• 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 / Webinar Recordings / Physio / Returning to school – tips and advice
Returning to school – tips and advice

Returning to school – tips and advice

8 September 2020 by Lynnette

Marion Main, expert Duchenne physiotherapist from Great Ormond Street Hospital shares her decades of expertise, covering important topics in the order below;

  • Introduction from Lynnette Ellison, Community Fundraising & Support Officer at Action Duchenne
  • Activity and inactivity (the effects from lockdown)
  • Reduced mobility and how to help
  • Physiotherapists and OTs in school
  • Changes to priorities in seating and physio needs
  • Social isolation and effects on the immune system (how to help)
  • Signs of deterioration, inactivity and growth
  • Adaptations, wheelchairs
  • Returning to in September to build immunity before flu season
  • Cough assist and Aerosol Generated Procedures
  • COVID-19 in excrement
  • PPE and fit testing
  • Getting over the fear
  • What to do if you think anyone in your family has COVID-19
  • Orthotics, getting back into action
  • Building your team back around you to review what is the priority NOW
  • Considering starting at reduced hours at school, building up to full time
  • Seeking help for your stress, sibling and other children
  • Avoiding sitting for a long time
  • Children wearing masks/visors
  • Minimising risk vs living and building up physicality
  • Hydrotheraphy
  • Horseriding
  • Tightness in the hips, flexors

Watch now

Who will benefit from watching the session?

  • Parents & carers of children and young people with Duchenne muscular dystrophy
  • Professionals involved in the care of young people with Duchenne
  • Teachers and 1-2-1 TAs
  • Community physiotherapists
  • Community occupational therapists

About the expert

Marion Main is long-standing friend of Action Duchenne and regular presenter at our Annual International Conference. Marion has an absolute wealth of knowledge from her role as Physiotherapist at world-renowned neuromuscular centre of excellence, Great Ormond Street Hospital for Children. Her presentations are always engaging, fun and interactive, sharing her vast experience in an easy to understand way.

Share this:

Category: Physio, Webinar Recordings

Previous Post: « Taking action and making an impact
Next Post: World Duchenne Awareness Day 2020 was a success »

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