Home Log in Contact us Jobs

Club - Gradient Header
spacer
Charities home page
BHF
Marie Curie
Family Start
Community awards
Schools awards
Family award
spacer
Candis Outstanding Family of the Year Award

Meet the winners

Earlier this year we launched our search to find Britain’s most outstanding family of the year. Entries flooded in from across the UK, bringing tales of triumph over tragedy; inspirational achievements; families who have worked together to make a difference and share their time, love and good fortune with those in need. After reading hundreds of entries and spending hours deliberating, we finally found the six winning families of the Candis Outstanding Family of the Year award for 2008.

Says Mike Tomlinson, one of our judges, “Reading about these families really makes you feel good. They’ve all chosen to focus on the positive in some way and in giving their time, energy and wisdom of experience, they are benefiting in return.”

Entries were of such a high standard that Mike and fellow judges Jane Asher and Denise Welch had their work cut out to choose the one family that shone above them all.
Says Jane, “For me, all of these families clearly belong in the outstanding category. I found reading each story both heartbreaking and inspiring. They have shown such extraordinary energy, selflessness and generosity that it was virtually impossible to choose a winner.”

Denise adds, “It was difficult because the entries were so varied and well written. After reading them I felt uplifted that there are so many good people in this world – something we don’t hear about enough.”

After much deliberation, six regional finalists were chosen and invited to a gala presentation lunch at Chester Zoo in July. Each family was presented with a £250 cheque and fantastic goody bag before the overall winner, who won an all-inclusive holiday courtesy of First Choice at the Holiday Village Aliathon in Paphos, Cyprus, was announced. So allow us to introduce the family both Debbie and our three celebrity judges unanimously deemed the most outstanding of them all

The overall winning family will enjoy an all-inclusive break to this fun-filled holiday village in Cyprus.


The Candis Outstanding Family of the Year 2008

The Murray Family
From: Fife, Scotland

In an era when time, patience and compassion seem to come at a premium – the Murray family really are unique. They have devoted their lives to helping the most vulnerable members of society – children who have been separated from their parents and are in need of a loving home.

As well as bringing up three of their own children, over the past 40 years Margaret and her husband, Ian, have adopted two others and have taken in over 60 children on foster placements ranging from one week to 18 years.

They have cared for children from all walks of life, many whose backgrounds mean they are considered ‘at risk’. But no matter what their story, the Murray’s top priority is to make them feel safe and secure.

“Children come to us for all kinds of reasons, mostly because their parents can’t cope, or because they’re struggling with problems such as mental health issues or addiction,” says Margaret. “But regardless of the reason, when they arrive at our home these children are always scared.

“We’ve had children who’ve been moved 27 times before coming to us. How frightening must that be?

“Our ‘tactic’, is to be as gentle with them as possible. Some of the children might have nits or worms or scabies but we don’t make them get in the bath or start dragging a comb through their hair. We show them to their room, let them know we’re here to talk if they want to, and let them find their feet. We’re simply kind to them and it works amazingly well.”

Margaret and Ian took the decision to become foster carers at just 23. As children they grew up in the same block of flats in Edinburgh and married at 16. After having two children, Donna, now 43, and Julie, 41, they decided that, rather than have another baby, they’d welcome a child in need into their home.

“There are so many children out there needing love and attention, and that’s what we had to give,” says Margaret. “At first we cared for mostly pre-adoption babies, or babies whose mums were having difficulty coping, maybe because they had post-natal depression.

“We took to it straight away and even decided to adopt a brother and sister, Bonnie and Paul, who had come to us on a foster placement.”

A few years later the couple added another child of their own, Lisa, now 23, to their brood. This meant that with up to three foster children at any one time the couple were caring for up to eight children at home.

“There was never a dull moment,” says Ian. “But Donna and Julie were old enough to help out too. Having these children at home was a great leveller for our girls. They got to see first hand the hardships other people go through and learned all about sharing.”
Adds Margaret, “We all had to work together and all the kids mucked in to help out. We had allotted shower times in the mornings and job rotas for chores, everyone did their bit and I think we are a stronger family for it.”

In fact the Murrays eldest daughter, Donna, has followed in their footsteps and is now also a foster carer. Inspired by her experiences at home, she and her husband Sid, 49 – who have two children of their own – are currently fostering two disabled children, a boy of 16 with spina bifida and a girl of seven who is deaf.

