Living with Hidden Disabilities

Living with Lyme disease is no small challenge, especially for those of us dealing with late-stage Lyme. We have to fight for the correct diagnosis and then fight for the adequate treatment. This complex illness requires us to be medical detectives, sourcing the most suitable practitioners to help us along […]

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Sophie Ward

What Does LDUK Mean To Me?

As part of LDUK’s birthday celebrations, I wanted to share what the community means to me, and how it’s helped shaped my life. LDUK means the world to me. It was a place that called me family before I really understood my health or anything about Lyme disease. There were […]

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A 5 Year Reflection

As Lyme Disease UK turns 5 this year, it only seems right to reflect on this period of time which spans half a decade and to take stock of what has developed organically over the years. I have to pinch myself every time I realise that a Facebook group which […]

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In the top 25 Lyme disease blogs

LDUK Receives Top Lyme Disease Blog Award

We’re thrilled to announce our inclusion in Feedspot’s top 25 Lyme blogs at number 14. So many fantastic global publications are on the list such as Lymedisease.org, CanLyme and Global Lyme Alliance. Our goal for the blog is to create quality posts about Lyme disease from a patient perspective. To help […]

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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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You never know – Jas Matthews

Happy new year! Our next guest blog is from UK patient and LDUK group member Jas Mathews and talks about living with chronic Lyme disease and how she meets the unique challenges it brings. Read more of her blog here http://lojango.blogspot.co.uk/. If you have a blog you would like featured, please […]

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