Thank you for registering to join the virtual #ADCONF20 over the weekend of 14 and 15 November.
We have received your details and are currently transferring your information into the Conference platform. You will have access to this platform the next working day.
(Having trouble entering the platform? Simply enter your email address, then reset your password, follow the email alert and you will be in!)
Let’s get started
Once you have access to the Conference platform, here are 3 things for you to do to help you get the most out of your time at the Conference.
Book 1-2-1 and small group sessions
There are many small group sessions or 1-2-1 private sessions to choose from.
Book time with a counsellor, get help with EHCPs and school, take part in a Mutation Masterclass, speak to a Duchenne researcher and find out more about the DMD Registry.
- FREE as part of your conference registration
- All are welcome
- Places are limited – book now to avoid disappointment
Watch the virtual guided tour
Lynnette talks you through the platform and shows you how to maximise your time at the Conference.
Get ready to watch LIVE
- First time at the Conference? Watch the newly diagnosed families/Conference newcomers recording – here.
- Check out the live agenda – here.
- Start to ask your questions for the live Q&A sessions – here.
- Add your photo and information to your profile – here.
- At 09.50 GMT Saturday 14 November enter the first session and enjoy! – here.
Pre-conference survey
It’s important for us to show the impact of the Conference on Duchenne families and the best way to measure the impact is to ask you, the people who are attending.
Please take 2 minutes to follow the link here and answer the questions about how you feel before the Conference.
You will have the opportunity to tell us how you feel again, after the Conference. The results are the way we measure impact.
We will then use these findings in our community reports, funding applications, impact reporting and it will help us to design and produce amazing events and projects in the future.
Any questions
As always, please contact us info@actionduchenne.org with any questions.
We are looking forward to seeing you online!
The Action Duchenne Team
