Tag: support

‘Grassroots music venues are in crisis’

A new levy on arena and stadium tickets and a cut in VAT are urgently needed to support grassroots music venues across the country as they struggle to cope with a crisis of closures and soaring costs, says a Westminster committee.

The recommendations are in a report from the cross-party Culture, Media and Sport Committee, which highlights how small local venues integral to the pipeline of professional creative and technical music talent are stopping performances or closing entirely at a rate of two per week.

The Committee also heard about how artists are facing a “cost of touring crisis”, while promoters are struggling to get shows off their spreadsheets and into venues.

On top of immediate financial help through a levy-funded support fund and a targeted temporary VAT cut to help stem the tide of closures, the report says a comprehensive fan-led review of live and electronic music should be set up this summer to examine the long-term challenges to the wider live music ecosystem.

The Committee inquiry, launched at the Music Venue Trust’s Venues Day in October 2023, heard from across the sector1 of the scale of the crisis facing venues and the impact this is having on artists and all those that rely on them for business.

The MVT described 2023 as the most challenging year for the sector since the trust was founded in 2014, while Creative UK said the grassroots music sector took a ‘battering’.

In total the number of GMVs declined from 960 to 835 last year, a net decrease of 13%, representing a loss of as many as 30,000 shows and 4,000 jobs.

The report says that given the urgency of the crisis, a voluntary levy on arena and stadium concert tickets would be the most feasible way to have an immediate impact, creating a support fund for venues, artists and promoters administered by a trust led by a sector umbrella body.

The Committee also calls for the industry to ensure the levy cost is not passed on to music fans. If there is no agreement by September or if it fails to collect enough income to support the sector, the Government should step in an introduce a statutory levy, the report adds.

On VAT relief, the Committee calls for a temporary cut based on venue capacity, with the Government undertaking analysis to assess the impact to inform future decisions.

Dame Caroline Dinenage MP, Chair of the Culture, Media and Sport Committee, said: “We are grateful to the many dedicated local venues who gave up their time to take part in our inquiry. They delivered the message loud and clear that grassroots music venues are in crisis.

“The ongoing wave of closures is not just a disaster for music, performers and supporters in local communities up and down the country, but also puts at risk the entire live music ecosystem. If the grassroots, where musicians, technicians, tour managers and promoters hone their craft, are allowed to wither and die, the UK’s position as a music powerhouse faces a bleak future.

“To stem the overwhelming ongoing tide of closures, we urgently need a levy on arena and stadium concert tickets to fund financial support for the sector, alongside a VAT cut to help get more shows into venues.

“While the current focus is on the many grassroots music venues falling silent, those working in the live music sector across the board are also under extraordinary strain. It is time that the Government brought together everyone with a stake in the industry’s success, including music fans, to address the long-term challenges and ensure live music can thrive into the future.”

Among the report’s other recommendations are for the Government and Arts Council to make it easier for the live music sector to apply for public funding and for stakeholders across the industry to continue to support the Featured Artists’ Coalition’s campaign to end punitive fees on artists’ merchandise.

Further information:

Charity calls for better understanding of neuromuscular conditions to speed up referral and improve vital support

  • Muscular Dystrophy UK voices concerns from the muscle wasting and weakening community in Scotland.
  • Study reveals possible signs of rare and progressive conditions are often missed and not investigated.
  • Speedy referral is essential due to complex diagnosis process and the urgent need to access vital healthcare and treatments as quickly as possible.

A recent study by Muscular Dystrophy UK reveals that people living with a muscle wasting or weakening condition are often misunderstood by healthcare professionals and are not referred at the earliest opportunity to specialist services.

The leading charity for more than 110,000 children and adults in the UK living with one of over 60 muscle wasting and weakening conditions, carried out a survey revealing key insights from the muscle wasting and weakening community.

Just under half of respondents (47%) faced being misdiagnosed at some point, with it taking four or more meetings with healthcare professionals for the majority (55%) of respondents to get a diagnosis. A significant majority of respondents (69%) waited in excess of a year to receive a diagnosis. 

The findings highlight the need to improve knowledge and understanding of neuromuscular conditions to ensure people are referred, as early as possible to a specialist neuromuscular team, to receive the right diagnosis and start on an appropriate care pathway to get the support and any available treatment required.

