Feb 292016
 

With thanks to Ian McLaren, PR account manager, Innes Associates

Scottish Bed Making Chmpionship 2016 launchIt will be pillows at dawn in Aberdeen next month as teams fight it out to be crowned Scotland’s best bed maker.
Organised by north-east children’s charity Cash for Kids, the Scottish Bed Making Championship will be held in the Granite City on Thursday, 31 March.

The competition is part of the Aberdeen-based charity’s annual Bed Appeal which runs throughout March.

It is hoped the appeal will raise £20,000 to enable the purchase of beds for around 150 disabled and disadvantaged children living in Aberdeen and Aberdeenshire.

This is the second time the unique competition has been held and this year will be staged at the Crowne Plaza Aberdeen Airport. Teams of four will to be tested on their bed making precision and speed, with points being awarded for each task. The two highest scoring teams will then go head-to-head in a bed race to be crowned Scottish Bed Making Champions.

Reigning champions are the staff at Crerar Thainstone House Hotel who showed that their hospital corners were a cut above the rest of the competition last year. The team is confident about their chances of retaining their title against a bigger field of competitors.

General manager Morag Clark said:

“The team at Thainstone are excited to again be involved in the Scottish Bed Making Championship and we hope to successfully defend our title.  It was great fun last year and it is fantastic way to support such a worthy cause.”

A number of the Aberdeen’s top hotels have already signed up to take part in the contest. The number of entries is already up on last year, but Cash for Kids is encouraging businesses from all sectors to get involved, including nursing and healthcare providers. Entries cost £100 per team of four, with all proceeds going to the Cash for Kids Bed Appeal.

Now in its fourth year, the month-long Bed Appeal aims to provide disadvantaged children with a bed of their own and disabled children with specialist beds. Over the last three years, the appeal has helped Cash for Kids provide new beds for over 350 local children.

The charity is also calling on the north-east public to fundraise for the Bed Appeal throughout March.  Cash for Kids is encouraging people to wear slippers to work for a month, organise breakfast bake sales, and hold onesie or pyjama to work days.  Employers are also being asked to consider raffling off an extra day’s holiday as a duvet day in support of the appeal.

Cash for Kids charity manager Michelle Ferguson said:

“The Scottish Bed Making Championship is open to anyone who wants to show off their bed making prowess.  Entries from businesses of all sizes and operating in all sectors are welcome.  It really is a fun event and great for teambuilding as everyone has to work together efficiently.

“The contest and the month-long Bed Appeal will once again highlight the issue of poverty in the region that is all too often hidden. We continue to be surprised by the number of applications we receive requesting beds for children who are forced to share beds with siblings or even sleep on a mattress on the floor.”

To register a team for the Scottish Bed Making Championship or for more information on the Bed Appeal visit www.northsound1.com/bed.

Cash for Kids is Northsound Radio’s listeners’ charity. It makes grants to individuals, families, children’s groups, organisations and projects throughout the Northsound transmission area.  All money is raised locally and spent locally to benefit local disabled and disadvantaged children and young people under 18. More information on Cash for Kids can be found at www.northsound1.com/cashforkids, or telephone 01224 337010.

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Feb 292016
 

CLAN logo2With thanks to Phil Moar, Account Manager, Citrus:Mix.

A glittering evening of music, hosted by Aberdeen woman Carol Norrie, has raised more than £12,000 for CLAN Cancer Support.

The dinner dance, which took place at the Chester Hotel in Aberdeen, was the first fundraising event that Carol has organised for the charity.

Following the success of the event Carol said:

“My father, Dave Allan, was diagnosed with lung cancer in June. Following his diagnosis and treatment, I visited CLAN Cancer Support in Aberdeen and was really impressed by the services offered to individuals and families affected by cancer. I came away determined to do anything I could to help to make a difference.

“Many people I spoke to who had been affected by cancer were unaware of the services that CLAN offers, and some believed CLAN provided respite care. I wanted to do anything I could to increase awareness of the services offered at CLAN House and CLAN Haven.

