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emily barker raised £4,304 from 176 supporters

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Closed 28/02/2021

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£4,304
raised of £3,000 target by 176 supporters

    Weʼve raised £4,304 to Fund research for Ataxia Uk - Wobble Walk 2020, all donations will be matched with the Big Give Christmas Campaign 💙 Find Mollie a cure 💙

    Funded on Sunday, 28th February 2021

    Don't have time to donate right now?

    Story

    We would love for everyone to join us to help spread awareness of Ataxia - a rare, usually progressive, neurological condition affecting balance, fine motor skill and speech.

    Our beautiful daughter Mollie was born with this rare disease that effects only 500 children and 10,000 adults in the UK and we are devastated that there is currently no treatment or cure.

    Mollie is amazing and puts a smile on everyone's face. Our happy, bubbly 4 year old who loves to dance and sing. The effects of Ataxia cause her to walk with a wobble and loose her balance often, our reality is that the symptoms usually progress and are similar to that of MS, Parkinsons disease and in some cases ALS - yet very few have heard of Ataxia

    We want to change this...

    We have created this virtual event the ‘Wobble Walk’ on Sunday the 6th December, we want to encourage you all to walk, wobble or wheel - everyone is included! There are no rules - just go outside, walk anywhere and any distance and please share your photos to show your support using #wobblewalk on social and please donate if you can.

    All funds will be donated to ‘The Big Give’ campaign who will be matching donations for Ataxia up to £30,000 towards much needed research and a helpline for people suffering with this rare disease.

    Please help us find a cure 💗

    ❤❤❤Any donations made for purchasing raffle tickets please email AJ Accounts and Taxation directly for your numbers - amy@ajat.co.uk Thank you ❤❤❤

    https://www.instagram.com/wobblewalk2020/

    https://m.facebook.com/wobblewalk/?ref=bookmarks

    Updates

    3

    • emily barker3 years ago
      emily barker

      emily barker

      3 years ago
      Update from the Page owner

      Share this update to help us raise more

    • emily barker3 years ago
      emily barker

      emily barker

      3 years ago

      Hi All!! we are overwhelmed with the support and generosity that is streaming in for this cause, from strangers, friends and family alike We have only a few days left to raise as much money as possible, therefore we have tweaked the target! :) Please keep it coming in and we hope to see all your pictures and hear your stories from your walk this weekend! all the best Dale, Emily and family x

      Share this update to help us raise more

    • emily barker4 years ago
      emily barker

      emily barker

      4 years ago
      Update from the Page owner

      Guy’s we are over a quarter of the way there 💙💙💙 Thank you to everyone that’s donated 💙💙💙

      Share this update to help us raise more

    4 years ago

    emily barker started crowdfunding

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    Page last updated on: 12/19/2020 15.44

    Supporters

    176

    • JB TRAINING ENTERPRISES LTD

      JB TRAINING ENTERPRISES LTD

      Dec 19, 2020

      £50.00

    • Anonymous

      Anonymous

      Dec 12, 2020

      Wishing you a happier future with lots to look forward to.

      £30.00

    • Nicola Clark

      Nicola Clark

      Dec 11, 2020

      Well done to all of you on your wobble walk xx

      £10.00

    • Liz Barker

      Liz Barker

      Dec 10, 2020

      £20.00

    • Anonymous

      Anonymous

      Dec 10, 2020

    • kevin lowne

      kevin lowne

      Dec 9, 2020

      Hope you raise lots of money and it will help find a cure.

      £20.00

    • Mary and Don Tillman

      Mary and Don Tillman

      Dec 8, 2020

      Well done Emily xxx

      £20.00

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    About Crowdfunding
    About the fundraiser
    emily barker

    emily barker

    Our beautiful daughter Mollie was born with Ataxia, a rare neurological disease that effects only 500 children and 10,000 adults in the UK and we are devastated that currently there is currently no treatment or cure - please help us try and change that 💙

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