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SMS Foundation UK

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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?

Smith-Magenis Syndrome Foundation UK – EGM Notice

October 3, 2019
New SMS Logo

The Trustees of the Smith-Magenis Syndrome (SMS) Foundation UK are calling an Extraordinary / Special General Meeting (EGM) for 10:30 am Saturday 16 November, at the Aldingbourne Country Centre in Chichester.

The meeting will be followed with an opportunity to join other SMS families at the centre. Booking details are below.

The purpose of the EGM is to vote on resolutions to change the status of the Foundation from an unincorporated registered charity to a Charitable Incorporated Organisation (CIO). This is a change of structure for the Smith-Magenis Syndrome (SMS) Foundation UK under which we continue as a charity regulated by the Charity Commission.

Details of the resolutions and an explanation are given in the documents below, together with a copy of the proposed constitution.

The trustees recommend voting in favour of all the resolutions. Voting can either be in person at the EGM or by returning the ballot paper as directed.

If you have any questions on the above, then please contact the Trustees.

SMS 2019 CIO Constitution for approval
SMS UK Postal Vote 2019 – CIO Constitution
SMS UK EGM Announcement

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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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