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Michael Gibson was just 18 when he became one of the youngest people ever to be diagnosed with Parkinson's Disease, a degenerative brain disorder that normally affects older people.
Now 25, Michael, a television presenter and film director who lives in London, tells LESLEY GIBSON his moving and inspiring story.
The doorman eyed me suspiciously and refused to let me soaring eagle casino players club levels the nightclub.
But the doorman didn't believe me when I told him.
I felt so upset, angry and frustrated that I gave up arguing and went home.
That was my first unpleasant taste of the ignorance and prejudice I would face over the next few years.
Although I felt angry about the doorman's attitude, I wasn't surprised other people couldn't accept I had Parkinson's, because, deep down, I couldn't accept it myself.
I will never forget the day I was diagnosed.
I'd been to see my GP four times because my hands had started to shake for no apparent reason.
He didn't take me seriously and kept saying it was nerves.
But I knew it wasn't; I'm not a nervous person.
So finally I'd taken my mother along, and she convinced him to refer me to a neurologist at Blackburn Royal Infirmary, near our home in Accrington, Lancashire.
A few weeks later, we sat in the specialist's consulting room, waiting for answers.
I'd spent half an hour doing tests that seemed pointless: drawing circles on a piece of paper, making pincer movements with my hands, walking up and down the room.
Then he said it: 'You have Parkinson's disease.
He said it was a degenerative brain disease and it wasn't curable.
But I didn't take in a word.
I didn't want to hear, didn't want to know.
Then my mother turned to me and said: 'Don't worry, love, we'll have the doors widened to accommodate your wheelchair.
It usually affected older people and was soaring eagle casino players club levels rare in the young.
Its cause was unknown.
Symptoms gradually worsened, leaving some patients wheelchair-bound.
But each case was different, and no one could say how quickly the disease would progress.
It wouldn't my life; Parkinson's isn't life-threatening, it would just affect my quality of life and I would need to take drugs every day to control it.
BY the time we'd arrived home, my shock was giving way to devastation.
I felt utterly heartbroken as we told my father and two brothers.
I just cried and cried as my family tried to comfort me.
One moment I'd been a normal teenager, with nothing more important to worry about than what I'd wear for a night out.
The next I faced a disability so terrifying I couldn't bear to contemplate it; a future I wanted to run away from.
Over the next few years, that was exactly what I tried to do mentally and emotionally, even though I couldn't escape it physically.
I went into denial, to the extent that most of the time I did-n't even take the pills I was prescribed to control my symptoms.
My father printed out masses of information from the internet for me.
And Mum bought me a book by Michael J.
Fox, who also has the condition.
But I stashed it all away without even looking at it.
I simply tried to forget about my condition and carry on as normal.
I was at college in Blackburn, studying video production.
I didn't tell my tutors slots cleopatra's gold the condition.
I didn't bingo jet international pity or special treatment.
I felt really angry about it and I'd release my aggression on nights out, by getting into fights.
It wasn't difficult to find trouble; in Blackburn you only had to look at someone twice and they'd think you wanted a fight.
I did a lot of sport, too, which helped my anger: badminton, volleyball, swimming and kickboxing.
Like any red-blooded young man, I enjoyed meeting girls.
I didn't tell them about my condition at first — if my hands began to shake I'd say I was nervous or cold.
But, of course, if I began seeing a girl regularly, I'd have to tell her the truth.
Girls always seemed sympathetic.
Yet it was always me who was dumped, and I couldn't help thinking: 'Did my disease frighten her away?
I couldn't forget I had Parkinson's for long.
One moment I'd be having a great time.
The next, a stranger would notice my hands shaking and make some stupid comment or make fun of me.
I'd get so upset that I'd go home early.
Yet I was determined not to let it stop me doing anything.
Far from holding me back, I think it's given me a lot of drive and made me more persistent.
My dream was to be a film director or a TV presenter and I never lost sight of that.
I worked so hard at college that I got a distinction.
Afterwards I spent a year doing a foundation course in video production; then I applied to Manchester Metropolitan University to do a degree in TV production.
When I was rejected, I rang the tutor and pestered him for an interview.
He agreed and asked me to take my show reel.
He loved it and I was accepted.
Again, I didn't mention Parkinson's — I wanted my achievements to be in spite of my condition, not because of it.
My three years at Manchester were great.
My illness didn't affect my course, but I still struggled with it mentally and emotionally.
I will never forget the day I graduated.
I got a first-class honours degree.
My father was with me when I found out.
He hugged me and we both cried: me with joy, relief and an amazing sense of achievement, and him with pride.
It felt great, like sticking up two fingers at my disease.
It was a turning point.
But my struggle to accept it was far from over.
After graduating, I spent six months working at a 999 call centre in Blackburn, to earn some money while I applied for jobs in TV.
It was high-pressured and often very upsetting, but the money was good.
Then, one day, we took a call from an elderly man who said his wife was dead.
He was told to give first aid and became terribly upset.
He said: 'She's my wife, and I love her.
I've been with her 60 years and I know she's dead.
He replied: 'She had Parkinson's disease and she's not shaking.
I thought: 'What am I doing here?
I applied to TV production companies for junior positions.
In December 2004 I got a job in London.
I was still working there when, late last year, I noticed my symptoms soaring eagle casino players club levels my legs were beginning to shake and sometimes I tripped and stumbled.
My older brother, Andrew, 27, had spent years nagging me to take my pills.
He couldn't understand why I wouldn't take them if they made me feel better.
But it wasn't as easy as that.
I'd always hated the idea that I would have to soaring eagle casino players club levels pills for the rest of my life that could give me side-effects such as nausea, sweating, and hallucinations.
They were meant to control my symptoms, but sometimes I thought the side-effects were worse.
