Our mission is to educate and inform physiotherapists regarding ME, and to support and advocate for people with ME. When the COVID-19 pandemic began in 2020, we recognised the potential increase of people suffering with Post Viral Fatigue Syndrome as well as ME, and the importance of spreading the message about appropriate management.  

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In September 2020 we wrote this blog post reflecting on COVID-19 and its impact on our work.

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In April 2021 we presented this poster at World Physiotherapy Congress to highlight the work we have done in education about Long COVID 

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Also in April 2021 our fantastic co-founder Natalie Hilliard presented "What we have learnt so far" which can be viewed here

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We regularly challenged inappropriate management advice that failed to acknowledge the precautions required. Together with Forward ME we produced an open access letter regarding Covid Rehabilitation, which aimed to raise awareness and/or challenge inappropriate advice.

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We are proud to be a member of the Long Covid Alliance.

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