Contacts

Volunteers Needed

The Branch is always interested in hearing from anyone who would like to join our committee. We are also looking for Association Visitors in Cheshire and would be delighted to hear from anyone who thinks that they might be interested in finding out more about this role.

Please contact Joel Millett on 01625 525 409 for more information.

To contact us about other volunteering opportunities please contact our Branch Secretary – details below.

Patron: Viscount Ashbrook

Branch Committee Members

 
Richard Webb

Richard Webb

Chair

We started supporting the Association in about 2006 when first told they were investigating my wife, Kathy, for MND, and I joined the committee after she was finally diagnosed in 2016.  I was asked to become campaigns contact, a job I thoroughly enjoyed until I was asked to take over the Chair in 2022.  After Kathy died in 2023 I became an Association Visitor and have been a member of the national peer support group on CHC since it started. 

Joel Millett

Joel Millett

Branch Contact

As well as my role as Association Visitor, I also act as the main point of contact for the branch. If you want to find out more about what we do, get involved yourself, or if you feel you could benefit from any of the support we offer, please do not hesitate to reach out.

Sally Hoare

Sally Hoare

Social Secretary

When my husband Mike was diagnosed with MND, we found meeting up with others who were going through similar experiences was a great help. I decided to help others to do the same and took on the role of social secretary for the branch. I am the person to contact for information about social get togethers and carers lunches and welcome any recommendations for accessible venues near you.

John Kinder

John Kinder

Treasurer

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

Rebecca Jackson

Rebecca Jackson

Secretary

After losing my step dad to MND I wanted to give something back to the association to thank them for the support and care they provided my mum and step dad. I’ve worked in administration and operations in my career and so the secretary role seemed a suitable post for me to support the branch with.

Steve Hopper

Steve Hopper

Campaigns

After losing a good friend in 2021, and my brother in 2022 to this awful disease I wanted to get involved & volunteer to raise awareness & support the charity locally by taking on the Campaigns Volunteer role.

Emma Edwards

Emma Edwards

Newsletter Editor

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.

Grace Kay

Grace Kay

Other Contacts

I am the Community Support Coordinator; I cover Cheshire and South Lancs Branches.  I am home based in Warrington and have been with the association since May 2023.  My role is primarily to support the volunteers to do their fantastic work.

Association Visitors

Jan Gates

Jan Gates

I think the work the MND association do is fantastic & I wanted to get involved in what way I could, supporting those living with MND in Cheshire & their families.

Allan Nicholles

Allan Nicholles

My wife was diagnosed with MND in 2019 and finally succumbed in 2023. During that period we had a lot of support from many sources including, of course, the Cheshire branch of the MNDA. After 2023 I felt that I had learned a lot about what patients and carers endured and so it seemed natural to offer to help out if the occasion arose. I took the Association Visitor training course in summer 2024 and look forward to helping others where I can.

Ros Graba

Ros Graba

I was an Occupational Therapist for 50 yrs. My special interest has always been Neurology. I have also been a Community Rehabilitation OT treating various conditions, including MND and have always been involved in Support Groups. When I retired 6 years ago I decided to train as an AV for the Cheshire Branch to support those living with MND and their families.

Richard Webb

Richard Webb

We started supporting the Association in about 2006 when first told they were investigating my wife, Kathy, for MND, and I joined the committee after she was finally diagnosed in 2016.  I was asked to become campaigns contact, a job I thoroughly enjoyed until I was asked to take over the Chair in 2022.  After Kathy died in 2023 I became an Association Visitor and have been a member of the national peer support group on CHC since it started. 

Joel Millett

Joel Millett

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.