For those of you who don’t use Facebook, below is a list of the external links shared within our Facebook Group during June:
Carers UK is organising this open letter on behalf of unpaid carers across the UK.
The ME association have created a new support pack for anyone with ME/CFS going to hospital.
Childhood trauma and risk for chronic fatigue syndrome: association with neuroendocrine dysfunction
https://pubmed.ncbi.nlm.nih.gov/19124690/
This series of podcast episodes complement the CPD accredited module on Myalgic Encephalomyelitis (ME/ Chronic Fatigue Syndrome (CFS).
AccessAble gives you the accessibility information you need to work out if a place is going to be accessible for you.
A blood test will diagnose fibromyalgia more reliably
The ME Association is funding a study led by Prof Sarah Tyson of University of Manchester (who also has ME) to develop a clinical assessment toolkit in collaboration with people with ME and clinicians who work in NHS ME/CFS specialist services.
https://www.qualtrics.manchester.ac.uk/jfe/form/SV_becvOoFYEA9WJTw