• 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

Inclusion and Equity

You are here: Home / Conference / Inclusion and Equity
Inclusion and Equity

11 November 2025 by Lizzie Cox

Inclusion and Equity

This stream will run on Saturday 15th November and will explore practical approaches to accessibility and equal opportunities for all in education, PE and employment.

Starting school: EHCP

Maria Sherwood and Emma Simmonds from Treloar School and College will share their expertise on navigating the complex EHCP process, as well as working alongside the Local Authority to ensure that your child’s needs are met.

Overview of inclusive activities for PE

Explore practical strategies in this session for making physical education accessible and engaging with experts neuromuscular physiotherapist Marion Main along with Paralympic double gold medal winner Rachel Morris.

Recognising emotional and educational needs of children and young adults

We are really excited to be joined by Dr Jo Finch, highly experienced social work educator and doctoral supervisor, Janet Hoskin, Associate Professor of Education at the University of East London, and Benjamin James, who lives with Duchenne and has worked with different Duchenne Charities as a patient advocate.

“We know from research that young people with DMD are at high risk of neuro-divergence and other educational needs. Many children with DMD find literacy and numeracy difficult, and some might struggle to pay attention or follow instructions. Others can find it hard to make and keep friends. In this session we will look at some of these established risks as well as share findings from our own research . We look forward to exploring and sharing ways in which young people with DMD can thrive at school and college and achieve their aspirations. “

Accessing Employment: Entering and Excelling in Work with a Neuromuscular Condition

This session will guide you through the full journey of finding and thriving in employment with a neuromuscular condition. We’ll start with the basics, how to read job adverts, tailor your CV, and write strong applications, before moving on to interview preparation and how to navigate workplace support once you’re hired. You’ll gain practical knowledge about your rights at work, including Reasonable Adjustments and the Access to Work scheme, and learn how to advocate for the support you need to succeed. We’ll also explore best practices for inclusive employment and how to build confidence in communicating your needs to employers. Whether you’re entering the workforce for the first time or looking to progress in your career, this session will equip you with tools, strategies, and insights to help you take the next step. The second half of the session will include time for questions, giving you the opportunity to raise specific concerns or seek advice tailored to your situation.

Please see the 2025 conference agenda here.

Share this:

Category: Conference

Previous Post: « Adapting to Change
Next Post: Givinostat Accepted for Restricted Use Within NHS Scotland for the Treatment of Duchenne in Patients 6 Years and Older »

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