Our Response to the Draft NICE Guideline

‘An Inadequate Tool for Doctors and Patients, Seriously Undermined by Lack of Evidence’ Lyme Disease UK is a registered stakeholder in the NICE Lyme disease guideline writing process. As the UK’s largest patient support network, taking part in this process has been an important priority because once finalised, the guideline […]

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AONM May 2017 Conference – Chronic Lyme Disease Uncovered

  LDUK were delighted to attend the AONM May 2017 conference titled Chronic Disease Uncovered – Lyme Disease, Viral Pathogens, Morgellons, Mould and More… on Sunday 14th May 2017 The conference was very informative with excellent presentations from key experts on the latest testing, treatment approaches and research into chronic […]

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bob miller lyme disease uk expert Q&A

Bob Miller – Expert Q&A Video

Bob Miller is an American practitioner with 20 years of experience and specialises in genetic variants and nutrigenomics. In this video he answers many questions from Lyme Disease UK members and explains his work in nutrigenomics and complimentary medicine. Robert Miller ND earned his naturopathic degree from Trinity School of […]

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rachel alban lyme disease and art

Lyme Disease and Art – by Rachel Alban

Rachel Alban is an artist living with Lyme disease in the North of England. In this guest blog post she discusses her illness and the effect it’s had on her art. You can find out more about her work from her website. http://www.rkalbanart.co.uk/ ‘When life gives you lemons, make lemonade’. This […]

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Lyme Ninja Radio Comes to the UK

Lyme Ninja Radio is ‘the #1 podcast for people with Lyme disease’. The well established show interviews experts and patients alike and this time, it has been the UK’s turn in the Lyme Ninja Radio limelight! They’ve recently featured two well known UK pracitioners and a UK patient. #121 Chantelle […]

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Lyme Disease Can Destroy Lives

For many people with ongoing health problems, life has changed since a diagnosis and they’ve had to adapt their work, adjust to medications and find ways to fit their illness around their lives. These are often the people you think of when you hear ‘chronic illness’. These are the people […]

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In My Blood – A Story of Lyme Disease in the UK

    In my Blood is an in depth look at the complex and baffling world of Lyme disease in the UK, as told by people whose lives have been shaped by it. The piece starts with the difficulties surrounding diagnosis and how many patients took years to finally get […]

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Letter to MPs and LDUK Response to Government Petition Statement

  LDUK group members signed and shared a petition demanding better testing and treatment for Lyme disease which generated over 10,000 signatures. The government then had to issue an official response which can be found here. LDUK members were dissatisfied with the official response and some prepared their own responses […]

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UK Lyme Disease Protest 2016

LDUK members were involved in two protests this year – one in Bath and one in London. The 10 aims of the protests can be found here. The events achieved unprecedented media attention with patients being interviewed around the country in newspapers, on TV and on local radio shows as […]

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