• Skip to main content
  • Skip to header right navigation
  • Skip to site footer
  • Home
  • Who we are
    • Our Vision, Mission, and Values
    • Meet the Trustees
    • Meet the Staff
    • Regional Parent Supporters
    • Our Professional Board
    • Policies and Documents
    • Annual Reports
  • How We Help
    • Carer Support Service
    • Education Support Service
  • Get Involved
    • Family Membership
    • Professional Membership
    • Donate
    • Regular Giving
    • Fundraising & Events
    • Volunteering
      • Become an SMS Awareness Ambassador
      • Become a Regional Parent Supporter
      • Become a Project Volunteer
      • Become a Community Supporter
    • Corporate Support
    • Trusts & Foundations
  • News & Events
Donate
Contact Us
SMS Foundation UK logo

SMS Foundation UK

Supporting SMS families for a positive future

  • What is SMS?
    • New Diagnosis
  • Support & Advice
    • Support for Parents & Carers
    • Support for Professionals
  • Information & Resources
  • SMS Stories
  • Home
  • Contact Us
  • Who we are
    • Our Vision, Mission, and Values
    • Meet the Trustees
    • Meet the Staff
    • Regional Parent Supporters
    • Our Professional Board
    • Policies and Documents
    • Annual Reports
  • How We Help
  • News & Events
  • New Diagnosis
  • SMS Explained
  • Support & Advice
    • Support for Parents & Carers
    • Support for Professionals
  • Information & Resources
  • SMS Stories
  • How You Can Support Us
    • Family Membership
    • Professional Membership
    • Donate
    • Become a Regular Donor
    • Fundraising & Events
    • Volunteering
      • Become a Regional Parent Supporter
      • Become a Project Volunteer
      • Become a Community Supporter
      • Become an SMS Awareness Ambassador
    • Corporate Support
    • Trusts & Foundations
  • Family Membership

We are a small charity that supports families living with Smith-Magenis syndrome (SMS)

Never feel isolated or alone. Call our helpline and leave a message: 0300 101 0034 (we aim to respond to messages within 48 hours).

Newly Diagnosed?

About the Author: George Fox

Black and white photo of George Fox smiling at camera

My career in specialist education began before I can even remember, growing up alongside my sister who had severe learning disabilities. Without realising it, she has always been my greatest inspiration and the reason I chose to dedicate my life to supporting people with learning disabilities.

My first professional step was at Prior’s Court, a school for children with autism. I was immediately inspired by Dame Stephanie Shirley’s vision and her drive to create something exceptional for her son, Giles. As a parent she had felt poorly equipped to deal with his challenges and as a result was made to feel like so many families that she was responsible for his intellectual disabilities.  The school broke new ground at the time, embracing families and focusing on every aspect of children’s lives to achieve the best possible outcomes. Her leadership continues to influence me deeply, shaping the way I lead and the values I bring to my work.

Over the years, I gained qualifications in Team Teach, Structured Teaching, PECS, and national leadership programmes. While the qualifications provided a foundation, it was the opportunity to learn from experts in the field that truly shaped my understanding of how to create meaningful impact for learners with complex needs.

My connection with Smith-Magenis Syndrome began in 2003, when I taught a young boy whose statement included the condition. Although at the time, little was known about it. He was seven, full of character, and taught me more than I could have imagined. His behaviours told a story of communication, emotion, and connection. Changes in routine or absence of familiar adults could unsettle him, while sleep difficulties and eating presented further challenges. Yet beneath it all was a remarkable capacity for empathy and awareness of those around him. That experience deepened my understanding of SEND and continues to guide my approach today.

With over 25 years of leadership and coaching experience across the public, not-for-profit, and independent sectors, I have since founded my own company to help leaders realise their potential – particularly those working to improve outcomes for people with learning disabilities. I now support individuals at all stages of transition, whether returning to work, changing direction, or stepping into new opportunities.

George Fox, Plain Thinking

SMS Foundation UK logo

Never feel isolated or alone. Call our helpline: 0300 101 0034

Please note: This is an answer phone service that will alert us as soon as a message is left. A member of the team will call you back as soon as possible – we aim to respond to messages within 48 hours.

  • Facebook
  • Twitter
  • LinkedIn
  • Instagram
  • YouTube
  • Mail

Become a Member of The SMS Foundation UK

Connect with SMS families in your region and be the first to receive updates on any social meetings, conferences, and fundraising events going on!

Family & Carer Membership
Professional Membership

Registered UK Charity (CIO) 1186647

Scottish Charity (SCIO) SC050921

Registered with the Fundraising Regulator

Copyright © 2021 Smith-Magenis Syndrome (SMS) Foundation UK CIO · Registered Charity Address: 61 High Street, Pewsey, Wiltshire SN9 5AF  
Privacy Policy · SMS Disclaimer · Terms and Conditions ·  Media and Logo Usage Guidelines ·  Social Media Usage and Policy · Policies and Documents