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Parent Carers

Parent

Who is a parent carer?

After all, arent all parents’ carers? Yes, we are, there’s no doubt that parents are carers for life. But what about when your child has additional needs? Unless you experience this for yourself or live with a family who has a child with additional needs, then how can anyone explain the difference between being a parent and being a parent carer?And how many of us can actually identify the extra caring, stressors and long term effects that being a parent carer has when compared to typical families? When we do, how many people tell us “what a good job you’re doing” and “keep up the good work”?

If you would like to be part of the Wirral Family Forum to meet other parents of children with additional needs, discuss local services and have your say in how services for your children are planned and delivered then please call the carers helpline on 0151 670 0777 and speak to a member of the carers team or contact us


Who is a parent carer?

Workers in ‘Serviceland’ often ask:

Where are the parents?
They are on the phone to the doctors and hospitals, wading through the red tape in order that their child’s medical needs can be properly addressed.

Where are the parents?
They are buried under a mountain of paperwork trying to make sense of a system that seems designed to confuse and intimidate all but the very savvy.

Where are the parents?
They are at home, putting nappies on their 15 year old son, or trying to lift their 100lb daughter onto the toilet.

Where are the parents?
They are spending an hour at each meal to feed a child who cannot chew, or laboriously and carefully feeding their child through a tube. They are administering medication, changing catheters and switching oxygen tanks.

Where are the parents?
They are sitting, bleary eyed and exhausted, in hospital emergency rooms, waiting for test results to come back, and wondering: is this the time when my child doesn’t pull through?

Where are the parents?
They are sitting patiently in hospital rooms as their child recovers from yet another surgery to lengthen hamstrings or straighten backs or repair a faulty internal organ. Grateful for the hospital allowing them to sleep on the floor on a mattress.

Where are the parents?
They are worried about their other children who are at home and have needs of their own.

Where are the parents?
They are worried about the weeks of recovery when they will have to support their child alone at home with no equipment.

Where are the parents?
They are sleeping in shifts because their child won’t sleep more than 2/3 hours a night and must constantly be watched lest s/he do harm to themselves or another member of their family.

Where are the parents?
They are sitting at home with their child because family and friends are either too intimidated or too unwilling to help with child care and the state agencies that are designed to help are suffering cutbacks of their own.

Where are the parents?
They are trying to spend time with their children who don’t have disabilities as they try to make up for the extra time and effort that is critical to keeping their child alive.

Where are the parents?
They are struggling to keep a marriage together because adversity does not always bring you closer.

Where are the parents?
They are trying to survive in a society that pays lip service to helping those in need, as long as it doesn’t cost them anything.

Where are the parents?
They are trying to patch their broken dreams together so that they might have some sort of normal life for their children and their families.

Where are the parents?
They are busy trying to survive.

Parent with kids Yes, there’s no denying it is hard work and at times can be difficult, but there are organisations, both voluntary and statutory, which have people who are able to offer support. The only thing is, you have to recognise what you need support with and what it looks like- not just what is available. The only person who can do this is you. Recognising you need support is not the same as saying you are a bad parent, can’t cope or don’t love your child. It is about doing your best for your child and yourself.

“I never knew there was so much out there. I must have been in a cocoon.”
But then “Troubles” always seem not so big when they are shared with someone who understands the situation to some extent. After the course, we have kept in touch and are using what we have learned to support other parent carers- and each other- in many areas of our lives, from carers of the very young to adults with additional needs. We are involved in the planning of services for those with additional needs and their families. We don’t forget that we are in the same position and not to put pressure on each other, but to support and encourage each other. We don’t trivialise the pressures on parent carers, and recognise there seems to be the added pressure from services for us to give our precious time to help them make policies and provide services which meet our needs. We think this is a positive move forward to improve servic es for parent carers and their families. But when they wonder why parents don’t turn up.

Lynne Elwell

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