Announcing our new network of regional representative to be there for families, who just ‘get it’ from lived experience of Smith-Magenis syndrome.
Use local knowledge to provide support and guidance to families. Build awareness of Smith-Magenis syndrome in your area. Help with regional events that bring our community together.
Volunteers wanted for some regions. Do you have 2+ years of SMS experience post-diagnosis? Are you ready to get involved? Then contact hazel@smith-magenis.co.uk
Scotland
| West Scotland: | Hazel Wotherspoon |
| East Scotland: | Lisa Gray |
| North Scotland: | Claire Woo |
England
| North-East & Yorkshire: | Richard & Dawn Arnold |
| North West: | Jo Martland |
| Midlands: | Emma Riddell |
| East of England: | Lorraine & Darrin Harwood |
| East of England: | Anand Kakad |
| London: | Anna Middleton |
| South East: | Mick Pearson |
| South West: | Jade May |
Wales
| North Wales: | Clare Barker |
| South Wales: | Nathalie Hughes |
Ireland
| N&W Northern Ireland: | Andrea Docherty |
| S&SE Northern Ireland: | Andrea Docherty |
Nigel Over ‘Terrific Trustee’ finalist in SCVO Awards
