Glasgow Times

‘There’s nothing you can do about it, you’ve got it. So you make the most of it’

- BY CAROLINE WILSON

KEITH Mitchell of Glasgow’s Golden Generation says there is still a perception that people affected by dementia are “completely incapacita­ted”. Reporter CAROLINE WILSON spent a day with the day centre charity that is helping people like live well with the illness into their 80s and 90s

“ONE of the biggest assumption­s is that dementia isn’t a terminal illness,” says Keith Mitchell, of Glasgow’s Golden Generation, where 80% of elderly clients at its three day centres have some form of the illness.

The city-wide charity estimates that attendance at the centres, where pensioners benefit from brain-stimulatin­g activities, companions­hip and a hot meal can delay admittance to care homes by 2-3 years. They follow the social care model that ‘society adjusts to those with incapacity’ and not the other way round so clients are picked up from their home and safely returned.

The centre give people “purpose and enjoyment in a safe environmen­t” says Keith, while offering crucial respite to relatives, particular if they are the primary carer.

He says the previous Labour-run council cut respite care offered to people with dementia from six weeks to two but it was re-instated by the SNP when they took control. However, according to Keith, families can face significan­t waits.

All those who attend the day centres are still living at home, staff at the resource tight charity can’t take clients if they are ‘prone to wandering.’

When the charity was launched 50 years ago it was people in their 60s and 70s attending the centres, but most are now one or two decades older, with the added demands of a dementia diagnosis. “We are at the lower end of social care,” says Keith. “We get people who are not long diagnosed. You don’t initially realise they have it but if you ask them, they won’t be able to find their way home. “There’s a lot of evidence that if you keep mind and body active it will delay the progressio­n.

“Everyone here is either lonely or isolated though, that’s the common thread.”

Clients pay a small amount of money each day to attend the centres, which are all run on a shoestring and badly in need of modernisat­ion but benefit from caring and devoted staff who know them inside out.

None more so than Keith, former day centre manager who now handles the centre’s database and marketing activities. He’s a reassuring presence for both the clients and their carers, always on hand to advise on benefits and care home recommenda­tions.

Most of those here who have dementia suffer a degree of impairment – they will repeat the same story to me several times but can hold a lucid conversati­on. Keith believes that staying mentally and physically active may have helped delay the worst effects of Alzheimer’s Disease for some.

However, he says all will finally succumb to the physical effects of the illness when they will require the 24-hour nursing care that can cost up to £1000 a week in care homes, which Alzheimer Scotland believes should be free.

At 87, Euphemia Lawrence, from Carmyle, comes to the Matty Carwood Centre five days a week and despite “not feeling her age” has very little shortterm memory.

Prompted by Keith she tells me she worked for the WD&HO Wills cigarette factory on Alexandra Parade, in Glasgow’s east end, which employed some 3,500 people and produced 260 million cigarettes a week. Her job was to peel the tobacco leaves off and she recalls wearing gloves to protect her skin from the resin.

“It’s a b ***** ” says Dorothy MacFadyen of the Alzheimer’s Disease she inherited from her mother.

A widow of 20 years, her husband died within a year of retirement from lung cancer, putting paid to all the plans the couple had. Dorothy, who is dressed smartly in bright yellow, and lives in sheltered housing on Crow Road will repeat that to me several times during our conversati­on.

She recalls her own mother suffering from Alzheimer’s to the point when she didn’t recognise her daughter but doesn’t recall the specifics of her own diagnosis.

She said: “I can cook, I can go out, I can bake. I can get drunk.

I’ve got my appetite. I can stand on my head if I feel like it,” she jokes.

“I just live my life normally. ‘I don’t go to bed at night thinking, oh that’s another day’. It doesn’t worry me. You just have to live with it.

“I like the company. My mother ended up in a home but she was 92 when she died. I’m heading that way.

“My daughter is a nurse at Hairmyres Hospital in East Kilbride and she will say are you breathing? If you need me, phone me. And I don’t phone her because I don’t need her.”

She tells me she worked as a typist for British Rail and then the Queen Mum’s maternity hospital, where she met her husband, who worked as a draftsman for the health board.

Her advice to others coping with a diagnosis? “Don’t worry about it, there’s nothing you can do about it, you’ve got it. So you make the most of it.

“This is Godsend. Two days a week, I know I’m coming here.”

Keith says: “People think if you have dementia you are completely incapacita­ted but the progressio­n of, and the manner in which the condition is manifest is different from individual to individual and users are at different stages of the “journey”.

“I think it’s important to remember that people affected by dementia retain capacity and are able to make decisions for themselves unless otherwise proven.

“At our centres for example, users, including those with dementia, are able to make their own determinat­ion on choice of activities and lunchtime menu for example -the crux of what the centres offer.”

Alfie Brown, 82, from Castlemilk, attends the David Cargill Centre, near Hampden stadium five days a week, giving his wife Rose and full-time carer, who is in her 70s, some respite.

He prefers male company but given that most of the clients are women, it’s not easy to cater for his preference­s. Keith admits his own father would have baulked at the idea of going to a day centre and says it can be more difficult to persuade men to attend its centres.

Alfie, who has a son and a daughter, tells me he worked as a telegraph boy then a postie for most of his life in Govanhill, describing it as a “fantastic job” and was an ardent supporter of Third Lanark Athletic Club before the club went out of business in 1967.

Dementia is “just one of those things,” he says cheerfully. Of the day centre he says:“It’s given me a lot of confidence. We keep each other going.”

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 ??  ?? Dorothy MacFadyen, who has Alzheimer’s Disease, visits the Fred Paton Centre two days a week, and below left, Keith Mitchell
Dorothy MacFadyen, who has Alzheimer’s Disease, visits the Fred Paton Centre two days a week, and below left, Keith Mitchell
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