Print

Print


I'm a clinical psychologist working in community learning disability team 
in London.  Hearing about this sort of situation is depressing.  Despite 
vaious government outpourings services are not becoming more 'person 
centred'.  In fact the fracturing and disaggregration of services in a 
mixed economy of care means that there is less flexibility; various 
automonous services just set their own rules and disabled people have to 
try and fit them.

I've also seen how difficult it is for young people like Cathy to 
negotiate the complex world of 'adult services' when they are moved on 
from childrens services where education, health and social care are more 
joined up.

However, a more practical answer to your query is that your friend will 
probrably need to access an assessment through her local learning 
disability team.  My experience chimes with Larry that psychiatrists are 
usually the ones who pronounce on autism issues, as autism is seen as an 
psychiatric/developmental disorder and defined in psychiatric diagnostic 
tomes such as DSM and ICD10.  They might just use 'clinical judgement', 
piecing information together from background information and someone's 
current presentation, or they might use a diagnostic tool, such as the ADI 
or DISCO.  The reports by psychiatrists I've read vary a lot in 
thoroughness and sensitivity.  A clinical psychologist is more likely to 
be asked to do an assessment of current abilities and support needs, maybe 
including an IQ test.  A learning disability social worker would then work 
out what sort of support this young woman would need, and should find ways 
to fund it.  This is separate from DLA and could be arranged through 
direct payments which means that Cathy and her family would receive the 
money to pay someone they choose to help her, for instance with travel or 
with her studies.

Another route might be to go to the GP and ask for a specialist assessment 
from a reputable psychiatrist (Pat Howlin in London for instance) or the 
National Autistic Society diagnostic service.  Though sorting out the 
funding for this can be complicated.

40 miles does seem a really long journey for anyone to do frequently.  
Maybe an social worker, advocate or service broker can help Cathy and her 
family look at different options.  

Good luck, I'd be happy to do some more thinking about this with you if 
you want to contact me off-list.

Deborah

________________End of message______________________
This Disability-Research Discussion list is managed by the Centre for Disability Studies at the University of Leeds (www.leeds.ac.uk/disability-studies). Enquiries about the list administratione should be sent to [log in to unmask]
Archives and tools are located at:
www.jiscmail.ac.uk/lists/disability-research.html
You can JOIN or LEAVE the list from this web page.