“As a guitarist and singer from the age of 12, my father has a great passion for music so I saw an opportunity to base an event around music and invite local artists to attend. I was delighted when Oliver Richards, Colin Newbury and Cameron Jay agreed to lend their support.”

Carol’s family also has a special connection with CLAN Cancer Support, with Carol’s parents Dave and Marion having been married in Rosemount Parish Church, CLAN’s former Aberdeen base, in 1971, and both Carol and her brother, David, were also christened in the church.

Carol added:

“Our family connections with CLAN just cemented the feeling that I needed to do all that I could to support this fantastic charity. I was overwhelmed by the support from friends, family and local companies, and to raise more than £12,000 was a wonderful feeling.

“I certainly won’t be stopping there though, my husband now volunteers at CLAN and I’m already looking towards my next fundraising challenge. I don’t know what that might be but I already have lots of ideas!”

Dr Colette Backwell, chief executive of CLAN Cancer Support, said:

“We are delighted that Carol’s dinner was such a success and wish to thank Carol and her family for selecting CLAN as the beneficiary for the evening. The enthusiasm and commitment shown by Carol, her family and friends, towards CLAN is inspiring.”

CLAN Cancer Support is an independent charity which provides comfort, support and information, free of charge, for anyone, of any age, affected by any type of cancer. CLAN aims to support people to reduce anxiety, stress and to increase their ability to cope with the effects of a serious illness.

Based in Aberdeen, the charity covers the whole of north-east Scotland, Moray, Orkney and Shetland. CLAN has a presence in Ballater, Banchory, Elgin, Inverurie, Fraserburgh, Lossiemouth, Peterhead, Stonehaven, Turriff, Kirkwall and Lerwick.

For further information about CLAN Cancer Support please call (01224) 647 000 or visit www.clanhouse.org

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Feb 252016
 

CLAN logo2With thanks to Phil Moar, Account Manager, Citrus:Mix.

A leading north-east cancer support charity is giving people the chance to come together this Mother’s Day by holding a special walk.

CLAN Cancer Support’s seventh annual Mother’s Day walk will take place within the grounds of Westburn Park in Aberdeen on Sunday, March 6.

The charity recognises that Mother’s Day can often be a difficult time for mothers who have lost a son or daughter or for individuals who have lost their own mother or wife and is giving people the chance to share part of what is a significant day for many with it.

The event is inspired by Macduff woman and CLAN supporter Marjorie Nicholson who organised a sponsored walk after losing her son to cancer on Mother’s Day in 2007. After raising more than £6,000 at the event, CLAN was inspired by her courage and began organising and hosting a similar walk in Aberdeen.

The 1km walk itself can be completed as many times as an individual chooses, with an opportunity to be sponsored to do so also available for participants.

Susan Crighton, CLAN’s fundraising manager, said:

“Our Mother’s Day walk is one of our most touching events throughout our year-long calendar and we’d be thrilled to welcome you along on a day that holds a special place for many.

“Westburn Park is a lovely location for the walk, which is open to anyone of all ages and abilities, with many choosing in the past to walk in memory of a loved one. We want to create a day that can often be viewed with a sense of fear into something positive, with the walk able to provide comfort and support to all those who attend.”

Registration on the day will take place between 9.30am and 10am in CLAN House on Westburn Road. The walk will start at 10am and continue until noon.

If you would like to take part adults cost £5 and children are free. Please contact Darren Hill at CLAN to register on 01224 651034 or email darren.hill@clanhouse.org

CLAN Cancer Support is an independent charity which provides comfort support and information, free of charge, for anyone, of any age, affected by any type of cancer. CLAN aims to support people to reduce anxiety, stress and to increase their ability to cope with the effects of a serious illness.

Based in Aberdeen, the charity covers the whole of north-east Scotland, Moray, Orkney and Shetland. CLAN has a presence in Ballater, Banchory, Elgin, Inverurie, Fraserburgh, Lossiemouth, Peterhead, Stonehaven, Turriff, Kirkwall and Lerwick.

