Looking at your needs as a carer – having a carer’s assessment

 

   DISC

   Oxford Dementia Centre

   Institute of Public Care

   Roosevelt Drive

   Oxford OX3 7XR

   Tel: 0845 120 4048

   www.disc.org.uk

   email: info@disc.org.uk

 

 

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This fact sheet offers information on who is a carer; the importance of recognising your own needs as a carer and having your own assessment as a carer with easier access to support and services.

 

You may also find the following fact sheets helpful:

 

·        What is dementia?

·        Assessment and diagnosis

·        Treatment and therapy for people with dementia

·        Making your home dementia friendly

·        Making the decision about future plans for care

·        Getting help through financial benefits

·        Finding out what help someone needs and who can provide

·        Paying for community care services

 

What is the actual definition of a carer?

 

You are defined as a carer if you look after a relative, friend or disabled child who needs support to live at home, provided the care is “substantial and regular”, and is having or will have, a central impact on your life either physically or mentally.  If a carer fulfils the above definition, they have a right to a carer’s assessment of their own needs.

 

What is the Carers and Disabled Children’s Act for?

 

The Carers and Disabled Children’s Act 2000 gives carers better access to services in their own right.  It also gives them the right to their own assessment, even if the person they are caring for has refused their own assessment.  It allows local authorities to provide some services to the carer directly and recognises that carers need support themselves eg counselling services.

 

There is provision for carers to receive vouchers, which either have a cash value or may be exchanged for services.

 

Local authorities have the power to make cash payments, known as ‘direct payments’, to allow carers to buy their own support and services.

 

 

 

 

 

How your caring role is affecting you – checklist for carers

 

Assessment - Department of Health Carers and Disabled Children's Act Practice Guidance

 

 

 

Breaks and social life

 

Can you regularly get a break to see friends, have time to yourself (not just for going to the GP, dentist or to do the shopping)?

 

 

Physical well being

 

What is your health like?

 

Is your sleep affected?

 

Do you undertake any tasks such as lifting (moving and handling) that affect your back?

 

 

Relationships and mental well-being

 

Is caring having an impact on relationships with the cared for person or other members of the family?

 

What are stress, depression and anxiety levels like?

 

Can the carer maintain their faith-related activities?

 

 

Care of the homes/s

 

Are there any issues about the care of the home/s?

 

Does it all fall to you as the carer?

 

Are there any problems with where the cared-for person lives?

 

Can equipment or adaptations help?

 

 

Finances

 

 

 

Are finances a problem?

 

Would advice on benefits or managing money or debt be helpful?

 

 

Work / Education and training

 

If you are working do you want to stay in work?

 

How could you be supported to stay at work?

 

What are the options?

 

Would you like advice on these issues?

 

Do you want to develop your skill, work related or otherwise?

 

Is it likely that you will have to give up because of your caring role?

 

 

Current practical and emotional support

 

 

Who/what helps you at the moment?

 

Is there enough support and are you satisfied with people who are providing the support you are receiving?

 

Are you aware of support groups, carers’ centres or counselling services in your area?

 

Wider responsibilities

 

 

What other wider responsibilities do you have, for example: other caring roles, work, looking after grandchildren, volunteering?

 

Is balancing these responsibilities causing you difficulties?

 

Are other family relationships suffering as a result?

 

 

Future caring role

 

How do you see your future?

 

What do you feel will affect your ability to care now?

 

What will affect your ability to care in the long – term?

 

 

 

 

 

Emergencies/alternative arrangements

 

 

If you suddenly became ill, what would happen?

 

What support could be called upon in an emergency?

 

Would you know who to contact in an emergency?

 

Would making an emergency plan ‘just in case’ help?

 

 

Access to information and advocacy

 

Are you aware of what organisations are out there who can offer you support?

 

Are there sources of support or advocacy locally that you could access?

 

 

What do you want the outcomes of the Carers Assessment to be?

 

In relation to your health and well-being, quality of life, your caring role?

Are direct payments appropriate for you rather than a service?

 

What would the difficulties be of obtaining these outcomes?

 

 

 

 

The Carer’s Assessment will determine:

 

·              Whether you are eligible for support as a carer

·              What services would be helpful to you

·              Your support needs to maintain your health and well-being

·              If a carer’s direct payment would be of benefit

 

Having an assessment at the same time as the person you care for

 

A Carer’s Assessment will often take place when the person you care for is being assessed or re-assessed.  Your assessment could take place at the same time, if you both agree that this is what you want.

 

Having a separate assessment

 

A separate Carer’s Assessment would mean that you have time alone with the assessor.  It could be an ideal time to discuss difficult issues, for example, if someone has mood swings or behaviours that you find difficult to cope with or embarrassing or confidential information that you do not wish to be shared with the person you care for.  This information will be kept confidential and not shared with the person you care for without your consent.

 

What if the person I care for refuses to have an assessment?

 

If the person you care for refuses to have an assessment of their needs, you still have the right to your own Carer’s Assessment.

 

What happens after the Carer’s Assessment?

 

The assessor will write the care plan.  If you and the person you care for had an assessment at the same time, your part of the assessment will appear on the care plan of the person you care for.  Where you have issues that you want to discuss confidentially, you will receive a separate care plan.

 

The plan will contain a clear statement of services and support intended for you and the person you care for.  This will be an important source of reference when implementing and reviewing your plan.

 

 

 

 

 

This fact sheet can be made available in large print.

 

We are constantly looking to improve our information.  It helps if you let us know whether the information in this fact sheet was/was not useful and if there are other fact sheets that you would have found helpful that we have not yet provided.

 

While the information contained in this fact sheet is believed to be correct, DISC does not accept liability for any error/s it may contain.