Middle daughter Julie, who also has two of her own children, always helps Margaret out when she needs a break while youngest daughter Lisa has recently completed a year-long course with Barnardo’s to be a respite carer, enabling her to care for foster children when their carers are not at home.

But the Murrays have also faced some serious challenges over the years.

“Almost all of the children who come to us have emotional baggage and it is often hard to get through to them,” says Margaret. “Sometimes they can be quite mischievous. I’ve had a microwave blown up, a game of noughts and crosses scratched into the paintwork on my car – and much worse!”

At present the couple are caring for a boy with challenging behaviour, often requiring Ian to attend school with him. “He finds school a difficult environment to be in,” Ian explains. “I accompany him to some of his lessons and as he’s bonded with me he finds it easier to behave while I’m there.” The Murrays think nothing of taking time out to do such things and have made many adaptations and sacrifices over the years to support their family, like moving into a bigger house to accommodate more children, finding innovative ways to stretch their budget and never enjoying a carefree social life. At an age when most people are looking to retire, Ian and Margaret have just committed to a long-term foster programme with Barnardo’s, which means the children will stay with them for years rather than months.

“We’re looking forward to it,” says Margaret. “People say we should be slowing down at this time in life but what would we want to do that for Fostering keeps us young.
“We were delighted to win the Outstanding Family of the Year Award, but the truth is, we don’t consider ourselves outstanding at all. We care for children because we love it. For all the trials and tribulations it brings, the rewards are tenfold. We’ll keep fostering for as long as we can – many of these children have no one. If we don’t care for them, who will?”


North East Regional winner

The Vasey family
From Burniston, Scarborough

On discovering two of their sons were suffering from a rare genetic disorder, Sue and Brian Vasey vowed they would enjoy as much quality of life as possible – whatever it took. Unlike their brothers, Alex, now 19, and Rio, ten, both Curtis, 16, and Taylor, 14, suffer from Alstrom Syndrome, an inherited disease marked by blindness, deafness, diabetes, the tendency to become obese and reduced life expectancy.

“The boys were toddlers when doctors told us about their condition,” says Sue. “Finding out they would never be able to see, and might not live to be adults was devastating, but our immediate reaction was to do everything in our power to help them.”

After discovering that maintaining a high level of fitness could help delay the progress of the condition, Sue and Brian trawled their local area for sporting activities for the visually impaired. With no such provision available in Scarborough where they live, the couple had to make weekly 200-mile round trips to enable their sons to take part in sport, often taking children from other families with them. Not surprisingly, such mammoth journeys took their toll. With two other boys to care for and a wholesale confectionery business to run, after six years, in 2005, the couple decided to set up their own group, Scarborough Actionnaires, to provide multi-sports sessions for blind and partially sighted children.

“It was hard work as it took a lot of organisation,” says Sue. “But it was better than all the travelling!”

Hundreds of families have benefited from the group, not least the Vaseys themselves – over the years, both Curtis and Taylor have maintained a healthy weight and with Sue, Brian, Alex and Rio’s help, manage to exercise every single day.

“Alex and Rio are great,” says Sue. “Anything Curtis and Taylor need, they’re there, from helping them clean their teeth to kicking a ball around. And I’m proud of Curtis and Taylor too. Considering what they deal with, they don’t complain.”

Looking to the future Sue says, ?“At the moment Curtis and Taylor are well, but the prognosis isn’t good. In addition to other health problems, Alstrom can also cause major organs to fail, which is a frightening prospect.

“But we don’t dwell on the possible hurdles of the future because we know that, as hard as it gets, we can get through it together.”

North West Regional winner

The Fairhurst family
From: Wigan, Lancashire


Sheila, 51, and Trevor Fairhurst, 54, were utterly devastated when their 19-year-old daughter Carly was killed by her partner of four years in a violent attack in 2006.
Overwhelmed with grief, Sheila came to depend on counselling from Victim Support Wigan, to which she says she owes her life. So, when the service was placed under threat because of a lack of money, the couple took action and set up the Carly Louise Fairhurst Fund raising more than £17,000.

“After Carly died I went downhill fast,” says Sheila.

“I was consumed with grief and even tried to take my own life; I just wanted to be with Carly and couldn’t bear the thought that I would never see her again.