For further information about CLAN Cancer Support please call (01224) 647 000 or visit www.clanhouse.org

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Feb 112016
 

There is a little-understood, little-known syndrome that strikes 1-2% of the population. Aberdeen Voice’s Suzanne Kelly, a sufferer, is joining with others around the world to raise awareness of this condition, particularly among health care professionals.

cyclical vomitingImagine an illness that works like this. You can be fine for weeks, months, and then with less than a minute’s notice, you get hit.

If you manage to take a preventative medication at absolutely the right moment, then chances are you’ll be lucky and avoid an episode. And if you’re not lucky?

Cyclical Vomiting Syndrome attacks see sufferers vomiting for anything from a few hours to a few days.

In rare cases some people have attacks that stretch to weeks, possibly months.

Looking back, I see that I had very infrequent attacks for at least 20 years; I always put these down to food poisoning. Then they increased in frequency and severity, until for a fortnight, I thought I was dying. I spent a day and a half on my bathroom floor, completely unable to get up except to hunch over and be ill again. The pain was searing; then I threw up bile; then I threw up blood.

I really thought ‘this is it’ and assumed I had some kind of cancer. I was either shaking with cold or burning up, or spending hours wondering if I could manage to get up to get any water, and if so, how long I’d keep it down.

Finally making it back to work a week later, I was straight onto my doctor, then a specialist. Being into research, yet knowing the stupidity of self-diagnosis, I came across this illness called ‘Cyclical Vomiting Syndrome’ – it struck people like me, who used to experience migraine headaches (I had them as a child and they abruptly stopped).

Little was known, there was no cure.

The specialist I went to talked to me for nearly an hour – this was after all the blood work was back and had ruled out any terminal illness.  He determined that it was CVS I had. The medicine I got to prevent attacks is not without potential side effects, but it seemed to work a charm. That is, if my attack was during the daytime. More often than not, this hits me between 2 and 4 am.

My first waking thought then is not to take a pill, and sometimes before I realise what’s happening, it’s too late. (I sleep with the medicine within reach, and have some stashed on me, and virtually every place I spend time).

I’m an extremely lucky person with this condition.

I’ve found a network of others with the illness. Many of them have it far, far worse than I do. I’ve never had to be hospitalised (although with hindsight, there were two attacks that I probably should have gone to the ER with). I’ve never had to be fed by IV. I’ve never had to plead with doctors or nurses for medicine, never been ridiculed, patronised or ignored.

My back teeth aren’t rotting from being ill as frequently as some of the other people I’ve come to know. And as I’m in a country with free health care (and am lucky enough to have additional health cover through my work), I’ve not had to spend thousands of pounds on treatment. And I’ve not had to have permanent feeding tubes put in me, either. And I’m not either a little child or an elderly person going through this. I am extremely lucky.

Being ignored at ER, being told ‘you’re just after drugs’, being sent home only to throw up blood on the way out of the hospital – this is how people are being treated by those in the health care profession who’ve never heard of CVS. My attacks, and most people’s attacks, have nothing to do with: drinking, emotions, stress, diet. One time I was walking down the street, felt a bit sick, and then that was that.

The worst occasion remains a quiet night in doing some work, and being sick for a week. In all of my attacks I’ve not had a care in the world, and oddly, I’ve never been sick when drinking. The worst parts of this illness is just that – no one really understands what sets it off, how to stop an attack, or how to cure CVS.

Here’s what some of the people with CVS say, and why they want to raise awareness.

“I’ve had CVS for 20+ yrs and still to this day get treated like a drug seeker. I’ve been left feeling tortured & in agony for hours laying in an ER bed more times than I can count.”
– Ryan

“Too many to count, not just medical staff, friends and family too! A few years ago, before I was diagnosed, my best friend in the whole world was bringing me to the ER in the middle of an attack and asked me if there is any chance that my symptoms were psychosomatic? It still hurts me to this day that that was a real question from her.”
– Jenna

“A specialist put me through every grueling test and when they were all negative, told me he could do nothing and I was obviously making it up to get sympathy. My daughter actually figured it out by watching Gray’s anatomy! Researched it, took it to my family Dr who researched further and here I am. Can only manage symptoms is what I get.”
– Susan

“I’ve lived in the same area (so, near the same hospital) since 2004. For 12 yrs. here in VA (20-yrs total with CVS), I’ve had to go to the ER only 2-3 times/year, and I’m STILL treated like a drug-seeker, by about 1/3 of the ER docs I’ve seen. When they do refuse my simple (approved & recommended) abort-meds, my cycle does not end. It can go for days. So, I have to return to the ER after having been kicked out 6-12 hours earlier.

