Hi, our names are Rob and Sharon. We are both 41 and live in Nottinghamshire,UK.

This site is about us and our experiences of living with Motor Neurone Disease/A.L.S.

Also known as M.N.D. or Lou Gehrig's Disease,after the famous baseball player who

had the disease. Please see the Links Page for more MND/ALS related sites or

Rob's Journal to read my own personal experience of living with MND.

Please take some time to leave a comment in our Guestbook below:

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Folding@home

The folding of proteins may hold the key to many diseases including Motor Neurone Disease.Click on the logo above to see how you can help.

 

What Is ALS.com

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John's Journey.
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Direct Enquiries is the home of the Nationwide Access Register, which provides access information for disabled people and parents. Use the search form below to try it out for yourself.

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www.build-uk.net - Building a motor neurone disease network for the UK

 

 

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DISCLAIMER: The information on this website is not an attempt to practice medicine.The content of Rob's Journal is my own personal experience and the information within it is not to be taken as medical advice.

 

------ Copyright © 2004 - 2007 Rob Marshall ------------------------------------------------------------------------------------------ Site Updated: 1st July 2007 -----

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