may also have Asperger Syndrome AS (a variant of autism) , or
high functioning autism, often the two are used
interchangeably however there are some differences
concerning the symptoms presented in the first few years of
life. I am at the very least effected by significant
autistic traits enough to have a profound effect upon my
life in general and my OCD. I believe that it is the
addition of AS that has made it difficult for me to cope
with my OCD or to sustain any improvements that I have made.
I believe that the addition of AS has compounded my OCD and
made it more difficult for me to cope with this
incapacitating disorder. There are a small number of people
with OCD for whom it appears no amount of therapy brings any
lasting relief from the torment, and I now consider that I
am one of these unfortunate few. Moreover I now believe that
the possibility of AS and other significant co-existing or
co-morbid disorders may have a role to play in such
intractability. Even if this is not the case in an obvious
proven way it cannot be denied surely that the presence of
any co-existing conditions results in complications and
impedes the sufferer’s ability to cope with or improve the
primary condition. Furthermore I believe that there is a
relationship between OCD and autism.
My doctor asked recently if it was important for me to
have an assessment to ascertain if indeed I do have AS. I
had consulted her about my migraine and had mentioned that I
thought that I may have AS. I had previously spent the last
two weeks prior to this appointment writing in detail why I
think that I qualified for a diagnosis of AS. The first
draft was thirty pages long the second was twelve and with
some editing from my son we got it down to nine pages, still
rather long to expect ones GP to read. I had wanted to ask
her to read at least the first three pages and thereafter to
browse the headings and I worried about this for days
rehearsing over and over how I would present his request. I
knew that I had to write it all down as I would never manage
to explain verbally because of my social interaction
difficulties which I will describe in due course. Despite
such rehearsal I never got to give her these papers and
instead attempted to explain the situation which is always a
dismal failure as I get tongue-tied, muddled and appear
socially inept. As is always the case when talking to others
I experienced communication difficulties both with
initiating a conversation and responding, it is as though I
process information at a different speed and as a result I
failed to explain why I need to know one way or another. I
found it difficult to articulate as though the words would
not form in my mind in order to clearly make this request in
any coherent manner. However after a somewhat garbled
attempt my doctor has agreed to look into this although
there may be no one locally who can undertake such an
assessment, and I am too anxious to travel any distance to
do so. I will include more here as the outcome of my request
progresses.
So why do I need a diagnosis of Asperger syndrome ? In
the next few pages I hope to answer some of these questions
for you. I hope that my comments and observations may be of
help to those of you who may be considering similar
possibilities and to help gain more understanding concerning
the complex natures of such conditions as AS, OCD and many similar conditions and
their interconnectedness.
The following quotation perhaps
describes the need for a diagnosis perhaps better than I am
able
"For some teens and adults, this is a tremendous relief:
it puts a name on a set of issues that has troubled them
throughout their lives. And it also opens the door to
support, treatment, and community.
Lisa Jo Ruby
About .com"
Knowing that I have AS, if appropriate, will help me make sense of my
difficult life , why I have always felt different. Sufferers
of any condition find comfort and a sense of belonging when
they are diagnosed, most people need to identify with others
who are experiencing similar difficulties or
circumstances. Most people need to put a label on why this or
that is happening to them, why they feel alienated and
different from others, why life does not seem to unfold the
way it does for other people. Without a formal diagnosis you
are simply not confident enough to present yourself for
instance at support groups or even on-line groups. I find it
disappointing that still after so many years mental health
professionals just do not understand this. Concerning
therapy if I do have AS therapy needs to be adjusted to
accommodate the presence of AS , for instance according to
Temple Grandin, a high functioning autistic,
medication needs to be administered in lower doses:
"People with autism have
very sensitive nervous systems. Some individuals may require
much lower doses of medications than people with a normal
nervous system. This will vary from individual to
individual. If some individuals are given too high a dose of
either an older tricyclic antidepressant or one of the newer
medications, such as Prozac or Zoloft, there may be side
effects."
Evaluating the Effects of Medication
Temple Grandin, Ph.D.
For me personally concerning AS; if appropriate this
diagnosis will help me to understand why I have experienced
difficulties with relationships and social interactions that
have left me feeling as though I am on the periphery of
society, like an outsider looking in but never
participating, isolated, alone and why I have had great
difficulty in coping with my OCD despite therapy. The last
consideration I will explain in more detail later in this
article . I like to label and categorise things - I
understand this in itself is an AS trait - and this is yet
another reason I need a diagnosis. I need to know if I have
AS without a formal diagnosis there will always be doubt. I need a diagnosis to see my situation in a complete
perspective in order to have understanding concerning the
difficult life I have had and it addresses questions about my
behaviours and attitudes and so on that are not answered fully by OCD. Most particularly social interaction
difficulties, generally speaking people with OCD do not have
this problem, it is not a part of the diagnostic criteria
for OCD. If it is present, as is the case for myself, it is
the result of another condtion such as AS, social phobia or
avoidant personality disorder. Last but not least I plan and
simply wish to know if I have an ASD in order to then use
this knowledge to find out about the condition in order
hopefully to improve the quality of my life.
It is important that I point out that OCD is my primary
condition which exists as a separate diagnosis rather than
part of AS. Obsessions and compulsions present as part of
the symptomatic criteria for many people on the autism
spectrum but usually not in quite such a disabling way and
indeed if such obsessions and compulsions present
significantly often the separate diagnosis of OCD is given.
I consider that the possibility of AS may explain not only
why it has been so difficult to explain my situation to get
effective treatment or to have friends or other
relationships and so on but it also explains why I have
sensitivity problems such as sensitivity to noise, (often
hearing noise that others are unable to hear) bright lights,
rough cloths and a whole range of other considerations which
I will explain in due course. These difficulties are not
part of OCD and indicate another disorder which I believe
may be AS.
So why do I believe that the presence of Aspergers has
made my OCD more difficult to treat.
It is my opinion that the existence of co morbid or
coexisting conditions greatly effects the primary condition.
It would seem obvious that the presence of
co-morbid or co-existing conditions will have an effect upon
the primary condition or indeed upon one another, yet little
has ever been done to treat some of these co morbid or
co-existing problems, clearly identify them or diagnose them. Other
disorders have greatly effected my OCD and have also had an
added impact upon other areas of my life which in turn also
indirectly effect my OCD. Such as in the case of AS my
inability to interact socially and make myself understood in
order to receive effective therapy. I believe that it may be
because of AS, particularly my social interaction problems
which cause significant anxiety in any social situation,
that my OCD is intractable. I think one of the greatest
difficulties that I have in getting help concerns my
inability to effectively relate my problems; difficulties
expressing myself have hindered my progress. Especially when
talking about health or emotional problems, I am unable to
think fast enough to form the words to convey my symptoms
quickly or clearly. I can explain such issues more easily in
writing. Moreover my social ineptitude means that I cannot
do things which distract from my OCD which require social
interaction such
as join clubs or associations, make friends and so on.
Moreover people on the autism spectrum experience a general
anxiety which adds to the anxiety created by OCD. In short I
have more to contend with, more conditions that create
anxiety which in turn increase my OCD because OCD breeds on
anxiety and stress and the more of either in your life will
result in an increase in OCD. OCD is rather a cyclical
condtion and while I believe that CD is neurological rather
than purely psychological OCD is nevertheless made worse by
the presence of anxiety, stress and depression while it
itself creates these condtions.
