Your future gift could give HOPE of a world free from MND.

My husband

Does not wish anyone to suffer from MND.

My husband

Pledged a gift in memory of her wonderful husband

To their partner

We need to find a cure so no one suffers.

A close friend

To help others in the future.

Sister-In-Law

My sister-in-law was diagnosed with MND 6 years ago...

Patients and their Families

As a respiratory physiologist I have seen the devastating impact of MND

My husband

I have pledged a gift to give hope and to find a cure.

Our darling friend Carol

It took so long for a diagnosis.

My Dad & Grandad

I have the weight of the risk on my shoulders.

My Mother

My mother, Annie, died in 1983.

For a Close Relation

A close relation died far too young...

My Mum

My biggest wish is to support other families.

My Wife

My wife fell ill, in summer 1997

My darling husband, Steve

My darling husband, Steve, was diagnosed with MND in April 2020 and passed away Dec 2021. We spent the Covid-19 pandemic in our family bubble, without the ability to make those 'last memories'. The help of the MNDA was invaluable, from the specific MND nurse at the hospital to the literature and small grant. Every penny is needed to help the MNDA in research and initial literature at diagnosis.

My Puppy Darby

I fostered a police puppy 3 years ago and her litter were named after MND heroes.

My Mother

I hope this gift will be used for research & medical education for all.

My Husband

Here we are nearly 10 years later.

My Father

Hope there will be a prospect of both prevention and effective treatment.

Our beloved son

In memory of our beloved son Darren

The bravery of Rob Burrow and his family

An Inspirational example of friendship and devotion.

Those with MND

I hope one day there is a cure.

Doddy and Family and Rob and Family

For their brave representation of the cause.

My Husband

My husband had MND for 12 years. He died at only 64 - Sandra

My Husband

Seeing him go through changes which we cannot stop is heartbreaking.

The MND Association

You know they are there for you in your hour of need.

All those fighting MND.

It takes away so much from the individual and their family!

My Dear Father

In hope that one day they will find a cure for this cruel disease.

My Favorite Aunt

It has always stayed with me.

All those fighting MND.

Funding for research to discover a cure is essential.

My Dad

If I can do anything to help others in a similar situation, I will if possible.

My Dad

I have supported MNDA since 1987 when my Dad was diagnosed

My Husband Martin

Fighting for an MND free world.

My Lovely Mum

She was a beautiful, caring, loving mum who did not deserve to be taken so young.

The MND Association

MND is close to our hearts.

My Wife

Your organisation helped me during my wife's illness.

Rob Burrow

We have been inspired by Rob Burrow.

In memory of my Mum

To find a cure for this dreadful disease.

My Uncle Vic

A dedication to my Uncle

Thank you the MND Association!

A gift to a cause close to my heart.

My Mum

I don't want others to have the same awful loss.

My Wife of over 46 years

I have written a book in her memory with all proceeds helping those with MND.

A close friend

A close friend suffered from MND. I'm very happy to support research for a cure for this debilitating disease.

My Husband

Myself and my family will always donate to MND.

My Mother

We must find a cure for this debilitating, horrendous and cruel disease.

Those living with MND

I feel privileged to support patients through the cruelest of journeys. We need to find a cure.

My Mum & My Nan

I lost both my Mum & my Nan to this devastating disease.

My Brother John

I pledged a gift in my Will because my brother John suffered with MND and I saw how it devastates your, and your family's lives.

Find a cure

I would like to support The MND Association to support others to find a cure.

My Dad

My Dad passed away from MND back in the 90s when I was in my 20s. The MND Association and RAF were very supportive to the rest of the family. - Joanne Downes

My Partner

I saw first-hand what a devastating disease it is.

My Dad

'I'm hoping that leaving a gift in my will will help to change this.' - Mandy Wood

My Dad

My Dad was told he had MND in January 2020, by July 2020 we had lost him - Tracey Horn.

My Wife & Work Colleague

My Wife died from MND and also a former work colleague who left a young family. The MND Association provided advice and help throughout my wife's illness. I hope this will help to find a cure, if not, help others with the illness and provide hope - Trevor.

Jacqui Hughes

One day we will be free of this terrible disease

In Memory of My Husband

My husband died from MND in 1981 after three years of suffering from this dreadful disease

Martin Gillies

When renewing my will, I realised the need to avoid inheritance tax

In Memory of My Mum

I really hope and pray that a time will come when those words change to 'yes we can cure and treat MND'

In Memory of My Wife

I lost my wife, Pauline 'Polly' Lambert, to MND in April 2019, 11 months after diagnosis. I want my gift to help prevent other families from suffering the pain we endured. - Michael Lambert

My Husband

My Husband, Reverend Richard W.A Dumville, died on 29.09.2000 after fighting MDA for 18 months - he was 54 years old. My Son Paul Woodhouse-Severn and myself have supported The MND Association ever since - Jean Dumville

