Hello everyone. My name is Daniel and I am 18 years old. For about a year, I have been having fasiculations that have progressively gotten worse.These happen everywhere on my body. In my calves they are 24/7. The rest come around my body like popcorn. Ive noticed that with movement, they increase. After strenuous research, I acknowledged that with no weakness, it would be unlikely for it to be motor neuron disease. I do have Obsessive Compulsive Disorder and Health anxiety, so I arranged with my family an appointment to see a neurologist. In september of 2015, My neurologist did a clinical examination and noticed no weakness and said that this was likely benign fasciculation syndrome but that she would like to have an emg done in the following months. I began to forget about these twitches recognizing that they were most likely benign, until the 9th of March where I had my EMG. The results shocked me. The man that did the EMG said the results were abnormal and wanted me to see my neurologist soon. My neurologist told me that my nerves were firing off too much and that it technically was a disease. She thought it was something along the lines of Spinal Muscular Atrophy but more on the benign end. The results of my EMG showed that I had widespread polyphasic units in every muscle tested some being very large (3+). They also all had increased duration and increased amplitude. There was no spontaneous activity, but fasiculations were present. She told me this was odd and that she wanted me to see a specialist in Boston (lahey clinic). About 3 weeks later I went to the lahey clinic where the neurologist there told me it was unlikely ALS (99% positive I don't have it) due to me having no weakness and the twitches being there for such a long time. Although he didn't really see my fasiculations there, which was frustrating. He did say that my emg was abnormal and that it showed Chronic Denervation. I'm very scared. He also the man that took my emg was very experienced so he would not expect much different results if I were to get another test. Never the less, he wants me to get a repeat test. He said if that comes back abnormal we will be in sort of a wait and see period. I have looked at these forums for posts on large MUPs on emus without spontaneous activity and I have been a little encouraged by seeing that its not the end of the world. I notice the love on these forums and every one of you suffering with MND are true fighters. I would appreciate some thoughts please