Muscle wasting and weakening conditions are progressive which means they will worsen over time and lead to an increasing level of disability. Care and treatments available will slow progression but there is currently no cure. 

The symptoms of muscular dystrophy, and the age at which onset occurs, will be different in each person.

Common symptoms could include muscle stiffness or pain, changes in mobility, such as difficulty walking, difficulty in lifting things and increased number of falls. Some muscle wasting and weakening conditions can affect the heart or the muscles used for breathing and in some severe cases, the condition may have life-threatening complications, and shortened life expectancy.

84% of respondents to the survey highlighted the need to increase understanding and awareness of muscle wasting and weakening conditions among non-specialist neuromuscular healthcare professionals as a key priority. With 56% of respondents highlighting that access to healthcare should be a further area of focus.

Respondents shared some of their diagnosis journey highlighting: “I was 14 when I knew something was wrong.

“At age 35 I was diagnosed. I was told I was lying and making things up.”

Another respondent said: “My first reported symptoms to my GP I was aged 35, then onwards from that, on a regular basis until eventual diagnosis at 65.

“I had in-patient assessments over those years, and no-one thought to look for Facioscapulohumeral muscular dystrophy (FSHD) even though my sister has it and I always disclosed this in my medical history.”

The findings show a lack of understanding of muscle wasting and weakening conditions within non-specialist neuromuscular healthcare professionals, either at the initial stages of a diagnosis or at different touch points throughout the management of the condition.

Muscular Dystrophy UK works with the NHS and the muscle wasting and weakening community to broaden knowledge and understanding of the different conditions and improve access to treatments. 

The charity is calling for improvements to be made, so people get a faster diagnosis and are better equipped to access appropriate healthcare sooner.

Catherine Woodhead, Chief Executive of Muscular Dystrophy UK said: “When you are living with a progressive condition that can affect vital muscles such as the heart and lungs, it is essential that you get a diagnosis quickly.  

“We know that neuromuscular conditions cover an incredibly wide range of rare and progressive conditions. The diagnosis journey is complex and it can take multiple appointments. It’s therefore crucial that we improve the understanding and knowledge of non-specialist neuromuscular healthcare professionals to ensure the referral process is quick and efficient to reduce the number of people being misdiagnosed.

People must be able to access the right support, management – and where available, treatment. Allowing people to remain independent, doing the things they enjoy for longer and more easily.”

A person holding a guitarDescription automatically generated

David Hick was diagnosed with Becker muscular dystrophy in July 2023. Photo credit: Muscular Dystrophy UK

David Hick, 35, a musician who lives in Glasgow, was diagnosed in July 2023 with Becker muscular dystrophy after years of not knowing. Despite having symptoms of fatigue and muscle aches in his teenage years he was told not to worry.

His symptoms progressed, following Covid, and the realisation came when he wasn’t able to continue with his motor trade job, that he had been doing for two decades. He got professional help and was diagnosed. A month after diagnosis, David joined the North Star Programme and is part of a clinical drug trial. David is now looking to move to closer to a specialist neuromuscular centre in Newcastle to ensure he can receive the best possible care.

He said: “Looking back it was apparent that something was wrong, but it was never properly investigated. I was told you’re a fit and healthy person. You’ve got nothing wrong with you. You’re just tall and skinny.

“It affected my mental health when I was in my early twenties, as I questioned why I couldn’t do certain things. Difficulties would come up in everyday life, but I just brushed it off.

“We were renovating our house and I lifted something heavy. As a result, I pulled several muscles, so went to a physio. This was the start of the diagnosis journey. I ended up being diagnosed with a rare and progressive condition. It was like a grenade going off – I’d never heard of muscular dystrophy before.”

Muscular Dystrophy UK provides a range of resources and awareness raising opportunities for non-specialist neuromuscular healthcare professionals, including an e-learning resource for General Practitioners, events, webinars and conferences and connections to local specialist services through its Regional Neuromuscular Networks.

Healthcare professionals who wish to access this support can email: 

campaigns@musculardystrophyuk.org

For more information about Muscular Dystrophy UK visit musculardystrophyuk.org 

or call our free helpline on 0800 652 6352 (open Mon – Thu 10am – 2pm).

Inspirational veteran dad inspires runner to achieve lifelong ambition

Teri Evans, 47, from Stevenston, recently fulfilled a lifelong dream by participating in the London Marathon.

