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Welcome to the holding page of Living with Glomuvenous Malformations GVM Our daughter Bethan-May was born with this rare condition. We along with Great Ormond Street Hospital are trying to find ways of management. Research is the way forward and the sharing of information. So we are in the process of building a Web Site about living with GVM, from information on the condition to our fundraising campaign. Please keep returning to this Web page for updates, to learn more about GVM and to join in our FUNdraising. Many thanks from Jacqui and Tim Slater In the meantime you might find these links useful:
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