How many here are members of the Registry? I've read that there are more than 20,000 enrolled. That's pretty impressive. I joined shortly after being diagnosed in 2000.
The reason that I ask is that I just got the latest issue of the MSQR newsletter. So it just got me to thinking
For those who are not familiar with the registry, here's a link to the CMSC-NARCOMS info (Consortium of Multiple Sclerosis Centers)-(North American Research Committee on Multiple Sclerosis)
The newsletter is a quarterly. I find it to be very informative with information on various studies and trials. Being a member of the registry, I get the newsletter for free. I occasionally get questionnaires to answer. That's all
Anyway, like I said, just curious