Contacts

I am very happy to support the Motor Neurone Association in this role and give something back with being involved in further charitable works.

We have supported the work of the Association for about 10 years but in 2016 my wife Kath was diagnosed with the disease. Having seen the support available from the Association I volunteered my help and was asked to stand as campaigns contact which I was happy to do.

My father was diagnosed with Motor Neurone Disease in March 2008. I made the decision to join the Committee to help provide support for people who have been diagnosed with this terrible, disabling disease.

As a former regional newspaper journalist now working in communications for a local hospice, I want to use my skills and experience to raise awareness of the condition in the Cheshire area and to inspire local communities to support the charity through fundraising and donations. My mum lived with MND for around 18 months and this is my way of doing something positive in her memory.

I volunteered in memory of my mum who we sadly lost to this terrible disease in 2014. Managing the newsletter means I can help to promote all the wonderful campaigns, fundraising events and local news.

In 2009 I completed my Association Visitor training. Previously I had cared for my mum, Erica who had MND. I am so proud to be part of such a dedicated, hard working and caring committee.

Paula is the Association’s Regional Care Development Adviser (RCA) working in the Branch area, who has detailed knowledge of the care and management of Motor Neurone Disease. Working very closely with local statutory services and community care providers she is able to provide support and advice to people with MND and their families.