“Our police liaison officer put me in touch with Victim Support who arranged counselling for me. I was in therapy at least twice a week for a year; usually people only receive six weeks.

“I couldn’t bear the thought that others may not have the same lifeline in future.”
The Fairhursts have channelled all of their energy into raising as much money for the Fund as they can, while also keeping awareness of domestic violence firmly in the public eye.

“We don’t want anyone to suffer in silence like Carly did. We just wish she’d spoken out,” says Trevor. “We know nothing will ever bring Carly back but anything we ?can do to stop the same thing happening to another young woman brings us comfort.”

Sheila and Trevor’s son Michael, 24, his partner, Shelley, 21, and her family are also involved in the Fund and assisted in the organisation of Concert for Carly, an annual event on her birthday in April.

All the money raised goes to the Victim Support counselling service, which has named a counselling room the Carly Fairhurst Suite, in honour of Carly and her family’s work.

“When we heard about the counselling room Sheila and I were reduced to tears, as we were when we heard we’d been shortlisted for this award,” says Trevor. “It’s nice ?to have the work we’re doing recognised but we do it as it gives us pleasure. We’ll be donating our £250 from Candis to the Fund so other victims of crime can receive the support they need.”

East Midlands Regional winner

The Matthews family
From: Goscote, Leicester

Like many ten-year-old girls, Celine Matthews loves to go dancing and to cheerleading classes. But Celine can only sit and watch as her twin, Rhia and elder sister Lacey, 12, jump, kick and twirl, as she has cerebral palsy, a condition affecting movement and co-ordination as a result of an injury to the brain.

Not content with sitting on the sidelines, Celine has become an ambassador for children with cerebral palsy through Scope’s In The Picture project – aimed at increasing the number of images of disabled children in books – and has spurred her whole family, including her sisters and mum, Jean, 48, and dad, Peter, 39, on to do the same.

Celine was just two when diagnosed with her condition, and a more specific analysis found that she was diplegic, meaning her body is affected from the waist down.

“We found different playgroups and resources for Celine,” says Jean. “One group, run by Red Cross, invited people to give talks. A lady from Scope came and brought along a book called Two Left Feet, about a little boy who has cerebral palsy and uses a walking frame, like Celine. She was only two and a half at the time but she was amazed there was a boy in a book like her. She’d never seen anything like it before and she just kept saying, ‘That’s like I am’.”

Following that meeting Scope launched In The Picture, citing Celine’s response to Two Left Feet as the inspiration behind it, and actively started looking for authors and illustrators to create books featuring disabled children. Celine, who was five by then, decided she wanted to write a book about her experiences of wearing splints and started working with Scope on developing it. 

“When Celine draws pictures they always feature a walking frame, or splints or a wheelchair,” says Jean. “They’re basic, typical children’s drawings, but they really reflect her and how she sees the world. Even the mermaids have mobility aids.

“Getting splints fitted can be quite a scary experience for children and there’s nothing that explains the process on their level. Celine’s New Splints is an amazing book, not just because our daughter wrote it, but because it gives children with cerebral palsy a starring role in ?a book any child can read. A few years ago there was a push for children’s books to be more inclusive of different ethnicities; it should be the same for disabilities.”

All the family have played a part ?in promoting In The Picture, and ?are kept motivated by Celine.

“What strikes everyone about Celine is how strong minded she is, she seems to know where she wants to go in life and nothing is going to stop her. Having cerebral palsy has never been an obstacle for her, and we all take inspiration from that.

“Every book, leaflet or poster she sees she points out where a disabled person could have been featured and how. Her ambition for the project is incredible, she’s definitely on a mission!”

West Midlands Regional winner

The Cullen family
From: Kenilworth near Coventry

Over the last four years, Ginny Cullen has raised over £20,000 for charity, by running four marathons, organising fashion shows, salsa nights and bring and buy sales. In addition she mentors at a local school and does voluntary work, including fundraising for local community projects and working at mental health charity MIND’s drop in centre. She also works part time in an estate agents.

All this, while being a single mum to Joshua, 16, and Daniel, 14, who suffers from Cystic Fibrosis (CF) – an incurable, hereditary disease that affects the internal organs, especially the lungs and digestive system, making it hard to breathe and digest food.

“People ask how I do it, but I don’t do it single-handedly. The boys are a great help. We work as a team, with everybody doing their part.

