Alzheimer’s Society Launches Emergency Appeal To Support Vulnerable People Affected By Dementia

Alzheimer’s Society has launched an Emergency Appeal to ask the public to help fund vital support for  people affected by  dementia in the UK, who may be isolated, alone and  without basic support to help them eat, wash and take medication during the coronavirus crisis.

  • Nearly 3,300 calls about coronavirus made to Alzheimer’s Society’s Dementia Connect support line in March alone – with an uplift of 60% last weekend.
  • Online community Talking Point sees 600% increase in sign-ups.

The current pandemic poses a significant risk for people living with dementia, and many are now facing the next weeks and months  cut off from the outside world and potentially essential care.  Around  95% of people with dementia are over 65, many with underlying health conditions, and they largely rely on social care for support.

Three fifths of homecare users and 70% of people in care homes have dementia. Social care, already in crisis, is only worsening as care worker numbers lessen and care homes have to close their doors to visitors, resulting in vital care, check-ups and support being reduced.

Coronavirus is making life much harder for people affected by dementia. People are unable to get essential care, confused by losing their much-needed routines, their symptoms are deteriorating because of a lack of social contact and carers are feeling isolated and struggling to get respite.

The Emergency Appeal will raise funds to help keep the Dementia Connect support line going and  extend  telephone  and virtual  support. People affected by dementia tell us this is a lifeline for them, with  thousands of them  now having to cope  with the suspension of all face-to-face services, stringent social distancing measures and  self-isolation.

The need for Alzheimer’s Society’s services has never been more urgent. Around  80% of calls to  our Dementia Connect support line  are about coronavirus issues  and in March alone,  nearly 3,300  calls were made*.   There’s been  an increase of 600% in people joining our online community Talking Point  in the last two weeks and  around 100 more posts made per day.

People with dementia are also telling us they’re absolutely terrified of going into hospital, because they aren’t confident they’ll receive the right care following the release of NICE Covid-19 guidelines two weeks ago.

Alzheimer’s Society’s asked NICE for an urgent review of these, as they suggest that all people with dementia, even mild, could be denied intensive care treatment, using the measure of those who can’t do everyday tasks like shopping, housework and managing medication on their own. We urge for the inclusion of guidance to make it clear that cognitive frailty is not discriminated against when having to make life or death decisions.

Alzheimer’s Society is working hard to continue existing services remotely, such as Singing for the Brain, and focusing on increasing  telephone support via the Dementia Connect support line,  by moving all frontline staff to respond to calls. The Dementia Connect support line will ensure people affected by dementia don’t have to face any challenges over the coming weeks and months alone.

Alzheimer’s Society is placing 20% of staff on either furlough or reduced hours in efforts to focus resources on frontline support. Furloughing is being kept to as low numbers as possible, while we aren’t able to top up salaries beyond the Government grant of 80%.

Like all charities our income has been affected by a whole range of challenges over the past two years, not least Brexit.  Prior to coronavirus, we were  therefore  already looking at  reshaping our  future  structure to  best  serve people affected by dementia and their greatest needs.

Alzheimer’s Society Dementia Adviser Helen Payton said:

‘This week I have had lengthy phone calls offering people support and access to the information they need.

‘Much of what I’m doing at the moment is emotional support – letting people talk and express their worries and frustration.’

‘Many are missing their family and worried about their care packages being reduced. One newly diagnosed person I spoke to cried when I told them I would phone them weekly to check in. They were so grateful to have someone there for them.’

Kate Lee, CEO of Alzheimer’s Society said:

‘We are hearing daily from people with dementia worrying how to cope, confused, isolated and unable to get food deliveries, families struggling to explain what’s going on and carers unable to visit vulnerable people in person.

 

 

 

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