LaurentHCH
Well-known member
I know that with my question about the contradictions in emg-infomation i have freaked up many among you, including myself. I just want to know the truth. In my research I have been told that this guy saying this is just a technician doing emg, not a professor of MND.Now i have asked in an ALS-forum if an EMG can be done too early, there are quite a few people with a tremendous knowledge over there, trying to hold on the facts, very rationally. Before I tell you what they said I now know that this bfs-forum is not a bfs-forum anymore. it is much more a forum for people with hypochondric and anxiousy disorders. Otherwise this forum would be more open and willing to know the truth about certain things, pe why it should be forbiden to do research and bring them from other sites here??? this is censur!!!! And this forum should be more rationally. It is to emotionally....everybody, i include myself, gets freaked out on every post, on every word that is just slightly questioning some positions from the nutshell. this is not a henhouse here!!!!Now, what is being said in the ALS-forum, from two people that have a lot of experience as well:1. Relax, you would have had some problems with your neuro exam.. Never ever heard of someo later being DX. with ALS that had a Clean Neuro exam... This is what get's everyone worked up, if you would have a problem your neuro exam would have shown problems. Everyone listen to this it is a fact. All worriers read this over and over.2. I am not an expert. My neuro told me that EMGs will detect symptoms of ALS before twitches or fasics even appear. So if you are having twitches and fasics and the EMG is extensive and comes out clean, then you are home free. You can't do it "too early." An EMG will pick up signs before symptoms even appear.Don't tell me it is a shame to go in ALS-forums, I have just been to a "is this ALS"-section. I am enough sensitive not to bother people who really have this terrible disease and who do not need to hear BFS-freaks. We who are people with BFS should donate for the research on ALS as even the very big and rich swiss chemical industry is not willing to invest in a disease so rare. Very sad....Laurent