• 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?

A huge “Thank You” to our Jeans for Genes fundraisers

September 29, 2017
Jeans for Genes Day

Jeans for Genes DayWe would like to say a huge “Thank You” to all those that helped to support last weeks Jeans for Genes Day and the Smith-Magenis Syndrome Foundation. The day was a huge success as schools and workplaces pulled on their jeans to raise awareness and funds for people with genetic disorders.

Some of the schools and workplaces involved in supporting Jeans for Genes in partnership with the SMS Foundation were:

Shevington High School
Total raised £520

Heskin Pemberton C of E Primary School
Total raised £191

Mossy Lea Primary School
Total raised £43

Pilkington Group LTD
Total raised £296

Wigan and Leigh College
Total raised £365

Marlborough St Mary’s CEVC primary school
Total raised £480

The Regis school
Total raised £1004

Network Rail
Total raised £300
If you know a school or workplace that supported the Jeans for Genes Day and partnered with the SMS Foundation please let us know so that we can add them to our list and include them in our thank you’s!

Share:

Share on Facebook Share on LinkedIn Share on E-mail
Category: Activities, News
Previous Post:Joanne Martland with her son LouieMum speaks of son’s genetic disorder for Jeans for Genes Day
Next Post:That Defining Moment – A Video about DiagnosisVideo front cover for film That Defining Moment

Sidebar

Copyright © 2026 Smith-Magenis Syndrome (SMS) Foundation UK · Privacy Policy · SMS Disclaimer | Terms and Conditions

Cultivating talent finalist for breaking the mould SCA Terrific trustee award badge  NUE Awards - Shortlisted Nomination

Smith-Magenis Syndrome Foundation UK

Connecting Families | Raising Awareness | Building Futures

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

MAKE A DONATION

Smith-Magenis Syndrome Foundation UK

Connecting Families | Raising Awareness | Building Futures

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

  • Home
  • Who we are
    • Our Vision, Mission, and Values
    • How We Help
    • Our Trustees
    • Our Staff
    • Our Regional Parent Supporters
    • Our Professional Board
    • Policies and Documents
    • Annual Reports
  • News & Events
  • Family Membership
  • Donate
donate
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