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Sarah's page

sarah lee is raising money for Motor Neurone Disease Association

Team: Remembering Bridget Simpson

In memory of Bridget Simpson
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Walk to d'feet* MND - Sarah Lee · 23 June 2012 ·

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

My mother was diagnosed in in 2004 with a rapidly progressing form of Motor Neurone Disease which took her life within a year. The M.N.D Association helped me with rest bite, talking to health professionals and providing some equipment. With out their support it would have been an even more difficult process for me and my mum. I had never heard of Motor Neurone Disease before my mum got i'll with it. I started organising walks as a way of dealing with grief as it's an illness that can make you feel that useless. Since then a team of four has grown into double figures, and I wish to thank all those who have contributed to the £3,800 raised so far xxx

 

Motor Neurone Disease Is a rapidly progressing fatal disease. It's a disease that attacks the upper and lower motor neurones leading to weakness and wasting of muscles, increasing loss of mobility in the limbs, and difficulties with speech, swallowing and breathing. The disease leaves people unable to look after them selves, and is very distressing for them and those who are close to them. Ther money from this event goes towards equpment, support and research into this illness. Every penny counts, even if you feel it's a small donation, it all makes a difference.

If you are in work and a tax payer, please gift aid your donation, as this adds 28p per pound. thank you xxxxx

 

 

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Donation summary

Total
£55.50
+ £7.50 Gift Aid
Online
£55.50
Offline
£0.00

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