Teri was inspired to run in the marathon by her army veteran Dad, Alexander Duncan, who started to lose his sight a few years ago due to macular degeneration and is now supported by Sight Scotland Veterans. ​

Teri explains: “My Dad has been incredibly fortunate to receive invaluable assistance and support from Sight Scotland Veterans since he began experiencing vision loss.

“The charity’s help and support has been so important in maintaining his independence and enabling him to engage in daily activities. It has provided him with essential equipment like screen readers, daylight lamps, driving glasses and a digital magnifier for reading that he uses regularly and is very grateful for.

“Additionally, he regularly attends the Seamill Veterans Sight Support Group, which he really enjoys as it allows him to connect with fellow veterans and individuals coping with sight loss.​

“I was so proud to be running the marathon for my dad and to raise money for Sight Scotland Veterans, it was great to give something back to the charity for all the help they have provided.

“We also arranged with Sight Scotland Veterans that all the money I raise would stay in Ayrshire, so that my dad and the group he attends could benefit, as he was in my thoughts a lot of the way round the 26.2 miles.”​

Alexander Duncan, who was in the 4th Royal Tank Regiment for 14 years adds: “I’m so proud of Teri for running the marathon and for raising money for Sight Scotland Veterans.

“The charity has helped me with lots of things and I love going to my group each month, I can’t thank them enough.”​

Teri’s love for running started when she was 40, when she decided to take part in a couch to 5K. She then built her way up to running a 10K, then a half marathon, and then ran the Edinburgh marathon 2 years ago.​

Teri, who works as a Student Experience Team Lead at Ayrshire College, says: “I never used to run, and would never have believed I would be running marathons a few years ago.

“But I have just built up my fitness and endurance and now regularly attend Irvine Running Club. It was through the running club that I got my spot in the London Marathon, as they got an entry, and my name was picked out of a hat.​

“Running a marathon takes over your life, as there are so many changes you need to make, like a strict training plan to follow and changing your eating habits, but it is definitely all worth it. London is the iconic marathon that every runner dreams of taking part in, so it was a lifelong dream! I also ran in 05:07:11 which was a personal best!”​

Teri has raised over £1000, plus gift aid, for Sight Scotland Veterans. Sight Scotland Veterans provides free support to armed forces veterans affected by sight loss in Scotland to help them regain confidence, restore their independence and make new connections.​

For more information please visit sightscotlandveterans.org.uk or call 0800 035 6409.

Foreign Secretary visits Ukraine 

Cameron reiterates UK’s ‘unequivocal support’ for the Ukrainian people

  • Foreign Secretary David Cameron was in Kyiv to reiterate UK support to Ukraine
  • The visit follows the Prime Minister’s announcement that the UK will spend 2.5% of GDP on defence, and commit to at least £3 billion a year on military support to Ukraine
  • The Foreign Secretary confirmed a £36 million package of energy support, including £20 million in new emergency funding following Russian attacks.

Visiting Kyiv, the Foreign Secretary reiterated the UK’s unequivocal support to Ukraine. Meeting with President Zelenskyy, Prime Minister Shmyhal and Foreign Minister Kuleba, he detailed how the uplift in defence spending announced by Prime Minister Rishi Sunak last week, including £3 billion multi-year funding for Ukraine and the largest ever donation of military equipment, would help ensure Ukraine has what it needs to win.

The Foreign Secretary announced that the UK’s donation of military equipment would include the provision of precision-guided bombs, and air defence missiles and equipment for 100 mobile air defence teams to enable Ukraine to shoot down Russia’s drones and missiles.

The UK also committed to doubling its domestic munitions production, by investing a further £10 billion over the next 10 years. This production will help ensure UK national security, whilst sustaining the UK’s weapons support to Ukraine, keeping Ukraine in the fight for as long as it takes.

Alongside domestic commitments, the Foreign Secretary also revealed that the UK intends to bring international partners together next month to attract additional contributions to the International Fund for Ukraine to meet Ukraine’s urgent capability requirements.

The Foreign Secretary also confirmed a £36 million package for Ukraine’s energy infrastructure and investments in future innovations to support Ukraine’s energy transition and recovery.

This includes £20 million of emergency funding following the recent barrage of attacks on national infrastructure as Russia intensifies its assault on Ukraine’s critical infrastructure, including power plants and gas storage facilities. This takes the UK’s total contribution to the Ukrainian energy sector since 2022 to £170 million.

