Monthly Archives: January 2013

How Norfolk’s carers beat the weather

When the bad weather sets in in Norfolk, taking a “snow day” is not an option for the county’s carers.

Carer Sue Hewitt visiting Norwich pensioner Helen Parker in her home. Photo: Steve Adams Carer Sue Hewitt visiting Norwich pensioner Helen Parker in her home. Photo: Steve Adams

By Victoria Leggett Saturday, January 19, 2013
12:45 PM

When the bad weather sets in in Norfolk, taking a “snow day” is not an option for the county’s carers.

For Sue Hewitt, home support worker for the Norfolk County Council-run Norfolk First Support service, dangerous roads and traffic jams simply mean abandoning her car and walking to the homes of the vulnerable people she needs to visit.

She said: “I would do everything in my power to make sure that person sees a carer. They really need them.

“Sometimes we are the only people they see. Even if they have family, they might not be venturing out because of the snow.”

Health and Clinical Commissioning Groups

Lee Stribling

Why do you need to know this?

You’ve probably realised by now that issues around types of care, funding, assessment and all things dementia related are not straightforward.  At some point the person you care for will have contact with Health professionals such as their GP. I thought it would be useful to explain the current structure (November 2012) so you could see how things are linked.  I’ll also talk about CCGs (the Clinical Commissioning Groups) as these are groups of doctors who decide how the budget is spent as well as signposting you to resources about how things will look from April 2013.


If there is a lack of provision for services for people with dementia in your area, you may wish to contact the CCG to highlight this gap so that they can make decisions as to whether this is a local need.  CCGs are comprised of other people too, including those who use services and you may wish to be involved in this.

We get there early and find Dad's dementia worse

As Dad struggles to lift his head, it’s clear how immobile he’s become since last time

 

Rebecca Ley with her dad, who has dementia.

The second time I visited Dad over Christmas was far less rosy than the first. It was Boxing Day but decorations at the home had already begun to wilt. And this time, instead of finding Dad sitting in the main room cleanly shaven, my husband and I are told he is still in his bedroom.

I walk down the corridor with trepidation. His bedroom scares me. While many of the residents have cosy rooms, personalised by their families with photographs, lamps and cushions, Dad’s is a barren, institutional space.

It’s not that we haven’t tried. When he first moved in, my mum and sisters took pictures and got a television mounted on the wall. But none of it lasted long. Dad’s habit of destroying things in the night meant that nothing was safe. Now there’s just an empty bracket where the TV was, and the walls are blank, save for pockmarks and the odd, unidentifiable smear.

The focus of the room is his bed, a hospital one with bars to stop him slipping out. And today he’s lying in it, his head tilted to the window and his bare torso only just covered by a sheet.