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SMS Foundation UK

Supporting SMS families for a positive future

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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?

Announcement of AGM

December 21, 2020

Announcement of the General Meeting for:

1186647 The Smith-Magenis Syndrome (SMS) Foundation UK CIOSC044841/1072573 The Smith-Magenis Syndrome (SMS) Foundation UK

The Board of Trustees hereby announce the calling of the General Meeting of these charities to take place on Tuesday 12 January 2021 at 6:30pm.

The voting members (the Trustees) shall consider statutory governance matters pertaining to:

  • Previous AGM/EGM minutes
  • Annual Report and Accounts to 30 June 2020
  • Appointment of Trustees and Board Members
  • Amendments to Constitutions
  • Any other relevant matters

Expressions of interest in joining the Board are invited from our wider membership/supporter community and should be submitted to Hazel Wotherspoon by 5 January 2021.

Any matters relating to the statutory operation or governance of the charities for consideration at the meeting should also be sent to Hazel Wotherspoon by 5 January 2021.

A separate report on the charities’ operations shall be prepared for the wider membership along with a virtual “Meet the Board and Senior Management Team” session subsequent to the formal General Meeting.

Hazel Wotherspoon
28 Kilbrennan Drive
Tamfourhill
Falkirk
FK1 4SG

Tel: 07952 047894
Email: Hazel@smith-magenis.co.uk

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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.

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Registered UK Charity (CIO) 1186647

Scottish Charity (SCIO) SC050921

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