Matthew Bennett

We hope more MND research can help detect rarer forms

David

For my Dad

My friend

We need a cure

My Mother

My Mother died of MND in 2005. My Father died of MSA (multiple system atrophy) in 2000. I do what i can to support research into these horrible conditions. - Gregory Jones

My Husband

My Husband passed away in April and I want no one to go through what he went through, therefore any donations that can help fight this disease are worthwhile - M Curran

My Husband

My husband and dearest friend of over 40 years first showed symptoms in March 2021. He deteriorated rapidly losing speech, mobility and swallowing. He was finally diagnosed in January 2022. He died March 2022. Throughout the MND Association supported us. Thank you

Gillian Ball

We need to find a cure for this terrible disease.

Janet Denny

My estate is divided equally among my family in my Will. My husband died of MND and my elder son of a brain tumour. They are still part of my family so their shares will go to MND Association and the Brain Tumour Charity

Polly Allen

I do my best to support the MND Association

Gaynor & Philip Davies

We've pledged to help find a cure

Maureen Robinson

My late husband Robert died from MND in July 2014 after being diagnosed in November 2012. I support the work of MND and all those working to find a cure for this terrible disease. I pray each day that this will happen in the near future.

Christopher Brown

This year I have witnessed for myself from two acquaintances with MND how devastating illness this is. It places intolerable pressures on both patient and family members. It is life-changing, life-curtailing and at the moment unrelenting. If I can make just a small contribution towards its extinction then a part of my estate will have been well-used.

Pam Eldridge

The help we received will never be forgotten

Gordon Tompkins

A cure is needed - I hope this helps

Andrew Watkins

In memory of my Mother

Carole Norman

My husband died with MND in November 2015. It broke my heart as MND took over his body.

Susan Heath

In memory of my husband

Gill Brader

A dear friend was diagnosed with motor neurone disease

Margaret Regan

I received so much support and kindness

John Long

My twin brother had MND

Anne Phillips

A world free from MND

Valerie Robinson

I will always be eternally grateful for the care and support given by the MNDA

Pauline Rowson

I lost my dear father to MND

For our son David Greaves

David died of MND in 2016, aged 31. He was an athlete. It is the most devastating disease and we were greatly helped by the MNDA. We hope so much that a treatment and a cure will be found soon.

Cath Muir

To give hope to other people with MND and to find a cure so they don't go through what I am.

Paul Kimber

This is for Catherine my girlfriend of 30 years, who passed away in August 2019. She died of MND and MNDA who have been very supportive to me. I want to tell the world about MND.

Anthony Pietka

Dedicated to my father

Delia Born

When I retired from social work I loked for ways to remain involved in helping others. MNDA was looking for volunteers and I find the work rewarding.

Michele Marshall

Supporting MNDA in our Wills is something we were pleased to do

Sheena Atkinson

My support for those with MND started many year's ago when I saw the result of the disease on a lovely, caring, vivacious aunt, mother of two teenage girls. On my last visit to her, before she died, she was unable to move and could only communicate by being shown words on a board which she acknowledged by blinking. It was heartbreaking. My aunt's grandson suffered from another genetic nerve/brain related disease, ALD & died aged around 7 years old. It was then that I wanted to remember them with a gift in my Will to support your work and research.

Bev Smith

My Husband Christopher has MND and we both feel not enough money is given to support the cause. My granddaughter aged 7 and her Mum raised over £1,000 by running 5k & 10k in Jan/Feb

Tim Proudman

I was diagnosed with MND nearly 3 years ago. I'm luckier than some as on-set is slow, but it is sadly changing my life. If I can help others overcome MND and live longer fulfilling lives, then I'm very happy to help support The MND Association with my pledge - Tim Proudman

Sue Cutler

In memory of my husband

Patricia Fenney

My Husband Glyn was diagnosed with MND in 2013 and sadly passed away in 2016 aged 57. The sooner we can find a cure for MND the better. My pledge is just a small amount, Glyn always wanted me to donate something to help research.

Sue Batten

I hope this will help in the fight to find a cure

I have left a gift in my Will in-memory of my darling husband

He sadly passed away from this cruel disease in 2018. We were both very grateful to the Association for all of the help we received during the six years he faught the disease and I hope the funds will go towards research and also help others suffering from the disease.

Mrs S Jackson

My Late husband passed away with motor neurone disease and I trained as an Association Visitor so I feel strongly to do all I can to help.

David & Liz

In memory of our brother-in-law

Alan Tabbush

My brother-in-law died from MND in 1995 and I have supported the MNDA every since

John Jefkins

My wife lived with MND for 5 years. During that time she received a lot of help from our local branch of MNDA and from the MNDA funded team at John Radcliffe. Hence my decision to leave a legacy.

Carolyn Wood

No cure has been found