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You are here: Home / Virtual talent show

Virtual talent show

Do you and your friends or local community have talent by the bucket load? Ever been told you have a lovely singing voice, or do you deliver punchlines like our very own Harry Hill? From budding magicians, karate kickers, pianists to poetry writers, you can include all talents in your online show.

Create fundraising page

How to make it happen?

  • Set a date, give your community at least a fortnight to get their talents perfected!
  • Set up your JustGiving page so you can ask for sponsorship for the event. We have a team page set up on JustGiving so your fundraising can contribute to the community total!
  • Decide how you are going to air the show. We use Google Meet for our online events, but you could use Facebook Live, Zoom, Gotomeeting or any other software which hosts online meetings/webinars. (Don’t let the tech put you off, we can help you set this up if you’re new to this).
  • Start to share your talent show, speak to friends, family, your local community. You may have a local community Facebook group, or groups which share things to do during the isolation time. Share your show far and wide.
  • Share your story, tell people WHY you are doing this, what is your connection to Duchenne muscular dystrophy? What does our charity mean to you?
  • Plan the event, work with the talented participants to allocate them time slots, find out what they are going to be doing and make sure they have access to the online log in details.
  • Send out log in details to everyone who wants to watch and take part. This is a great opportunity for Grandparents and family in isolation to watch their precious little ones sharing their talent!
  • Remember, share your JustGiving page far and wide to get maximum fundraising for your hard work!
  • Have fun on the day and share your photos with us!

More information

  • Why support us during COVID-19
  • Advice for the Duchenne community
  • Our vision
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From our community

Blue Monday Blog: Hear from Victoria, our Fundraising Officer and Duchenne Mum

Written by Victoria Edwards, Action Duchenne’s Fundraising Officer and mum to Dougie (who lives with Duchenne) and Allie. Feeling Blue “This Monday was Blue Monday, and wow… I really felt it. It was grey, drizzly, my son was up half the night and ended up off school from sheer tiredness. My daughter went in to …

“Making contact with Action Duchenne provided a lifeline”

“Making contact with Action Duchenne provided a lifeline”: Find out why Ben Dolling decided to run the London Marathon dressed as a parrot! Harry was diagnosed with Duchenne muscular dystrophy in 2019 Ben and his wife have 3 children: a daughter in year 3 and a son in his first year of university and Harry, …

The Power of Shared Experience: “Honestly, it would’ve been a much harder road without having joined this group.”   

Action Duchenne have monthly online meet-ups for Duchenne dads, mums and grandparents, facilitated by our Family Support Officers and designed to enable connection with those who truly understand. A Duchenne diagnosis can often set people apart from the support systems they usually rely on. Our support groups mean you can meet people who know exactly …

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Action Duchenne
5th Floor, Mariner House
62 Prince Street
Bristol
BS1 4QD

07535 498 506
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