“You must go back; dehydration is no joke. I’ve had to call an ambulance for some of these return trips when I’m completely disoriented. I don’t see how a hospital can bill you for the 2nd stay when treatment was REFUSED during the 1st stay. I’ve fought that before & won – I think everyone should contest billing for any repeat-visits that are due to malpractice: neglect of duty.

“They see me coming back, the nurses at least recognize me, and viola(!) the new doc is suddenly ready to take things seriously. I have much less trouble if someone is with me, “vouching” for me. To summarize, I am luckier than some patients who have more frequent episodes. But, only 2-3 trips to the ER per yr & they think I’m drug-seeking?! (Yes, I’m a 3-time-a-year addict. So dumb!)

“I’m a 40 yr old mom, nothing “wild” looking about me at all. (Not that it should matter, but some advice to others: I’m treated like a drug-seeker more often if I look really messy/out of it. I actually prepare an outfit & hair ties, etc. every night before bed in case an episode starts & I have to go to the ER.)

“I had an episode last weekend & encountered a doc I’ve had the misfortune of seeing in the past. He has a line he loves to use, and he YELLS, no, BELLOWS at me:

“I’m not going to distribute narcotics as they are not indicated for CVS!!!!!”

“The nurses stare in horror at HIM. My preventative meds are anti-anxiety meds. At the ER, to abort an episode, I need 2mg (yes, only 2!!) dilaudid, 25-50mg phenergan (over time), & Ativan or similar & at least 1 bag of fluids. Dr. Pain here should be avoided at all cost. I went back the next day with my father, and there was no delay in giving me that exact Rx to stop the episode. I was very dehydrated by then, however, so the IV was extremely hard to establish & left 10+ huge, black/purple bruises all over my arms & hands.

“I’ve had the great honor of emailing with Dr David Fleischer, “The Father of CVS.” He expressed to me in 2010 that my episodes seemed to require very little to abort, & he added that dilaudid is preferred over morphine bc it is not likely to create nausea – like morphine does.

“I was diagnosed by a GI in Manhattan after every test known to man & even gall bladder removal. I was referred by him to a Neuro back here in VA, who then passed me off to a shrink who only did my Med. Mgmt for anti-anxiety meds & then said I should just have my Primary taking care of this. My Primary is pretty lazy about it, though. On occasion the ER has tried to contact her by her emerg svc, but she’s not very forceful in her care of me, her patient. None of them care!!”
– Emily

The aim of the initiative is to raise awareness in the medical profession of the seriousness – and painfulness of this condition.

A support group is there to help. Colleen from CVS Speaks said:

CVS Speaks actively works raising awareness and helps support Facebook support groups. We currently have 14 groups teamed up helping suffers in the day to day struggles. We have groups by age kids thru adults, caregivers to suffered only, men’s groups, women, mothers. You name we probably have a group to fit sufferers diverse needs.

“CVS patients often need safe place to feel validated, accepted and learn from others what helps relieve symptoms. Medical professionals often do not have much experience with CVS. So along with groups like CVSA www.cvsaonline.org, we help get them in touch with the most up to date treatment options and research to talk with their providers about.”

More information can be found here: https://www.facebook.com/CVS.Speaks/

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Feb 012016
 

With thanks to Esther Green, Tricker PR.

NDCS-Small-Jo-Donaldson_Photography-96

Offering support to families when they need it the most. National Deaf Children’s Society is running a families weekend in Edinburgh this month.

Families of young deaf children from across Scotland who gather in Edinburgh later this month to learn that deafness is no barrier to preventing a child achieving their dreams. Peer support, expert advice and professional information will be available for families getting to grips with a baby or toddler’s diagnosis during a weekend course organised by the National Deaf Children’s Society (NDCS) and funded by Aberdeen Asset Management.

