I've recently had some visits to neuros with mixed results. The first thing is that my EMG is not normal. The first neuro's report was that there was no evidence that it was ALS but he could not rule it out and the only option was to wait and see. He asked if I wanted a second opinion and recommended someone to me.I went to see the one he recommended and his assessment was that in his view ALS is unlikely and that he thought the more likely diagnosis is Cramp Fasciculatory Syndrome (CFS). Obviously I prefer this assessment, but I did have more confidence in him as he has experience of over 300 ALS cases and was considerably older than the first neuro and I suspect has more experience. For now I'm accepting that CFS is the most likely cause. The symtoms are getting worse and I'm suffering increasing muscle pain. I've cut down on exercise but it is now taking longer to recover. I'm interested to hear from anyone who has been diagnosed as having CFS and can tell me what sort of variation and change I can expect in the symptoms.As you can appreciate, every time there is a change it triggers further anxiety.Chris