We currently have 2 projects you can sponsor, for more information go to our
If you are living with MND or are a Carer of someone Living with MND or are someone who knows someone living with MND and you are reading/visiting this site for the first time or second time or ......... and have not had any contact with the Branch.
Would you like to speak to someone or like a copy of our quarterly newsletter?? Our branch contact is Marion (07929 732958) and if you have a question that she cannot answer she will know someone who can. If e-mailing is easier why not contact her on firstname.lastname@example.org
Would you like to meet us at one our informal get togethers for tea and cake in and around Cheshire – two of our venues are Hotels and one is a Garden Centre. These are very friendly and positive meetings with an exchange of ideas and hints and tips.
We would love to meet you, and if you think this is for you please contact Marion
Always look at 'Diary Dates'
for news of forthcoming events
Stay in touch by signing up now to our online community to hear the latest Association news!
You''ll receive e-newsletters, including exclusive research updates, our most recent activities and campaigns. Sending e-mails is a cost effective way for us to stay in touch.
The more Friends we have, the more powerful we'll be in our fight towards a world free of MND.
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Find out more on our Volunteer Page
A Date for your Diary
at Eaton Hall Gardens Charity
Open Day on 28th July 2013
Hall Gardens are open to the public four times a year in order to raise
funds for local charities, and the Branch have been allocated,this date
to host the Open Day, by the Duchess of Westminster,.
88 acres of gardens, Scented Rose Garden, the Chester Wind Band,
falconry displays, Shetland Carriage Driving Displays, Katie the Steam
Train, family history room and Carriage Museum, it will be a fabulous
day out for all the family.
For more information on the open days go to
Our MND Charter 3 minute campaign calls on everyone to spare three minutes or less to show support for the Charter.
We have got to stop the ignorance surrounding this disease and have to make sure that when a patient is first diagnosed with MND, they must have access to good co-ordinated care and services.