The gathering, on 27 and 28 February, will be attended by families from Angus, East Lothian, Orkney, Argyll and Bute, Midlothian, Glasgow and other parts of Scotland.

Over 90% of the 3,850 plus deaf children in Scotland are from hearing families with no previous history or experience of deafness, so for  many parents the diagnosis comes as a devastating and overwhelming shock.

The NDCS supports deaf children and young people, but in the early years of a child’s development, it is parents who need the charity the most.  With the low incidence of deafness in Scotland, families often find themselves to be unique within their immediate communities, leading to feelings of isolation and uncertainty.

Heather Gray, NDCS director for Scotland and Northern Ireland explains:

“The NDCS Early Years weekends empower and inform parents at a crucial stage in their child’s development, and offer vital support and advice at a time when parents are still getting to grips with their child’s diagnosis.

“Families receive clear, unbiased information from audiology, education and from local sources of support over the course of the weekend, giving parents the opportunity to explore the options that are available to their child and ask the questions they have been unable to ask in busy everyday situations.

“Through receiving this information in a safe and relaxed environment, parents are able to gain an understanding of childhood deafness and develop a network of support which can assist them now and in the future.”

By bringing families together, parents have the opportunity to share their experiences and access vital peer support that can often exist far beyond the weekend itself. In addition, families also find reassurance in the shared experiences of parent volunteers, and inspiration and encouragement through speaking to young deaf role models.

The impact of NDCS Early Years weekends is clear – parents have indicated they felt more confident in working with professionals to ensure the right support for their child as a result of becoming informed and connected.

One parent said:

“I have learned more about my child’s hearing loss in the past two days than I have in the past two months. It was eye opening to hear other people with similar or even more difficult circumstances. Great to share stories about struggles.”

Karin Hyland, of Aberdeen Asset Management’s Charitable Foundation said:

“The weekend will help 12 families; enabling parents to become part of a positive community network of mutual self-support. Families will also be informed about access to services which encourage improved community relations, reduce isolation and improve peer support through this valuable outreach work by the NCDS.”

The Aberdeen Asset Charitable Foundation was established in 2012 to formalise and develop the Group’s charitable giving globally. The Foundation seeks partnerships with smaller charities around the world, where funds can be seen to have a meaningful and measurable impact and the firm encourages its employees to use their time and skills to support its charitable projects.

For more information visit http://www.aberdeen-asset.co.uk/aam.nsf/foundation/home

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Jan 282016
 

Future Choices GarthdeeWith thanks to Future Choices.

Local disabled Charity Future Choices, which is based at Inchgarth Community Centre, Garthdee has come forward to
help the Primary 7 pupils of Kaimhill with their fundraising
efforts.

The Charity which provides social inclusion became aware of the pupils’ fundraising efforts and wanted to do all they could to help, so they donated £100 to help boost their efforts.

Chairman of Future Choices, David Forbes said:

“As a completely self funded charity, we absolutely know how difficult it is to fundraise, so anything we could do to try and help the children, we aim to.”

The P7 pupils are currently fundraise to go on a school trip to Cromdale Outdoor Centre later on in the year ut need much needed funds to make this dream a reality. They have made this trip an annual one so want to continue with the trip this year.

David added:

“Seeing the pupils so happy, that’s what it’s all about and as a charity, we strive to get Vulnerable adults out enjoying themselves, so to be able to help local school children  try to reach their goal is simply a positive thing.”

If you feel you can contribute to the fundraising efforts to help the pupils of P7, please contact David by email on info@future-choices.org.uk or freephone 0800 5668728

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Jan 282016
 
CLAN8 (2)

Carol Norrie and CLAN chief executive Dr Colette Backwell at CLAN House in Aberdeen.

With thanks to Phil Moar, Account Manager, Citrus:Mix

An Aberdeen woman is to hold a charitable dinner dance next week
after her musical father’s cancer diagnosis moved her to organise an event.

