Supporting people and families affected by motor neurone disease

MND Foundation Summer Gala Ball

Our mission

Built around three core pillars

Get involved

Take part. Raise funds. Help change lives.

Our events bring people together to raise vital funds for practical care, crucial research and clearer guidance for people affected by MND.

  • Summer Gala Ball

    A magical summer evening in support of the MND Foundation, with welcome drinks, live saxophone, a three-course dinner, silent auction, DJ and dancing until midnight.

    Get your tickets
  • Quiz Night

    An evening of quiz night fun in support of the MND Foundation, with trivia, brain teasers, bonus rounds, friendly competition and plenty of laughs along the way.

    Get your tickets
  • Golf Day 2026

    Join us at The Heron Golf & Country Club for a special day of golf, food and fundraising in support of the MND Foundation.

    Get your tickets

Latest news

Stories, updates and progress

Read the latest news from the MND Foundation, including updates on our work, fundraising activity, research support and the people helping us make a difference.

Why we exist

The reality of Motor Neurone Disease

MND is a progressive condition with no cure. People affected by it need timely support, coordinated care and clear guidance from diagnosis through to end of life.

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    Average life expectancy is just 27 months from diagnosis.

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    Around 50% of people diagnosed with MND die within 12 months.

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    Approximately 5,000 people are living with MND in the UK.

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    Around 1,100 people are newly diagnosed each year in the UK.