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The Society For Mucopolysaccharide Diseases

“Girl Gone” fundraiser for The Society For Mucopolysaccharide Diseases. Support the MPS Society. Difficult to pronounce. Devastating to live with.

Thank you for taking the time to visit my page.

After a successful head shaving fundraiser during December and January for MPS, I am thrilled to continue fundraising for The Society For Mucopolysaccharide Diseases (The MPS Society)!

This will be through my various solo adventures, be it trail running, hiking, wild camping, surfing and bouldering/ climbing. My biggest and most personal challenge would be aiming to solo ”bikepack” around Europe. As I embark on these journeys, I am reminded of the individuals and families affected by MPS diseases who face their own daily challenges. Through my advocacy, I hope to raise awareness and funds for this incredible organisation that provides support, education, and research for those impacted by MPS diseases.

Your donation will make a significant impact in the lives of those affected by these rare genetic disorders. Join me, GIRL GONE on

Instagram-

Facebook-
https://www.facebook.com/Girl.Gone78, in making a difference today.

Your donation through Go Fund Me is simple, fast, and secure. Let's come together to support The MPS Society and their mission to improve the lives of those affected by MPS diseases.
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Donations 

  • Anonymous
    • £14
    • 10 mos
  • Anonymous
    • £13
    • 10 mos
  • Anonymous
    • £5
    • 10 mos
  • Anonymous
    • £40
    • 10 mos
  • Tracy Colcombe
    • £10
    • 10 mos
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Organizer

Tracey Cotterell
Organizer
Wales
Society for Mucopolysaccharide Diseases
Beneficiary

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