I wish I could! I’m always very interested in their meetings! They always get great guests speakers, good subject talks and my doctor, Dr Kaul runs the Q&A sessions. But I’m in South West Wales! I’ve started a lupus support group here but no doctors, nurses or consultants have shown any interest in attending one of our meetings, let alone speak at one. I guess it’s easier in London to build up relationships with support groups and experts, as the doctors are there. Hopefully one day I’ll be able to get to one of these. Would love to meet up with fellow HU lupies too. Let us know how it goes, if you attend. Wendy
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