There are additional symptoms other than social
interaction which lead me to strongly believe that the
problem is due to an AS rather than the other conditions
such as social phobia or avoidant personality disorder.
These symptoms I once put down to my OCD such as sensory
problems being the result of anxiety but now in light of
recent events and much research on the net I now consider
otherwise. I have some doubts though as some of the
diagnostic criteria doesn’t fit. However my son having
recently had a diagnosis of AS, which I understand may be
genetic, adds weight to the possibility that I may have AS.
In many families of a person with autism there will be a
family member with OCD. The possibilty of some form of ASD
or significant traits thereof may be present in people with
OCD. It is something that medical professionals need
to take into consideration when making an assessment a
consideration which in all fairness would not have been a
available when I was assessed when I went into a psychiatric
hospital in the early eighties.
I will first list the symptoms which I manifest and than
the symptoms which I do not.
The following symptoms lead me to consider the
possibility that I may have Asperger syndrome in addition to
my OCD.
To begin with here are the results of on-line tests.
These test are available on-line and may be taken by
anyone.
"Psychologist Simon Baron-Cohen and his colleagues at
Cambridge's Autism Research Centre have created the
Autism-Spectrum Quotient, or AQ, as a measure of the extent
of autistic traits in adults."
To take the AQ test go to Wired magazine's website where
you can take the test and calculate your results.
Wired 9.12: Take The AQ Test
I scored 35 the last time I took this test.
The Geek Syndrome The Aspergers
Syndrome Test.
To take the test go to the left hand column and click
Geek test
I scoured 32
(The symptoms I have listed relate to the
DSM
BehaveNet® Clinical Capsule™:
Asperger's Disorder
and similar diagnostic criteria and other symptoms which
I feel may be relevant to the possible diagnosis of AS or
other ASD, along with characteristics which people with AS
appear to have and which I have read about in books and in
internet forums such as
Wrong Planet - Asperger and Autism
Community)
Difficulties with social interaction
The title of Robert Heinlein’s science
fiction novel “A Stranger in a Strange Land” nicely
describes how I feel for most of the time.
I have difficulties initiating,
maintaining and ending a conversation.
For as long as I can remember I have
experienced hampered conversational ability. I do not fit in
socially. I am unable to think fast enough to form the words
to communicate quickly or clearly, neither can I think or
process information quickly enough to respond in the way
people expect. I am often therefore unable to express my
thoughts, or say what I wish to say or even to formulate
thoughts quickly enough to respond. I cannot think of
anything to say, sometimes there are no thoughts there no
matter how much time I have to respond. I find speaking to
anyone difficult. I find it very difficult to express myself
verbally and this is especially so if I need to discuss
health issues or emotional problems as already described.
However any type of verbal communication does not come
naturally, even the most simple of social interaction is
difficult. I am hopeless at small talk. I have difficulties
communicating, not knowing what to say, the words often
coming out all jumbled and inarticulate. In a group of
people I will remain silent feeling awkward, conspicuous,
tongue-tied. I become quietly panicky, wanting to say
something but not able to do so. I invariably feel awkward
not just because of my inability to participate or initiate
conversation but also in a way not easy to describe as
though I feel physically out of place, clumsy and awkward
with unnatural movements, and I feel as though this is
noticeable. It is as though there is an barrier between me
and others, as though there is no connection with others. As
already described these communication difficulties I
believe, have been a detriment in getting mental health
professionals to understand my OCD problems, particularly now
that they are so complicated and interwoven. Although I find
it easier to write than talk there is still a problem with
writing. I do write prolifically but it does take inordinate
lengths of time not only because of the OCD checking and
rumination problems but also because it is difficult for me
to find the correct words to express myself.
I rehearse expected conversations, impromptu
conversations leave me tongue-tied. I do not know how to
interact with others; I am socially inept and don’t fit in.
With very few exceptions I have had few
close relationships. At the present time I have no friends.
Childhood was a lonely experience of social isolation, I
avoided unnecessary contact with other children.
Now in adulthood I have no idea
whatsoever how to speak with a child. With my own son it was
less difficult however I tended to talk with him in much the
same way as I would with an adult and in some ways of course
this meant that I did not talk to him enough due to my own
inabilities over which I felt guilty not of course realising
that I may AS or other
condition. Yes social phobia explained why I was anxious in
social circumstances but it did not explain the more complex
issues such as my inability to know what to say in any
situation. Baby talk was impossible, it was something I just
could not do as I had no idea how to do this. To compensate,
when he was a baby and a toddler I read to him nursery
rhymes and children's stories very frequently. It is of
interest to note that this was done following the advice of
my health visitor and the paediatrician at the hospital
because there was concern that my son who had been premature
might as a result be delayed in his development. Therefore
when he appeared not to be the same as other babies it was
concluded that this was due to a developmental delay as a
consequence of his premature birth. I had no experience with
other people’s babies as indeed until I had my son I had
never even picked up a baby. It was only the expertise of
the health care visitor that alerted me to these differences
which we hoped he would grow out of and indeed as time went
on he appeared to catch up but was still nonetheless somehow
not quite the same as the other kids. And it would not be
for many years until we found out that he had AS. In fact my
son discovered this quite by accident whilst studying for A
level psychology when he recognised himself in a case study
of AS. This answered a lot of questions that had been
troubling him concerning his relationships with other people
and other issues relating to AS.
During adulthood my attempts to be normal
with rehearsed conversations and contrived attempts at
fitting in produced some superficial friendships but little
else. Notwithstanding such social ineptitudes I met my
husband and we are soul mates and this, believe it or not,
may be due to the fact that he also may have some autistic
disorder along with attention deficit disorder.
To reiterate I used to consider my social inabilities as a form of
social phobia. Now however I think my social inabilities may
be due to AS and the phobic element arises
from fears concerning rejections by society who fail to
understand my social interaction problems.
When I am involved in conversation, which sadly is
becoming less often, I find it difficult to maintain a flow
of conversation and often not knowing when to change
subjects - I usually leave that to the other person who
finally gets bored with my inability to change topics. I
just do not know when a subject has concluded and how to
introduce another without an abrupt change. I repeat things
over and over. Knowing when a subject has concluded is
ambiguous and awkward. Also there is the problem of not
knowing what to say unless the conversation is about
something which I am interested in or have a passionate
opinion about such as politics and religion. My husband and
I have an acquaintance. I refer to her as an acquaintance
because both my husband and I experience great difficulty in
knowing who can be counted as a friend and who is an
acquaintance. I assume that because we see this person only
about half a dozen times each year for a chat that she is an
acquaintance rather than a friend, but who knows I sure
don’t. Suffice it to say we meet up for a chat occasionally,
either we go to her home or she to ours. We met at tai Chi
which we no longer attend. This lady who is of similar age
is easier to talk with than most. Unlike many people she
listens while we talk and we do likewise. Although the urge
to say something, get excited or on my soap box as my mother
use to say when I rambled on with passion about social or
political subjects, is difficult to control and I have to
focus my awareness on this and we seem to conduct a
reasonable conversation. This is because we have similar
interests in common. For instance our interest in China, its
history and present situation and political and social
issues. There is very little small talk. Often
though social pleasantries are forgotten, such as how are you.