Now, with my shak-shortening spreading and worsening, I couldn't deny my illness any longer.
That's when I came up with an idea for a documentary about Parkinson's disease.
Although I'd been aware I had Parkinson's for six years by then, I knew very little about it and had no idea what the future might hold.
It occurred to me that, in learning about the illness, I could inform other people, too.
There's so much ignorance about it, and especially about the fact it can affect young people.
I wanted to show what it's like for a young man like me to have to live with it.
So I pitched my idea to the TV company.
They thought it was great, so late last year, I sat at a big table at Channel 4' s offices in London with nine experienced film makers who also had ideas they wanted to develop.
Mine was the only idea that was commissioned.
I felt incredibly proud.
But I was terrified, too: I knew I'd finally begun the journey towards accepting my illness.
As part of the film-making process, I went out on the streets and asked people what they thought Parkinson's disease was.
It was very disturbing.
One young man about my age said 'They're spastics, aren't they, people with Parkinson's disease?
I said: 'I have Parkinson's disease,' soaring eagle casino players club levels watched his face drop.
Older people said I couldn't have Parkinson's because I was too young.
I did a lot of things I'd been too afraid to do before.
I sat down for the first time with my family for an honest discussion.
I told them my symptoms were getting worse, and how frightened I was.
They were really supportive and tried to reassure me they hadn't noticed any deterioration.
I admitted I'd tried to shield them from my condition in the past.
I finally read Michael J.
Fox's book, which I found really inspiring, and I went to see other people with Parkin-son's disease — something I'd flatly refused to do before.
It was terrifying to see people in wheelchairs, or unable to walk properly, and think: 'Will I be like that in a few years?
I want to marry and have children one day, and I talked about my fears that I might never marry because my disease could frighten off any woman I fall for.
For the first time, I also went to see my consultant alone.
In the past, my mother had come with me, and I hadn't been honest about my symptoms because I didn't want her to know they were getting worse.
The consultant told me more about the disease but admitted no one could say what the future held for me; it affects everyone differently and there was no way of knowing how quickly my symptoms would develop.
Finally, I decided to take my pills to control my symptoms and give soaring eagle casino players club levels as much normality as possible, for as long as possible.
These days, I wake up to take my pills at 8am, and swallow soaring eagle casino players club levels with lots of water, which seems to min-imise side-effects.
I eat regularly and healthily, and get plenty of sleep.
I'm lucky, because my symptoms haven't got drastically worse since I was first diagnosed.
I have constant shaking in my hands and also, more mildly, in my legs.
Sometimes I stumble because of it.
Slurred speech is a common symptom; I don't slur my words but sometimes I mumble.
My balance isn't as good as it was; if someone hugs me, I feel like I'm going to fall over.
I think the worst symptom is an internal feeling of constant movement that's difficult to describe.
It's horrible — like snakes moving inside you or a train that can't stop.
But my symptoms have been brought under control in the past nine months, since I've been taking my tablets Cabaser properly.
The drugs, which work by mimicking dopamine, have camouflaged my symptoms a lot.
I'm hopeful that my symptoms won't worsen and I won't need a wheelchair.
I don't like to think about the future; I prefer to focus on the present.
But if I do get much worse, there are other treatment options, such as brain surgery.
AT THE moment, given the chance to get rid of Parkin-son's, I don't think I'd take it.
My disease is a constant reminder to enjoy each day and get the most out of life.
It gives me so much motivation and determination.
Recently, I soaring eagle casino players club levels a job as a presenter on MTV Select, a programme for young people, broadcast live every day.
I did-n't mention my disease until I'd been offered the job, and the team were fine about it.
To cap it all, I'm in a wonderful relationship.
I met Paola, a 27-year-old Italian model, six months ago at a nightclub.
I thought she was out of my league, so when she agreed to let me take her for a drink I was thrilled.
I told her about my disease straight away.
To my immense relief, it didn't put her off.
We look after each other: when she comes to stay, I make her breakfast and she brings me my pills and water.
As well as being stunning, she's the sweetest girl I've ever known.
I've come a long way since that day when, as an immature 18-year-old, I was diagnosed with Parkinson's disease.
Not only have I finally learned to accept it and enjoy the present rather than worrying about the future; I'm living my dreams and loving my life.
¦ I'M All Shook Up: Parkinson's At 25 is on Channel 4, tonight at 11pm.
The Parkinson's Disease Society has a free helpline on 0808 8000303, Mon to Fri, 9.
The average age of onset is 55 to 60, but about one in 20 people diagnosed are under 40.
It can affect all activities including talking, walking, swallowing and writing.
Parkinson's occurs when cells in the part of the brain that controls movement die.
These cells produce dopamine, a chemical messenger that enables people to perform smooth co-ordinated movements.
It is not known why these cells die.
Once about 80 per cent of these cells have been destroyed, symptoms of Parkinson's appear.
The three main symptoms leading to the diagnosis are tremors, muscle stiffness and slowness of movement, although not everyone will have all three.
Other symptoms that may later develop include a lack of facial expression, an altered posture, tiredness, difficulties with balance and depression.
It is believed that Parkinson's results from a combination of genetic susceptibility and an external trigger, such as toxins from food or the environment.
In most cases, however, Parkinson's is not thought to be inherited.
The main aims of drug treatments are to increase the level of dopamine that reaches the brain.
Deep Brain Stimulation DBS is a form of surgery used to treat some of the symptoms.
Some 760 soaring eagle casino players club levels with Parkinson's have had DBS in the UK, including well-known London chef Fergus Henderson.
The procedure involves the implantation of a wire, with four electrodes at its tip into the brain.
A neurostimulator and extensions are also implanted in the patient's chest.

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