The Courier & Advertiser (Fife Edition)

Angus man welcomes funding to help people with rare brain disease

Keith Swankie praised for campaign to appoint dedicated manager

- JANET THOMSON jathomson@thecourier.co.uk

A campaignin­g Angus man battling a progressiv­e neurologic­al condition has welcomed Scottish Government funding for a new developmen­t worker.

Keith Swankie, 47, from Arbroath, was diagnosed with the debilitati­ng disease progressiv­e supranucle­ar palsy (PSP) in 2012. As part of his fight for greater awareness, he held talks with Conservati­ve MSP Miles Briggs and PSP Associatio­n chief executive Andrew Symons.

This led to a cross-party parliament­ary meeting in Holyrood where MSPs discussed what could be done to make people more aware of the disease.

The Scottish Government has now said it will provide £25,000 to the PSP Associatio­n to support a new developmen­t manager post.

The worker will raise awareness of PSP and corticobas­al degenerati­on (CBD) across Scotland in collaborat­ion with charities and health care profession­als.

Mr Swankie has campaigned for years to raise awareness of his uncommon brain disorder which affects movement, control of walking and balance, speech, swallowing, vision, mood, behaviour and thinking.

He said: “I am absolutely delighted the Scottish Government has co-funded this position as I know costs are tight.

“Miles Briggs hosted a cross-party round table meeting in Holyrood last November. Jenny Marra MSP also wrote to the Scottish Government to ask what support they could lend.

“So it’s a massive thanks to Miles for making the meetings happen and to Jenny working across parties with Miles to get us to this fabulous result which will only benefit both sufferers of PSP/CBD and their families in Scotland.”

Andrew Symons said: “We are really pleased the Scottish Government has recognised the need for this role and supported it with a generous grant after several years of tireless campaignin­g by Keith Swankie.

“The developmen­t manager will work at the strategic level to raise the profile of PSP and CBD with the Scottish Government, NHS Scotland and other neuro-degenerati­ve charities to educate health and social care profession­als in best practice treatments.”

Iam absolutely delighted the Scottish Government has co-funded this position as I know costs are tight.

KEITH SWANKIE

Life dealt Keith Swankie a devastatin­g blow when he was diagnosed with progressiv­e supranucle­ar palsy (PSP) in 2012. The debilitati­ng neurologic­al condition is relatively unknown, meaning he struggled to get the support he needed.

Lesser men might have buckled. Mr Swankie knuckled down and campaigned for greater awareness and has now been credited with helping to secure Scottish Government funding for a new developmen­t worker. His strength is an inspiratio­n.

 ?? Picture: Kris Miller. ?? Keith Swankie, from Arbroath, who suffers from PSP, has welcomed Scottish Government funding for a new developmen­t manager to help raise awareness of the disease.
Picture: Kris Miller. Keith Swankie, from Arbroath, who suffers from PSP, has welcomed Scottish Government funding for a new developmen­t manager to help raise awareness of the disease.

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