Our history

2016

Doddie is diagnosed with MND in December 2016, though he doesn’t publicly reveal it until June 2017.

2017

Our first fundraising dinner is held at Battersea Power Station in November, raising over £600,000.

2017

In November, My Name’5 Doddie Foundation is officially registered as a charity, with Jill Douglas MBE becoming our CEO.

2021

Doddie Aid is created by former Scotland rugby captain Rob Wainwright. Since then, we’ve run the challenge every January, encouraging people to get active and raise money.

2022

Doddie’s Clubhouse is introduced, enabling members to make monthly payments to support our work.

2022

On 26 November, Doddie Weir dies, aged 52, almost six years after his diagnosis, and less than two weeks after attending his last match against the All Blacks at Murrayfield.

2023

My Name’5 Doddie Foundation is registered as an official charity in Hong Kong, raising money for research and supporting people living with MND there.

2023

We are named JustGiving UK Charity of the year, reflecting the incredible hard work of our whole community.

2023

We become an Introductory Member of the Association of Medical Research Charities (AMRC). This allows us to receive practical help and support aligning our funding processes to those recommended by the AMRC, and ensures that we fund the highest quality of research.

2023

Our five-year research strategy “Catalysing a Cure”, is launched, setting out our mission to fund, guide and enable the smartest, most efficient research to accelerate the development of new treatments.

2024

After a successful partnership in 2021, The British & Irish Lions Trust choose us again as one of their charity partners, for a two-year partnership.

2024

We achieve full AMRC membership in March 2024, confirming our dedication to high-quality, peer-reviewed research funding for MND.

2024

Our Year One Catalysing a Cure report is published, outlining our investment of over £3 million to a range of exciting and ambitious projects.

2025

Building on the success of the previous year, we share our Year Two Catalysing a Cure report, and invest a further £8 million to 26 new projects, including launching two new funding programmes.

2026

To date, we have committed £24 million to cutting-edge MND research. Our community makes it all possible. Together we’ve filled stadiums, baked, walked, ran, and hiked. We’ve done it dressed in a tartan as bold as our approach, and echoing Doddie’s message: “MND isn’t incurable, it’s just underfunded.”

Our founder

About Doddie Weir OBE

With a personality as vibrant as his iconic tartan suits, Doddie was one of rugby’s most recognisable and beloved names. Earning 61 caps for Scotland, he represented the British and Irish Lions on their iconic 1997 tour of South Africa. Whether winning championships with Melrose, Newcastle, or Scotland, Doddie did everything with infectious charisma.

Much more than his trophy cabinet, Doddie was a character larger than life. And anyone who knew him will have a story about the first time they met. 

In June 2017, Doddie announced his motor neuron disease (MND) diagnosis. 

For a man used to finding his way through the toughest defensive lines, his diagnosis came as a deadlock. At the time, there was only one drug option available and no new treatments on the horizon. For many people living with MND today, this is still the case. This isn’t good enough. And Doddie knew he had a platform to do something about it. 

Drawing on the strength of his family for support, his wide network of friends, and his public profile, Doddie wanted to change the narrative for people affected by MND. He understood that this could only happen through world-class research. That’s why he launched My Name’5 Doddie Foundation in November 2017. In typical Doddie style, he helped raise MND awareness and funds with a relentless drive and a signature spirit of love, fun, and hope.

As we move forward, together, we will create a world free of MND.

It’s the people behind the scenes that have been truly inspirational. They’re doing the dinners, they’re doing the walks, they’re doing the tractor rallies, to raise awareness and funds. Together we’re going to get a cure.

Doddie Weir OBE

Our founder

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