NMC
President Matthew Kelly
"The
NMC is a fantastic project which I have been involved with for some
years now - my wife Sarah is one of the two co-founders of the charity.
I
am all too aware that, in the past, there was very little opportunity
for young people with muscular dystrophy to realise their potential
- the chances and choices available to others were just not open to
them.
But
then The Neuromuscular Centre was created. User led, and increasingly
user run, the Centre answers as many of the needs of those with Muscular
Dystrophy in the region as it can.
I
am proud to be the Centre's President and I have watched with delight,
and respect as the Centre has gone from success to success. The dream
has become a reality, and the extraordinary and unique work that the
Centre does must be encouraged and sustained.
This
web page has been designed for you by young people at the NMC. At long
last, they have been able to realise their potential. NMC North West
is a prototype, and so that it may continue to flourish and develop,
and in time, be replicated elsewhere, helping countless others, I would
urge you to join with me in supporting this unique initiative offering
hope and a sense of purpose and worth where before there was none."