Today we received a visit from this lady and it is not until
now that I have remembered that we all three of us forgot
such displays of politeness. It was pouring with rain when
she arrived and because of this we soon got on to the topic
of global warming, social graces seemingly forgotten. But
somehow with this person it seems not to matter. Eventually
I remembered to ask after her health about half way through
the visit. No this is not because no one cares it is simply
that we get carried away with what we wish to say as though
there is some urgency to say what is on our minds. I can’t
of course know what is going on in our visitor's mind and
what follows is only my assumption. Her Grandson has ADHD which is on
the spectrum so ... maybe she has at least some autistic
traits. But autism is a spectrum meaning that everyone has
the odd trait or behaviour and perhaps the forgetting of
such social etiquette is hers for indeed in other ways her
social skills are excellent and for the most part I do not
feel too much awkwardness or anxiety in her company. The only problem here
though is eye contact which is
awkward but with effort I think it is not noticed that much.
However after a while I become exhausted and my eyes feel
strained as though the effort of trying to make eye contact
actually puts strain on my eyes. Perhaps it is the tension
of not knowing when it is appropriate to look at someone in
the eyes and when it is appropriate not to do so. I would
much prefer not to look at people in the eyes and cannot
understand why it is important to do so. After all in the
case of other animals to look them in the eye is interrupted
as a challenge and when confronting a dangerous animal it is
not a good idea to look him in the eye. Even our
domesticated cat will attack if you look him in the eye. It
has also been found that most confrontations between people
come as a result of staring at one another, making eye
contact. To me eye contact is unnatural. And quite frankly
so what ! What does it matter if you can’t do this. Perhaps
it is other people who should change their behaviours. With
this lady a visit does not bring with it much anxiety other
than the eye contact thing. However with most other people
conversations are nightmare of dysfunction.
Moreover during mundane conversations my mind wanders off
somewhere and I look spaced out and miss what has been said.
All in all the aforementioned are significant impairments in
all areas of social function either with friendships or even
simply to make complaints or an enquiry . Telephones are the
worst means of communication and is more difficult than a
face to face conversation. Letters and email are much
easier, however instant messages can be a problem though
there is at least more time to think.
However sometimes this can be problematic as a result of
my inability to spell, my lack of coordination using the
keyboard resulting in typing errors. After all for someone
such as myself it is a complex procedure: first trying to
think of what to say, than trying to form the sentence in my
mind in a coherent way whilst so doing and at the same time
trying to think how to spell
the words whilst hitting the correct keys. in addtion to the
consideration of AS I am not coordinated, which in fact is
another presentation of some AS people, and have
symptoms of ADD and am in general prone to errors. I was the
child at school who had red inked comments all over my
written work concerning spelling errors but also what was
described as careless errors which were considered so
particualry if this work was copied off the blackboard. I can’t touch
type I often hit caps lock and not notice so my typing ends
up rather like the example below, which was how part of this
section first appeared. It took approximately ten minutes
to write, edit and correct this paragraph. And often after a
few readings I will come across mistakes. Sometimes such
mistakes are not noticed.
however sometimes this can be problemati as a result of
my inabilty to spell, my lack of corination suing the
keyboard result in typing rros . After all fro soemone scu
as myslef it is a complex procedure: first rying to think of
what to say. that rying to form the sentence in my mind in a
choherant way , tryin to spel the wros whislt hitting the
corect keys , I CANT TOUCH TYPE i often hit caps lock and
not notice so my typing ends up rahter like this whcih was
how the above appeared before editing and correction.
Internet forums are not that easy either and I always
have difficulties knowing when to end the conversation so to
speak , when the thread
is finished, when to reply to someone who has responded to
me and when it is not necessary to do so. I have had to
abandon two forums in recent times because somehow or other
I managed to cause upsets, not of course intentionally it
was a misunderstanding amongst the group concerning forum
protocol . It is a long story and not that interesting.
Suffice it to say I just could not articulate even in
writing what I was trying to say and thought it best in
everyone interest if I stopped participating. There was no
unpleasantness and really I still do not understand what all
the fuss was about obviously I missed something. But these
things which may seem to others of no consequence can be
very depressing and one can feel lonely and isolated as
though I don’t fit in anywhere.
I lost a job many years ago; I was told that because I
did not join in conversations that I made the atmosphere
uncomfortable for my
co workers. There are so many similar examples which have
occurred throughout my life.
During conversations I cannot process information fast
enough to respond. To use computer analogy: It is as though
I am working with Pentium 1 while everyone else is on
Pentium 4 sometimes I just freeze and cant think of any
response.
I used to desire social interaction with others but have
trouble knowing how to make it work. At the present time I
now seem less keen to do this as it is exhausting and
anxiety provoking to such a degree that my ability to
converse with others has deteriorated, the ordeal of social
interaction is stressful to the extreme.
I once belonged to a computer club, my husband had to go
with me even though he has no interest in computers. The
other members where of similar age most older than I. But I
could simply not fit in. I felt conspicuous awkward and for
most part both of us where excluded, left out. I know enough
about computers to join in intelligently, even enough to
perhaps help others with their problems but no I simply do
not know how to integrate, social interaction does not come
naturally at all not like it appears to do for many others
who mix and converse without a thought as naturally as the
way that we breathe, without any forethought or anxiety.
Part of the problem lies in the fact that I do not share
with others my interests. For instance I could have
mentioned my son’s website which I created for him in the
beginning. I could not of course mention this one they
simply would not understand. But no there is something that
prevents me from doing so, something I cannot quite put my
finger on. I find it difficult to tell people much of
anything perhaps I simply do not know how. I see a situation
that allows for an opening but often I let such situations
pass overcome by a hesitancy, the reason for which is often
very difficult to define. Mostly I am lost for words. For
instance one day another member was sitting there looking at
a front-page manual, the same software I have used to create
both websites. Now I could have said to him something like:
Have you created a website? Are you in the process of
creating a website. I have used front page to create my
website... There are any number of things I could have said
to initiate conversation yet I did not as at the time I
could not think how to say these things and the moment
passed as so often it does. Maybe it is that I have to
organise what I say and even after doing so when I open my
mouth to speak it is unnatural and comes out muddled and I
often stammer and than the eye contact problems adds even
more difficulties. Yes there is no doubt that others can
tell that I have a problem with eye contact.
In recent years my inability to interact with others has
increased quite dramatically. I no longer answer the
telephone leaving this task to my husband. I will use the
telephone to make a call if absolutely necessary as I know
the person whom I am telephoning and have some idea what to
say having rehearsed this and I sometimes I write it all
down first. Nonetheless I am anxious when making a phone
call and often procrastinate until I really am compelled to
do so, often until it is too late. For instance the
insurance ran out on my computer before I made the phone
call concerning a fault with my monitor now I will have to
buy a new one.
Other social interaction difficulties include
difficulties in accepting criticism feeling this is a
personal attack.
I am naïve and tend to
trust others and often miss their devious intentions. This
has resulted in a certain level of paranoia inasmuch as I
trust no one.
