When stroke survivors go home, they often rely on others to help them with everyday activities. These people, the carers, are also affected by the stroke. 
 
No one plans on becoming a carer.  If you are a carer it is important that you don’t feel alone – especially if you don’t have family members to give help and support.

The changes in your life and relationship with the person you are caring for may be very frightening and stressful.  You may have mixed feelings about being a carer and feel resentful about the changes in your life.  These are normal feelings and reactions.
 
Although there will be changes in your life it is important to remember your own needs.  You should continue to do the things that you did before your life was affected by stroke, making sure to keep the person who has had the stroke involved in, or at least aware of what is happening.  Share other carer's stories.

Carers often manage the health care and medications of the person they care for. You may also have a lot to do with health care professionals as part of your caring role.  Think of yourself as being part of the team working with the stroke survivor to make the best recovery possible. 

Do not be afraid to ask your General Practitioner or the Stroke Team for guidance and support or contact one of the following organisations:

Carer Respite Centres
Provides information on respite accommodation facilities for those with a disability. Contact 1800 059 059 (freecall).

Commonwealth Carer Resource Centre
The Commonwealth Carer Resource Centre provides referral to services and practical written information to support people who are carers. Contact your Commonwealth Carer Resource Centre on 1800 242 636.