'Just For Joe' Bridgnorth Walk page

Emma Hiller is raising money for The Society For Mucopolysaccharide Diseases (The MPS Society)

Participants: Emma Hiller, Kate Coady, Sam Burrows, Louise Hales, Mia George, Charlotte Cains, Sophie Crooks, Hannah Elkes, Holly Wainwright, Liam Cains.

Story

Thanks for taking the time to visit our JustGiving page.

I (Emma Hiller) am delighted to be joined by Kate Coady, Sam Burrows, Louise Hales, Mia George, Charlotte Cains, Sophie Crooks, Hannah Elkes, Holly Wainwright and Liam Cains on the annual 22 mile Bridgnorth Walk. Together we are hoping to raise money for the MPS Society under the group name 'Just For Joe'.

The MPS Society has been an amazing support to me and my family since my son, Joe Hiller, was diagnosed with the rare, genetic, life limiting condition called Hunter Syndrome (MPSII).

Children with Mucopolysaccharidosis, or MPS, are missing an enzyme which means their bodies cannot break down certain molecules called GAGS. The GAGS build up in every cell causing progressive damage. The MPS Society supports families, raises awareness and helps to fund research into the cures so desperately needed.

We would be very grateful if you could donate some time by sharing this link and raising awareness for the Society and MPS, or by sponsoring us so we can be ever closer to finding a cure. Thank you!

For more information about MPS please visit www.mpssociety.org.uk

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