I have difficulty with reciprocal displays of
pleasantries and greetings and congratulatory responses,
feeling awkward not knowing quite how to go about this in
particular expressing congratulations or enthusiasm that
people expect, for instance when they announce the birth of
a baby. This frankly leaves me cold and I am thinking so what
I am not really interested or have any emotion one way or
another but will for the sake of the another perosn try to
feign such interest and the expected enthusiasm and
sometimes my clumsy attempts are often ignored. The only
exception to this concerns the announcement of a new baby
and took place when a neighbour told me that their new baby
had been born by a surrogate mother not for money but simply
done so as an act of friendship. I was bowled over that
someone should have such a close friendship with another to
be prepared to the child of another couple. I was amazed to
have or be such a friend to someone, such intense feelings
towards a friend are beyond my comprehension.
Failure to develop peer relationships appropriate to
developmental level
DSM criterion 1 2) failure to develop peer
relationships appropriate to developmental level
I have throughout my life virtually found it impossible
to form relationships with people of my own peer group. With
very a small number of exceptions I have had few close
relationships; I could count the number of friends upon one
hand and still have fingers remaining. Childhood was a
lonely experience of alienation. I always preferred the
company of much older people, both my sister and I avoided
unnecessary contact with other children. Neither she nor I
could fit in. This was particularly the case at puberty, the
interest in boys ,pop music and the usual teenage
preoccupations were absent particularly interest in boys. I
tried to have interest in other things and for a time
vaguely likely the current pop music but it was never with
the same fervour as my contemporaries and was perhaps mostly
to appear similar to others. If I consider my behaviour in
those days I really had no interests appropriate for the
typical teenager and had no real friends for any length of
time after leaving infant school. I could not interact with
other children at all to play imaginary games or to become
part of any group. I could just about manage ball games and
that was about it and that was only casual games in the
playground. I could not participate in team sports or any
other kind of sport for that matter. Doing things in groups
was impossible for me. I recall with some horror having to
play housewife for a week with another girl in the forth
year at secondary school. This was a requirement for pupils
in the final year of school. Two girls would get together
and be housewives for a week sharing the duties of such in
an apartment set aside for this purpose. This would also
include having two teachers of ones choice for dinner. What
a nightmare! I recall this so vividly, the fear, anxiety and
awkwardness experienced by my social ineptitude. I simply
could not participate and interact with this girl whom I
barely knew and who had only selected me because there was
simply no one else. No one ever selected me as a partner for
anything and I had no friends at this time in my life. It is
a long time ago now but I recall this particular incident
which was one of many, I was and still am simply incapable
of any kind of co-operative teamwork. I should point out
with family members my husband and son such coordinated
endeavours are not such a problem.
Anything that required team work found me left out as I
simply could not interact with others and this of course
continues today in adulthood, Groups of people are more
difficult to interact with than individuals and I am always
the quiet one who invariably feels left out and conspicuous
by my silence. In heated discussions I get really confused,
such rapid conversations and the need to think quickly cause
more difficulties and my conversation becomes mixed up and
muddled and it is difficult for me to get the other person
to understand. I get angry and frustrated my voice raising
and it often appears that I am becoming verbally aggressive
and the other person senses this and feels they ‘re being
attacked and it than becomes personal. Moreover it is
frustrating and anxiety provoking. Also during conversations
my mind seems to go blank even with rehearsed conversations.
I tend to talk about such things as politics and religion,
the type of conversations upon matters of which I am
interested but which often cause discord with others. Even
when talking about such matters it can be difficult. I often
repeat myself in conversions covering the same ground two or
three times but I have noticed others tend to do this also
Difficulty with eye contact
The DMS criterion A (1) states : 'Marked impairments in the
use of multiple nonverbal behaviors such as eye-to-eye gaze,
facial expression, body postures, and gestures to regulate
social interaction.'
The word marked might be the key here in deciding if I
have the degree of eye contact difficulties that constitutes
AS.
Eye contact is for me a significant problem I find eye
contact difficult even with my husband and son. Eye contact
or lack thereof is one the most prominent features of my
inability to interact socially as such is sometimes very
significant and people I know feel considerable discomfort
when speaking with me. I simply have no idea when to look
someone in the eye; for how long and when it is appropriate
to look away. Most of the time I either look away repeatedly
or whilst trying to be normal stare into someone’s eyes for
too long resulting in an obvious discomfort as the person
with whom I am conversing turns their gaze a way with marked
uneasiness.
Difficulty with physical contact
I tend to shy away from physical contact and if it does
happen I do not know how to reciprocate. For example my
mother in law would embrace and kiss me and I could never
return the affection particularly when we first met. I never
know how to react in such situations particularly when this
happens with people I am not comfortable with, which is just
about everyone except my husband and son and than at times
that also feels unnatural as if it is a learned response. I
would always stiffen if my sister embraced me and my mother
claims that whenever she picked me up for cuddle as a baby
and later as a child I would push her away and become stiff
and rigid. I recall no physical contact ever with my mother
until I left home at twenty one. I can only assume that she
grew cold towards a child who could not reciprocate
affection. This is not to say I do not love or care for
anyone it is simply I cannot display such physical emotions.
I am able to cuddle my husband and indeed clung to him
during times of intense fear due to OCD but otherwise just
lately I am finding it difficult to be touched by anyone and
this makes me depressed. The problem with physical contact
is caused by the effect of overwhelming sensory feelings
whenever I am touched and more so of course If I am hugged
or cuddled. Most bizarre of all is now as I'm thinking about
it the sensations are there now, right now precipitated by
merely the thought of being hugged. These overwhelming
sensations when anyone touches me are difficult to describe
. Today I still stiffen and become rigid whenever I am
hugged.
Inability to share achievements
DSM criterion A (3) states: a lack of spontaneous seeking
to share enjoyment, interest or achievements with other
people, (e.g.. by a lack of showing, bringing, or pointing
out objects of interest to other people.
This has always been a problem and my hesitancy to share
achievements, as described in the previous example
concerning the computer club, I have previously put down to
modesty and lack of self esteem thinking that no one will be
interested. I do however try to at least pretend to be
interested in other peoples interests but at times I overdo
this and it then can seem obviously insincere.
Sharing interests and pointing out things of interest to
other people is difficult and in fact after so long of never
doing this it has become a habit not to do so and I tend not
to think about it. I will sometimes point out things of
interest to my husband and son but with others,
acquaintances and strangers, I would never point out
anything of interest even if I knew that the person
concerned was interested. Why I do not know, I simply feel
uncomfortable or I simply cannot express myself articulately
to do so and often in many conversations I can’t get a word
in sometimes, and I do not know how to interrupt other than
abruptly. It appears to me that with very few exceptions
most people talk and talk. My brain gets overloaded I can’t
focus on what they‘re saying, particularly if the
conversation is mundane or trivial. This is one of the most
difficult problems I have conversing with others other than
actually not knowing what to say, most times in situations
were the other person is talking incessantly I either never
say a word or I have to blurt out what I am going to say and
the person than seems surprised.
I understand that many people with AS
will talk incessantly about their interests but more like a
monologue rather than a proper conversation. For me with
anyone other than my husband or son this is something I
never do as I cannot communicate sufficiently well enough to
do so. Even with my husband and son I really do not talk
much about my interests.
Moreover I most likely fail to notice
things in my environment that are of interest to others as I
am usually absorbed in my own interests and preoccupations.
