Joint Committee on the Draft Mental Health Bill Written Evidence


DMH 01 Memorandum from Sandra Banawich

Chairman,

I would like to comment on the Governments Draft Mental Health Bill and include some of my personal experiences of Mental Health Services. In particular I am concerned with Government proposals for compulsory medication in the community and extending powers to cover people who may commit an offence, on the off chance they might Government proposes to 'treat' them. How does this stop these people making a decision to hurt or kill someone? In my experience Medication doesn't stop you thinking, many Sane people carry out crimes everyday if someone on Medication still commits a crime what will the Government do next to the Mentally ill community? This Bill is misguided and drawn in haste as an answer to a Media driven Psycho-phobic public. If you want to punish someone who has committed an offence already then we have Laws for that but to do it by way of medication seems barbaric make Life mean Life and protect our right to innocence until proven guilty.

Compulsory treatment in the community is in my opinion as a Schizophrenic service user and former councillor with responsibility for chair of Social Care and Health Scrutiny is both not needed and flawed. Medications for my condition are at best unpleasant and sometimes harmful. In my case I was prescribed Zyprexa (olanzepine) for schizophrenia and developed type 2 diabetes in using it. I now have a very serious illness as a result of taking my medication, if it were to be forced on me what redress would I and thousands of others have. Will there be a compensation fund for victims of damage caused by forced Medication? Will we have redress through the courts via Human Rights freedom from torture legislation? I am serious about these questions as this issue affects my life on a daily basis. The playing field between psychiatrists and service user is already not level why put more mistrust and helplessness into the balance, we need better and safer drugs and people who treat us as responsible people with choices and freedoms that other mainstream patients have. Sectioning already exists if necessary the whole point of being in the community is to live a normal life not be in a form of oppression. It is o.k. for professionals to argue about these things but I would urge you to consider the service users themselves and how these decisions affect them we are real people with real lives not the Schizo knifeman as portrayed by the media.

September 2004





Annex

In Addition to my e-mail could you also include this article that appear online in the Guardian news site in 2001


Mental health | Social care

Time to take a whole-life approach to mental illness

Mental health service users deserve a treatment strategy that addresses their need for support but allows a certain level of freedom, writes Sandra Banawich

Tuesday April 17, 2001

Schizophrenia is a serious illness, one that has an impact on every aspect of the sufferer's life. When drawing up a strategy for treatment, we need to address the effects of the illness on a person's life and develop a whole-life strategy.

A whole-life approach should look at the user's relationships and family. It is stressful for relatives to support a mentally ill person, and relationships can break down. In these circumstances, advice on relationships for all members of the family would be helpful, along with support groups or befriending schemes when these relationships are no longer working.

Mental health service users can lead productive, well-ordered lives, if they are given opportunities and support. It is time for the government and mental health service providers to put resources into real choices and opportunities - to commit to providing real inclusion and equal opportunities for the service user, and to protect their human rights.

Of course, treatment and hospitalisation play a vital role under the Mental Health Act 1983 - and are a necessary evil at times. Voluntary treatment in the community, however, gives service users greater control over their own lives and is more beneficial in the long term.

At present, there is a delicate balance of trust and confidence between service users and providers. This could be undermined by government proposals, set out in the recent mental health white paper, for compulsory community treatment.

Where medication is concerned, there should be room for negotiation between the service user and provider. Being allowed to lower or increase medication levels or try different medication is vital in finding a solution that works for the sufferer.

Mental health crisis teams provide valuable support in the community and often prevent the need for hospitalisation. If the government goes ahead with the white paper on mental health, then it must be supported by a commitment from all involved in the mental health field to train service users as advocates and mentors.

Advocates need to have a legally recognised status, which is stronger than next of kin, so that the service users' opinions are heard and carry weight with officials.

Mental health groups, charities and drop-in centres can provide a safe environment for service users - but are we creating a mental health sub-culture? Is this really what we mean by social inclusion?

We need more schemes centred on encouraging the mentally ill to rejoin the rest of society, providing links to community groups, education and employment. Such schemes would offer real opportunities to mental health service users.

  • Sandra Banawich was diagnosed with schizophrenia 10 years ago and was treated under section in hospital. She is married with four children and is receiving treatment from a local community mental health team. She is a Labour councillor on St Helens borough council, Merseyside, and a member of Mind.






 
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