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Volunteer ME sufferer saves shop

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Published Date: 31 July 2008
A SHOPKEEPER whose business has survived thanks to the generosity of an ME sufferer is launching a charity to help him and people like him.
Sandra Majboudoub, 47, only opened Royal Artizana in Leith Walk last September, but loss of business from the tram works had almost forced her to close.

However, John Garner, 44, one of her earliest customers, stepped into the breach, offering to
work for free to keep it afloat.

The two or three days his illness allows him to work has given Mrs Majboudoub the opportunity to do temp work and bring in another wage.

Now the pair have launched a fundraising drive to fund the charity ME Endurance, which they hope will be a lifeline to sufferers in the city.

Mr Garner, who lives in Lorne Street, said: "We want to help people get things like proper cooked meals, bus passes and showers fitted in every sufferer's home.

"We are hoping to receive donations of cars and other transport and have a phone line operating until 10pm, so we can collect shopping and cook meals, and even provide holidays and days out.

"Some people with ME can become very isolated. I've been helping out in the shop since the middle of March. I do it because it's good to be a member of society, I want to work.

He added: "I'm extremely grateful to Sandra as I've been talking about starting this charity for years and now it is finally happening."

ME, or chronic fatigue syndrome as it is also known, results in tiredness and muscle fatigue. Mr Garner's condition leaves him unable to get out of bed some days.

Despite a 2002 report by the Chief Medical Officer for England concluding that ME is a genuine and disabling condition, some people still believe it is all in the mind, which can make it difficult to raise funds and provide support for sufferers.

Mr Garner, who previously worked as a cleaner and carer, developed the illness five-and-a-half years ago. He says it is the result of a bout of glandular fever and a mystery illness which left him with a low white blood cell and red blood cell count.

He has been able to work part-time at Royal Artizana because Mrs Majboudoub is understanding about his condition and accepts that sometimes he will call her up and say he is unable to come in, forcing her to make new arrangements.

Mrs Majboudoub, a mother-of-one from Lasswade, said: "John came in to buy a tea set when we opened last September. We got to know each other and have become good friends.

"We've had a very difficult time because of the trams and were considering shutting up shop.

"John started working for us – had it not been for him the shop would no longer be here."

Anyone who would like to offer support to ME Endurance should call 0131-555 3999

www.edinburgh.gumtree.com/edinburgh/40/26360340.html



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  • Last Updated: 31 July 2008 11:34 AM
  • Source: Edinburgh Evening News
  • Location: Edinburgh
 
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31/07/2008 11:59:03
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31/07/2008 13:11:46
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31/07/2008 13:11:57
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4

Hmm?,

31/07/2008 13:29:23
Trollllllllllllllll in the dungeon!
5

alex paterson,

edinburgh 31/07/2008 13:34:24
Well done John Garner,more people like you would make a happier and better world.
6

Smiffy83,

Somerset 31/07/2008 21:05:56
Well done John Garner and Sandra Majboudoub for wanting to help the mostly overlooked sufferers of the horrible, excruciatingly painful neurological illness Myalgic Encephalomyelitis, & especially to John for using his precious energy in this way.

I have been housebound with M.E. for 20 lonely years & in all that time the government have spent no money on biomedical research, testing or treatment; all money has gone to the psychiatric profession. This is not the case with any other neurological illness.

80% of M.E. sufferers never recover. 25% are bed or housebound, some so severely affected they spend their lives in darkened rooms unable to talk or swallow. M.E. has been found to shorten life by an average of 25 years because the heart is usually affected. People who have died of M.E. have been found to have viruses in their hearts, muscles, guts, brains, spinal cords and brains. One dedicated UK doctor, using a powerful darkfield microscope, is finding parasites and bacteria in the blood of most M.E. patients he tests.

Despite the fact that it is a physical illness, the only NHS treatment available is psychiatric - cognitive behaviour and graded exercise 'therapies' that actually worsen symptoms, sometimes permanently. Some severely affected patients are being sectioned under the mental health act - one young woman, Sophie Mirza, tragically died as a result of such sectioning.

The treatment of M.E. patients in this country as if they have a mental disorder is a national scandal.
7

DNN,

UK 31/07/2008 23:27:22
I persuaded fellow workers to work for two weeks without pay. We had to keep moving our stock of steel and our machines between various premises to dodge our bosses creditors until he gained a new contract and saw it through to completion. We saved the company and our jobs. It was one of the most rewarding but hilarious escapades I have ever been party to.
8

DNN,

UK 31/07/2008 23:39:34
I also wish the very best for these sufferers of this nasty physical condition, which is horrible to read about, let alone to suffer in such dreadful isolation.
9

truthsleuth,

04/08/2008 00:21:14
ME

Clinical Depression for Yuppies
10

linda mccafferty,

Glasgow 04/08/2008 00:35:55
Your just an idiot #9

 

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