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ME Research UK and the ME Association have announced funding for a study that aims to create a diagnostic test for ME/CFS using the electrical signature from a simple blood test: bit.ly/doreystudy

Please contact me if you would like to get involved in this study. We know that some #pwME have high levels of lactic acid but there are no studies that identify what is normal during every day activity. We want to compare #pwme and healthy comparators. Thanks

This is a great book

#WorldMEDay - we hear you, we see you, we do everything we can to advocate and support you. Wish we could do more. Physios For ME

A thread of resources for physiotherapists and all Allied Health Professionals for #WorldMEDay You might work with someone with #MyalgicEncephalomyelitis in ANY specialism. 1. For those in specialist services, an in-depth book on understanding and management (with 25% off)

If someone is bedbound with #longcovid & hospitalised, withholding urine bottles will not make them walk to the toilet. They will wet the bed. Withholding feeding will not make them eat. They will starve. Sometimes this job hurts my soul at the lack of human rights.#NHS

So many issues including the big impact on the climate crisis

First year anniversary of our book. So proud of what we produced.

V helpful and informative book. Got me started on my #ME journey.

Great piece on BBC Breakfast Physios if you want to know more about working with people with ME visit our Physios For ME website Important to recognise that the type of pacing that is needed for people with ME is different to our usual approach physiosforme.com/resources-for-… Chartered Society of Physiotherapy (CSP)

Yes 👇🏻