I can't help but notice the amount of people posting who ultimately end up reassured that they don't have ALS. After Thursday, when I have my 2nd EMG in 3 months (upon my request) I hope to be one of them. I'm 26 and I've actually become quite close with another poster who is 25 who also thought he had ALS. We have been talking off the forums about how we can give back, how we can help. I know there are national organizations and such but for the people here who have spent so much time calming the fears of others, what can others do to help fight ALS and most of all to help you? We're looking ways to give back. Thanks!