UK funding will provide equipment to repair damaged energy infrastructure, help physically protect existing infrastructure, and provide back-up support – including generators and distributed renewable generation – for use if Russian attacks destroy more infrastructure.

Speaking from Kyiv, the Foreign Secretary, Lord Cameron, said: “Ukraine is fiercely defending itself against Russia’s illegal invasion, making a war Putin thought would last days, take years. But this war is the challenge of our generation and Ukraine cannot fight it alone.

“We must all step up to ensure Ukraine has what it needs to win. Through our multi-year military funding, weapons provision and vital support to protect and repair Ukraine’s energy infrastructure, the UK is standing with Ukraine and we will stand with Ukraine for as long as it takes.”

A further £16 million was awarded to winners of the UK’s Innovate Ukraine Green Energy Competition, at a reception hosted by the Foreign Secretary and Ukrainian Minister for Energy, Minister Galushchenko.

The 13 winning projects, made up of UK and Ukrainian innovators, partners, businesses and NGOs, launched their innovations to help Ukraine rebuild a greener and more resilient energy grid. This funding was previously announced at the Ukraine Recovery Conference in London and has now been awarded to recipients. 

In Kyiv, the Foreign Secretary saw how Ukrainians are continuing to show resilience in the face of Russian attacks, witnessing first-hand how Ukraine is pushing forward with innovative drone development.

The Foreign Secretary also kicked off negotiations with Ukraine on a 100 Year Partnership – a new agreement that will build enduring links between our two countries across the spectrum of trade, security and defence cooperation, science and tech, education, culture, and much more.

The UK’s commitment to developing this Partnership is a clear signal of its intent to build close and enduring cooperation with Ukraine, and the Ukrainian people, for decades to come.

Letter: You’re not alone …

Dear Editor

This May we celebrate Deaf Awareness Week (6-12 May).

Did you know that nine out of ten deaf children are born to hearing parents? A great many parents tell us they knew very little or even nothing at all about deafness before they had a deaf child.

So it’s hardly surprising that many such parents find themselves feeling confused, unprepared and worried about what the future might hold.

The National Deaf Children’s Society is here to help you give your deaf child the very best start in life. With the right support, there’s absolutely no reason why they shouldn’t grow up confident, happy and fulfilled.

We’re here for you. We can provide support for all of you who are new to the journey, through our extensive resources – from our Helpline, 0808 800 8880, and our wealth of expertise, right through to the friendship and reassurance of our fantastic community.

Find out more by visiting our website www.ndcs.org.uk

Susan Daniels OBE,

Chief Executive, the National Deaf Children’s Society

What is Power of Attorney?

A few places still available at LifeCare’s free info event to help local people simplify the future

Thinking about what would happen in the future if our, or our loved ones, faculties deteriorated can be stressful and worrying. How would someone manage our affairs, access our accounts to set up the right care for us, or pay the bills? Without the right processes in place, an already very emotional situation can be made worse with often very serious consequences.  

Local charity, LifeCare Edinburgh understands how daunting and complex these situations can be and will next month host a free information giving event to help debunk the complexities and help people put the right practical support in place to ensure someone trusted can quickly make decisions on behalf of a loved one if they’re not able, or no longer able, to make them themselves.  

Power of Attorney is a legal document where someone – while they still have mental capacity – nominates a trusted friend or relative to look after their affairs if they later lost capacity in the event of an emergency, illness or accident.

It is not limited to people who are older or unwell, everyone needs to consider setting up a Power of Attorney at any stage of life to avoid any future complications. For example, due to having a stroke, serious accident or dementia.  

Delivered in partnership with experts from Lindsay’s Legal Services team, LifeCare will host its first information giving event designed to encourage people to stop and think about what they need to put in place to help simplify the future.  

Sarah van Putten, Chief Executive of LifeCare said “Unfortunately at LifeCare we are well aware of how stressful life can be when people don’t have the right documents in place.  No one can predict when they may face an unforeseen illness, accident or other debilitating event that may render them incapacitated.  

“As one of Edinburgh’s leading charities providing practical care support we know how emotional these situations can be at the best of times but we also know how much worse they can be when family members and loved ones are locked out of helping access the support for the people they care for. 

