Mark Maddox

Mark's Mime for MND

Fundraising for Motor Neurone Disease Association
£467
raised of £1,000 target
by 41 supporters
Donations cannot currently be made to this page
We fund care, campaigning and research to achieve a world free from MND

Story

Thanks for taking the time to visit my JustGiving page 

I was diagnosed with Motor neurone disease MND in 2010, or as it's known in America amyotrophic lateral sclerosis ALS. in reality I should be dead now that's how serious MND is. It's an illness that kills 50% of people diagnosed within two years and the rest are given between 2-5 years. You will lose all use of you're muscles in you're body before you die including you're voice. I feel extremely lucky that I'm still here, 

#MimeForMND is an idea I had because I used to sing but unfortunately MND has stolen my voice. The next best thing is miming. All you have to do is write on a piece of paper or card why you're doing it and if you know someone with MND who your are miming for, show it to the camera. Choose you're favourite song Film it, mime it, donate and post online. Simple. so please get onboard and spread the word. 

http://youtu.be/jJ6JZPpTlIU here's our #MimeForMND I'm the one with the inflatable saxophone! Please have fun with it life's too short to be serious. 

http://youtu.be/q6zWei3zY2I Here's another brilliant example by the fabulous Lily Scott. Please get the kids involved. 

For more information go to www.markmaddox.co.uk or Twitter @lastofadying1 

Thank you for you're support 

Mark #MNDWarrior 

About the charity

The MND Association focuses on improving access to care, research and campaigning for those living with or affected by MND in England, Wales and Northern Ireland. If you or a loved one need practical or emotional support, call our Connect Helpline on 0808 802 6262, Mon to Fri between 10am and 4pm.

Donation summary

Total raised
£466.68
+ £88.75 Gift Aid
Online donations
£466.68
Offline donations
£0.00

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