• 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

Easter Card and Invitations sent to UK SMS Members

April 14, 2021

In the lead-up to our next virtual event, the ‘Teddy Bears’ Picnic’ on the 1st and 2nd May, the SMS Foundation has recently sent out approximately 300 Easter cards to every person on our UK membership with Smith-Magenis syndrome. Also included with the Easter cards was a written personal invitation for the virtual picnic event.

The aim was to reach as many members as possible within our SMS community, encouraging people to join in and connect with other families.

We were also very lucky to receive the eager help of SMS’er Lily Stevenson, who was in charge of labeling and stamps!

The Teddy Bears’ Picnic is scheduled over the course of the bank holiday weekend with relaxed family-friendly online activities that our community can dip in and out of. Some of the activities include the return of the Scavenger Hunt, by popular request, and a magic show by Magical Mayhem who have performed at previous conferences.

Click here for more information about the picnic and schedule.

Share:

Share on Facebook Share on Twitter Share on LinkedIn Share on E-mail
Category: Activities, 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: « Impact of COVID-19 on SMS Population Survey
Next Post: 300 picnic boxes make their way to UK SMS members Genny Bear packing boxes »

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