Hi i am some times finding it very hard to opening the door and i just keep looking at it , its like my brain has not toll me to open it. I have the some thing going on getting in the shower , can anyone tell me what this mite be thank you
Hi i am some times finding it very hard to opening the door and i just keep looking at it , its like my brain has not toll me to open it. I have the some thing going on getting in the shower , can anyone tell me what this mite be thank you
Unfortunately nobody knows.... Most research on autism is about finding a cure or supporting people in childhood and adolescence. As recent figures have shown upwards of 95% of funding on research goes on finding a cure (well more chance of getting a Chair or a Nobel Prize - lifestyles research is for wimps).
NAS has a campaign "Getting on? Growing older with autism" under living with autism - adults with autism and asperger's syndrome - autism and ageing. But it doesn't have much in the way of answers. It just seems to be a knee-jerk response to realising autism continues after transition to adulthood.
The original diagnosed children are now in or approaching middle age, but while some adults have been diagnosed, as all can testify there isn't much support around, so how can anyone use adult diagnoses to study autism and ageing?
Added to that you have to look at the outcomes for many adults with autism - secondary complications like depression and schizophrenia, alcoholism (a scary number) and drug addiction, homeless including in hostels and on the streets, in prison or otherwise in trouble with the police. Any of us with a job find ourselves brushed off by GPs and other health professionals as delusional and immature, and those without a job are treated as benefits scroungers. So where on earth they are going to collect data on growing older with autism beats me...
I blame parents groups (and NAS originates from parents groups) which are more about the trials and sufferings of parents bringing up children and adults on the spectrum. Go to a parents group meeting anywhere in the UK and in the unlikely event of seeing an adult on the spectrum, he/she will be with the parents - there's nothing provided for adults on the spectrum in their own right. Its the parents that matter.
So all I can say is if you've survived intact to 51 its a miracle in itself. Many people on the spectrum experience minor motor control based stalling/hesitancy, and the chances are that's all you've got. Known cases of catatonia with autism have been young.
The fact is though we don't know how autism affects dementia - will the dementia drugs respond adversely with autism? At 64 I'm nearer finding out than you, but I've already almost died twice in my late 50s from entirely different medical problems, so my philosophy is largely see how it goes.
My main concern is as a loner with social difficulties I don't know what happens when I can no longer support myself - living in a communal environment like a care home would be hell on earth.
Unfortunately nobody knows.... Most research on autism is about finding a cure or supporting people in childhood and adolescence. As recent figures have shown upwards of 95% of funding on research goes on finding a cure (well more chance of getting a Chair or a Nobel Prize - lifestyles research is for wimps).
NAS has a campaign "Getting on? Growing older with autism" under living with autism - adults with autism and asperger's syndrome - autism and ageing. But it doesn't have much in the way of answers. It just seems to be a knee-jerk response to realising autism continues after transition to adulthood.
The original diagnosed children are now in or approaching middle age, but while some adults have been diagnosed, as all can testify there isn't much support around, so how can anyone use adult diagnoses to study autism and ageing?
Added to that you have to look at the outcomes for many adults with autism - secondary complications like depression and schizophrenia, alcoholism (a scary number) and drug addiction, homeless including in hostels and on the streets, in prison or otherwise in trouble with the police. Any of us with a job find ourselves brushed off by GPs and other health professionals as delusional and immature, and those without a job are treated as benefits scroungers. So where on earth they are going to collect data on growing older with autism beats me...
I blame parents groups (and NAS originates from parents groups) which are more about the trials and sufferings of parents bringing up children and adults on the spectrum. Go to a parents group meeting anywhere in the UK and in the unlikely event of seeing an adult on the spectrum, he/she will be with the parents - there's nothing provided for adults on the spectrum in their own right. Its the parents that matter.
So all I can say is if you've survived intact to 51 its a miracle in itself. Many people on the spectrum experience minor motor control based stalling/hesitancy, and the chances are that's all you've got. Known cases of catatonia with autism have been young.
The fact is though we don't know how autism affects dementia - will the dementia drugs respond adversely with autism? At 64 I'm nearer finding out than you, but I've already almost died twice in my late 50s from entirely different medical problems, so my philosophy is largely see how it goes.
My main concern is as a loner with social difficulties I don't know what happens when I can no longer support myself - living in a communal environment like a care home would be hell on earth.