Also OCD plays a role here and often the task of trying to
cope with it's pervasive intrusion absorbs my focus to a
huge extent along with my preservative thinking where I am
mentally still concentrating on my interests even though for
all intents and purposes I am otherwise occupied. To say I
do not give anyone my undivided attention would be very very
accurate indeed.
I lack social or emotional reciprocity
DSM criterion A (4) states: lack of social or
emotional reciprocity
This is a diagnostic criterion from the DSM the meaning
of which is unclear the following is my interpretation which
I feel is perhaps incorrect but which nonetheless expounds
my difficulties further. And part of this criterion has been
covered earlier concerning social etiquette.
I realise when someone is attempting to socialise however
I am unable to respond particularly if the situation arises
spontaneously and I have not had time to rehearse and
consider what I will say and how I will react. For example
if a stranger or even an acquaintance or relative initiates
a conversation for which I am not prepared I become
tongue-tied. Mostly this is of course much worse if the
person is a stranger and it is a conversation which has been
forced upon me unexpectedly. Mostly I barely respond and if
I do my comments are brief and uncoordinated and
inarticulate. For example recently a little girl whom I
actually suspect as having some problem or other herself
suddenly appeared and said to me: “ It is uncomfortable
walking upon the stones?” We were in the ruins of an old
abbey and the floor was paved with cobbles. I could think of
nothing to say and responded with “yes yes” and walked on. I
felt just awful but I simply was unable to respond quickly
without preparation. This has been the way all my life and
has caused much loneliness and pain. Incidentally I have
always had difficulty speaking to children. I managed with
my son’s few friends but it was always when and only as
necessary. I had no idea about baby talk and do not in any
case approve of talking down to children . I spoke to his
friends the same way as speaking to an adult
Concerning Emotional responses, these are often out of
proportion to the situation, they are basically more intense
and mostly negative.
Concerning other people’s feelings and my attempts at
responding to such: I believe I have some empathy - at least
what I assume is empathy and not some kind of emotional transference.
My emotions and empathy it seems are all or nothing. It
appears that I have only empathy for people whom I consider
are experiencing the same emotions as myself :unhappiness,
pain, stress and other negative emotions . Indeed I am very
sensitive to negative emotions and feel profoundly the
sorrow and misery of others even those I do not know, in
fact more often than not when the person is known to me such
emotions tend to diminish with the exception of my son and
husband, Also the pain and misery of animals whose suffering
causes me immense sadness.
I do have empathy and this was one of the reasons that I
doubted I had AS. However I think that with AS one has
emotions but perhaps they are not the same as for NTs (
neurotypicals people not on the autism spectrum) or are more
exaggerated or intense, but only in certain situations
whilst remaining cold and aloof in other circumstances where
everyone else's emotions are intense . For instance the the day whilst
visiting a website someone had the most endearing Avatar of
the cutest sweetest creature you can imagine. I am not even
sure what kind of animal it was but it had just the
loveliest innocent face and I was overwhelmed with such
emotions for this creature which I would describe as love.
I once saw a homeless person in the street crying. I
offered help but my inarticulate manner made matters worse,
I then cried myself. Often I am overwhelmed completely by
the sorrow of the entire world - at least my perceived
sorrow of the entire world. However, and this is the crux of
the matter, I have no empathy for the more joyful emotions
of others. For instance as I have
already explained I cannot
get all excited if someone announces a wedding or pregnancy
the way other people do, such events leave me cold. I just
don’t have the emotions and find it hard to fake them for
the benefit of others. Furthermore I cannot express what
empathy I do have (or perhaps it’s my transferred misery
which I think is empathy) to another. Someone I once knew,
a former friend (I use the term here loosely as in reality
I had no real emotions towards this person she was someone I
tried to relate to but as usual failed miserable to do so) whom I no longer see now because friendships
do not last, was very distressed. I could see her tears but
could not feel her pain and I did not know how to respond.
She asked me:” can you not see how upset I am?” Yes I could
and indeed I wanted to reach out to her but I did not know
how. I think she thought that I did not care perhaps in this
instance this was true I cannot recal, but yet in other instances I care
deeply and the pain of others effects me profoundly, yet I
cannot express this and reach out to another to share my
empathy or comfort them as I do not know what to say or how
to react.
Touching people except my husband and son seems totally
alien and I rarely know when it is appropriate to do so and
I experience such awkwardness if I attempt to do this. Even
if I care to admit it the same feelings occasionally occur
with both my son and husband and contact feels strange and
unnatural even though I love both deeply. It is important to
note that I would like to be able to socialise in a normal
way, I am not reclusive, the problem simply lies in the fact
that I cannot interact with others in the usual way.
To reiterate: It is important to note that I do have
emotions, rather an abundance in fact I am an extremely
hypersensitive person and feel the pain of others, but not
universally in any situation and at times I can be very cold and emotionless for reasons
not easy to understand. I also feel the pain of other
animals more keenly right down to the lowliest of creatures.
Yes I even feel sorrow if a plant dies or a tree is cut down
. However I have difficulties expressing and showing such
emotion and empathy to most people as in the aforementioned
example. My empathy or emotions are simply not the same as other
people’s appear to be, mine are perhaps inappropriate, for
instance I recall many years ago during a bad time with my
OCD how I genuinely cried when hearing a commentary on the
radio about Robbie Burns, who died in his thirties and how
on the day of his funeral his wife gave birth. I recall
actually crying, I mean seriously crying, as it felt so sad.
It has to be said if I am to be entirely honest, there
are times when my emotions towards others seem dead as
though they have been turned off and I feel cold and
indifferent. I feel ashamed for on a different level, a non
emotional level, I do care about this person and what
happens to them and should they be in dire straits I often
go out of my way often at detriment to myself to offer help,
yet the actual emotions are non existent.
I prefer animals to most people, at least I have stronger
feelings towards animals. In the same way as I have more
feelings towards disadvantage people.
Concerning sensitivity: I feel more empathy for people or
other creatures who are suffering. I have no empathy
whatsoever for happiness or positive emotions of any kind. I
feel a more keen empathy for the suffering of people I do
not know, as for instance the starving in Africa. Individual
people well ... when I see an individual who is clearly
suffering such as a disabled person I feel profound sorrow
and I really feel very depressed and hopeless that my son
is depressed and his life is a misery and I always sense
straight the way any change in his mood. The same applies
also to my husband and recently I can sense a very
significant change in his mood as he becomes more withdrawn.
However displaying emotions borne of empathy is difficult
for me and I come over as uncaring and rather cold.
The only emotion I can display is anger and than it can
take a while to erupt but when it does I most certainly let
go. In adulthood apart from throwing things usually at the
door , walls and so on I have not physically attacked
another. Although at school I did so if sufficiently
provoked. Having said all that I do admit that it does take
a lot to cause real anger or should I say in all honesty I
do well in suppressing this emotion for in truth my anger is
easily provoked. I should not confuse this with a tempter
tantrum borne of OCD frustrations, irritability or
heightened stress levels. In recent years this anger is
there like a kettle ready to boil, often I seethe with
overwhelming anger difficult to control. I feel as though I
am becoming like my mother who always exhibited an
underlying aggression which with increasing age become more
palpable.
