Lyme disease is still widely misunderstood by the medical profession. Through our awareness work, it is our wish that people are diagnosed more quickly so that they don’t miss the crucial window for early treatment but so many members of our Online Community have suffered for years on end, often […]
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What is the most challenging part of living with Lyme disease? Let’s face it, there are enough physical symptoms that would be deserving answers to this question. Feeling so fatigued that lifting your arms to brush your hair is a struggle, irregular heartbeats thumping you from the inside your chest, […]
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I was aware that this question could cause some upset but I think it’s so important to keep goals and dreams alive in order to foster hope and instill a sense of purpose into our fight by having something to work towards, keeping the light at the end of the […]
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In July, John Caudwell pledged over £1 million to fund research into Lyme disease on condition that the Department of Health also invests. Mr Caudwell asked Lyme disease patients and their friends and families to write to their MPs and the media to make some noise and ensure that our […]
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Hi my name is Kelly Williams and last year I started a campaign called Spreadalittlesunshine. I wanted to raise £60 000 for someone called Sol who lives in Argentina and suffers from Chronic Lyme disease. I didn’t even know Sol, she was a friend of a friend who I was […]
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2018 has been an incredible year for LDUK. Our community has grown bigger by the day and we continue to be inspired by all the hard work and determination we see. So much has been going on, from new local support groups popping up to the fantastic efforts lobbying support […]
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Many Lyme patients hit a brick wall when we are faced with doctors who belittle our suffering and who are not knowledgeable about Lyme disease and its devastating effects. We asked our Online Community what they would like doctors to understand when it comes to living with Lyme disease: “That […]
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One of the hallmarks of Lyme disease is the dreaded ‘brain fog’ which can lead to some rather embarrassing mishaps. Sometimes, laughter is the best medicine and so we asked our Online Community to share some of their foggy moments by finishing the sentence ‘You know you’re a Lymie when…’ […]
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Each year we host a Children’s Poster Competition as part of our ‘Wake Up to Lyme’ campaign and strive to get Lyme disease education into schools using our school awareness packs. We are delighted to announce our winner and runners up and thank you to all the children who took […]
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What Is The One Thing You Wish People Would Understand About Lyme Disease? Lyme disease is still widely misunderstood. As a Lyme patient, being dismissed and encountering astonishing ignorance is the norm. We asked our Online Community to share what they wish people would understand about Lyme disease. ‘We don’t […]
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