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CFS/LC ADVOCACY

Chronic Fatigue Syndrome has permanently changed my life and the life of millions of others worldwide. There are an estimated 17-24 million people with our condition. 

 

As a result of the Covid-19 pandemic, it is estimated that there may be around 65 million people with Long Covid. 

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The two conditions share many similarities, including hugely diverse symptoms that can be difficult to diagnose. The effects of both can have a devastating impact on both  individuals and families. 

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It feels right to hold this space for sharing information about CFS and LC with those who are interested. This should not be taken as medical advice, but a way of collating information and research, with links to support groups.

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Useful links 

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Action for ME

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The ME Association 

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Solve ME/CFS Initiative

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Long Covid Support

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24 September 2024 

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Temperatures are about to drop towards the end of the week, so I thought I'd share this piece about temperature sensitivity in CFS/fibromyalgia that has also been shown in LC patients. 

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Cold Weather & Pain in Fibromyalgia & Chronic Fatigue Syndrome

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17 August 2024 

 

Long COVID: a clinical update published by The Lancet. 

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5 May 2024 

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I found this page that hosts links to a range of CFS related articles on The Guardian website, check it out, if you are interested. 

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5 March 2024 

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Insight into mechanisms of ME/CFS by National Institutes of Health.

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15 February 2024

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Chronic fatigue syndrome: Number of patients is expected to double due to long-term effects of the COVID-19 pandemic by the Medical University of Vienna.

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3 December 2023

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This is a link to an older Kings' College London study from 2018, but worth linking via the Telegraph article. There is a direct link towards the end of the piece. It suggests a link between CFS and a hyperactive immune system. 

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10 August 2023 

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Very welcome news as government plan aims to improve understanding, research and care for those living with CFS. 

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Government announces new plan to help those impacted by ME/CFS 

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