Carol Norrie will hold The Allan CLAN Red Carpet Charity Ball, in aid of CLAN Cancer Support, at the Chester Hotel, Aberdeen on Friday, Feb 5.

The night, which will include a three-course dinner and live performances from local artists Oliver Richards, Colin Newbury and Cameron Jay, has been devised by Carol after her father Dave Allan was diagnosed with lung cancer in June.

Dave’s diagnosis was then followed by a bout of pneumonia before further tests showed he required a double heart bypass before he could properly start his cancer treatment.

With her Dad’s cancer treatment now underway, Carol felt that she needed to focus on something that was positive and was looking for a distraction. She struck upon the idea of organising a charitable event and on recommendation from her friends, she visited CLAN Cancer Support at its CLAN House base in Aberdeen to see first-hand the work they do with individuals and families affected by cancer.

After being so impressed by the facility and the services the charity provides, it was an obvious choice for her to link-up with for her special evening.

Carol said:

“Dad has had a bit of a tough time of it recently, overcoming both pneumonia and a heart bypass in the days and weeks after being diagnosed with cancer in June last year. It’s been difficult for him and our family but his strength has been amazing. He’s managed to remain so positive throughout it all.

“With this in mind, I was looking for a bit of a distraction to take my mind off things. Some friends told me about CLAN and on learning more about the charity, I was immediately taken in by its spread of services and comfort and care it provides to people affected by cancer. It just seemed right to hold an event on its behalf.

“The night itself will have a strong musical element which was a key consideration given my Dad’s love for music throughout his life so far. He has played in various bands from the age of 12 up until a few years ago and we’re still hopeful that he might be able to play a song on the night; we’ll just have to wait and see.”

Ticket sales for the dinner dance have been strong, with all funds raised set to go towards CLAN’s provision of free support services to anyone affected by cancer throughout the north-east of Scotland, Moray, Orkney and Shetland. Monetary donations are still being sought to help cover lighting and sound costs.

Carol added:

“The support we’ve had from friends, family, members of the public, my work and local businesses such as The Chester Hotel itself and SIGNAL2NOISE has been fantastic so far and it really has helped create a feeling of positivity around something which is undoubtedly a tough time for us all. Not everyone is lucky enough to have the support network that my Dad has had so the work of charities like CLAN can bring an added importance to many.

“We’re delighted to be supporting the charity with the event and we can’t wait to invite attendees to a night of musical fun.”

Dr Colette Backwell, chief executive of CLAN Cancer Support, said:

“Carol’s enthusiasm and passion for helping CLAN is there for all to see and we’re so delighted to have been selected as the beneficiary for what is sure to be a fantastic night of entertainment.

“CLAN is there to help all those affected by cancer; whether it is the person directly affected, a family member, a friend or even a carer. Carol, her Dad and their family have an obvious close bond and for them to turn what is sure to be a difficult time into something so positive is testament to their character and approach to life.”

Those interested in getting involved with the evening or those who would like to donate funds to the night are asked to contact Carol Norrie on carol.norrie572@btinternet.com

CLAN Cancer Support is an independent charity which provides comfort support and information, free of charge, for anyone, of any age, affected by any type of cancer. CLAN aims to support people to reduce anxiety, stress and to increase their ability to cope with the effects of a serious illness.

Based in Aberdeen, the charity covers the whole of north-east Scotland, Moray, Orkney and Shetland. CLAN has a presence in Ballater, Banchory, Elgin, Inverurie, Fraserburgh, Lossiemouth, Peterhead, Stonehaven, Turriff, Kirkwall and Lerwick.

For further information about CLAN Cancer Support please call (01224) 647 000 or visit www.clanhouse.org

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Jan 282016
 

acsha logoWith thanks to Eoin Smith, Senior Account Executive, Tricker PR

A group of Aberdeen hoteliers has been working tirelessly to raise funds for a leading dementia charity, and is set to reach a five figure fundraising goal. Aberdeen City and Shire Hotels’ Association (ACSHA) has raised over £13,000 for Alzheimer Scotland so far, and is confident that it will increase this to £20,000 by its AGM in April.

