Hi everyone, I thought I would post an update on my neurologist appointment. He did a few basic tests and is confident I don’t have MS but that I have Myasthenia Gravis as well as my fibromyalgia. He took blood that’s getting specialist testing down in Oxford so I have a couple of weeks wait for those results but he said that if they don’t come back positive the physicals tests he did and my facial features (I have a drooping eyelid and face on one side) were a clear sign of it.
I feel somewhat relief at getting an answer but then it’s another diagnosis to add to the already long list. The fact it’s on top of my fibromyalgia makes it harder but I will be ok.
I just wanted to say a massive thank you to you all for answering my questions and worries over the past few weeks. I wish all of you the best.