 “CF is an illness that you can’t get better from, so when I found out Daniel had it, it was a real blow. But having someone like Daniel in your family makes you realise that you have to make the most of every minute of every single day, because life really is precious.”

Daniel requires two sessions of physiotherapy every day as well as nebulisers, medication and a very high calorie diet.“Mornings are quite full-on and we get up very early but it’s all part of our routine so we just get on with it. It makes the juggling act of being a mum – which every mum has to perfect – that little more taxing, but it works because we pull together as a family to help Daniel with his illness.”

The family have found one of the best ways of dealing with Daniel’s illness is by helping others.

“Daniel desperately wanted a dog, but due to my work we couldn’t get one full-time so we compromised and began looking after guide dogs waiting to be matched with new owners,” Ginny explains.

The boys have also played an integral part in organising fundraising concerts at school ?that have raised £20,000 for the inhabitants of Bo in Sierra Leone and Uyogo in Tanzania, the latter being twinned with Kenilworth where the Cullens live. And Daniel, a gifted poet, often performs his poetry at such events, which expresses what it is like to live as a teenager with CF.

Joshua, meanwhile, has recently completed the bronze Duke of Edinburgh Award and is currently working towards silver. A talented basketball player, he represents Warwickshire and Coventry and also acts as a school basketball coach, helping staff coach younger pupils.

Says Ginny, “I’m so proud of both of my boys, Daniel, for his bravery and creativity, Joshua for his total selflessness. CF is a very demanding illness and a lot of my time is devoted to Daniel’s care, so I’m not there for Joshua as much as I would like. But never has he complained.

“I would give anything for Daniel to be healthy, but he’s not, so we concentrate on staying positive, and we’ve found by helping others we actually help ourselves.”

Southern Regional winner

The D’Lima family
From: Whetstone, London

Jack D’Lima was a remarkable little boy. With a winning smile and witty quips, his parents, Beverley and Albert, describe him as the kind of ‘cheeky chappy’ you couldn’t help but love. Jack loved nothing more than having a kick about with his brothers, Tom, and Charlie in the back garden.

Anyone watching them would never have realised the little boy was battling a brain tumour, discovered when he was just 15 months old.

“Jack was one of life’s fighters,” says Beverley, 39. “He took strength from being with those he loved.”

As Jack’s illness worsened, both Beverley and Albert, 43, gave up their jobs to care for their son and Tom, now 15, and Charlie, 9, spent every moment they could at his side.
“They’d wait on him, feed him and never tire of trying to cheer him up. When he was too ill to move, they’d play football with him on the couch, and when he was too poorly to do that they’d hold him and chat for hours on end,” says Beverley.

Sadly, following a nine-year battle with cancer, Jack passed away just after his tenth birthday in March 2005. Afterwards, Beverley arranged counselling sessions with The Grief Encounter Project for her boys.

“While Charlie, who was only six at the time, wanted to talk about Jack, I could see Tom, who was 12, holding back,” says Beverley.

“He co-ordinated the funeral service, cleared Jack’s belongings, took on chores, but inside he was consumed by grief. Seeing his counsellor Shelley really helped him deal with his feelings and thoughts.”

Adds Tom, “After we lost Jack I felt as though nobody could ever understand how I was feeling. I felt lonely and confused but I didn’t want to talk about my feelings in case I upset people. On the first visit to Grief Encounter I felt a bit awkward but it soon became something I looked forward to. Finding out someone understood me made everything much easier.”

Tom began writing and giving speeches at fundraising events for Grief Encounter. He has written for their website and he and Charlie have taken part in workshops to improve the lives of other bereaved families.

As for Beverley and Albert, in January 2006, they set up a charity called Jack’s Goal – to raise funds for research into discovering the causes, advancing the treatments and finding a cure for childhood brain tumours. Through bingo nights, sponsored dinner parties, a gift sale (by Tom), a sponsored walk (by Charlie) and publishing a recipe book they have raised over £36,000.

“Our work for Jack’s Goal and The Grief Encounter Project has been our therapy,” says Beverley. “It is lovely to think we might spare another family the agony of losing a child along the way.”
spacer
spacer
   © Newhall Publications Limited
Check out this NEW feature on the Candis website and view previous issues of Candis Magazine Online... click here

Book ahead with Candis Club and save up to 33% on great family days out at some of Britain's biggest and best attractions... click here