Well, here I am, over a year later and, finally, I have a diagnosis of MS (probably relapsing remitting), possibly been affecting me unnoticed for many years. I’ve seen an absolutely fantastic neurologist who has listened and discussed and is arranging a care plan. Plenty of things to consider - not least, the offer of DMTs. I’m so grateful for our NHS - if only Cameron et al would realise what this means to people, ordinary people like me.
To those of you still looking for answers - keep the faith xxx