• 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

Supporting SMS families for a positive future

  • Home
  • General
  • Guides
  • Reviews
  • News
  • 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?

Private 24 12 10 Alexa Flexy And Sophie Weber A... Direct

On December 24, 2010, a private session took place involving Alexa, Flexy, and Sophie Weber. The details of this session are not publicly available, but it appears to have been a unique gathering.

If you could provide more context or clarify what this write-up should be about (e.g., a event, a meeting, a project), I'd be happy to help you create a more informative and accurate piece. Private 24 12 10 Alexa Flexy And Sophie Weber A...

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

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
Private 24 12 10 Alexa Flexy And Sophie Weber A...

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

© 2026 Green Matrix