• Donate
  • About Us
    • Our Purpose
    • What We Do
    • Our Impact
    • Our Team
    • Work For Us
    • Volunteer
    • The DMD Registry
    • Action Duchenne Policies
  • Get Support
    • Support Calendar – What’s On
    • Register for Support
      • Time Out – A Space for Mums
      • Dads Against Duchenne
      • Grandparents Together
      • Online Group Counselling Programme
    • Recently diagnosed
    • Children and Young People
    • In-Person Support Events
    • Schools
    • End of Life and Bereavement
  • Annual Conference
    • Save the Date for the Action Duchenne Community Summit 2026 (Previously known as Annual International Conference)
    • Highlights from the Action Duchenne Conference 2025
  • News, Webinars and Blogs
    • News
    • Webinar Series 2026
    • Webinar recordings
    • Bite-Sized Duchenne Science Live
      • Facts about Duchenne muscular dystrophy
      • Signs and Symptoms of Duchenne Muscular Dystrophy
      • Diagnosis of Duchenne Muscular Dystrophy
      • Crucial Genetic Terminology
      • Genetics – Blueprint of Duchenne Muscular Dystrophy
      • How is Duchenne Muscular Dystrophy Inherited?
    • Hear From Our Community
  • Support Us
    • Friends of Action Duchenne
    • Upcoming Events and Challenges
    • Give in memory and help us support every family, every time.
    • Organise your own event
    • Fundraising at school
    • Donate by cheque and post
    • Welcome to our Runner Hub
  •  0 items - £0.00
  • Menu
  • Skip to right header navigation
  • Skip to main content
  • Skip to secondary navigation
  • Skip to primary sidebar
  • Skip to footer

Before Header

  • My account
  •  0 items - £0.00

Action Duchenne

Header Right

  • Donate
  • About Us
    • Our Purpose
    • What We Do
    • Our Impact
    • Our Team
    • Work For Us
    • Volunteer
    • The DMD Registry
    • Action Duchenne Policies
  • Get Support
    • Support Calendar – What’s On
    • Register for Support
      • Time Out – A Space for Mums
      • Dads Against Duchenne
      • Grandparents Together
      • Online Group Counselling Programme
    • Recently diagnosed
    • Children and Young People
    • In-Person Support Events
    • Schools
    • End of Life and Bereavement
  • Annual Conference
    • Save the Date for the Action Duchenne Community Summit 2026 (Previously known as Annual International Conference)
    • Highlights from the Action Duchenne Conference 2025
  • News, Webinars and Blogs
    • News
    • Webinar Series 2026
    • Webinar recordings
    • Bite-Sized Duchenne Science Live
      • Facts about Duchenne muscular dystrophy
      • Signs and Symptoms of Duchenne Muscular Dystrophy
      • Diagnosis of Duchenne Muscular Dystrophy
      • Crucial Genetic Terminology
      • Genetics – Blueprint of Duchenne Muscular Dystrophy
      • How is Duchenne Muscular Dystrophy Inherited?
    • Hear From Our Community
  • Support Us
    • Friends of Action Duchenne
    • Upcoming Events and Challenges
    • Give in memory and help us support every family, every time.
    • Organise your own event
    • Fundraising at school
    • Donate by cheque and post
    • Welcome to our Runner Hub
You are here: Home / Conference / LEGO Quest 2021
LEGO Quest 2021

LEGO Quest 2021

12 October 2021 by Lynnette

Calling all LEGO master builders

We are super excited to launch the second annual Action Duchenne LEGO Quest.

What you need to do

  • Take a look at the list of Quests and prizes below
  • Pick your Quest (it’s free to enter and you can take part in as many Quests as you like)
  • Create your build
  • Take photos of your build and share on Facebook

The Quests

Quest 1: Design and build your dream home (PRIZE – Lego City Family House 60291)

Quest 2: Build a robot (PRIZE – Zane’s Titanium Mech 71738)

Quest 3: Build your own LEGO game (PRIZE – Harry Potter Chess Set 7632)

Quest 4: Make a LEGO mosaic (PRIZE – Flower Bouquet 10280)

Quest 5: Build a musical instrument (PRIZE – Avengers End Game Final Battle 76192)

Quest 6: Create a scene for your favourite minifigure (PRIZE – Hogsmeade Village Visit 46388)

Quest 7: Build a bridge (PRIZE – The Pig House 21170)

Quest 8: NASA needs you to build a new rocket (PRIZE – Boba Fett’s Starship 75312)

How to enter

Upload your entries on Facebook (or ask a parent) and make sure you include the following in the post;

  • the Master Builder’s first name and age
  • the hashtags #ADConf21 #ADLegoQuest
  • Quest number
  • photos of the build

Voting for the winners

Your builds will be uploaded into our Conference platform for attendees of the virtual Action Duchenne International Conference to vote for their 8 Quest winners. Hundreds of people from across the globe will judge the entries across the weekend of 13 and 14 November!

Deadlines and timings

The deadline for entries is 6pm on Friday 5 November and winners will be announced at the Conference on Sunday 14 November and on social media Monday 15 November.

Prizes will be delivered to our Quest winners in time for Christmas.

GOOD LUCK EVERYONE! Have fun and let your imagination run wild!

Get, set….BUILD!

(prizes are proudly brought to you by the The Paskin Childrens Trust)

Check out last year’s winners

Share this:

Category: Conference, Hear From Our Community

Previous Post: « Brain Involvement  in Dystrophinopathies (BIND) Study
Next Post: Sam’s 2nd Conference blog »

Primary Sidebar

From our community

Turning Challenges into Change – Our Story with Action Duchenne

I was introduced to Action Duchenne by the Muscle Team in Newcastle shortly after Oliver’s diagnosis in 2017. In those early, overwhelming days, their support meant everything. Members of the Support Team would call just to let me talk, vent, cry — whatever I needed. They were simply there, and that’s why I choose to support them every …

Louise’s London Marathon Story

Louise’s London Marathon Story Written by Louise Ruddick “My relationship with Action Duchenne came about very spontaneously at the beginning of January this year. My brother, George, was diagnosed with Duchenne back in 1992, just before his third birthday. He was obviously too young to be aware however the impact that it had on our …

Parent Story: Scott and Vicki share their story of their son’s diagnosis of Duchenne and their family’s journey.

Parent Story: Scott and Vicki share their story of their son’s diagnosis of Duchenne and their family’s journey. “I was just sitting in the room and the doctor’s mouth was moving but I couldn’t hear anything that was coming out of it”  Parents Scott and Vicki have two children, Josh and Layla. When Josh was just …

Footer

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

07535 498 506
info@actionduchenne.org 

 

 

 

 

 

 

 

 

Subscribe to our mailing list

Do you consent to receiving regular email updates? *
Email Format
  • Accessibility
  • Privacy Policy
  • Terms & Conditions

© Action Duchenne - Registered Charity No 1101971 - Scottish Charity No SC043852