West Surrey Branch support volunteer
West Surrey Branch, Motor Neurone Disease Association (MNDA)
We are a small, friendly group of volunteers who work to support those living with and affected by Motor Neurone Disease in West Surrey.
What we do…
- We raise awareness of MND and the needs of people living with the disease.
- We offer grants which allow families to access essential equipment and help as they need it.
- We support individuals and hold a pub afternoon tea group, where people can meet up for friendly conversation and advice.
- We assist individuals and groups who raise vital money for us, by helping at events, giving talks and chatting to people about our work.
Would you like to be part of our team?
- Are you good at listening and talking with people? We need people who can spare a couple of hours once a month (Thursday’s) to join our pub afternoon tea group.
- Could you support our fund raisers, by attending some events and being a representative of the branch?
- Would you like to organise some fund-raising activities?
We are looking for volunteers who would like to be part of a team and wish to make life better for our families. Full online training is available, which can be done when convenient for you.
If you can spare a few hours a month, we would love to hear from you!
The MND Association was founded in 1979. Our mission is to improve care and support for people with MND, their families and carers. We also fund and promote research that leads to new understanding and treatments and brings us closer to a cure for MND. The Association also campaigns and raises awareness so the needs of people with MND, and everyone who cares for them, are recognised, and addressed by wider society.
“I am extremely honoured to be a volunteer for the MND Association. The most rewarding thing is knowing that I have helped people to access the services, equipment and support they need.” Jo-Ann, Volunteer
What’s involved?
- Offer support and provide information to people affected by MND
- Help people affected by MND make informed choices and access appropriate services / support
- Explain to people affected by MND how the MND Association can support them
- Record information following the MND Association guidelines and local protocols
- Develop and maintain relationships with our local branch or group
- Attend support and supervision meetings as well as development events
This role will suit me if I:
- Have good listening skills and am a good communicator
- Am able to develop and maintain supportive relationships with people affected by MND
- Am non-judgmental and respectful of diverse lifestyles
- Am prepared to increase my understanding of MND and its impact on families
- Understand the need for confidentiality and the importance of data protection
- Am able to assess when extra support is needed
What’s in it for me?
- Become part of a friendly and dedicated team
- Make a positive impact to the lives of people affected by MND
- Get access to a range of workshops and events
How flexible is the role?
The time required is flexible
What sort of training/induction will I receive before starting?
You’ll be inducted into the role and informed about the Association.
We encourage and welcome applications from all backgrounds and all communities
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