As part of its fundraising effort, ACSHA recently auctioned a bottle of Pol Roger Vintage Cap 1943 champagne for an impressive £800.

The prize, which also included a meal at Ardoe House Hotel & Spa and a bottle of White Label Pol Roger, was won by Calum Richardson, who runs The Bay Fish & Chips, Stonehaven. After placing the winning bid, Mr Richardson offered an additional lot comprising of outside catering which raised an additional £1,000.

Mariner Hotel owner Mike Edwards, who donated the champagne, is spearheading ACSHA’s fundraising effort, and believes the organisation is well on its way to reaching its target. He says,

“It’s incredibly heart-warming to see so many hoteliers working together to raise funds for a cause as worthwhile as dementia care and research.

“We are delighted to have raised so much money from auctioning the champagne, and hope to continue in a similar vein as we push closer to our £20,000 target over the next few months.

“I hope that Calum enjoys the champagne, and that he celebrated his winning bid in suitable style – with fizz and chips!”

ACSHA will continue its fundraising efforts over the coming months, starting with a 24 hour endurance relay on static bikes which will take place in a number of hotels across the region. The organisation has also partnered with the Deeside Brewery to create a specially labelled lager which will be sold in local hotels with all profits going to Alzheimer Scotland.

Alzheimer Scotland is ACSHA’s nominated charity for 2015/16, and it is hoped that the money raised will go some way to funding its operations in the north east, including a newly opened resource centre in Aberdeen city centre. In addition to monetary donations, a number of ACSHA members have joined the Dementia Friends initiative, which seeks to make all venues more welcoming and hospitable for those with dementia and their carers.

Mr Edwards’ father, David, was once a familiar face in the hospitality trade in Aberdeen, and was diagnosed with vascular dementia in 2008 at the age of just 59. There are currently around 90,000 people across Scotland diagnosed with dementia, including around 3,500 under the age of 65. In Aberdeen alone there are almost 300 people living with dementia under the age of 65.

Aberdeen City and Shire Hotels’ Association represents 49 independently operated hotels and conference venues, along with a further nine associate members. These hotels provide around 4,500 bedrooms in Aberdeen and Aberdeenshire. ACSHA is committed to improving the quality and standard of hotel services and to furthering the overall standards of excellence and hospitality within the region.

To make a donation to ACSHA’s fundraising pot for Alzheimer Scotland, visit www.justgiving.com/ACSHA

For more information about Aberdeen City and Shire Hotels’ Association, visit www.aberdeenhotels.org

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Jan 282016
 

Mental Health Aberdeen (MHA) has forged a link with an innovative charity which offers a therapeutic animal service. With thanks to Jessica Murphy, Senior Account Executive, Citrus:Mix.

MHA owl and pussycat1The leading north-east charity recently visited The Owl and The Pussycat Centre in Maud, which gives people the chance to have a positive experience with birds of prey, including the owl stars of Harry Potter, Eral and
Hedwig.

Service users in MHA’s Companions Befriending Service and their companions had a magical time on the visit, which was used as an opportunity to get out and about in the community, have fun and build relationships with peers.

Flora Todd, manager of MHA Companions Befriending, is currently looking for volunteers to take on a befriending role within the charity.

She said:

“Our service users and their companions thoroughly enjoyed themselves at The Owl and The Pussycat Centre, and we would like to thank everyone there for making us so welcome. We would love to repeat visits like this as they are so beneficial in helping our service users combat feelings of isolation and embrace day to day life. Interaction with animals and birds is a great tool for improving a person’s wellbeing.

“Companionship can make an incredible difference to a person’s wellbeing and it was fantastic to see our befrienders and service users interacting with the owls and having such a good time. We are currently on the look-out for volunteers to join our pool of befrienders in Peterhead, Fraserburgh, Banff, Turriff and surrounding rural areas. It is a fantastically rewarding role to take on and while it has its challenges, the transformation it can bring about to someone’s life is incredible.

“Volunteers befrienders can help in so many different ways, from going out for coffee, helping build their self-confidence and learning new skills to attending local activities such as exercise classes and arts or cultural groups. They are also very much a listening ear. We would urge anyone interested to get in touch with us and find out more about becoming a befriender.”