Perserverations and repetitive behaviours
The DSM Criterion B
states Restricted repetitive and
stereotyped patterns of behavior, interests, and activities,
as manifested by at least one of the following:
(1) encompassing preoccupation with one or more stereotyped
and restricted patterns of interest that is abnormal either
in intensity or focus
Well as a sufferer of OCD there is of course some overlap
however the preoccupations, in other words obsessions that I
refer to here are intense and addictive like interests and
they are
not the same as the OCD obsessions, and I do know the
difference. Although OCD rituals and obsessive
behaviours interfere with my interests as they do with every
other aspect my life. For me there has always been some
intense and obsessive preoccupation with some interest, idea
or activity. Right now in the last few yeas it has been the
computer including this website site, graphics programs, the
internet and so on. I have other interests such as art but
this is not such an obsession and quite often a good deal of
my art work has something to do with the computer anyway,
such as my attempts to make hand drawn clip art. I often
resent having to do other things to the extent that my
depression becomes more profound and I become irritated. I
am up and on my computer as soon as I wake between 4 and
5am. Yes I have insomnia and this is how this routine came
about but there are times when perhaps I do get up early
just to work on my computer. It has taken on the quality of
an addition and I have to really force myself to do other
things and sometimes it is only the OCD rituals, the needs
of others and pressures of society that one should not
indulge ones time in such things so intensively that I turn
often reluctantly to other pursuits. I have a long deep and
abiding religious preoccupation however this may have more
to do with the OCD part of my personality. Nonetheless
religion as a comprehensive interest in all religious belief
is indeed one of my interests and you would be hard pressed
to find a book in my home which belonged to me that was not
about religion, philosophy, metaphysics or esoterica.
I can’t recall the unusual collections of odd items
associated with sufferers of AS in childhood but in
recent years I have collected huge numbers of stuffed sheep,
ornamental sheep, pictures of sheep and after buying a
digital camera well I of course take endless photographs of
sheep. I do seem to be rather be obsessed with sheep not in
an OCD way as I have said before I do most certainly know
the difference. However my husband does likewise hence all
the sheep photographs in the gallery section on his page.
However since giving all this thought to whether of not I
have Asperger syndrome I now consider that my husband indeed
has some form of autism himself! Well of as unlikely as that
may seem it is of course not impossible and as the saying
goes like attracts like and this may be the reason that
unlike many who have been married for over thirty years we
are still together.
Apparently inflexible adherence to specific, nonfunctional routines or rituals
The DSM Critrion b (2) : apparently inflexible adherence
to specific, nonfunctional routines or rituals
Well I had plenty of these as a child however this is
really where there is rather a grey dividing line between
routines and rituals connected with OCD. I recall having
such routines as a child and will mention those which have
no fear as such attached to them and where not motivated by
intrusive thoughts of an OCD nature. For instance in the
bath if I washed one leg I immediately had to wash the other
in exactly the same way immediately afterwards in a routine
way. If I scratched one part of my body I had to immediately
scratch the opposite site in the same place. I had set
routines in my everyday life such as going to go to bed at
exactly the same time. I had hand washing rituals before
going to bed and these had to be done . No in retrospect
these were not OCD rituals and had no connection with either
germs or something bad happening however there was some
anxiety if this ritual was not performed so there may be
some cross over there with my OCD. Most daily activities
were undertaken in a routine manner and although there was
no fear attached if such was not possible, nonetheless I did
not like changes to my habits and would become stressed or
agitated if I was unable to abide by these routines. If
major and irreversible changes did occur I would adapt other
routines to take their place. This area is very confusing to
separate from my OCD and I had numerous religious rituals
which were more of an OCD nature. And now after all this
time it is of course not easy to recall which were which as
of course at the time no distinctions were made although
there was obviously problems , problems which were noticed
at school and for which I was referred to a psychiatrist
from the age of three and again at eight. I have no personal
recollections. I recall the sedative which I later learned
tasted like gin and looked like gin, ummmm I wonder.....
Interestingly gin was used in the eighteenth century as a
sedative. My mother told me the sedative was advised because
I would scream in the street and was generally disposed to
crying and moaning all day and generally being a misery. I
do recall screaming whenever confronted with a turnstile and
this may have been one of the reasons my parents stopped
going to football matches. Crowds also caused problems
although for the most part I have no other clear
recollections of screaming in the street. I do have the
vague feeling that I was terrified of passing building sites
the noise and the equipment producing feelings of being overwhelmed as did steam
trains, also escalators caused problems and I do recall
anxieties about using them. I recall screaming whenever I
had to have my hair washed. I can recall my mother trying to
wash my hair, my reluctance to lean my head back, the
ceramic sink seeming hugely scary . I recall screaming when
confronted with a turnstile at football matches and this may
have been the reason my parents stopped attending. Moreover my mother said
that the school were concerned as I did not play with my
toys in the normal way. I have no idea what this period in
my life was really all about my mother claimed to have few
memories. However as social services were involved I find it
very difficult to believe that she could not recall much
other than what I have told you above.
I do not like changes in routine and changes in plans
really upset and confuse me. After five years I am still not
settled in my new home and I have not completely recovered
from the shock of this huge change in routine. I do not like
changing immediate plans. This however is two fold first
because it simply makes me uneasy and anxious for reasons
not easy to define. However plans which involve travelling
have an extra OCD component concerning my fears that
changing plans may change circumstances with dire
consequences. I like to know each day what I am doing and
when. I am not at all spontaneous and cannot cope with
ambiguity.
Repetitive motor mannerisms
The DSM
Critrion b (3) stereotyped and repetitive motor
mannerisms (e.g., hand or finger flapping or twisting, or
complex whole-body movements)
I have the involuntary compulsion to rock backwards and
forwards without realising this and was teased for this at
work in my late teens where it was first bought to my
attention. I continue to do this today. Other less noticed
mannerisms include swinging my leg or foot when sitting
cross legged and also swaying from side to side.
This criterion below is described in detail in the
explanations above and therefore need no further
elaboration.
C. The disturbance causes clinically significant
impairment in social, occupational, or other important areas
of functioning
Developmental delay
DSM Criterion D.
There is no clinically significant general delay in
language (e.g., single words used by age 2 years,
communicative phrases used by age 3 years)
At my age now it is impossible to recall if I had
cognitive abilities suitable for my age I have no
recollection as to whether or not there were any delays in
self help abilities, such as dressing myself, feeding
myself, and so on or my curiosity about my environment.
There where delays in reading and I have never been able to
spell. The only problem I recall clearly relating to the
possibility of AS for as long as I can remember is my social
integration difficulties. There were some problems at school
with play and other matters indicating a rebellion against
authority at the age of eight, at least according to a
couple of letters in my medical files. And also the problem
with screaming in the street referred to earlier .
Following is list of other diagnostic criteria associated
with Asperger syndrome or other ASD which seem not to be
included in the DSM but which many people with AS seem to
have.
