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


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.