Jacqueline Horsfall

Rok Torquay Team Fundraising Page

Fundraising for The Society For Mucopolysaccharide Diseases (The MPS Society)
£1,700
raised
Donations cannot currently be made to this page
The Welsh 3000's, 17 June 2009
Participants: Intrepid Torquay Team Explorers: Andy Braund; David Bray; Danny Mitchell; Sam Welch; Jon Gledhill; David Champion; Vicki Dean; Gareth Lewis; Andy Gulley; Elaine Tucker; Richard Allen; Steve Cutland.
The Society For Mucopolysaccharide Diseases (The MPS Society)

Verified by JustGiving

RCN 1143472 and Scotland SC041012
We support affected individuals & families to raise awareness of rare conditions.

Story

Dear friends and colleagues, once again we are sending out an appeal for your valued support and generosity.

Following on in the tradition of the last five years or more, the Torquay Team,  have set themselves yet another gruelling charity challenge this year:

Over the weekend of Friday 26th June to Sunday 28th June 2009
The mixed team of men and women will be attempting to climb 15 no. Snowdonia Mountain ranges over 3000 ft high!

The team is also pleased to welcome to the charity team this year three members of NPS (South West) Ltd, Architects.

This is the most physically challenging event that the team has undertaken to date!  They are very serious about completing this challenge successfully and each member has committed their own time each week to take part in rigorous group fitness training, aside from any other personal regimes they are undertaking.

This year our plea is even more heartfelt and personal as Corey Jeffery, aged 9 months, has recently been diagnosed with Hurler Syndrome.  Corey’s Daddy, Shane Jeffery, is a member of the South West Construction team in Exeter.  Corey’s Grandfather and Uncle, Brian and Jason Jeffery, are long serving members of the Torquay Build Team.

PLEASE HELP US TO TRY TO MAKE A DIFFERENCE!

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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
£1,700.00
+ £363.85 Gift Aid
Online donations
£1,700.00
Offline donations
£0.00

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