Count me in too.
Amgen's head office is in southern california.......Not too far from where I am..

I was just diagnosed at the time Amgen thing was going on and was in my own world of hallucinations, thanks to requip.
I sort of know what happened, but donot know the details. Any websites that would give me an accurate picture of what happened. Amgen site??/.......may not be the best!

I just sent a email to MJFF regarding NYC conference and who can/cannot attend it. I know this is not an issue of great importance when you are looking at a bigger picture of cure for PD, but I like to know. I cannot understand why researchers dont want patients to be at the meeting listening and asking questions. Paula, i was wrong, it is registration not an application.
Debi, (if you are reading this post) I didnt want to ask you questions about the policy of MJFF in an open forum. But if you want to comment on it........thank you.


Thanks
Girija