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Simon Enger

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Help Me Raise Some Much Needed Funds by Supporting My Ride for Muscular Dystrophy

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Hi,
 
This year I am fundraising for young people living with Muscular Dystrophy.
 
Muscular Dystrophy is a devastating neuromuscular disorder which weakens and wastes the muscles.  The most common form is Duchenne Muscular Dystrophy which mainly affects boys.  Onset of this condition is between 3 and 5 years of age and the disorder progresses rapidly with most boys completely dependent on an electric wheelchair by their early teens. Life expectancy for this disorder is usually only early twenties. There is no treatment, there is no cure and no boy survives.
 
Muscular Dystrophy NSW’s (MDNSW) goal is to improve the quality of life for all people affected by Muscular Dystrophy.  A dedicated, skilled and enthusiastic team of staff continually work to improve the range of services, programs and events available for those living with the condition as well as their families and carers. MDNSW provides critical life-changing support and assistance people living Muscular Dystrophy including our innovative Duke of Edinburgh's Award program, counselling, family retreats, children’s camps, medical, accessibility and communication equipment and access to sport and special interest programs.
 
Please share my page above or comment below so more people know about this wonderful cause and hopefully support as well.

Simply click 'Donate Now' to make a secure online donation.


Thank you so much for your support!  Young people with Muscular Dystrophy will benefit enormously from your generous support.

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Muscular Dystrophy NSW

Muscular Dystrophy is a devastating neuromuscular disorder, which results in the progressive deterioration of muscle strength and function. Muscular Dystrophy is the name of one of more than 75 different types of neuromuscular conditions. There are more than 40,000 people in Australia who have some form of neuromuscular condition, 13,000 of whom live in NSW.

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