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MND Matters by the MND Association
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MND Matters by the MND Association

Author: Motor Neurone Disease Association

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The MND Matters podcast offers people living with and affected by motor neurone disease access to information, informal advice and expertise.

Created by the MND Association, the podcast will explore a wide range of subjects alongside people affected by MND. As well as being an extra information source for the MND community, MND Matters will also be  a new tool for the Association to use to raise awareness among the wider community.

Find out more on our website www.mndassociation.org.
45 Episodes
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When someone is diagnosed with MND, the effects can ripple across the whole family. Lindsay shares her experience of living with PLS – a form of MND – and how her daughter, Cally, struggled with anxiety and uncertainty following the diagnosis.  Joined by Emily from the MND Association's Children, Young People and Families Service, the episode highlights the emotional challenges young people can face, from worries about a loved one’s health to balancing school, friendships and future plans. We also discuss the tailored support available from the Association, including counselling, school support, one-to-one guidance, grants, resources and ongoing help for children and young people up to age 25. For more information about our support for families: https://www.mndassociation.org/support-and-information/children-and-young-people/support-families-children-and-young-people 
In this episode of MND Matters, we explore the world of voice banking and how rapidly evolving technology is changing the way people stay heard. Guided by questions from you - the MND community - Steph and speech and language therapist Jen Benson unpack why our voices are such a core part of who we are, and how voice banking helps preserve that identity. Jen shares when to get started, what to do if your voice has already changed and how AI is creating increasingly natural digital voices. We also highlight support available, funding options and the wide range of devices and access methods now available - even for those with limited movement. Find out more about our financial support:  Contact our MND Connect helpline on 0808 802 6262 or email [email protected]  
“Sometimes the companionship of a dog is better than human company. They don't judge you. You don't have to sort of speak. They're just there. And sometimes that's all you want, because it's hard.” Through every chapter of our lives, our pets are right there beside us. We look after them, and they look after us. They’re not just animals we live with - they’re family.  In this episode of MND Matters, Domonique sits down with Lizzie from Woodgreen Pets Charity and Channel 4’s The Dog House. Lizzie’s husband Chris was diagnosed with MND at just 34. In this episode she discusses the challenges of being a carer while raising young children, but how bringing puppy Betty into the home gave the family comfort, routine and companionship.  Drawing on her personal and professional experience, Lizzie also shares practical advice for caring for pets while managing the changes MND might bring. You may hear the very occasional bark during the episode – Lizzie’s dog Bumblebee couldn’t resist getting involved in the episode too.  
Meet Rick and Ali – our hosts for this special episode of MND Matters. Rick is a biologist, educator, advocate and artist living with PLS - a slow progressing form of MND. Ali is a licensing officer for local government. Her mum, Sheila, died in March 2025 soon after being diagnosed with MND.  Together, Rick and Ali put MND research under the microscope with Mike Rogers, the Association’s Director of Research and Innovation. The trio discuss the development of the Association’s new five-year research strategy, how it resulted in four key aims: understand, detect, discover and innovate, and how the MND community shaped the strategy from the very beginning.   
In this powerful episode, host Domonique is joined by Lorraine Redmond, who lives with MND, Emma Wood, a clinical lead dietitian, and Jonathan Phang, a cook and MND Association ambassador. Together, they explore the emotional and practical challenges of eating and drinking with motor neurone disease. The conversation is rich with practical tips - from modifying food textures and using feeding tubes flexibly, to managing social anxiety around eating in public. It’s also a reminder that food is more than fuel - it’s love, culture and togetherness. For more information about eating, drinking and swallowing with MND, see our guide, Eating and drinking with motor neurone disease (MND). You can request a free printed copy from our helpline MND Connect. 
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