Before anyone starts to think that my ego is getting just a 'wee' (Scottish for small!) bit too big, this section is not just so I can boast about what I've done (well, maybe that's part of the reason..). I thought by putting up some of the press cuttings I've been in, it'd let you see a side of me from another perspective - even if it is a journalists'! I'll add a few of the articles I've been featured in in the past at a later date, but for now, here the latest 'outing'!

Newspaper: Evening Times (A West of Scotland, daily newspaper)Date: Saturday, 10th January, 1998
ROBERT SOFTLEY has achieved more in his 17 years than most people have in a lifetime. His arms and legs jerk uncontrollably, he can't stand upright or walk on his own and his speaking is always slurred. But never once has Robert let his cerebral palsy - which was caused by a lack of oxygen at birth - get in the way of his life. It affected his balance and means that he can only move around in a wheelchair or by crawling around on his hands and knees. But Robert is blindingly optimistic about everything he does. In recognition of his efforts he has just been given a Young Achiever Award by East Dumbartonshire Council. He has never asked for sympathy, he hates relying on others and he doesn't want to be treated any differently.

But he is starkly honest about what he can and can't do physically. He has battled endlessly to control his erratic movements. Now he can get himself dressed, move swiftly about the house without help and can even use the mouse to operate his computer. And although his mum, Bet (54), never thought it possible, Robert passed his driving test last July.

Now he speeds around Glasgow and Kirkintilloch in his hand-operated mobility car. "My life was great before hut now it's heaven," beams Robert, at his home in Adamslie Drive, Kirkintilloch. "I'm the only one of my friends with a car, so we drive into Glasgow and go to clubs and pubs. "On New Year's Eve we went to the Hogmanay street party in George Square and had a great time. "Some of my friends had too much to drink and were joking that they could do with a wheelchair to get them home. But they're brilliant ...they don't treat me as anyone special. "To them, I'm just Robert and it's not important how I look ... they forget that I'm in a wheelchair. "Everyone near my home knows me. People are always saying hello to me in the street and I often haven't got a clue who they are, but I'm a happy person and love talking to people." Until a year and a half ago he was plodding along at Ashcraig special needs school in Stepps. He was top of the class but he still felt as though he wasn't learning enough.

HE MADE up his mind to go to a mainstream school and battled against all the odds to get into Lenzie Academy. Robert, in his typical direct manner, told the head teacher that ramps were needed to get up stairs and a lift had to be installed. Major changes were needed to make classrooms and corridors accessible for his wheelchair. Although it took some time, the changes were made and the school doors have been permanently opened to pupils with disabilities. Robert is under no illusions about the difficulties faced by people like himself. "There's a path laid out for disabled people and it's very difficult to do anything different" says Robert. "But if it's only money that's stopping people like me from having the same chances as everyone else, then it's not a very good reason. "Just because I'm disabled doesn't mean I don't have any rights and can't decide for myself what I want to do with my life. "I can't help but fight to do the things I want to do and have a right to do." Robert has been at Lenzie Academy for nearly two years and is preparing for his Highers. He plans to study computing science at university, but unlike anyone else thinking about where to go, he has to choose the place very carefully. "I visited one university and when I told the woman what subject I wanted to do, she said there was no way I would be able to get inside the building," he says. "I've already done work experience setting up web sites fur a company in America."

ROBERT set up Boab's Bio web site to explain a bit about his Iile and what it was like to live with cerebral palsy. He had so much response that he decided to research the condition and extended the site even further ... now there are 50 pages. When the English charity Scope saw what he had written, he was invited tn speak at a conference in London about cerebral palsy. "Everything has really taken off," laughs Robert, who has a sister, Julie (25) and a brother Scott (29). "And although I don't need special help, some people do "Ive travelled to Blackpool and London to speak about the rights of disabled children. "I've been like this all my life, but I'm happy, I have friends, a great family and I've got lots of plans for the future ... what more could I need?" Roderick McLelland, head teacher at Lenzic Academy said: "His determination, good humour and positive, attitude have been an inspiration to us all."

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