“Relatives can’t just walk into a bank and access your money, even if it is to pay for your care. Unless you’ve a Power of Attorney, loved ones would need to apply through court, which can be long and costly. 

“We understand that thinking about the future can be upsetting and frightening. Our free and informal information giving event delivered in partnership with Lindsays is designed to simplify matters; there will be no jargon and there will be plenty of time for questions and discussions and an opportunity to discuss any concerns with legal experts for free.”

LifeCare’s ‘What is Power of Attorney’ event, delivered in partnership with Lindsay’s, will take place at 2pm on Wednesday 1st May in the charity’s fully accessible community café, CafeLife at 2 Cheyne Street, EH4 1JB. 

Free tea and coffee will be available along with the opportunity to find out more about LifeCare’s vital services for older people and the community overall.  

The charity is encouraging people to register via Eventbrite in advance of the meeting: https://www.eventbrite.co.uk/e/lifecares-power-of-attorney-information-event-tickets-856970821797?aff=oddtdtcreator

or visit the LifeCare website https://www.lifecare-edinburgh.org.uk/

or call 0131 343 0940 to register interest.

Parliament Committee backs Bill which would introduce safe access zones around abortion services

After carefully considering views from a broad cross-section of stakeholders, the Scottish Parliament’s Health, Social Care and Sport Committee has agreed to the general principles of the Abortion Services (Safe Access Zones) (Scotland) Bill.

The recommendation comes as part of the Committee’s Stage 1 report. The Committee say the evidence it has gathered has led it to conclude that the creation of safe access zones around abortion services are necessary to protect women’s rights so they can access healthcare services without experiencing harassment and undue influence. 

At the same time, the report acknowledges evidence on the potential impact the Bill will have in restricting the human rights of those who engage in anti-abortion activity outside abortion services. The Committee says it recognises the right to protest and private thought are cornerstones of a free democracy, but concludes that the restrictions on human rights imposed by the Bill are proportionate to achieving its aims.

The report highlights a difference in views amongst the Committee on the issue of silent prayer. It says it could be difficult for the police to decide whether a law has been broken by people silently praying and that this issue requires further consideration.

The Committee stress that the Bill’s implementation needs to be subject to ongoing post-legislative review to ensure that these restrictions continue to be proportionate and kept to a necessary minimum, as well as being subject to continuing parliamentary scrutiny. The Committee has made several recommendations to strengthen the Bill to ensure the provisions reflect this and said any future changes to safe access zones should be subject to additional human rights considerations.

The Committee also say it is vital that individual cases are assessed according to their particular circumstances and that how the legislation is enforced will have a critical role to play in ensuring its appropriate implementation.

Speaking on the publication of the report, Clare Haughey MSP, Convener of the Health, Social Care and Sport Committee, said: “Our Committee is united in backing the Abortion Services (Safe Access Zones) (Scotland) Bill.

“We recognise the strong views it has generated and that not all are in favour of its introduction. But ultimately we believe the creation of safe access zones around abortion services is necessary to enforce the principle that everyone should be able to access healthcare free from intimidation or harassment.

“We understand there are competing human rights at play but we have concluded this Bill strikes an appropriate balance.

“We held extensive discussions on the issue of silent prayer and while some Members felt this should be exempt from the provisions in the Bill, other Members felt an exemption would fundamentally undermine its purpose and that silent prayer can be intimidating to those accessing services. This will need further consideration if the Bill proceeds to Stage 2.

“We’d like to thank all who shared their views with us and helped inform our recommendations.”

Some of the other key conclusions in the report include:

  • The Committee has concluded that, due to the very clear and narrowly defined scope of the current Bill, there is no potential for its provisions to be applied more widely to anything other than abortion services. 
  • The Committee seeks further explanation as to why the default radius of safe access zones has been set at 200m when evidence suggests a radius of 150m would be sufficient for all but one protected premises currently providing abortion services in Scotland.
  • The Committee say they are satisfied that the penalties in the Bill are appropriate and proportionate to achieving the aims of the Bill. 
  • The Committee has called on the Scottish Government to put in place the necessary funds for Police Scotland to develop and deliver specialist training on the enforcement of offences created by the Bill, and that the financial memorandum be updated to reflect that commitment.

