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Our Story

Our founder was Robert Sinclair Davidson who was diagnosed with Motor Neurone Disease in 2015 shortly after he got married. He knew his terminal condition would cause a steady decline in his faculties and that, as time went on, he would need increasing assistance and expensive equipment.

 

He appreciated that his needs were by no means unique and were shared by many young families such as his, many of whom were less fortunate than he in terms of meeting those material needs. He was determined to leave a legacy that provided for those families. Thus, was born the RSDF.

 

Robert died in 2016 aged 34 leaving a young wife and a baby daughter. But, as he wanted, his legacy lives on in the help that his charity has given to families like his.

 

Today the charity is run by his mum and dad, close family members and some of his close family friends, all of whom respect entirely what Robert wanted his charity to achieve and strive very hard to make sure that he would be proud of us.

 

As a charity we depend entirely on donations but we recognise that what is important is to make sure that those donations are properly spent and don’t just languish in a bank account.  That is why we welcome any request for funding. If it meets our criteria then we are not just prepared to help, we positively want to help. It’s what Robert set up his charity for.

 

If you are a young family where one of you has a life limiting or terminal condition or are a professional, such as an occupational therapist, please get in touch if you think we can help make life a little bit more comfortable for you or your client. We can reach decisions quickly and there are no strings attached. We just want to help.

 

Incidentally, you might get a feel for what a unique and caring person Robert was by listening to a poem, introduced by Eddie Redmayne, which Robert composed shortly before his untimely death. You can find it on this website.

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Meet The Team

Who We Are

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Dr Edward H Davidson

Chair Of Trustees

As Robert’s brother, it was privilege to have been there at his conceptualization and the through the genesis of this unique charity,  and it continues to be a privilege to serve now as a trustee to the Foundation that is his living legacy after an illness fought with great courage, dignity and humour.

Robert's enduring wish was to help other young couples and families going through similar circumstances to take back some control in their life.

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Leah Berke

Trustee

​My name is Leah, and I’m proud to serve as a trustee of the RSDF. Robert was my first cousin, and together with Edward, we shared a close childhood. His diagnosis was a heartbreaking moment for our entire family, but the courage he showed throughout his journey was nothing short of inspiring. His strength and determination left a lasting impression on everyone who knew him. The RSDF carries forward that same spirit—offering hope, support, and tangible help to those facing unimaginable challenges. It’s both a privilege and a deeply personal honour to contribute to a cause that makes such a meaningful impact.

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Robert Brosgill

Trustee

Rob and I were longtime friends and shared many milestones and adventures along the way - he was always one to celebrate life, even as his own became more difficult. 
It’s a privilege to honour my old friend, by supporting this incredible charity. 

Andrew Saffer

Chair

My name is Andrew Saffer, and I have the privilege of serving as Chairman of The Robert Sinclair Davidson Foundation. My journey with the charity began in 2016, when I joined as a volunteer at its inception.

Robert was my best friend. I witnessed firsthand the remarkable strength and dignity with which he faced his battle with Motor Neurone Disease (MND). Even in the most difficult moments, Robert never lost his sense of humour or his zest for life. Supporting him through his illness was both humbling and deeply inspiring.

When I was invited to become a founding member of the committee, I was honoured to help launch a charity dedicated to supporting others who, like Robert, are facing life-limiting conditions—often when they have nowhere else to turn.

In late 2022, I was humbled to be appointed Chairman. I continue to lead the Foundation with the same commitment I made to Robert: to honour his legacy and do everything I can to ensure that those who need our support receive it with compassion, dignity, and hope.

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His Honour Andrew Saffman

Vice Chair

​​​I am Andrew Saffman, a retired judge. Mike and Suzanne Davidson have been close friends of mine for over 50 years. I saw Robert grow up and I also saw first hand how his terrible illness can turn a life and a family upside down. It is an honour to be involved in a charity that aims to ease the burden that life limiting or terminal illness can bring to a family

Adam Levinson

Treasurer

It has been an honor to serve on the committee of Robert’s charity, having been his friend for many years. Supporting people in their time of greatest need is deeply meaningful, and knowing that our work brings real relief to families allows Robert’s legacy to live on in a powerful and lasting way.

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Alexandra Myers

Secretary

My name is Alexandra Myers 
I became a member of this committee because I was approached by Suzanne & Michael - and knowing Roberts tragic story - I wanted to be able to help young families in any way during their time of need - it’s such a wonderful feeling to be able to do so. 

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Michael Davidson

Volunteer

​I am Michael Davidson but my son Robert always called me Mick.
I am totally committed to honouring his memory by putting my heart and soul into the Charity he established in the months before his untimely death at the age of 34.

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Suzanne Davidson

Volunteer

I am Suzanne Davidson 
My son Robert Davidson set this charity  up as he was dying of MND 
It is humbling and an honour  to be a member of this charity and help as best I can.

Amanda Berwin

Volunteer

My name is Amanda Berwin. 
I have been on the RSDF committee now for about 2 years and I have found it to be one of the most rewarding experiences of my life. Mike and Suzanne are very close friends of my family. Their loss was very keenly felt but their desire to continue Robert’s  legacy is inspiring. 
It is a real privilege to help improve the lives of families struck with very serious illness by the support that RSDF has to offer through the generosity of those kind people who support us. 
I never ceased to be amazed at the kindness of our supporters and the resilience of those we help. It is really humbling.

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Neil Brosgill

Volunteer

My name is Neil Brosgill. I have served as a committee member for over one year. I have been a friend of Mike Davidson since primary school. My son (also called Robert; now a trustee) and Robert Sinclair Davidson were at university and law school together, graduated together, played football together and shared digs. Robert’s diagnosis, his fortitude and Mike and Suzanne’s loss have left a lasting impression. I am pleased to be able to help young families who are going through similar experiences and make their lives a little more comfortable in some small way whilst continuing Robert’s legacy.

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