The following are characteristics of AS or other ASDs
which do not appear in the DSM but are nevertheless
experienced by many on the autism spectrum
Sensory problems:
Sound for me is greatly amplified at least by comparison
to the reactions of others. I am overwhelmed by noise and
often hear noises or am disturbed by noise that is either
not heard by others or does not effect others. With the
occurrence of music just about anywhere and everywhere in
virtually every public building, I can barely cope I
sometimes feel like a child once again and there are times
when I reach up to cover my ears and feel like screaming. My
sensitivity to noise seems to becoming more enhanced. Sudden
noise is anathema and brings about an almost phobic reaction
if I suspect such is likely to occur. For instance if I see
a child with a balloon I immediately become tense should the
balloon burst suddenly. I react by covering my ears even now
in adulthood when really loud noises occur suddenly, such as
fire alarms, fireworks, low flying air craft and the like.
Noises such as people eating, swallowing and sniffing drive me
crazy and even the noise of people moving about, fidgeting
is extremely irritating jarring my nerves, for instance my
husband fidgeting with his glasses or licking his fingers to
turn a page which I don’t like anyway because of my OCD
anxiety about salvia and contamination. I don’t like the
sound of appliances such as vacuum cleaners and the washing
machine. I am significantly disturbed by a constant low
frequency hum from the local factory.
Physical sensation of touch and clothing etc.
Clothing irritates me particularly underwear, bras and
pants. Anything tight or made of rough material is
impossible for me to wear. I can’t wear wool next to my skin
or even synthetic knitted garments. I am sensitive to cloths
labels and seams which are bulky and crinkly materials. I
change very early in the evening into loose flowing night
clothes, I can’t stand my day clothes and can’t wait to
discard them. Sometimes I can’t sleep even with these lose
fitting clothes as such irritate when I become entangled in
them such as a nightdress wrapping round my legs.
Bright lights are a problem particularly florescent.
This problem could also be related to my chronic daily
headaches and migraine. Brilliant sunshine during the summer
months seems now far too bright. I am more comfortable with
sunglasses. I can’t cope with fluorescent lights.
A mixture of all the above such as in a cafe where there
is music, bright lights, background noise - such as from
coffee machines, the rattle of cutlery, the babble of
background conversations, children yelling or crying and the
pressure to make conversation is overwhelming. In such
conditions I can barely think, my nerves are heightened, my
stress levels rise and difficulties with conversation are
more accentuated and I can barely hear or concentrate on
what the other person is saying. I can become completely
overwhelmed.
I don’t like crowds. Particularly when mixed with noise,
bright lights. For instance a shopping trip is nightmare of
misery screaming children, thumping music florescent lights
and the hustle and bustle of crowds is overwhelming
Outburst of anger
I am prone to tantrums for want of a better word such as, screaming, throwing things, yelling,
ranting and raving, sometimes over a small issue others
would not be so angst about. Shouting at the TV mostly about
social injustice, politics, animal rights and so on is a
regular occurrence I am constantly angry for reasons both
personal and non personal.
Other peoples opinions
I rarely if ever understand another’s point of view
although I attempt to tolerate such opposing opinions no one
will ever change my mind and I appear as bigoted, self
opinionated and intolerant. I tend to think others are
stupid and shallow and cannot image how on earth they can
possibly think or behave the way that they do. I find it
difficult to accept that other people do not think the way I
do.
Multitasking
This is of course is impossible. I can only concentrate
upon one thing at a time and often times even that is difficult. For
instance I can’t do something when someone is talking to me,
I either ignore them or stop what I am doing. Using the
typewriter key board is difficult because I cannot do this
quickly while trying to think what to type which includes
such difficulties as trying to think how to express what I
intend to say, which of course is a problem in itself ,than
to construct it according to grammar and than trying to
spell correctly , so what I write is full of mistakes and
needs to be corrected considerably therefore it takes a long
time to write anything. Even preparing the dinner if it is
complicated is impossible now, just lately I cannot co
ordinate all the different stages both of these examples are
further complicated by my OCD.
Concentration
My ability to concentrate and focus is greatly impaired.
I cannot take in verbal instruction easily and on some
occasions not at all. I have always learnt better from books
than from a teacher for this reason. I tend to hurry things
and can’t cope with reading instructions and cannot
comprehended them
particularly if they are boring and I have
no interest. For instance I learnt to use a computer but
don't know which switch on the TV control to use to turn it
on! I am intensely interested in the former and have little
interest in the latter.
My short term memory is poor. I cannot even recall a
series of numbers such as if I were trying to copy a phone
number from the computer onto a piece of paper it would take
several tempts to do so accurately. The same goes for
copying words. I am a poor speller and often need to copy a
word letter by letter and like copying numbers this is
difficult and I make numerous mistakes and most of my
writing is inaccurate, Bizarrely sometimes I do not even
notice maybe for weeks than all of sudden I see a mistake
which would surely have been hard to miss. I check written
work over and over due to my OCD checking compulsions and
also because of this tendency as it makes me anxious that I
have made mistakes which in fact I do and which may have
gone unnoticed for ages despite all the checking.
However my concentration is keen on what would be
described as my preservations, my intense interests or
occupations as for instance I have sat here for hours
involved in the final editing of this account to the degree
that I am irritated by any interruption even the necessity
of going to the toilet
Information overload
After a while my brain fogs over and I cannot think
straight. I am overwhelmed and often incapacitated by too
much information at one time in rapid succession or if under
pressure to react to such information. Too much talking also
has this effect, by which I mean whenever I am being
subjected to too much talking by another person who does not
allow you to get a word in. Conversations exhaust me and
intensive occupation requiring complex thinking such as
studying and writing something like this does likewise and my
thinking becomes muddled and I feel confused despite my
ability to concentrate upon matters of interest.
Face recognition
I find it difficult to recognise people unless I have
known them for years or see them everyday. This problem is
more accentuated whenever the person concerned is seen out
of context as it where; if they are somewhere I do not
expect to meet them and this occurs even if I have known
them for years.
Tuning out, going blank
This has occurred for all my life. I go into what was
once referred to as a day dream and yes I do day dream.
However sometimes I just tune out so to speak or go blank as
though I am in a trance. I suddenly stop what I am doing, my
eyes glaze over and I stare into space - at least this the
way that people who have observed me describe what happens.
Some times I can be watching TV, reading, or even listening
to someone talking and I have no idea what I have seen, read
or heard. it is as though I were not there yet I do not
black out as such. It is difficult to explain quite what
happens.
Perfectionism
I cannot tolerate mistakes. This brings about much
torment in my life and often impedes progress to such an
extent that I procrastinate the commencement of a task
because of the fears of making mistakes. Such as with
painting or my writing for my website I will delay starting
either of these endeavours because of the torment I know
that I will endure because of my perfectionist tendencies
which in themselves are impeded by my attention deficits and
and tendency to make errors. And
concerning my art plain and simply lacking the talent to
paint in the detailed manner that I seem not to be able to
edit out so to speak the way many artist do. I struggle to
include in a painting or drawing all the detail, every blade
of grass every leaf, which I do not have the talent to do
successfully.
I have difficulty generalising
for example this
explanation which is in fact only a third of the original
length. I am told what I write is over detailed and rambling
but to me it appears inefficient, as to my way of thinking
all the details matter or at least I have difficulty knowing
which do not. This very account of my writing is over
detailed and repetitive I have tried several time to
describe the situation in a more concise manner but have
failed to do so and this must therefore remain as it is
otherwise I will never be able to publish it to my website.
I cannot be concise. As already mentioned this occurs with
my artwork and along with perfectionist anxieties my
inability to generalise interferes with painting concerning
the inclusion of too much detail, if I try to point from a
photo I try to add every detail I do not have the knack of
painting the general aspects thus art is frustrating.