Read the report: 

Stage 1 report on the Abortion Services (Safe Access Zones) (Scotland) Bill

£30 million paid this year to help households with higher energy bills

Number of winter payments passes 400,000 mark 

 People in Scotland have received more than £30 million via two Scottish Government benefits to help them deal with increased energy costs this winter, new statistics have shown.   

Winter Heating Payment supports households on low incomes, including older people, disabled people and families with children under five.    

Child Winter Heating Payment helps families of the most severely disabled children and young people.     

The official figures show more than 400,000 Winter Heating Payments of £55.05 were issued between November last year and the end of March. More than 30,000 Child Winter Heating Payments of £235.70 were made in the same spell.    

Winter Heating Payment replaced the UK Government’s Cold Weather Payment in 2023. Most people getting it receive more money on average than via Cold Weather Payment. 

People receive Winter Heating Payment whatever the weather, unlike Cold Weather Payment when the temperature needs to drop to a specific level.  

Child Winter Payment, introduced in 2020, is not available anywhere else in the UK. There is also no cap on the number of children who can get it in the same family. 

 Cabinet Secretary for Social Justice, Shirley-Anne Somerville, said:   “The £30.2 million paid over the course of winter provides support to those who need it most. It is being paid quickly and effectively to help mitigate the worst of the cost of living crisis.  

“Winter Heating Payment guarantees those who qualify will get a payment every year – in contrast to the UK Government approach which needs the weather to be under a certain temperature for a sustained spell.    

“Both Winter Heating Payment and Child Winter Heating Payment have recently been increased in line with inflation which means we will be getting more money into people’s pockets in 2024/25. I am pleased that we are getting the vast majority of these payments to people in good time.   

“I urge anyone who is struggling during the cost-of-living crisis to visit the Scottish Government’s Cost of Living website for support and advice.”    

Cadenza concert in support of Kindred

Cadenza Spring Serenade in support of Kindred

Date: Saturday 11th May 2024

Time: 7.30 pm

Tickets: £12 (Children free) available on

Eventbrite https://www.eventbrite.co.uk/e/cadenza-spring-serenade-tickets-862646728587?aff=ebdssbdestsearch or on the door

Venue: Inverleith St Serf’s Parish Church, 280 Ferry Road, EH5 3NP

One of Edinburgh’s leading mixed voice choirs, Cadenza, celebrates sunny days, starry nights and air filled with birdsong, in works by Ravel, Elgar, Saint-Saens and more …

Funding to support refugee integration

Ensuring access to information and advice

Refugees and people seeking asylum who live in Scotland will be supported to settle into local communities through new funding for Scottish Refugee Council.  

Scottish Government funding of £3.6 million will support Scottish Refugee Council’s Refugee Support Service, which helps people access health, housing, welfare and employment support. It also provides information and resources, as well as encouraging social connections.

The funding will ensure this support can continue, after EU funding the service had previously received came to an end in 2023.

Migration and Refugees Minister Emma Roddick said: “Scotland welcomes refugees and people seeking asylum. Supporting them to settle into communities from day one of arrival, and ensuring they can access information and advice, is key to helping people integrate successfully.

“This Scottish Government funding will ensure that Scottish Refugee Council can continue their vital work to help people begin to rebuild their lives here, particularly as EU funding is no longer available to the service after Brexit.

“Respect and compassion underpin our approach to supporting people displaced by conflict or other circumstances beyond their control. While the UK Government pursues harmful policies on asylum and immigration, we will continue to do everything we can to mitigate their impact.”

Chief Executive Officer of Scottish Refugee Council, Sabir Zazai said: “We welcome this timely investment in a Scotland-wide Refugee Support Service to ensure people seeking protection across Scotland feel welcomed and supported and can start rebuilding their lives in their new communities. 

“This integrated service will be available and accessible to everyone who needs it, wherever in the country they are based.  

“With a focus on collaboration and partnership, we will work with local authorities, grassroots organisations and communities to build a better future for refugees and people seeking asylum. This approach builds on our extensive expertise of delivering vital integration services over the years.  

“Scotland is known around the world for being a warm and welcoming country. We look forward to building on this proud reputation in the coming years as we aim to make Scotland the best place for refugees to thrive, challenge injustice, achieve their ambitions and empower their communities, no matter where they have come from or how they arrived.” 

The Refugee Support Service supports refugees, people seeking asylum and other groups of displaced people.

More information, including on how to access advice and support, can be found on Scottish Refugee Council’s website.