People who self-diagnose gaining access to services

A major autism organisation is giving access to groups/services for adults with Asperger's and high functioning autism to adults who self-diagnose.

Those who self-diagnose are highly motivated, unlike many adults with autism where motivation can be an issue.  They are more likely to attend groups than those with significant problems. These self-diagnosed adults as service users have a say in how services are run.  In this organisation, they want groups set up that exclude those with Asperger's and high functioning autism who have more problems than they do.

This mirrors what has happened in some online groups for people with Asperger's that have been dominated by those desperately seeking a diagnosis.

What other condition allows those that self-diagnose to be given access to services?  It could be argued that everyone as some autisitic traits i.e. is on the autism spectrum.  But surely the point of diagnosis is to identify those that are in need of support services.  To be given a diagnosis, there must be 'significant impairment'.  Many of those desperate for a diagnosis do not meet the criterea.  For many 'Asperger's Syndrome' seems a trendy diagnosis - it doesn't have the baggage of many conditions linked to the mind/brain.  They have little awarenees of the many difficulties faced by those living with Asperger's/high functioning autism.

I believe allowing people who self-diagnose access to services makes diagnosis meaningless.  In the long term, it is likely to have a negative affect on funding for services for adults.

What are your thoughts?

 

Parents
  • Not at all Longman. I am a case in point. I have AS but my symptoms  have improved as I have older, and I am far from dependant on anyone, although I require support to help me  make progress. Support has enabled me to volunteer in the community and to be an active citizen.  I do not believe that people with AS are doomed to suffer, will inevitably be helpless or dependant. We are agents and not simply victims of our fate, and I have never argued to the contrary, so I think there has been a misunderstanding.

    There is no private-members club, but there must be a wider debate about the potential pitfalls of private medicine.

Reply
  • Not at all Longman. I am a case in point. I have AS but my symptoms  have improved as I have older, and I am far from dependant on anyone, although I require support to help me  make progress. Support has enabled me to volunteer in the community and to be an active citizen.  I do not believe that people with AS are doomed to suffer, will inevitably be helpless or dependant. We are agents and not simply victims of our fate, and I have never argued to the contrary, so I think there has been a misunderstanding.

    There is no private-members club, but there must be a wider debate about the potential pitfalls of private medicine.

Children
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