An example recently of my inability to generalise arose
when for an assessment for CBT I was required to fill in
automatic response forms . This is done in order for me to
begin to look at my thoughts, take the situations and, with
the help of my psychologist, try and find a more rational
approach. Now on some level I knew that this would only work
with the situations we would discuss during the session.
When the time arrived for me to carry this method over to my
daily life I knew that I would not be able to apply the
thinking I had been taught in the examples to any situation.
Every situation would appear to be different and the same
methodology would not apply. Lets look at a simple example
from my OCD. When I was receiving exposure prevention
therapy I would expose myself to a situation which involved
contact with a dog, this means I would
touch the dog and not wash my hands and than go on to touch
my cloths and my possessions and everything in my day to day
environment. The idea was to sensitise my fear of dogs and
catching rabies. However when nothing happened and no one
died because the dog did not have rabies this did nothing to
alleviate my OCD concerning contamination by dogs because I
could not generalise. The dog I came into contact with may
not have had rabies but that would not mean that in general
dogs did not have rabies: because one particular dog did
have this disease did not mean that other dogs did not. No
matter how many dogs I came into contact with this fear
could not be generalised therefore the therapy failed.
I don’t like learning new tasks I have impatience following
instructions.
I have no patience to read manuals unless it is to do
with my interests such as a computer manual than I will sit
and read this much in the same way as some people would read
a novel . But for boring things such as how to work
the video or how to assemble flat packed furniture the
instructions are ignored and I tend to try to manage without
and get irritated and impatient if this is not possible and
I have resort to the tediousness of reading the instructions
which are read with some considerable irritation and
impatience. I can only learn new tasks which interest me.
Other general characteristics of mine which may be
relevant towards deciding if a diagnosis of AS is
appropriate or otherwise.
These characteristics have been mentioned by others who
are on the autism spectrum but are not specifically
mentioned in any diagnostic criteria.
Hyper-critical tendencies and other negative presentations
I am generally very critical of others, negative and unforgiving,
fixating on bad experiences with people or events for an
inordinate lengths of time.
I adhere to rules perhaps too
rigidly.
I am mainly a serious minded person everything has
to have some meaning or purpose. I can do few things for
sheer enjoyment. My artwork for instance is sheer torture
for the reasons described above and the only reason it is
undertaken is so that I can feel I have done something useful,
the same applies to my website. Although in the beginning
this was not the case and there was some satisfaction if not
enjoyment, but enjoyment is relative is it not and depends
on your perspective, but since OCD has intruded with its
anxieties about everything I write and also checking
compulsions it is now not as satisfying as it once was.
I become upset when things do not work out the way I
expect them to do, sometimes excessively so even in minor
disappointments that others would more easily take in their
stride. My temper will erupt over trivial issues. Any
inconvenience I become extremely annoyed, with shouting,
swearing, hitting something such as thumping on the door or
throwing things . My volatile temper would exploded
sometimes for the least little thing during disagreements
with family members.
I have an extreme dislike of being interrupted particularly if
intensely occupied in my preservations. My whole body tenses
I become irritated snapping or I ignore the person who has
interrupted. if indeed it is a person. Sometimes I find
myself extremely irrationally irritated if I have to
interrupt what I am doing to for instance use the toilet or
get on with tasks such as preparing a meal. Such can induce
anger and indeed depression.
I experience an Inability to deal with people assertively
- unless I get angry.
I also tend towards being paranoid. I trust no one and
this is due to having been taken advantage of, because of my
sensitive nature and not willing to hurt another, always
wanting to keep the peace and also because of my trusting
naivety because I cannot read the intentions of others.
However once I have been taken advantage of I never forgive
even after decades have passed.
Difficulty it transitions for instance from one task to
another.
Not knowing how to finish conversations or written
accounts such as this account which, after the section
concerning aspects of AS that I do not have, is now provisionally
concluded but may be added to or altered as the situation
warrants.
AS characteristics I do not have, at least not in an obvious way.
The most notable of these is
the nerdy symptoms. I have the kind of interest typical of
AS such as science but I do not have the good memory for all
the facts. often I can understand an idea or scientific
principle and know that if I had the correct terminology I
could understand more complex things but the problem lies in
my inability to remember. Moreover I can understand
something while I am reading but cannot articulate this
understanding in either words or writing. I find more
serious often obscure subjects fascinating and for years was
always rather non-pulsed when people would exhibit some
surprise at the nature of my interests. For instance I found
myself feeling a quite keen interest and looking forward
with anticipation about reading an article in the New
Scientist about the big bang, and looking reward to anything
these days is a rarity for me no doubt due to depression and
OCD however things of this nature do spike my interest
perhaps more than is usual for many people. However I could
not now relate to you much of anything I have read other
than the very basics. Moreover I could not give you
the long rambling monologue which seems typical of AS as I
simply cannot coherently articulate what is in my mind. And
even with simpler subjects it would take enormous amount of
time to do so even in writing, and it has taken weeks to
explain this problem, this makes me appear stupid even
though I can understand quite complex issues. Also there is
this bizarre phenomenon which may be OCD related where I
basically know I understand something yet doubt that I do
and continue to seek information to clarify for myself that
I do indeed understand. If I make a concerted effort I can
recall facts such as the highway code of which I answered
correctly very question for my during test yet failed to
pass the actually driving.
Memory
Most people with AS appear to have
an excellent memory, it is one of the more noticeable
aspects of this condtion. My memory however is poor as I
have already explained. It is at the very least selective.
For instance the other day I picked up a book of which I was
interested in and could recall the exactly when I had bought
it even though it must ahve been about fifteen years
ago, I could see in my mind the situation and recalled the
circumstances along with other related mental images.
However it can happen that I can be looking through my stuff
and come across a possession and it is as though I have
never seen it in my life although I know it is mine. I can
recall facts if I make an effort to do so with accuracy but
it takes persistent and determined effort . I am a slow
learner but I get there in the end but only if the subject
is of interest to me.
(4) persistent preoccupation with parts of objects
Not a problem this is one manifestation I do not have
unless of course I am missing the point, often diagnostic
criteria such as the DSM can seem somewhat vague, ambiguous
and open to misinterpretation by anyone other than a
professional.
less Specific considerations: IBS
Many people on the autism spectrum have gastrointestinal
problems. I for instance have IBS.
It is a known that the intestines have the highest
concentration of nerve cells second only too the brain,
resulting in a stream of constant communication with the
brain and the gut and it is likely therefore if you
have a neurological disorder, a malfunction of the
brain you are more likely to suffer with IBS and other
gastrointestinal diseases, such neurological dysfunctions
include depression, anxiety, panic attacks, OCD and of
course autism including AS it is important to note that this
communication between the brain and the intestines involves
the neurotransmitter serotonin which is also important in
mood regulation, dysfunction of serotonin result in all the
conditions above. My problems with IBS which although are
only relatively recently diagnosed in the last tens years
have been a steadily increasing problem right from
childhood. However this disorder could also be the result of
my depression or OCD rather than AS nonetheless it does add
to the possibilty of the presence of AS.
If you would
like to contact me concerning this article please e-mail at
Wanderingmind54@aol.com
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