A relative of mine has offered to help me work with a doctor (i.e financially support medical stuff). They have not heard of ME/CFS and neither had their functional medical medical doctor. I would like to send them 1 or 2 key pieces outlining the illness from a medical perspective rather than me rattling off terms like 'PEM', which makes me feel like a fraud because of how makeshift the terms we use on here sound. Is there something I can forward them? I need to temper their optimism about curing the illness and make them aware of the reality of the disease they are dealing with.