A committed network of befriending volunteers has served the north-east through MHA for a number of years but the charity is working to expand the service.

Full training is provided to all volunteers, who must be aged 18 and over, and the charity has an experienced team leading the programme. All out of pocket expenses are reimbursed and the next induction training course will begin in February.

MHA was founded in 1950 and provides support services, counselling and advice to people affected by challenges related to mental health and wellbeing. Services are available for children from the age of 12 and adults. The organisation was among the first to provide community care – with its first residential project, a group home for discharged psychiatric patients, opened more than 35 years ago. MHA has also been providing day services continuously for over 60 years.

For more information on the befriending scheme and volunteering opportunities contact Flora Todd on 01779 470122 or visit www.mha.uk.net.

For more information on The Owl and Pussycat Centre visit www.owlandpussycatcentre.co.uk

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Jan 142016
 

With thanks to Esther Green, Senior Account Executive, Tricker PR.

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Deafness is no barrier to children achieving great things, parents will learn on a weekend course run by NCDS and funded by Aberdeen Asset Management’s Charitable Foundation.

Parents will learn that deafness is no barrier to preventing their child achieving their dreams on a weekend course dedicated to providing peer support, expert advice and professional information for families getting to grips with a diagnosis.
Over 90% of deaf children in Scotland are from hearing families with no previous history or experience of deafness, so for many parents the diagnosis comes as a devastating and overwhelming shock.

Help is on hand from the National Deaf Children’s Society (NCDS) which, with a grant from Aberdeen Asset Management’s Charitable Foundation, is organising a weekend gathering for 12 families with deaf babies or toddlers living in Scotland to share experiences and learn more about the help and support available to them.

From birth through to independence, the NCDS supports deaf children and young people but in the early years of a child’s development, it is parents who will need the charity the most. With the low incidence of deafness in Scotland, families often find themselves to be unique within their immediate communities, leading to feelings of isolation and uncertainty.

Heather Gray, NDCS director for Scotland and Northern Ireland explains:

“The NDCS Early Years weekends empower and inform parents at a crucial stage in their child’s development, and offer vital support and advice at a time when parents are still getting to grips with their child’s diagnosis.

“Families receive clear, unbiased information from audiology, education and from local sources of support over the course of the weekend, giving parents the opportunity to explore the options that are available to their child and ask the questions they have been unable to ask in busy everyday situations.

“Through receiving this information in a safe and relaxed environment, parents are able to gain an understanding of childhood deafness and develop a network of support which can assist them now and in the future.”

By bringing families together, parents have the opportunity to share their experiences and access vital peer support that can often exist far beyond the weekend itself. In addition, families also find reassurance in the shared experiences of parent volunteers, and inspiration and encouragement through speaking to young deaf role models.

The NCDS has its Scottish headquarters in Glasgow, and the families weekend, open to families from across Scotland with a deaf child from birth to two years old, will take place in Edinburgh in February 2016.

The impact of NDCS’ Early Years weekends is clear – all parents who attended weekends in 2014 said they felt more positive about their child’s future, and all agreed that the weekend helped them to make positive decisions and choices. 100% of families also felt more confident in working with professionals to ensure the right support for their child. Over the two days, families become informed, empowered and connected, three characteristics that stay with them long into the future.

One parent said:

“I have learned more about my child’s hearing loss in the past two days than I have in the past two months.’ It was eye opening to hear other people with similar or even more difficult circumstances. Great to share stories about struggles.”

Karin Hyland, of Aberdeen Asset Management’s Charitable Foundation said: “The weekend will help 12 families; enabling parents to become part of a positive community network of mutual self-support.

“Families will also be informed about access to services which encourage improved community relations, reduce isolation and improve peer support through this valuable outreach work by the NCDS.”

The Aberdeen Asset Charitable Foundation was established in 2012 to formalise and develop the Group’s charitable giving globally. The Foundation seeks partnerships with smaller charities around the world, where funds can be seen to have a meaningful and measurable impact and the firm encourages its employees to use their time and skills to support its charitable projects.

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