Scottish Government’s National Care Service plans will not work: COSLA

The Scottish Government’s plans for a National Care Service as they currently stand will not work for service users or communities, COSLA said yesterday.

COSLA also warned that, as the Bill stands, it would have a significant impact on councils’ ability to deliver not only social care services but other critical councils services that our communities rely on.

In a meeting of Council Leaders yesterday there was unanimous and cross-party concern that the National Care Service (Scotland) Bill as published will see decisions around locally delivered social care services moved from communities to Scottish Government Ministers in Edinburgh.

The powers set out in the Bill would potentially lead to the transfer of 75,000 local government employees from local authorities to care boards.

It was the strong view of Leaders that local authority services, staff and resources should remain the responsibility of locally elected members, a view that has been echoed by all the main Local Government trade unions.

COSLA Leaders also fear that the transfer of public protection duties from local authorities risks losing local expertise and knowledge, with implications for safety within our communities.

COSLA, which represents every council in Scotland, has also cautioned that the Scottish Government’s National Care Service Bill will create significant uncertainty and further division for the Local Government workforce, at a time when there are already significant recruitment and retention challenges.

Councillor Paul Kelly COSLA’s Health and Social Care Spokesperson said: ““All Council Leaders were in agreement that as it stands, the National Care Service Bill with the power to transfer local authority functions, staff, property and liabilities to a National Care Service, poses a serious risk to councils’ ability to deliver a wide range of services for communities including non-social work and care services.

Leaders were very clear that this approach would result in destabilising the Local Government workforce and potentially impacting on the sustainability of some councils to carry out their functions and responsibilities.

COSLA is committed to the change, improvement and investment needed in our social care system and will continue to work with the Scottish Government and partners to better the experiences of both those using and delivering social care services now and in the near future and not wait until a National Care Service is in place.

COSLA will seek further engagement with the Scottish Government in an attempt to ensure that there is no disruption to local services by ensuring that local authority staff remain in local authorities.”

Lifelong support for Thalidomide survivors in Scotland

Thalidomide survivors will now receive lifetime funding from the Scottish Government.

The measure extends the previous 2013 agreement which granted survivors £14.2 million over ten years to help meet their health and living costs.

There are currently 50 known survivors of the drug in Scotland, most of whom are now in their 60s, and grants will be allocated on a needs-basis, as assessed by the Thalidomide Trust.

Thalidomide was prescribed to expectant mothers between 1958 and 1961 to relieve morning sickness and insomnia  but was withdrawn after thousands of babies were born worldwide with disabilities, including limb damage, sensory impairment and internal damage.

Mr Yousaf said: “This funding is used to give thalidomide survivors as much assistance as they need to maintain their independence. It has been a vital support in helping people adapt their homes and manage their pain.

“I hope this lifelong commitment to continue this support will reassure recipients and help them deal with any challenges they face.”

Jean, 61, was born with damage to all four of her limbs as a result of thalidomide. She said: “This is such great news. The Health Grant from the Scottish Government has really helped me over the years – my kitchen, for example, is now completely accessible from my wheelchair and I have been able to build a little gym in the garden which has helped me so much in terms of my physical strength, fitness and my mental health.

“Due to thalidomide, I live with chronic pain and if I don’t move around my body would stiffen and seize up. The grant also allows me to pay for a personal trainer who understands my disabilities and can keep me fit and flexible, without causing further damage. 

“Knowing this funding is going to continue indefinitely has given me, and many other Thalidomiders living in Scotland, such peace of mind.”

Deborah Jack, Executive Director of the Thalidomide Trust added: “This is fantastic and very welcome news. Sadly, as our beneficiaries age they are experiencing multiple health problems, in addition to their original thalidomide damage, and the costs of meeting their complex needs are significant. Many of them have been really anxious about the prospect of this much-needed funding coming to an end.

“We are really pleased that the Scottish government has recognised this by committing to lifetime financial support and also agreeing to review the level of funding regularly to ensure it is meeting their changing needs.”