I think the problem is the elephant in the room, r
Post# of 148165
I looked at 4-5 of the sites we are supposedly running the CD12 trial at and can find no mention of LL or the trial. On almost every one of them, they mention giving Rem.
I think it is very hard for the sick pateint or relatives to see and or pick LL.
I spent a couple of hrs looking for LL on their web sites and the Drs running each site anything I could troll and found nothing.
I would like people here to show me were they can find it mentioned anywhere.
I did not check Dr JL's hospital or website. Nor Dr. Recknor's, was looking at the other sites.
Patients need to know about LL at these sites, I don't think they do.