Assessment Help

After work sent me to a psychologist after I was suffering from stress, they strongly suggested that I have Aspergers/HFA (July 15). Since then I have considerable research into Aspergers and it does seem to fit some of my "issues" and also I have done a number of Aspies tests and it does appear that I probably have Aspergers.

Since then I have seen my Mental Health specialist at my GP (Sept 15) who referred me on.

I then saw a junior doctor at the local Mental Health Department who went through a few things and as the tests suggested Aspergers I have now carried on, and have what I think will be a full assessment on the 21st Jan 16.

In many ways this is pretty good progress and I am quite happy with the service I have been getting.

However there is an issue here, they have made a number of requests, both of which make complete sense.

1. They have requested my school reports, I have kept some but I am not fully sure what they would need. I am also not sure how to get them, I would think from the local council.

2. The doctor has also requested that a parent attends; this is a major issue as I have not told my parents about any of this, however they are aware that I have depression and that I have a meeting but have no idea about Aspergers, as I am unsure how they would react and whether or not it could upset them, they have enough going on.

What information would the doctor require, could it be asked for in advance and would Aspergers be mentioned in the interview? (It has been mentioned it would last approx 2 hours.)

Would I be able to ask in advance some of the questions.  

Any help that anyone could provide would be massively welcomed. Thanks in Advance.

Parents
  • Hiya. I must take issue with you for calling AS a 'developmental disorder', it is nothing of the sort. I resent being called 'disordered' and so do many of us. We have a condition known to be on the autism spectrum, which simply describes our differences to NTs. You were (assuming you do get diagnosed as autistic) born that way. Your development, like anyone else's, was subject to your environment, but you were in that environment as an AS person.

    There is absolutely no need whatsoever for either your school reports or any input from your parents. The assessement is of you, the other information helps to inform the process when it is available, but many people have neither of those things to offer. This doesn't affect your asessement, although we do sometimes hear from posters telling us that they have been told it is essential. This is simply not true.

    Depression and anxiety go with our condition, mainly due to trying to function in a world that we have no control over, largely populated by people who cannot understand our difference. We have 'troubled minds' because of the way our brains work, but that doesn't mean that we are incapable, incompetent, or untalented. Quite the reverse, but the depression and anxiety that we get because this is not understood simply adds to the pool of negativity that is our experience when out in the NT world.

    A 2 hour asessemnt is sufficient, in the hands of a properly qualified assessor, to make the diagnosis. There is nothing that you can be pre-warned about because it is a dynamic process -  it is a tailored discussion, not a question and answer tick-box filling exercise. No two such assessments can ever be the same because no two people are ever the same.

    Remember, this is your assessment. Some of us have had very good experiences, some of us have had very bad experiences. You cannot take either example as indicative of how yours will go.

    However, let me assure you that the session will not be painful or harmful to you. The (typical) anxiety you are feeling over it is perfectly normal for anyone, the intensity of it is very much AS in nature. Relax into the session - two hours seem long, but my own two hours were over in about 5 minutes, it seemed. I can't remember any of the discussion, apart from a few odd snippets, and I'm still amazed that that was all it took.

    I did an AQ questionnaire, it meant little to me at the time and I can't remember any of that either, but on the strength of it I was put straight to the assessemnt, although I had to wait a year for it to come around. I didn't come to this website untill after I'd been diagnosed, and frankly I'm glad. I think that if I'd asked questions and got the range of answers that commonly arise, I'd have been thouroughly confused and even more anxious.

    You're an individual, you make your own choices and decisions, and I sincerely hope that you get the answers that you deserve whether you decide to include your parents or not - you know them better than any of us so we cannot advise you either way. Your answers will come from your diagnosis, not from us. All we can do is welcome and support you, understand who you are and what you're going through, and do discussions like this with you. I think that if you spend time going over old threads on here, it will give you a much greater understanding of our range of experience when we are faced with questions such as yours.

    I wish you all the best

Reply
  • Hiya. I must take issue with you for calling AS a 'developmental disorder', it is nothing of the sort. I resent being called 'disordered' and so do many of us. We have a condition known to be on the autism spectrum, which simply describes our differences to NTs. You were (assuming you do get diagnosed as autistic) born that way. Your development, like anyone else's, was subject to your environment, but you were in that environment as an AS person.

    There is absolutely no need whatsoever for either your school reports or any input from your parents. The assessement is of you, the other information helps to inform the process when it is available, but many people have neither of those things to offer. This doesn't affect your asessement, although we do sometimes hear from posters telling us that they have been told it is essential. This is simply not true.

    Depression and anxiety go with our condition, mainly due to trying to function in a world that we have no control over, largely populated by people who cannot understand our difference. We have 'troubled minds' because of the way our brains work, but that doesn't mean that we are incapable, incompetent, or untalented. Quite the reverse, but the depression and anxiety that we get because this is not understood simply adds to the pool of negativity that is our experience when out in the NT world.

    A 2 hour asessemnt is sufficient, in the hands of a properly qualified assessor, to make the diagnosis. There is nothing that you can be pre-warned about because it is a dynamic process -  it is a tailored discussion, not a question and answer tick-box filling exercise. No two such assessments can ever be the same because no two people are ever the same.

    Remember, this is your assessment. Some of us have had very good experiences, some of us have had very bad experiences. You cannot take either example as indicative of how yours will go.

    However, let me assure you that the session will not be painful or harmful to you. The (typical) anxiety you are feeling over it is perfectly normal for anyone, the intensity of it is very much AS in nature. Relax into the session - two hours seem long, but my own two hours were over in about 5 minutes, it seemed. I can't remember any of the discussion, apart from a few odd snippets, and I'm still amazed that that was all it took.

    I did an AQ questionnaire, it meant little to me at the time and I can't remember any of that either, but on the strength of it I was put straight to the assessemnt, although I had to wait a year for it to come around. I didn't come to this website untill after I'd been diagnosed, and frankly I'm glad. I think that if I'd asked questions and got the range of answers that commonly arise, I'd have been thouroughly confused and even more anxious.

    You're an individual, you make your own choices and decisions, and I sincerely hope that you get the answers that you deserve whether you decide to include your parents or not - you know them better than any of us so we cannot advise you either way. Your answers will come from your diagnosis, not from us. All we can do is welcome and support you, understand who you are and what you're going through, and do discussions like this with you. I think that if you spend time going over old threads on here, it will give you a much greater understanding of our range of experience when we are faced with questions such as yours.

    I wish you all the best

Children
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