• Skip to main content
  • Skip to header right navigation
  • Skip to site footer
  • Home
  • About Us
    • Our Vision, Mission and Values
    • How We Help
    • Our Trustees
    • Our Staff
    • Our Regional Parent Supporters
    • Our Professional Board
    • Newsletters
    • Annual Reports
  • News
    • News
    • SMS Family Events
    • Activities
    • Conferences
    • Research
    • Blog
    • Newsletters
  • Get Involved
    • Fundraising Events
    • Become a Member
    • Ways to Donate
    • Become a Regular Donor
    • Payroll Giving
    • Fundraising Ideas
  • Shop
    • Basket
  • Contact
  • Membership
  • Donate
Smith-Magenis Syndrome Foundation UK logo

Smith-Magenis Syndrome Foundation UK

Connecting Families, Raising Awareness, Building Futures

  • What is SMS?
    • Overview of SMS
    • New Diagnosis
    • A Guide to SMS Booklet
    • SMS Behaviours
    • Sleep in SMS
    • Living with SMS
    • Health
    • Facts about Smith-Magenis syndrome
    • Videos about SMS
    • Frequently asked questions
    • Find Support for SMS
  • Spotlight on SMS health
    • Vision
    • Sleep
  • Find Support for SMS
    • Small Grant Applications
    • Newlife’s Emergency Equipment Loan Service
    • Emergency hospital documents for download
    • Other Support Organisations
    • Scientific Papers
    • SMS Research
  • Our SMS Community
    • SMS Conference 2022
    • Become a Member
    • Regional Parent Supporters
    • Stories from our SMS Community
  • Home
  • About Us
    • Our Vision, Mission and Values
    • How We Help
    • Meet the Trustees
    • Meet the Staff
    • Regional Parent Supporters
    • Our professional board
    • Newsletters
    • Annual Reports
  • SMS Conference 2022
  • News
    • SMS Family Events
    • Activities
    • Conferences
    • Research
    • Blog
  • Get Involved
    • Events
    • Become a Member
    • Ways to Donate
    • Become a Regular Donor
    • Payroll Giving
    • Fundraising Ideas
    • Support My Smile Campaign
  • Shop
    • My Basket
  • What is SMS?
    • Overview of SMS?
    • New Diagnosis
    • SMS Behaviours
    • Living with SMS
    • Sleep and SMS
    • Health
    • Facts about Smith-Magenis syndrome
    • Frequently asked questions
    • Find Support for SMS
  • Spotlight on SMS health
    • Vision
    • Sleep
  • Find Support for SMS
    • Small Grant Applications
    • Newlife’s Emergency Equipment Loan Service
    • Emergency hospital documents for download
    • Other Support Organisations
    • Scientific Papers
    • SMS Research
    • Videos
  • Our SMS Community
    • Become a Member
    • Regional Parent Supporters
    • Stories from our SMS Community
  • Contact

CEO Announced for The Smith-Magenis Syndrome (SMS) Foundation UK

January 12, 2020
Nigel Over, CEO Smith-Magenis Syndrome Foundation UK

Nigel Over, CEO Smith-Magenis Syndrome Foundation UKFor over 35 years, Nigel Over has been involved in the running of, or contributing towards numerous charities where he holds a personal interest. His dedication has seen him devote a considerable proportion of his time and effort to the benefit of the widest communities actively contributing to national and local charities including, the British Science Association, ENABLE Scotland, REMAP and, of course, the Smith-Magenis Syndrome (SMS) Foundation UK. So much so, that for almost 20 years Nigel has split his time equally between a career in project management and compliance and the third sector in order that he could commit to charitable endeavours; a change in part instigated from becoming the main carer for his son, Matthew, who has Smith-Magenis syndrome.

Nigel’s passion enthuses others to become involved, irrespective of whether he is championing, leading, contributing or supporting these good causes.

Announcing his appointment as Chief Executive Officer for the Smith-Magenis Syndrome (SMS) Foundation UK, Hazel Wotherspoon, Chair of the Board of Trustees commented

Persuading Nigel to join our Board in 2012 has been one of the best moves we have made in the leadership of the charity. His has been at the heart of the organisation connecting families, raising awareness and building futures for our families. Nigel has led our governance and development strategy review that now sees our evolution into a well-supported, sustainable charity ensuring the long-term benefits for our community.

In 2008 Nigel’s efforts were recognised with the Volunteer of the Year Award predominantly for activities relating to the public understanding and engagement with science. Through chairing committees he has delivered highly accredited festivals of science, events and conferences. A particular highlight was a national award for an inclusive communication conference delivered by university researchers, care health and education professionals, voluntary organisations, people with learning disabilities, and those with communication challenges.

As a campaigner, Nigel has been influential in changes to legislation and practice with a particular focus on education and care. A number of these campaigns, primarily with ENABLE have gone forward to receive many charity awards recognising the significant contributions being made towards equality in society and improving the quality of life for those with disabilities.

Nigel says,

I am absolutely delighted to be given this opportunity to take the Foundation forward working with and for our SMS families and supporters to meet our vision that every person with Smith-Magenis syndrome shall have a fulfilling life within a supportive and understanding community.

Nigel will formally take up the position of Chief Executive Officer upon the completion of our transition to a Charitable Incorporated Organisation. In the meantime he shall continue as a Trustee on the Board devoting time to implementing our strategy and organisational development.

Share:

Share on Facebook Share on Twitter Share on LinkedIn Share on E-mail
Category: News

Like this article?

Sign-up with your email address below and we’ll keep in touch, sending you our latest news and articles about Smith-Magenis syndrome.

Previous Post: « Registered CIO Charity Certificate Charity Commission approval for CIO
Next Post: Information and Communications Manager Announced for Smith-Magenis Syndrome (SMS) Foundation UK Information and Communications Manager Leeann Stevenson »

Join our Community

Join as a family member and we can connect you with families living near you. You will also receive updates of any social meetings, conferences, and fundraising events going on! Joining is quick and easy!

Join
View the international map of families diagnosed with SMS

Never feel isolated or alone.
Call our helpline: 0300 101 0034
Other ways to Contact Us

Please note: This is an answerphone service that will alert us as soon as a message is left. A trustee will call you back as soon as possible – we aim to respond to messages within 24 hours.

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

The Smith-Magenis Syndrome (SMS) Foundation UK CIO

Connecting Families, Raising Awareness, Building Futures

Sign-up to receive the latest news and information direct to your inbox

Please enter your email address below if you would like us to send you emails with our latest news, articles, and information about SMS.
To join as a full member, please click here.
Your data will be processed in accordance with our privacy notice.

Proud finalist of Keele University Breaking the Mould awards
SCA Terrific trustee award 2020
NUE Best Student contribution

Registered UK Charity (CIO) 1186647   ·  Scottish Charity (SCIO) SC050921    

Copyright © 2021 Smith-Magenis Syndrome (SMS) Foundation UK CIO · Privacy Policy · SMS Disclaimer · Terms and Conditions