Skip to main content

The Sinking Agenda

Dame Jane Campbell is Chair of the EHCR Disability Committee. Guardian Society today published a feature by her which is essential reading. For years I have known her as one of the ‘goodies’ and my admiration and respect for her says that she would not betray her role.

I have then written to her in response to her speech:

Dame Jane Campbell,
Chair,
EHCR Disability Committee,
3 More London,
Riverside Tooley Street,
London, SE1 2RG

Hello Dame Jane.
This letter is in response to the extract from your Cambridge speech printed in Guardian Society today.
I would like to say at the start that since, as a then active member of the BASW Mental Health Special Interest Group, I heard you speak at a BASW AGM fringe meeting at Malvern many years ago, you have been something of an icon for me and your words encouraged and stimulated my broader interests in disability rights and independence and greatly reinforced my belief in the value of service user involvement.
In the Guardian Society article, talking about the the merger of the gender, race and disability commissions, you say: “...as chair of the commission’s disability committee, I feel a tremendous responsibility not to lose all we have gained.”
From early retirement in 1999 (after successfully taking my employer to an Employment Tribunal for failing to make reasonable adjustments under DDA), as a disabled service user myself, I have done much voluntary work in mental health and disability rights and service user involvement. However, dismayed and disaffected yet again by yet another example of double talk by a public authority I wrote in pplog on 24th April:
“I’ve taken several steps back to have a proper think: weary of the vacuous and sometimes downright deceitful words of government and their QUANGOS and angry at public body tokenism which cynically exploits the good will of volunteers and service user involvement...there are many indications that some local authorities, PCTs and hospital trusts are also doing the absolute minimum to comply the Disability Discrimination Act 2005. Having published their Disability Equality Schemes they are conveniently forgetting they exist or burying them in amongst generic policies under the name of “diversity.”
All this really makes mugs of those people who in good faith give their time, skill and knowledge in a voluntary capacity.”

Yes, this is happening in Norfolk and the disability agenda is sinking out of sight in the sea of generic diversity. All done in the name of organisational convenience - paraphrasing what you said in your speech it is: “...a politics aimed at erecting barriers that prevent all individuals, families and communities participating as full members of society.”

The reality is that disabled people and their carers have varieties of needs different and distinct from those of the no less important issues of gender and race (just a glance through the pages of research findings by the Norfolk Police Authority in preparation for their Disability Equality Scheme underlines this). Additionally, there are differences in the legislation which can become obscured by this lumping together, e.g.:

the requirement that organisations commissioned by public bodies to carry out their functions must observe the Disability Equality Schemes which should be in contracts;

the requirement that the “involvement” of disabled people must not just be “consultative” or “advisory”: “This involvement must be planned, structured and significant. It will not be acceptable for public authorities simply to consult disabled people. The involvement with disabled people will need to be a much more active process.” (Bert Massie, Chairman, Disability Rights Commission, in the introduction to ‘The Disability Equality duty and Involvement’ 31.08.06.)

The same dilution and blurring applies indeed to the merger of the DRC with the Equality and Human Rights Commission (onomatopoeically ERK). My own experience with this new conglomeration has been dismal. In November 2007 I contacted EHRC (via their helpline e mail form) and as well as another query asked: “I am of the opinion that the use of eligibility criteria for the provision of services may also be a breach of the Disability Equality Duty. Can you also please advise on this.”

I received nothing in reply. I tried again, and again. Nothing. I had some correspondence with an ERHC lawyer but who still didn’t answer my query. I sent a Freedom of Information Act request. Nothing. I haven’t referred the matter to the Information commissioner because it would take too long for it to be dealt with. I would not have had this tardy treatment from the DRC.

So all in all, this is one very disaffected service user who is giving up the battle to lose myself in music and family history.


Heddwch. Mike Llywelyn Cox.

Comments

Popular posts from this blog

Self Advocate’s Support and Action Group Wednesday 08 February 2023 Time: 12:30pm-2:30pm https://us06web.zoom.us/j/97471173675 Meeting ID: 974 7117 3675 1. Present Andrew Ray Olcay Russell Phil Sarah 2. Apologies: Jenny Firielle Chris Peter Vicky Andrew welcomed everyone to the meeting. Our last meeting was 8th February. 3. Check-in Andrew asked how everyone was feeling. Everyone shared how they were feeling and their news. 1 Firielle: told us about her acting work. She finished her tour with the play Milk and is now doing a performance with Dark Horse. They are currently touring. Russell: said he had just been to a face-to-face speaking up meeting, which was really good. He also told us that Joanne won the Derek Russell Award for Outstanding Leadership at the North West Self |Advocate’s conference. Peter: said he has been well. He told us about some of the jokes and play on words that he works on. He shared some that he had worked on earlier. Ray: said he has h

SURVIVOR HISTORY NEWSLETTER

>From Andrew Roberts Secretary Survivors History Group http://studymore.org.uk/ studymore@studymore.org.uk telephone: 020 8 986 5251 home address: 177 Glenarm Road, London, E5 ONB Survivor History Group Summer 2012 Newsletter The July London meeting of the Survivors History Group will be held on Wednesday 25.7.2012 from 1pm to 5pm at Together, 12 Old Street, London. Everybody is welcome and refreshments will be provided. The September meeting has had to be moved from a Wednesday to Thursday 27.9.2012 (subject to approval by this Wednesday's meeting) because of the availability of a room at Together.   -------------------------------------------------------------------- The agenda for the July meeting will be drawn up at the beginning of the meeting, but it will include Peter Campbell's regular report back on the research he is leading on the history of Survivors Speak Out and discussion of material received from other people about Survivors Speak Out.  Rick Hennelly has sen

inappropriate!!!

I tried to respond to a Patient Citizen Exchange blog by Laura Greene today. I said: Hello Laura. Welcome - and my admiration? for you "single-handedly representing the entire health voluntary sector and 1000+ PCX membership..." My first question has to be: what is the composition of the Strategic Advisory Board? And my second question: what proportion of service users to professionals is there on that Board? There are indeed millions of impatient citizens out there. They are called Service Users (primarily because 'Patient" carries the labels 'One that has things done to her/him'; 'One that is subservient to the "We know what is best for you" approach'; 'One that is at the wrong end of an imbalance of power.' etc). The Americans prefer the term 'consumers', but whatever, we should avoid the term with the negative connotations. I was listening to the 5 Live debate this morning on the Strictly Come Dancing row about whether