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The Nick Smith Foundation
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    • Motor Neurone Disease
    • Bereaved Children
    • Rugby League
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Welcome to The Nick Smith Foundation

In the 38 years before his death from Motor Neurone Disease (MND), Nick ‘Smudger’ Smith made a huge impact on many people’s lives.

We pledge to ensure his legacy lives on and that he continues to have a huge impact on people’s lives.

We’ll do this by:

  • Supporting research into the disease that took Nick from us – MND, and look at how we can improve the help available for those diagnosed and their families.

  • Supporting children who have had to face the death of a parent at a young age – as Nick and his sister faced aged 6 and 4, and now Nick’s children have to face aged 5 and 2.

  • Supporting amateur rugby league which played such a significant part in Nick’s life from childhood to adulthood.

We hope we can make a difference. In Nick’s memory. In Nick’s name. #ForSmudger

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Latest News

  • The Calderdale Community Spirit Awards – An open letter to you from our Chair
  • Fixby and Brighouse WI support charity’s efforts to help children facing the death of a parent
  • Annual Report 2018/2019
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The Nick Smith Foundation

Registered charity remembering Nick Smith who died at 38 from Motor Neurone Disease (MND). Supporting MND research, bereaved children & rugby league

Email – contact@nicksmithfoundation.org.uk

Telephone – 03333 446 406

Latest News

  • The Calderdale Community Spirit Awards – An open letter to you from our Chair
  • Fixby and Brighouse WI support charity’s efforts to help children facing the death of a parent

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© The Nick Smith Foundation 2019. A registered charity in England and Wales - number 1178182