• 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?

Information and Communications Manager Announced for Smith-Magenis Syndrome (SMS) Foundation UK

February 1, 2020
Information and Communications Manager Leeann Stevenson

The Smith-Magenis Syndrome (SMS) Foundation UK introduces Leeann Stevenson as our Information and Communications Manager.

For the past eight years, Leeann has been at the heart of our communications, information and branding as a Trustee of the charity. The transformation of the charity in this time has been exceptional. Leeann’s dedication has resulted in the Foundation becoming the go-to organisation for information on Smith-Magenis syndrome not only for the United Kingdom but across the world.

Nigel Over, CEO (Designate) says, “I am delighted that Leeann is becoming a core member of our senior management team. This transition is a natural development that will help strengthen the charity with greater focus on information and communication. Leeann also brings in valuable business experience vital to the successful management of the charity especially in this stage of our evolution.”

Leeann is the mother to three children, Lily who is 13 (SMS), William who is eight, and Teddy who is five. Leeann is coming from being a director of a small Web Design agency in Marlborough, Wiltshire that specialises in charity websites and marketing.

Hazel Wotherspoon, Chairperson, adds “During the time Leeann has been involved in the Foundation she has used her design skills to breathe new life into the charity branding, logo, website and digital marketing platforms. She has also been responsible for the publication of our booklet, guidance literature, awareness videos, and leading the Support My Smile campaigns. It is fantastic that Leeann is now able to devote more time to the charity as she moves into the position of Communications Manager.”

Leeann is continuing to provide Pro Bono support to the Foundation as a Trustee and will take up the position of Communications Manager once we have completed our transition to a Charitable Incorporated Organisation.

Share:

Share on Facebook Share on LinkedIn Share on E-mail
Category: News
Previous Post:Nigel Over, CEO Smith-Magenis Syndrome Foundation UKCEO Announced for The Smith-Magenis Syndrome (SMS) Foundation UK
Next Post:The Smith-Magenis Syndrome (SMS) Foundation UK introduces Helen Hargrave as our Fundraising ManagerHelen Hargrave - Fundraising Manager
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