Ann and Peter’s story
Ann and her husband Peter share how Farleigh Hospice has supported them to adapt to life with motor neurone disease, helping Ann stay independent, live at home, and feel supported for the future.
Supporting people living with motor neurone disease
At Farleigh Hospice, we support people living with motor neurone disease (MND) and their families from the point of diagnosis onwards. Our approach is centred on the individual, focusing on what matters to them, how their needs change over time, and how we can help them live as well as possible.
We work closely with GPs, community health teams, specialist services and the MND Association to provide joined-up care. This helps ensure people receive the right support at the right time, whether that is managing symptoms, accessing practical support, or having space to talk things through.
MND affects everyone differently. Our role is to listen, respond and adapt care so it remains appropriate, compassionate and responsive as needs change.
Jo’s story: living with MND
Watch Jo share her experience of living with motor neurone disease (MND). In this short video, she reflects on her diagnosis, the changes she has had to adapt to, and the care and support she has received from Farleigh Hospice. She also talks about the difference this support has made to both her and her family.
This story offers a personal insight into life with MND and highlights the importance of compassionate, joined-up care provided by Farleigh Hospice.
This story offers a personal insight into life with MND and highlights the importance of compassionate, joined-up care provided by Farleigh Hospice.
Information and support
If you or someone you care about has been affected by MND, there are a range of trusted resources available to help you understand the condition and access support:
- Information about motor neurone disease and what to expect
- Guidance for families and carers
- Emotional and practical support services
- Links to specialist organisations and support networks
- Advice on planning ahead and making informed choices
Our team is also here to talk through what support might be helpful for you or your loved one. If you’re unsure where to start, please get in touch.
To view the list of resources, click here.
You may also find this leaflet helpful.
A day in the life of Tessa, our MND Coordinator
Supporting people living with motor neurone disease requires time, coordination and a highly personalised approach. At Farleigh Hospice, our MND Coordinator, Tessa, plays a key role in ensuring care is responsive to changing needs. Here, Tessa gives us a glimpse into a typical day supporting patients and families at Farleigh Hospice.
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Patient stories
Laura and Terry’s story
Laura and her husband Terry shared their experience of living with motor neurone disease (MND) and the support they received from Farleigh Hospice during a time of significant change.
Richard and Moira’s story
Richard and Moira share how Farleigh’s support helps them navigate life with motor neurone disease, giving them confidence, comfort and practical guidance at home.
Support for people living with MND
If you have been affected by motor neurone disease, support is available. At Farleigh Hospice, we work alongside people living with MND and their families to provide practical, emotional and clinical support tailored to individual needs.
If you would like to find out more about our services, please get in touch.