Motor Neurone Disease Research
Motor Neurone Disease
MNDR EBS UK Ltd Information
CD Christmas Single
CD Christmas Single
MNDR Facts
Motor Neurone Disease facts
EBS UK LTD. Profile
Professor Karen Morrison
Professor Karen Morrison
Molecular Genetic Studies in Motor Neurone Disease
Molecular Genetic Studies in Motor Neurone Disease
Thank You Letter 2006
MNDR.Thanks for support and for funds raised
G & T & a Slice
Details of the band, with Gary & Tim & Sandra
MNDR Charity Lunch 2010
Charity lunch event 2010 for 21st November 2010
Christmas Charity Song by Gary Saunders
MNDR 15th Annual Charity Lunch Sunday 6.11.2011
Details of the annual Charity Lunch at Moor Hall Hotel, Sutton Coldfield

Motor Neurone Disease Research




Welcome to the web site of Gary Saunders and Motor Neurone Disease Research (MNDR)
at the QE Hospital, Edgbaston. For the last 15 years I have raised awareness and funds for MNDR at the QE Hospital which is headed up by Professor Karen Morrison, with a Trust Fund designed specifically for MND Research, so there is no wastage for administrative costs etc. The funds are utilised for both genetic and clinical patient support.

This work has been completed in a variety of ways.

* Talks and presentations given to various Groups on raising PR via Charity work and specifically MNDR.

* Contribution towards MNDR via Telecom Division of EBS UK Ltd as per attached information sheet.

* Lectures given to third year student nurses on “living with terminal illness.” from a patients, carers and nursing aspect.

* Producing two CD’s composed and written by Gary Saunders, with the most recent being titled “Christmas Love, Christmas Magic.” See information sheet attached.

Holding an Annual Charity Lunch at Moor Hall Hotel, Sutton Coldfield, with musical entertainment, auction, raffle and Irish Bingo. A thoroughly entertaining and enjoyable afternoon. See attached information sheet.

If you would like to make a donation at any time, I will be pleased to organise this for you, with official acknowledgement via Professor Karen Morrison. I can also organise information or advice on fund raising event for MNDR.

Equally I will be available to speak to on a private and confidential basis if you just need some advice or someone to talk to who can relate to individual and personal difficulties faced by a person with MND. My simple advice is always to be positive and look to explore alternative medicines if it can provide some form of hope or opportunity in the face of this terrible disease. This is not always easy to do or say, especially as MND progresses in a person, but the mind set and being mentally positive is I feel essential.

Lastly I would like to express my heartfelt thanks to all those people that have supported me over the last 15 years in a variety of ways as I have raised awareness and funds towards fighting MND. There is currently no government funding into MND so every effort or contribution no matter how small or large is wonderful. Thank you one and all.

Gary Saunders
Business Development Manager. 
EBS is supporting the fight against Motor Neurone Disease.


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