Daniel Walker

Daniel, Kate & Daniel cycling London to Brighton for Marfan Trust

Fundraising for The Marfan Trust
£2,392
raised of £2,500 target
by 56 supporters
Donations cannot currently be made to this page
Event: London to Brighton Cycle Ride 2021, on 19 September 2021
Participants: Kate Rennoldson Daniel Blander
The Marfan Trust

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RCN 328070
We fund medical research to aid diagnosis & treatment

Story

Daniel Blander, Kate Rennoldson and I are taking part in the London to Brighton cycle ride this year in order to raise funds for the Marfan Trust.

Marfan syndrome is a little known, but severe and life-threatening disorder. In the UK around 18,000 people are known to suffer from Marfan syndrome and there are certain to be many more that have not been diagnosed. Implications of Marfan syndrome vary from family to family but can include blindness, spinal curvature requiring surgery, lung disease and sudden cardiac death due to aortic dissection.

My own family was unaware of Marfan syndrome until 1990 when my mother suffered a sudden aortic dissection (a partial split in the main artery carrying blood from the heart) in 1990. In the surgery that followed she received an artificial, mechanical heart valve and part of her aorta was replaced by a dacron tube.

After my mother's surgery I too was diagnosed and have been actively monitored ever since. In 1999 my mother died from an aortic rupture caused by Marfan syndrome.

In our family the key consequence of Marfan syndrome is its effect on the heart and arterial system. In particular the aorta can expand and stretch until it thins and potentially splits.

The year after my mother died I had preventative open heart surgery to replace my aorta with one made from dacron and, in what was then a fairly rare procedure, to re-suspend my own heart valve in the new plastic artery. Since then I have been regularly monitored both by the Royal Brompton Hospital (where I had my surgery) and the Marfan Trust.

I have been lucky enough to be diagnosed in good time that I can be effectively monitored and treated. However, there is much more to be done to better understand the condition and potential treatments. Marfan Trust is the only charity in the UK funding it's own laboratory undertaking medical and analytical research into Marfan Syndrome.

I am particularly keen to raise awareness of Marfan syndrome in the rowing world: Marfan sufferers are commonly tall and slim, the ideal build for rowers.  I had been rowing for eight years before my family became aware of our Marfan story.  I still row today but at a much lower intensity!  If you know about Marfan it can be monitored and managed very effectively.

Do you want to join us in making a difference? The money we raise will go to the Trust and every donation will help. Thank you in advance for your contribution.

You can learn about the Trust and their work here: https://www.marfantrust.org/

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About the charity

The Marfan Trust

Verified by JustGiving

RCN 328070
Marfan syndrome is a disorder of the body's connective tissues, affecting the eyes, heart and skeleton.As the sole charity in the UK dedicated to improving and saving the lives of those with the syndrome we provide personalised support, undertake research into improved treatments, & raise awareness.

Donation summary

Total raised
£2,391.19
+ £465.00 Gift Aid
Online donations
£2,141.19
Offline donations
£250.00

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