So today I had a consultation with the Neurologist who, due to my Lumber spine test results being clear, has ruled out MS for me and has verbally confirmed CFS/ME.
I’m relieved I don’t have MS as I know it can be a nasty illness but I also know I now face an uncertain future. With ME having no treatment, it’s like falling into a void of the unknown. I can’t accept this is my life forever as I live in hope that a boom in research (thanks to Covid 19 and Long Covid being post viral fatigue) will bring some form of medication in the near future. I hope.
For now I will continue on. I have a family trip to look forward to and then we’ll see what the rest of this year brings.