After the spot yesterday on SENDirect I thought this letter in the Weekend's Guardian was very interesting. I might contact the author.
The juxtaposition of David Mitchell's article and the story of Gloria Foster's death is important. Families need support to cope. Trained staff who understand the needs of a child (or adult: autism is a lifelong condition) do not and should not come cheap. Increasingly, families are given "personal budgets" that are inadequate to fund specialist care. The marketisation of care means that the poorest families who cannot "top up" these budgets will have the poorest provision. Care on the cheap carries with it huge risks, and the most vulnerable and those who love them are suffering.
Liza Dresner
Director, Resources for Autism, London NW11
I think, although DPs offer control which LAs don't want to give, this move to 'brokerages' suggests that control may not be left in our hands for very long. I wonder if we will just be told we can have services only if we go through brokerages? Will there be a list of acceptable providers? Will you ge on that list of you start saying a child needs more care than the LA want to offer?
Have these charities thought this through? This in particular worried me from the SENDirect site - one aim is to
"Provide support across sector?s to develop products to meet identified needs and therefore create a sustainable marketplace of provision."
Aim of reform: marketisation of SEN provision? We know how that ends up.
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Here are some suggested organisations that offer expert advice on special needs.
SN children
Children and families bill: marketisation of SEN provision
29 replies
inappropriatelyemployed · 07/07/2013 08:13
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