Hello, first time posting here. Nice to meet you all.
I was diagnosed with FM in 2013 but have had the symptoms since 2011. It's been a tough thing to come to terms with, but as the years have gone on I have become more and more accepting of it. Anyway, I'm not really here to share my story...
I have been experiencing various symptoms for a long time now and am one step away from a diagnosis of M.E. I have seen a neurologist, rheumatologist and M.E. specialist. Everyone seems to think I have M.E.
I'm worried it could be something else, like ALS, and I wondered if you could...