Dale Vigus

MPS Society TCS London Marathon 2023

Fundraising for The Society For Mucopolysaccharide Diseases (The MPS Society)
£2,434
raised of £2,000 target
Donations cannot currently be made to this page
Event: London Marathon 2023, on 23 April 2023
In memory of Emma Vigus
The MPS Society has a great team of runners for the TCS London Marathon 2023 which takes place on Sunday 23rd April. Our runners are raising money for our members affected by MPS, Fabry and related lysosomal diseases.

Story

I'm running the TCS London Marathon for the MPS Society, a charity which supports children and families affected by rare genetic conditions. Donate today and help this wonderful charity. 

My sister, Emma, was diagnosed with Sanfilippo syndrome at the age of 6. The syndrome is a rare genetic metabolism disorder. A change in a single gene makes a child's body unable to break down certain carbohydrates, which leads to serious problems in the brain and nervous system. 

The illness is terminal, with a cure yet to be found, and made my sister spend the large majority of her life in 24/7 care which was undertaken by, mainly, my mum and dad, as well as me, my brothers and sister. 

Going to Treliske hospital was a regular occurrence growing up as Emma spent a lot of time needing professional care and treatment. There were many times we thought we'd lost her, including one year when she spent 10 consecutive weeks in hospital.  

Emma lost her life on 21st December 1999 when she was just 18 years old. 

I know it's a hard time for everyone at the moment, but any donations, big or small, would be greatly appreciated to help me on my journey to run in the memory of my sister. 

Those of you that know me knows I've been doing anything I can to avoid exercise at all costs for the last few years... so give me some money because we all know I'm going to suffer physically for the next four months!

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About the campaign

The MPS Society has a great team of runners for the TCS London Marathon 2023 which takes place on Sunday 23rd April. Our runners are raising money for our members affected by MPS, Fabry and related lysosomal diseases.

About the charity

The Society For Mucopolysaccharide Diseases (The MPS Society)

Verified by JustGiving

RCN 1143472 and Scotland SC041012
The MPS Society provides specialist support to children, adults and families in the UK who are affected by MPS, Fabry and related lysosomal storage diseases and we fund research into treatment and therapies. These diseases are rare, genetic, life-limiting conditions with no cure.

Donation summary

Total raised
£2,433.20
+ £382.75 Gift Aid
Online donations
£2,433.20
Offline donations
£0.00

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