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Amy and Katie's page

Amy Campbell is raising money for Motor Neurone Disease Association

Participants: Amy and Katie Campbell

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Motor Neurone Disease Association · 18 April 2010

Motor Neurone Disease moves fast. It takes away time, it takes away independence and it has no cure. Every day we support people affected by MND. We fund ground-breaking research. We campaign for better care. We’re here for everyone who needs us. Because with MND, every day matters.

Story

Thanks for taking the time to visit our JustGiving page.

As most of you know and for people that don't our Dad 'Dave' has recently been diagnosed with Motor Neurone Disease (MND) and therefore we have decided to do a sponsored Skydive to try and raise as much money as possible for the MND Association. This will help provide the essential services that people with MND rely on and fund research projects to bring hope for a future without this devastating disease, as currently there is no cure.


The jump will be now take place on ***FRIDAY 23rd APRIL*** in Lancaster. Please feel free to come along for support and to have a great day out while we both do one of the stupidest things we have ever done and 'jump out of a plane' ahhhhh lol!


We will be grateful for any donations however large or small :-) 


Many Thanks


Amy and Katie x x



P.S. We are currently in the process of organising a Charity Night in June for MND! You are all invited and we will let you all know as soon as possible when we have a fixed date!!!!

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So please dig deep and donate now.

Donation summary

Total
£1,097.80
+ £229.87 Gift Aid
Online
£1,097.80
Offline
£0.00

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