Fulfilling Futures – We need your help
Supporting families for nearly 30 years Since 1992, the SMS Foundation UK has helped over 300 …
Teddy Bears’ Picnic Feedback – Survey closes on 16th May
Our Teddy Bears’ Picnic survey ends on Sunday 16th May and we need your help! Can you spare …
Teddy Bears’ Picnic – schedule for the weekend
You are invited to join us for our Virtual Teddy Bears’ Picnic. We have lots of activities over the …
300 picnic boxes make their way to UK SMS members
300 picnic boxes are gradually making their way to all the people with Smith-Magenis syndrome on our …
Easter Card and Invitations sent to UK SMS Members
In the lead-up to our next virtual event, the ‘Teddy Bears’ Picnic’ on the 1st and …
Impact of COVID-19 on SMS Population Survey
This survey is being conducted by the Smith-Magenis Syndrome (SMS) Foundation UK with the purpose of …
This week’s community Zoom drop-in chat with Jayne Dainty of SOS Care Services
This week’s community Zoom drop-in chat is with Jayne Dainty of SOS Care Services. Jayne will …
SMS Foundation UK Conference Cancelled for 2021
At the start of this week the UK Government announcements placed the UK into the highest COVID-19 …
December Newsletter
Connecting Families | Raising Awareness | Building Futures Our December 2020 newsletter is here! …
Natasha Craven Shortlisted for ‘Best Student Contribution’ to a Small to Medium-sized Employer award!
Natasha Craven, who joined the Smith-Magenis Syndrome Foundation UK team in October 2020, has …
Announcement of AGM
Announcement of the General Meeting for: 1186647 The Smith-Magenis Syndrome (SMS) Foundation UK …
Conference 2021 Announcement
A Conference Like No Other Yes, we are still planning to hold an in-person conference on 1st & …