Lyme disease is a complex condition that can leave many of us feeling alone. We don’t always know where to turn, doctors don’t understand our symptoms; family members can’t always relate, and friends often struggle to see our pain. That’s why LDUK is so important – we have an amazing […]
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Raising awareness is a proactive and productive dose of medicine. It can give us a real buzz, provide us with a sense of a purpose, and make a real difference at the same time. You don’t have to go to extreme lengths to raise awareness, simply sharing your story with […]
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As 2018 marks LDUKs 5th birthday and Christmas is on the horizon, we’ve been talking about celebrations and how to best manage our symptoms when trying to enjoy ourselves. The Christmas period can often leave us feeling stressed. There are so many people to see, so many events, so much […]
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Over the past 5 years, the Lyme Disease UK’s Online Community has grown from two founding patients, Natasha Metcalf and Louise Dean, to a community of over 9,500 members from across the UK and further abroad. Whilst it is wonderful that so many patients and their loved ones who are […]
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